Biological Control of Weeds (DPI Vic)
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Beetles from Sălaj County, Romania (Coleoptera, Excluding Carabidae)
Studia Universitatis “Vasile Goldiş”, Seria Ştiinţele Vieţii Vol. 26 supplement 1, 2016, pp.5- 58 © 2016 Vasile Goldis University Press (www.studiauniversitatis.ro) BEETLES FROM SĂLAJ COUNTY, ROMANIA (COLEOPTERA, EXCLUDING CARABIDAE) Ottó Merkl, Tamás Németh, Attila Podlussány Department of Zoology, Hungarian Natural History Museum ABSTRACT: During a faunistical exploration of Sǎlaj county carried out in 2014 and 2015, 840 beetle species were recorded, including two species of Community interest (Natura 2000 species): Cucujus cinnaberinus (Scopoli, 1763) and Lucanus cervus Linnaeus, 1758. Notes on the distribution of Augyles marmota (Kiesenwetter, 1850) (Heteroceridae), Trichodes punctatus Fischer von Waldheim, 1829 (Cleridae), Laena reitteri Weise, 1877 (Tenebrionidae), Brachysomus ornatus Stierlin, 1892, Lixus cylindrus (Fabricius, 1781) (Curculionidae), Mylacomorphus globus (Seidlitz, 1868) (Curculionidae) are given. Key words: Coleoptera, beetles, Sǎlaj, Romania, Transsylvania, faunistics INTRODUCTION: László Dányi, LF = László Forró, LR = László The beetle fauna of Sǎlaj county is relatively little Ronkay, MT = Mária Tóth, OM = Ottó Merkl, PS = known compared to that of Romania, and even to other Péter Sulyán, VS = Viktória Szőke, ZB = Zsolt Bálint, parts of Transsylvania. Zilahi Kiss (1905) listed ZE = Zoltán Erőss, ZS = Zoltán Soltész, ZV = Zoltán altogether 2,214 data of 1,373 species of 537 genera Vas). The serial numbers in parentheses refer to the list from Sǎlaj county mainly based on his own collections of collecting sites published in this volume by A. and partially on those of Kuthy (1897). Some of his Gubányi. collection sites (e.g. Tasnád or Hadad) no longer The collected specimens were identified by belong to Sǎlaj county. numerous coleopterists. Their names are given under Vasile Goldiş Western University (Arad) and the the names of beetle families. -
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. -
Host-Plant Genotype and Other Herbivores Influence Goldenrod Stem Galler Preference and Performance
Oecologia (1999) 121:392–404 © Springer-Verlag 1999 James T. Cronin · Warren G. Abrahamson Host-plant genotype and other herbivores influence goldenrod stem galler preference and performance Received: 26 January 1999 / Accepted: 2 June 1999 Abstract Ecologists have labored to find an explanation suitability as a host to the stem gallers. One possible ex- for the lack of a positive correlation between host prefer- planation for why spittlebugs caused a significant reduc- ence and offspring performance in herbivorous insects. tion in preference, but not in performance, was that spit- This study focuses on how one herbivore species can in- tlebugs had very few long-term effects on the host plant. fluence another herbivore species’ ability to accurately Flower number, flowering phenology, and the allocation assess the suitability of different host-plant genotypes for of the ramet’s biomass to different structures (below- larval development. In particular, we examined the role ground organs, stems, leaves, and flowers) were un- that an early season xylem-feeding homopteran (meadow changed with respect to spittlebug density. The only ef- spittlebug, Philaenus spumarius) has on the preference- fect of spittlebugs was a 3–4% decrease in ramet height performance correlation of a late-season dipteran stem at the end of the growing season. We argue that the lack galler (Eurosta solidaginis) among different goldenrod of a positive correlation between host-plant preference genotypes. In a greenhouse, we released adult stem gall- and larval performance may reflect a constraint on the ers into replicate cages that contained ramets from four discriminatory ability of female stem gallers. -
Preliminary Results on the Phytophagous Insect Fauna on Onopordum Acanthium (Asteraceae) in Bulgaria
Pestic. Phytomed. (Belgrade), 25(4), 2010, 301-309 UDC: 591.617:632.51 Pestic. fitomed. (Beograd), 25(4), 2010, 301-309 Scientific paper * Naučni rad DOI: 10.2298/PIF1004301H Preliminary Results on the Phytophagous Insect Fauna on Onopordum acanthium (Asteraceae) in Bulgaria Vili Harizanova1, Atanaska Stoeva1, Massimo Cristofaro2, Allesandra Paolini2, Francesca Lecce2 and Franca Di Cristina2 1UAgricultural University-Plovdiv, Plovdiv 4000, Mendeleev 12, Bulgaria ([email protected]) 2ANEA C.R. Cassacia UTAGRI-ECO Via Anguillarese 301, 00123 S. Maria di Galeria (Rome), Italy Received: August 5, 2010 Accepted: November 3, 2010 SUMMARY The Scotch thistle, Onopordum acanthium (Asteraceae) has the Eurasian origin and represents an invasive weed in the USA and Australia. It is a serious problem in pastures, along roadsides, rangeland, etc. The weed is very common in Bulgaria and in 2009-2010 several sites with large populations of O. acanthium have been located. The weekly sur- veys of some of the sites, mainly in