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Bulletin No. 206-Treehopper Injury in Utah Orchards
Utah State University DigitalCommons@USU UAES Bulletins Agricultural Experiment Station 6-1928 Bulletin No. 206 - Treehopper Injury in Utah Orchards Charles J. Sorenson Follow this and additional works at: https://digitalcommons.usu.edu/uaes_bulletins Part of the Agricultural Science Commons Recommended Citation Sorenson, Charles J., "Bulletin No. 206 - Treehopper Injury in Utah Orchards" (1928). UAES Bulletins. Paper 178. https://digitalcommons.usu.edu/uaes_bulletins/178 This Full Issue is brought to you for free and open access by the Agricultural Experiment Station at DigitalCommons@USU. It has been accepted for inclusion in UAES Bulletins by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. Bulletin 2 06 June, 1928 Treehopper Injury in Utah Orchards By CHARLES J. SORENSON 3 Dorsal and side views of the following species of treehoppers: 1. Ceresa bubalus (Fabr.) ( Buffalo treehopper) 2. Stictocephala inermis (Fabr.) 3. Stictocephala gillettei Godg. (x 10 ) UTAH AGRICULTURAL EXPERIMENT STATION LOGAN. UTAH UTAH AGRICULTURAL EXPERIMENT STATION , BOARD OF TRUSTEES . ANTHONY W. IVINS, President __ _____ ____________________ __ ___________________ Salt Lake City C. G. ADNEY, Vice-President ____ ___ ________________________________ ________________________ Corinne ROY B ULLEN ________ __________________________ _______ _____ _____ ________ ___ ____ ______ ____ Salt Lake City LORENZO N . STOHL ______ ___ ____ ___ ______________________ __ ___ ______ _____ __________ Salt Lake City MRS. LEE CHARLES MILLER ___ ______ ___ _________ ___ _____ ______ ___ ____ ________ Salt Lake City WE S TON V ERN ON, Sr. ________________________ ___ ____ ____ _____ ___ ____ ______ __ __ _______ ________ Loga n FRANK B. STEPHENS _____ ___ __ ____ ____________ ____ ______________ __ ___________ __.___ Salt Lake City MRS. -
Coleoptera: Chrysomelidae)
Acta Biol. Univ. Daugavp. 10 (2) 2010 ISSN 1407 - 8953 MATERIALS ON LATVIAN EUMOLPINAE HOPE, 1840 (COLEOPTERA: CHRYSOMELIDAE) Andris Bukejs Bukejs A. 2010. Materials on Latvian Eumolpinae Hope, 1840 (Coleoptera: Chrysomelidae). Acta Biol. Univ. Daugavp., 10 (2): 107 -114. Faunal, phenological and bibliographical information on Latvian Eumolpinae are presented in the current paper. Bibliographycal analysis on this leaf-beetles subfamily in Latvia is made for the first time. An annotated list of Latvian Eumolpinae including 4 species of 3 genera is given. Key words: Coleoptera, Chrysomelidae, Eumolpinae, Latvia, fauna, bibliography. Andris Bukejs. Institute of Systematic Biology, Daugavpils University, Vienības 13, Daugavpils, LV-5401, Latvia; [email protected] INTRODUCTION (Precht 1818, Fleischer 1829). Subsequently, more than 15 works were published. Scarce faunal The subfamily Eumolpinae Hope, 1840 includes records can also be found in following other more than 500 genera and 7000 species distributed articles (Lindberg 1932; Pūtele 1974, 1981a; mainly in the tropics and subtropics (Jolivet & Stiprais 1977; Rūtenberga 1992; Barševskis 1993, Verma 2008). Of them, 11 species of 6 genera are 1997; Telnov & Kalniņš 2003; Telnov et al. 2006, known from eastern Europe (Bieńkowski 2004), 2010; Bukejs & Telnov 2007). and only 4 species of 3 genera – from Fennoscandia and Baltiae (Silfverberg 2004). Imagoes of Eumolpinae feed on leaves of host plants; larvae occur in the soil, feed on In Latvian fauna, 3 genera and 4 species of underground parts of plants; pupate in the soil Eumolpinae are known. In adjacent territories, the (Bieńkowski 2004). number of registered Eumolpinae species slightly varies: Belarus – 5 species are recorded (Lopatin The aim of the current work is to summarize & Nesterova 2005), Estonia – 3 species information on Eumolpinae in Latvia. -
