Biology and Biological Control of Yellow Starthistle
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Coleoptera: Curculionidae, Lixinae)
J. Entomol. Res. Soc., 14(2): 71-85, 2012 ISSN:1302-0250 New Faunistic Data on Selected Palaearctic Species of the Genus Larinus Dejean, 1821 (Coleoptera: Curculionidae, Lixinae) Levent GÜLTEKİN1 Attila PODLUSSÁNY2 1Atatürk University, Faculty of Agriculture, Department of Plant Protection, 25240 Erzurum, TURKEY. e-mail: [email protected] 2Hungarian Natural History Museum, H-1088 Budapest, Baross utca 13, HUNGARY. e-mail: [email protected] ABSTRACT Faunistic data regarding 50 species of the weevil genus Larinus Dejean, 1821 (Curculionidae: Lixinae) from the Palaearctic region are registered. New country records are: Larinus elegans Desbrochers, 1897 and L. puncticollis Capiomont, 1874 for Iran; L. filiformis Petri, 1907 for Georgia; L. fucatus Faust, 1891 and L. rectinasus Petri, 1907 for Syria; L. hedenborgi Boheman, 1845 for Cyprus; L. idoneus Gyllenhal, 1835 and L. darsi Capiomont, 1874 for Turkey; L. carinirostris Gyllenhal, 1835 for Bulgaria; L. curtus Hochhuth, 1851 and L. minutus Gyllenhal, 1835 for Croatia; L. leuzeae Fabre, 1870 for Spain; L. modestus Gyllenhal, 1835 for Syria and Israel; L. nubeculosus Gyllenhal, 1835 for Greece, Hungary, Slovenia; L. gravidus Olivier, 1807 and L. rectinasus Petri, 1907 for Greece; L. serratulae Becker, 1864 for Turkmenistan; L. sibiricus Gyllenhal, 1835 for Macedonia; L. sulphurifer Boheman, 1843 and L. ochreatus (Olivier, 1807) for Tunisia; L. syriacus Gyllenhal, 1835 for Croatia and Macedonia; L. vitellinus Gyllenhal, 1835 for Israel; L. vulpes (Olivier, 1807) for Bulgaria, Croatia, Serbia and Turkey. Keywords: Curculionidae, Larinus, new records, faunistic data. INTRODUCTION The weevil genus Larinus Dejean, 1821 (Coleoptera: Curculionidae: Lixinae) contains many species which are closely associated with thistles, knapweeds or other noxious weeds belonging to the tribe Cardueae (Asteraceae) in the Palaearctic (Ter-Minassian, 1967; Zwölfer et al., 1971). -
2007 Annual Report Summary
BIOLOGICAL CONTROL PROGRAM 2008 SUMMARY Developed by: Jim Brown Kris Godfrey Syed Khasimuddin Charles Pickett Mike Pitcairn William Roltsch Baldo Villegas Dale Woods Lue Yang CALIFORNIA DEPARTMENT OF FOOD AND AGRICULTURE PLANT HEALTH AND PEST PREVENTION SERVICES INTEGRATED PEST CONTROL BRANCH Cite as: Dale M. Woods, Editor, 2009, Biological Control Program 2008 Annual Summary, California Department of Food and Agriculture, Plant Health and Pest Prevention Services, Sacramento, California. 69pp. CDFA CONTRIBUTING PERSONNEL Mr. Jim Brown Dr. Kris Godfrey Dr. Syed Khasimuddin Dr. Charles Pickett Dr. Mike Pitcairn Dr. William Roltsch Mr. Baldo Villegas Dr. Dale Woods Mr. Lue Yang CDFA Technical Assistants Ms. Penny Baxley Ms. Kathleen Cassanave Ms. Lia Chase Ms. Leann Horning Ms. Chia Moua Ms. Viola Popescu Ms. Nancy Saechao Mr. Ciprian Simon County Co-operator Acknowledgement The CDFA Biological Control Program greatly appreciates the many biologists and agriculture commissioners throughout the state whose co-operation and collaboration made this work possible. FOR OFFICIAL USE ONLY This report contains unpublished information concerning work in progress. The contents of this report may not be published or reproduced in any form without the prior consent of the research workers involved. Cover developed by Baldo Villegas, Dale Woods, and John P. Mattia (Orange, CT). Infestation of perennial pepperweed east of Susanville, California. (Photo courtesy of Lassen County Weed Management Area). Inset photo shows severe infection of perennial pepperweed by the plant pathogen, Albugo candida. (Photo by Villegas and Woods) COOPERATING SCIENTISTS Ms. Jodi Aceves, Siskiyou County Department of Agriculture, Yreka, California Dr. Pat Akers, CDFA, Integrated Pest Control Branch, Sacramento, California Dr. -