Evolution of Insect Color Vision: from Spectral Sensitivity to Visual Ecology
EN66CH23_vanderKooi ARjats.cls September 16, 2020 15:11 Annual Review of Entomology Evolution of Insect Color Vision: From Spectral Sensitivity to Visual Ecology Casper J. van der Kooi,1 Doekele G. Stavenga,1 Kentaro Arikawa,2 Gregor Belušic,ˇ 3 and Almut Kelber4 1Faculty of Science and Engineering, University of Groningen, 9700 Groningen, The Netherlands; email: [email protected] 2Department of Evolutionary Studies of Biosystems, SOKENDAI Graduate University for Advanced Studies, Kanagawa 240-0193, Japan 3Department of Biology, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia; email: [email protected] 4Lund Vision Group, Department of Biology, University of Lund, 22362 Lund, Sweden; email: [email protected] Annu. Rev. Entomol. 2021. 66:23.1–23.28 Keywords The Annual Review of Entomology is online at photoreceptor, compound eye, pigment, visual pigment, behavior, opsin, ento.annualreviews.org anatomy https://doi.org/10.1146/annurev-ento-061720- 071644 Abstract Annu. Rev. Entomol. 2021.66. Downloaded from www.annualreviews.org Copyright © 2021 by Annual Reviews. Color vision is widespread among insects but varies among species, depend- All rights reserved ing on the spectral sensitivities and interplay of the participating photore- Access provided by University of New South Wales on 09/26/20. For personal use only. ceptors. The spectral sensitivity of a photoreceptor is principally determined by the absorption spectrum of the expressed visual pigment, but it can be modified by various optical and electrophysiological factors. For example, screening and filtering pigments, rhabdom waveguide properties, retinal structure, and neural processing all influence the perceived color signal. -
The Importance of Behavior and Venom System Morphology in Understanding Its Ecology and Evolution
Toxins 2019, 11, 666; doi:10.3390/toxins11110666 S1 of S11 Supplementary Materials: The Diversity of Venom: The Importance of Behavior and Venom System Morphology in Understanding Its Ecology and Evolution Vanessa Schendel, Lachlan D. Rash, Ronald A. Jenner, and Eivind A. B. Undheim Table S1. Independently evolved venomous animal lineages and the primary ecological roles of their venoms. Taxa for which no direct support of their venomous nature could be found are shown in grey font. General Venom System Animal Group Venomous Lineage Primary Role References Morphology Predation, defense, Cnidarians All Nematocysts [1] intraspecific competition Coleoid Posterior and anterior glands, cephalopods, venom injected through salivary Predation [2,3] including octopus papilla. and squid Long duct/venom gland, venom Cone snails and injected through hollow radular Predation, [4] relatives (Conoidea) tooth on proboscis by a distal defense venom pump. Tritons, helmet Two-lobed salivary (venom) Molluscs shells, etc. glands that open through Predation [5] (Tonnoidea) common duct into buccal mass. Dwarf tritons, Single-lobed salivary (venom) including vampire glands that open through Predation [6] snails common duct into buccal mass. (Colubrariidae) Primary and accessory salivary Murex snails (venom) glands that open Predation [7] (Muricidae) through common duct into buccal mass. Proboscis with venom secreting cells, sometimes with stylet to Nemerteans Ribbon worms facilitate venom delivery Predation [8] (Enopla), or pseudocnidae with a potential role in venom delivery. Toxin-producing “lappets” secreting venom into large Blood worms muscular and glandular venom Predation [9] (Glyceridae) reservoir, which is presumably Annelids also involved in venom expulsion. Secretory cells dispersed along Predation, Leeches (Hirudinea) the buccal cavity in jawed [10–12] blood feeding leeches (Arhynchobdellida); Toxins 2019, 11, 666; doi:10.3390/toxins11110666 S2 of S11 presence of two paired salivary glands in jawless leeches (Glossiphoniidae). -
Diptera, Tabanoidea, Tabanidae) Dorian D
Dörge et al. Parasites Vectors (2020) 13:461 https://doi.org/10.1186/s13071-020-04316-7 Parasites & Vectors RESEARCH Open Access Incompletely observed: niche estimation for six frequent European horsefy species (Diptera, Tabanoidea, Tabanidae) Dorian D. Dörge1*, Sarah Cunze1 and Sven Klimpel1,2 Abstract Background: More than 170 species of tabanids are known in Europe, with many occurring only in limited areas or having become very rare in the last decades. They continue to spread various diseases in animals and are responsible for livestock losses in developing countries. The current monitoring and recording of horsefies is mainly conducted throughout central Europe, with varying degrees of frequency depending on the country. To the detriment of tabanid research, little cooperation exists between western European and Eurasian countries. Methods: For these reasons, we have compiled available sources in order to generate as complete a dataset as possi- ble of six horsefy species common in Europe. We chose Haematopota pluvialis, Chrysops relictus, C. caecutiens, Tabanus bromius, T. bovinus and T. sudeticus as ubiquitous and abundant species within Europe. The aim of this study is to esti- mate the distribution, land cover usage and niches of these species. We used a surface-range envelope (SRE) model in accordance with our hypothesis of an underestimated distribution based on Eurocentric monitoring regimes. Results: Our results show that all six species have a wide range in Eurasia, have a broad climatic niche and can there- fore be considered as widespread generalists. Areas with modelled habitat suitability cover the observed distribution and go far beyond these. This supports our assumption that the current state of tabanid monitoring and the recorded distribution signifcantly underestimates the actual distribution. -
Grape Insects +6134
Ann. Rev. Entomo! 1976. 22:355-76 Copyright © 1976 by Annual Reviews Inc. All rights reserved GRAPE INSECTS +6134 Alexandre Bournier Chaire de Zoologie, Ecole Nationale Superieure Agronornique, 9 Place Viala, 34060 Montpellier-Cedex, France The world's vineyards cover 10 million hectares and produce 250 million hectolitres of wine, 70 million hundredweight of table grapes, 9 million hundredweight of dried grapes, and 2.5 million hundredweight of concentrate. Thus, both in terms of quantities produced and the value of its products, the vine constitutes a particularly important cultivation. THE HOST PLANT AND ITS CULTIVATION The original area of distribution of the genus Vitis was broken up by the separation of the continents; although numerous species developed, Vitis vinifera has been cultivated from the beginning for its fruit and wine producing qualities (43, 75, 184). This cultivation commenced in Transcaucasia about 6000 B.C. Subsequent human migration spread its cultivation, at firstaround the Mediterranean coast; the Roman conquest led to the plant's progressive establishment in Europe, almost to its present extent. Much later, the WesternEuropeans planted the grape vine wherever cultiva tion was possible, i.e. throughout the temperate and warm temperate regions of the by NORTH CAROLINA STATE UNIVERSITY on 02/01/10. For personal use only. world: North America, particularly California;South America,North Africa, South Annu. Rev. Entomol. 1977.22:355-376. Downloaded from arjournals.annualreviews.org Africa, Australia, etc. Since the commencement of vine cultivation, man has attempted to increase its production, both in terms of quality and quantity, by various means including selection of mutations or hybridization. -
Novel Bacteriocyte-Associated Pleomorphic Symbiont of the Grain