Alhagi Maurorum
Prepared By Jacob Higgs and Tim Higgs Class 1A EDRR- Early Detection Rapid Response Watch List Common crupina Crupina vulgaris African rue Peganum harmala Small bugloss Anchusa arvensis Mediterranean sage Salvia aethiopis Spring millet Milium vernale Syrian beancaper Zygophyllum fabago North Africa grass Ventenata dubia Plumeless thistle Carduus acanthiodes Malta thistle Centaurea melitensis Common Crupina Crupina vulgaris African rue Peganum harmala Small bugloss Anchusa arvensis Mediterranean sage Salvia aethiopis Spring millet Milium vernale Syrian beancaper Zygophyllum fabago North Africa grass Ventenata dubia Plumeless thistle Carduus acanthiodes Malta thistle Centaurea melitensis m Class 1B Early Detection Camelthorn Alhagi maurorum Garlic mustard Alliaria petiolata Purple starthistle Cantaurea calcitrapa Goatsrue Galega officinalis African mustard Brassica tournefortii Giant Reed Arundo donax Japanese Knotweed Polygonum cuspidatum Vipers bugloss Echium vulgare Elongated mustard Brassica elongate Common St. Johnswort Hypericum perforatum L. Oxeye daisy Leucanthemum vulgare Cutleaf vipergrass Scorzonera laciniata Camelthorn Alhagi maurorum Garlic mustard Alliaria petiolata Purple starthistle Cantaurea calcitrapa Goatsrue Galega officinalis African mustard Brassica tournefortii Giant Reed Arundo donax Japanese Knotweed Polygonum cuspidatum Vipers bugloss Echium vulgare Elongated mustard Brassica elongate Common St. Johnswort Hypericum perforatum L. Oxeye daisy Leucanthemum vulgare Cutleaf vipergrass Scorzonera laciniata Class 2 Control -
Yellow Starthistle Management with Grazing, Mowing, and Competitive Plantings
California Exotic Pest Plant Council 1996 Symposium Proceedings Yellow Starthistle Management with Grazing, Mowing, and Competitive Plantings Craig D. Thomsen, William A. Williams, and Marc P. Vayssieres Dept. of Agronomy and Range Science, University of California, Davis, CA 95616 1. Using livestock to manage yellow starthistle in annual grasslands Introduction Livestock grazing has been recognized as a major driving force for noxious weed invasions in pastures and on rangeland (Parker 1949). Livestock alter botanical composition and contribute to weed proliferation by reducing plant cover, dispersing seed, concentrating nutrients, compacting soil, and selective grazing (Burcham 1957). Many weeds that occur on grazing land possess anti-herbivore traits such as spines, stiff awns, high silica and lignin content, or secondary compounds such as alkaloids and glandular exudates. Because animals selectively graze some plants and avoid others, species that have grazing deterrents are favored on grazing lands and often increase relative to those eaten by livestock. Paradoxically, some noxious weeds that flourish on grazing lands have some stages of growth that are palatable to livestock, and with alterations in grazing management, can be suppressed by livestock. For example, medusahead (Taeniatherum caput-medusae) (Lusk et al. 1961), Klamath weed (Hypericum perforatum) (Murphy et al. 1954), spotted knapweed (Centaurea maculosa) (Kelsey and Mikalovich 1987), leafy spurge (Euphorbia esula) (Johnston and Peake 1960), tansy ragwort (Senecio jacobaea) (Mosher 1979) and yellow starthistle (Centaurea solstitialis) (Thomsen et al. 1993) have all been suppressed by livestock grazing. Some invasive species are absent from grazing land because they are highly palatable to livestock. In maritime areas, the palatable sweet fennel (Foeniculum vulgare) can reach dominant status in ungrazed grasslands, but is usually entirely absent from adjacent grazed land. -
Multi-Trophic Level Interactions Between the Invasive Plant
MULTI-TROPHIC LEVEL INTERACTIONS BETWEEN THE INVASIVE PLANT CENTAUREA STOEBE, INSECTS AND NATIVE PLANTS by Christina Rachel Herron-Sweet A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Land Resources and Environmental Sciences MONTANA STATE UNIVERSITY Bozeman, Montana May 2014 ©COPYRIGHT by Christina Rachel Herron-Sweet 2014 All Rights Reserved ii DEDICATION To my parents and grandparents, who instilled in me the value of education and have been my biggest supporters along the way. iii ACKNOWLEDGEMENTS Special thanks go to my two advisers Drs. Jane Mangold and Erik Lehnhoff for all their tremendous support, advice and feedback during my graduate program. My two other committee members Drs. Laura Burkle and Jeff Littlefield also deserve a huge thank you for the time and effort they put into helping me with various aspects of my project. This research would not have been possible without the dedicated crew of field and lab helpers: Torrin Daniels, Darcy Goodson, Daniel France, James Collins, Ann de Meij, Noelle Orloff, Krista Ehlert, and Hally Berg. The following individuals deserve recognition for their patience in teaching me pollinator identification, and for providing parasitoid identifications: Casey Delphia, Mike Simanonok, Justin Runyon, Charles Hart, Stacy Davis, Mike Ivie, Roger Burks, Jim Woolley, David Wahl, Steve Heydon, and Gary Gibson. Hilary Parkinson and Matt Lavin also offered their expertise in plant identification. Statistical advice and R code was generously offered by Megan Higgs, Sean McKenzie, Pamela Santibanez, Dan Bachen, Michael Lerch, Michael Simanonok, Zach Miller and Dave Roberts. Bryce Christiaens, Lyn Huyser, Gil Gale and Craig Campbell provided instrumental consultation on locating field sites, and the Circle H Ranch, Flying D Ranch and the United States Forest Service graciously allowed this research to take place on their property. -
Thistle Identification Referee 2017
Thistle Identification Referee 2017 Welcome to the Thistle Identification Referee. The purpose of the referee is to review morphological characters that are useful for identification of thistle and knapweed fruits, as well as review useful resources for making decisions on identification and classification of species as noxious weed seeds. Using the Identification Guide for Some Common and Noxious Thistle and Knapweed Fruits (Meyer 2017) and other references of your choosing, please answer the questions below (most are multiple choice). Use the last page of this document as your answer sheet for the questions. Please send your answer sheet to Deborah Meyer via email ([email protected]) by May 26, 2017. Be sure to fill in your name, lab name, and email address on the answer sheet to receive CE credit. 1. In the Asteraceae, the pappus represents this floral structure: a. Modified stigma b. Modified corolla c. Modified calyx d. Modified perianth 2. Which of the following species has an epappose fruit? a. Centaurea calcitrapa b. Cirsium vulgare c. Onopordum acaulon d. Cynara cardunculus 3. Which of the following genera has a pappus comprised of plumose bristles? a. Centaurea b. Carduus c. Silybum d. Cirsium 4. Which of the following species has the largest fruits? a. Cirsium arvense b. Cirsium japonicum c. Cirsium undulatum d. Cirsium vulgare 5. Which of the following species has a pappus that hides the style base? a. Volutaria muricata b. Mantisalca salmantica c. Centaurea solstitialis d. Crupina vulgaris 6. Which of the following species is classified as a noxious weed seed somewhere in the United States? a. -
Biological Control of Yellow Starthistle