Okude et al. Zoological Letters (2017) 3:13 DOI 10.1186/s40851-017-0073-8 RESEARCH ARTICLE Open Access Novel bacteriocyte-associated pleomorphic symbiont of the grain pest beetle Rhyzopertha dominica (Coleoptera: Bostrichidae) Genta Okude1,2*, Ryuichi Koga1, Toshinari Hayashi1,2, Yudai Nishide1,3, Xian-Ying Meng1, Naruo Nikoh4, Akihiro Miyanoshita5 and Takema Fukatsu1,2,6* Abstract Background: The lesser grain borer Rhyzopertha dominica (Coleoptera: Bostrichidae) is a stored-product pest beetle. Early histological studies dating back to 1930s have reported that R. dominica and other bostrichid species possess a pair of oval symbiotic organs, called the bacteriomes, in which the cytoplasm is densely populated by pleomorphic symbiotic bacteria of peculiar rosette-like shape. However, the microbiological nature of the symbiont has remained elusive. Results: Here we investigated the bacterial symbiont of R. dominica using modern molecular, histological, and microscopic techniques. Whole-mount fluorescence in situ hybridization specifically targeting symbiotic bacteria consistently detected paired bacteriomes, in which the cytoplasm was full of pleomorphic bacterial cells, in the abdomen of adults, pupae and larvae, confirming previous histological descriptions. Molecular phylogenetic analysis identified the symbiont as a member of the Bacteroidetes, in which the symbiont constituted a distinct bacterial lineage allied to a variety of insect-associated endosymbiont clades, including Uzinura of diaspidid scales, Walczuchella of giant scales, Brownia of root mealybugs, Sulcia of diverse hemipterans, and Blattabacterium of roaches. The symbiont gene exhibited markedly AT-biased nucleotide composition and significantly accelerated molecular evolution, suggesting degenerative evolution of the symbiont genome. The symbiotic bacteria were detected in oocytes and embryos, confirming continuous host–symbiont association and vertical symbiont transmission in the host life cycle. -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
Catalogue of Latvian Leaf-Beetles (Coleoptera: Megalopodidae, Orsodacnidae & Chrysomelidae)
Latvijas Entomologs 2013, 52: 3-57. 3 Catalogue of Latvian leaf-beetles (Coleoptera: Megalopodidae, Orsodacnidae & Chrysomelidae) ANDRIS BUKEJS Vienības iela 42-29, LV-5401, Daugavpils, Latvia; e-mail: [email protected] BUKEjS A. 2013. Catalogue OF Latvian LEAF-BEETLES (COLEOPTERA: MEGALOPODIDAE, ORSODACNIDAE & Chrysomelidae). – Latvijas Entomologs 52: 3-57. Abstract: Critical catalogue of Latvian leaf-beetles (Megalopodidae, Orsodacnidae & Chrysomelidae) is presented. In the current work all available bibliography on Latvian leaf-beetles are reviewed and analyzed. In total, 326 species are confirmed from Latvia till now, although few of them are known from the old records only, and their occurrence in the local fauna should be confirmed by new material. All doubtful species recorded till now from Latvia are commented and removed from the list. Key words: Coleoptera, Megalopodidae, Orsodacnidae, Chrysomelidae, Latvia, fauna, bibliography, catalogue. Introduction Kaliningrad region (Russian enclave in Central Europe) – 280 (Alekseev 2003; Leaf-beetles, represented by 30 000–50 Bukejs, Alekseev 2009, 2012; Alekseev, 000 species, are one of the largest families of Bukejs 2010, 2011; Alekseev et al. 2012). the order Coleoptera worldwide (Bieńkowski The first information on leaf-beetles 2004; Brovdij 1985; jolivet 1988). They (Chrysomelidae s. l.) from the present territory are phytophagous: imagines mostly occur of Latvia was published in the second half of on leaves and flowers, larvae mostly feed the 18th century in the works of j.B. Fischer on leaves and roots, occasionally larvae are (1778, 1784, 1791). In the first edition of saprophagous or carpophagous. Some species his monograph describing nature of Livland of leaf-beetles are considered serious pests (Fischer 1778), three species of leaf-beetles, of agriculture and forestry (Kryzhanovskij Cassida viridis LINNAEUS, 1758, Phratora 1974; Lopatin, Nesterova 2005). -
Pseudotsuga Menziesii
SPECIAL PUBLICATION 4 SEPTEMBER 1982 INVERTEBRATES OF THE H.J. ANDREWS EXPERIMENTAL FOREST, WESTERN CASCADE MOUNTAINS, OREGON: A SURVEY OF ARTHROPODS ASSOCIATED WITH THE CANOPY OF OLD-GROWTH Pseudotsuga Menziesii D.J. Voegtlin FORUT REJEARCH LABORATORY SCHOOL OF FORESTRY OREGON STATE UNIVERSITY Since 1941, the Forest Research Laboratory--part of the School of Forestry at Oregon State University in Corvallis-- has been studying forests and why they are like they are. A staff or more than 50 scientists conducts research to provide information for wise public and private decisions on managing and using Oregons forest resources and operating its wood-using industries. Because of this research, Oregons forests now yield more in the way of wood products, water, forage, wildlife, and recreation. Wood products are harvested, processed, and used more efficiently. Employment, productivity, and profitability in industries dependent on forests also have been strengthened. And this research has helped Oregon to maintain a quality environment for its people. Much research is done in the Laboratorys facilities on the campus. But field experiments in forest genetics, young- growth management, forest hydrology, harvesting methods, and reforestation are conducted on 12,000 acres of School forests adjacent to the campus and on lands of public and private cooperating agencies throughout the Pacific Northwest. With these publications, the Forest Research Laboratory supplies the results of its research to forest land owners and managers, to manufacturers and users of forest products, to leaders of government and industry, and to the general public. The Author David J. Voegtlin is Assistant Taxonomist at the Illinois Natural History Survey, Champaign, Illinois. -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying -
Proceedings of the United States National Museum
: BEETLE LARVAE OF THE SUBFAMILY GALERUCINAE B}^ Adam G. Boving Senior Entoniolotjist, Bureau of Etitomology, United States Department of Agricvltwe INTRODUCTION The present pajxn- is the result of a continued investigation of the Chrysomelid hirvae in the United States National Museum, Wash- ington, D. C. Of the subfamily Galerucinae ^ belonging to this family the larvae are preserved in the Museum of the following species Monocesta coryli Say. Trirhabda canadensis Kirby. TrU'habda hrevicollis LeConte. Trirhabda nitidicollis LeConte. Trirhabda tomentosa Linnaeus. Trirhabda attenuata Say. Oalerucella nymphaeae Liiniaeus. Oalerucella lineola Fabrleius (from Euroiie). Galerucclla sagittarUu' Gylleuhal. Oalerucella luteola Miiller. Galerucclla sp. (from Nanking, China). Galcrucella vibvrni Paykull (from Europe). Oalerucella decora Say. Oalerucella notata Fabricius. Oalerucella cribrata LeConte. Monoxia puncticolUs Say. Monoxia consputa LeConte. Lochmaca capreae Linnaeus (from Europe). Qaleruca tanacett Linnaeus (from Europe). Oaleruca laticollis Sahlberg (from Europe). Oalcruca, pomonae Scopoli. Sermylassa halensls Linnaeus. Agelastica alnl Linnaeus.^ 1 The generic and specific names of tlie North American larvae are as listed in C W. Leng's " Catalogue of Coleoptera of America north of Mexico, 1920," with corrections and additions as given in the "supplement" to the catalogue published by C. W. Leng and A. J. Mutchler, 1927. The European species, not introduced into North America, are named according to the " Catalogus Coleopterorum Europae, second edition, 1906," by L. V. Heyden, E. Rcitter, and .7. Weise. 2 It will be noticed that in the enumeration above no species of Dinhrlica and Pliyllo- brotica are mentioned. The larvae of those genera were considered by tlie present author as Halticinae larvae [Boving, Adam G.