Biological Control of Yellow Starthistle Lincoln Smith, USDA-ARS-WRRC, 800 Buchanan St, Albany CA 94710 Joe Balciunas, USDA-ARS-WRRC, 800 Buchanan St, Albany CA 94710 Michael J. Pitcairn, California Dept. of Food and Agriculture, 3288 Meadowview Road, Sacramento, CA 95832 Yellow starthistle (Centaurea solstitialis L.) is an alien plant that probably originated from the eastern Mediterranean. It was first collected in California in 1869, and now infests 42% of the state’s townships. It interferes with land use such as grazing and recreation, displaces native species, and is toxic to horses (Sheley, et al. 1999 and papers cited therein). This weed is much less invasive in its land of origin. This is presumably because natural enemies, such as insects, plant diseases, animals or competing plants help to keep it under natural control. We are exploring for insects and pathogens that attack this plant. They are tested for host specificity to make sure they do not attack other plants. After evaluation and approval by state and federal agencies, these agents will be released to try to reestablish the natural control that occurs in the land of origin. So far, six species of insect biological control agents have been introduced to control yellow starthistle (Turner et al. 1995; Rees et al. 1996; Jette, et al. 1999). All six attack the seedheads. The most promising agent is the hairy weevil (Eustenopus villosus), which is well established in California and occurs in high densities, attacking 25 to 80% of seedheads. Adults damage young flower buds by feeding on them, and lay eggs on later-developing flower buds. -
Том 4. Вып. 2 Vol. 4. No. 2
РОССИЙСКАЯ АКАДЕМИЯ НАУК Южный Научный Центр RUSSIAN ACADEMY OF SCIENCES Southern Scientific Centre CAUCASIAN ENTOMOLOGICAL BULLETIN Том 4. Вып. 2 Vol. 4. No. 2 Ростов-на-Дону 2008 Кавказский энтомол. бюллетень 4(2): 209—213 © CAUCASIAN ENTOMOLOGICAL BULL. 2008 Hibernation places and behavior of the some weevil species (Coleoptera: Curculionidae) Места зимовки и поведение некоторых видов жуков- долоносиков(Coleoptera: Curculionidae) L. Gültekin Л. Гюльтекин Atatürk University, Faculty of Agriculture, Plant Protection Department, Erzurum 25240 Turkey. E-mail: [email protected]; lgultekin@ gmail.com Университет им. Ататюрка, сельскохозяйственный факультет, кафедра защиты растений, Эрзерум 25240 Турция Key words: hibernation places, behavior, Curculionidae, Eastern Turkey. Ключевые слова: локализация диапаузы, поведение, Curculionidae, Восточная Турция. Abstract. Hibernation places and behavior of перед зимовкой. Cleonis pigra (Scopoli), Larinus onopordi the 40 species of weevil from subfamilies Lixinae, (Fabricius), L. inaequalicollis Capiomont, L. ochroleucus Ceutorhynchinae, Baridinae, Gymnetrinae and Entiminae Capiomont, L. sibiricus Gyllenhal, L. sp. n. pr. leuzeae Fabre, (Curculionidae) were determined in Eastern Turkey during L. filiformis Petri, Herpes porcellus Lacordaire и Mononychus 1997–2007. Larinus latus (Herbst), L. fucatus Faust, punctumalbum (Herbst) часто образуют скопления под Lixus ochraceus Boheman, L. furcatus Olivier, L. obesus камнями, корой растений или в почве. Conorhynchus Petri, L. siculus Boheman, L. korbi Petri, and Mononychus hololeucus (Pallas), Mecaspis incisuratus Gyllenhal, schoenherri Kolenati prefer to migrate by flight before Leucophyes pedesteris (Poda), Otiorhynchus brunneus hibernation. Cleonis pigra (Scopoli), Larinus onopordi Steven, O. latinasus Reitter зимуют под растительными (Fabricius), L. inaequalicollis Capiomont, L. ochroleucus остатками и под камнями. Gymnetron netum (Germar) Capiomont, L. sibiricus Gyllenhal, L. sp. n. pr. leuzeae и Larinus puncticollis Capiomont заселяют на зимовку Fabre, L. -
Weed: Yellow Starthistle (Centaurea Solstitialis L.)
Weed: Yellow starthistle (Centaurea solstitialis L.) Family: Asteraceae (Sunflower family) Images: Brief Plant Description: (Summarized from Healy, E. and J. DiTomaso, Yellow Starthistle Fact Sheet, http://wric.ucdavis.edu/yst/biology/yst_fact_sheet.html) The seed leaves (cotyledons) are oblong to spatulate, 6-9 mm long and 3-5 mm wide, base wedge- shaped, tip +/- squared and glabrous. First few rosette leaves typically oblanceolate. Subsequent rosette leaves oblanceolate, entire to pinnate-lobed. Terminal lobes largest. Later rosette leaves to 15 cm long and are typically deeply lobed +/- to midrib and appear ruffled. Surfaces +/- densely covered with fine cottony hairs. Lobes mostly acute, with toothed to wavy margins. Terminal lobes +/- triangular to lanceolate. Mature plants have stiff stems, openly branched from near or above the base or sometimes not branched in very small plants. Stem leaves alternate, mostly linear or +/- narrowly oblong to oblanceolate. Margins smooth, toothed, or wavy. Leaf bases extend down the stems (decurrent) and give stems a winged appearance. Rosette leaves typically withered by flowering time. Largest stem wings typically to ~ 3 mm wide. Lower stem leaves sometimes +/- deeply pinnate-lobed. Foliage grayish- to bluish-green, densely covered with fine white cottony hairs that +/- hide thick stiff hairs and glands. Flower heads ovoid, spiny, solitary on stem tips, consist of numerous yellow disk flowers. Phyllaries palmately spined, with one long central spine and 2 or more pairs of short lateral spines. Insect- pollinated. Flowers mid-summer to fall. Corollas mostly 13-20 mm long. Involucre (phyllaries as a unit) ~ 12-18 mm long. Phyllaries +/- dense to sparsely covered with cottony hairs or with patches at the spine bases. -
Fire Controls Yellow Starthistle (Centaurea Solstitialis) in California Grasslands
California Exotic Pest Plant Council 1996 Symposium Proceedings Fire Controls Yellow Starthistle (Centaurea solstitialis) in California Grasslands. Burns timed to prevent seed maturation have nearly eliminated this exotic, and increased natives within test plots at Sugarloaf Ridge State Park, CA Marla S. Hastings and Joseph M. DiTomaso [Editor's note: the following article, Hastings, Marla. "Fire Controls Yellow Starthistle." RESTORATION AND MANAGEMENT NOTES, Volume 14, number 2 (Winter, 1996), is reprinted by permission of The University of Wisconsin Press. It summarizes the talk given at the 1996 CalEPPC Symposium in San Diego. Adapted according to Guidelines for Preparation of Manuscripts for Publication in the Proceedings of the California Exotic Pest Plant Council 1996.) Marla S. Hastings California State Parks, Silverado District 20 E. Spain Street, Sonoma, CA 95476 Joseph M. DiTomaso Coop Ext. Non-Crop Weed Ecologist Vegetable Crops/Weed Science Program, Robbins Hall University of California, Davis, CA 95616 Yellow starthistle (Centaurea solstitialis) first invaded open grassland sites within the San Francisco Bay Area sometime before 1869 when a specimen was collected in Oakland. Native to Eurasia, it was apparently introduced in association with livestock use during the Mexican and post-mission period (Maddox and Mayfield 1985). A fast-growing, aggressive annual herb, yellow starthistle reaches a height of 0.3 to 2 meters, and often grows in dense stands, mainly in grasslands. It rapidly crowds out less-aggressive natives. At present it is the most widely distributed weed in California, infesting over 4 million hectares, or approximately 10 percent of the total surface area of the state. In addition, it has infested large areas in Washington, Oregon and Idaho, and is present in smaller numbers scattered throughout much of the United States and Canada (Maddox 1981). -
Flora Mediterranea 26
FLORA MEDITERRANEA 26 Published under the auspices of OPTIMA by the Herbarium Mediterraneum Panormitanum Palermo – 2016 FLORA MEDITERRANEA Edited on behalf of the International Foundation pro Herbario Mediterraneo by Francesco M. Raimondo, Werner Greuter & Gianniantonio Domina Editorial board G. Domina (Palermo), F. Garbari (Pisa), W. Greuter (Berlin), S. L. Jury (Reading), G. Kamari (Patras), P. Mazzola (Palermo), S. Pignatti (Roma), F. M. Raimondo (Palermo), C. Salmeri (Palermo), B. Valdés (Sevilla), G. Venturella (Palermo). Advisory Committee P. V. Arrigoni (Firenze) P. Küpfer (Neuchatel) H. M. Burdet (Genève) J. Mathez (Montpellier) A. Carapezza (Palermo) G. Moggi (Firenze) C. D. K. Cook (Zurich) E. Nardi (Firenze) R. Courtecuisse (Lille) P. L. Nimis (Trieste) V. Demoulin (Liège) D. Phitos (Patras) F. Ehrendorfer (Wien) L. Poldini (Trieste) M. Erben (Munchen) R. M. Ros Espín (Murcia) G. Giaccone (Catania) A. Strid (Copenhagen) V. H. Heywood (Reading) B. Zimmer (Berlin) Editorial Office Editorial assistance: A. M. Mannino Editorial secretariat: V. Spadaro & P. Campisi Layout & Tecnical editing: E. Di Gristina & F. La Sorte Design: V. Magro & L. C. Raimondo Redazione di "Flora Mediterranea" Herbarium Mediterraneum Panormitanum, Università di Palermo Via Lincoln, 2 I-90133 Palermo, Italy [email protected] Printed by Luxograph s.r.l., Piazza Bartolomeo da Messina, 2/E - Palermo Registration at Tribunale di Palermo, no. 27 of 12 July 1991 ISSN: 1120-4052 printed, 2240-4538 online DOI: 10.7320/FlMedit26.001 Copyright © by International Foundation pro Herbario Mediterraneo, Palermo Contents V. Hugonnot & L. Chavoutier: A modern record of one of the rarest European mosses, Ptychomitrium incurvum (Ptychomitriaceae), in Eastern Pyrenees, France . 5 P. Chène, M. -
Population Buildup and Combined Impact of Introduced Insects on Yellow Starthistle (Centaurea Solstitialis L.) in California
Proceedings of the X International Symposium on Biological Control of Weeds 747 4-14 July 1999, Montana State University, Bozeman, Montana, USA Neal R. Spencer [ed.]. pp. 747-751 (2000) Population Buildup and Combined Impact of Introduced Insects on Yellow Starthistle (Centaurea solstitialis L.) in California MICHAEL J. PITCAIRN1, DALE. M. WOODS1, DONALD. B. JOLEY1, CHARLES E. TURNER2, and JOSEPH K. BALCIUNAS2 1California Department of Food and Agriculture, Biological Control Program, 3288 Meadowview Road, Sacramento, California 95832, USA 2United States Department of Agriculture, Agricultural Research Service, 800 Buchanan Street, Albany, California 94710, USA Abstract Seven exotic seed head insects have been introduced into the western United States for control of yellow starthistle. Six are established; three are widespread. Preliminary evaluations suggest that no one insect species will be able to reduce yellow starthistle abundance in California. Rather, a combination of the current, and possibly, future natu- ral enemies may be necessary. Studies were initiated in 1993 to evaluate the population buildup, combined impact, and interaction of all available biological control insects on yellow starthistle. Three field sites were established in different climatic regions where yellow starthistle is abundant. Four insects, Bangasternus orientalis, Urophora sirunase- va, Eustenopus villosus, and Larinus curtus, were released at each site in 1993 and 1994 and long-term monitoring was initiated. The accidentally-introduced insect, Chaetorellia succinea, was recovered in 1996-98 at these sites. Four years after the first releases, we have evidence that these biological control agents are having an impact on yellow starthistle seed production that may translate into a decline in mature plant populations.