the region of Plovdiv, revealed a significant diver- sity of phytophagous insect species, some of which had very high population density. More than 30 species have already been identified and observations on the phenolo- gy and biology of some of them have been conducted. For some of the species, such as endophagous Larinus latus, Lixus cardui, Eublemma amoena, Trichosirocalus briesei, or ectophagous Cassida rubiginosa etc. found during our surveys, there are reports in the lit- erature describing them as having been already introduced as successful biocontrol agents in Australia. Endophagous species like lepidopteran Myelois circumvoluta and Pyroderces argyrogrammos which feed on the stems and the head, and the tephritid flies Tephritis pos- tica and Chaetostomella cylindrica which feed on the capitula, seem quite destructive for the weed, but need to be further studied regarding host specificity. -
OBCL Newsletter, December, 2020 (Pdf)
December 2020 OBCL Newsletter Overseas Biological Control Laboratories Edited by Michael Grodowitz U.S. Department of Agriculture, Agricultural Research Service Previous newsletter editions are available at: In This Issue www.ars-ebcl.org Introduction ...............................................................................................1 ABCL - Australia ......................................................................................1 Australian Biological Control Aquatic Weed Biological Control and COVID................................. 1 Trichilogaster Bud Gall Wasp: A Priority Biocontrol Agent for Laboratory - ABCL Earleaf Acacia.................................................................................... 2 Aquatic Weed Biological Control and COVID Sino-ABCL - China.................................................................................... 4 Matthew Purcell, Nathan Harms and Bradley Salivary Gland Secretome Analysis Reveals A Novel Mechanism of Horizontal Gene Transfer in the Brown Marmorated Stink Bug ...... 4 Brown FuEDEI - Argentina................................................................................... 5 Little Fire Ant ...................................................................................5 Much of the exploration for biological control of Improving the Success and Perception of Biological Control Through aquatic weeds conducted by ABCL has been performed Community Engagement and Awareness.......................................... 6 in the Asian native range of several invasive -
The Phytophagous Insect Fauna of Scotch Thistle, Onopordum Acanthium L., in Southeastern Washington and Northwestern Idaho
Proceedings of the X International Symposium on Biological Control of Weeds 233 4-14 July 1999, Montana State University, Bozeman, Montana, USA Neal R. Spencer [ed.]. pp. 233-239 (2000) The Phytophagous Insect Fauna of Scotch Thistle, Onopordum acanthium L., in Southeastern Washington and Northwestern Idaho J. D. WATTS1 and G. L. PIPER Department of Entomology, Washington State University, Pullman, Washington 99164-6382, USA Abstract Scotch thistle, Onopordum acanthium L. (Asteraceae: Cardueae), a plant of Eurasian origin, has become an increasingly serious pasture, rangeland, wasteland, and roadside weed in the western United States. Prior to the implementation of a biological control agent acquisition and release program, a domestic survey was carried out at 16 sites in five southeastern Washington and northwestern Idaho counties between 1995-96 to ascertain the plant’s existing entomofauna. Thirty phytophagous insect species in six orders and 17 families were found to be associated with the thistle. Hemiptera, Homoptera, and Coleoptera were the dominant ectophagous taxa, encompassing 50, 20, and 17% of all species found, respectively. The family Miridae contained 60% of the hemipteran fauna. Onopordum herbivores were polyphagous ectophages, and none of them reduced popula- tions of or caused appreciable damage to the plant. The only insect that consistently fed and reproduced on O. acanthium was the aphid Brachycaudus cardui (L.). A notable gap in resource use was the absence of endophages, particularly those attacking the capitula, stems, and roots. Consequently, the importation of a complex of nonindigenous, niche- specific natural enemies may prove to be a highly rewarding undertaking. Key Words: Onopordum, Scotch thistle, weed, biological control, entomofauna Scotch thistle, Onopordum acanthium L. -
Coleoptera: Curculionidae, Lixinae
© Entomologica Fennica. 6 June 2007 Oviposition niches and behavior of the genus Lixus Fabricius (Coleoptera: Curculionidae, Lixinae) Levent Giiltekin Gultekin, L. 2007: Oviposition niches and behavior ofthe genus Lixus Fabricius (Coleoptera: Curculionidae, Lixinae). — Entomol. Fennica 18: 74—8 1. Oviposition places in the host plants of23 Lixus Fabricius species in eastern Tur- key were identified. Lixus nordmanni Hochhuth, L. subtilis Boheman, L. in— canescens Boheman, L. brevipes Brisout, L. sp. n. pr. brevipes Brisout, L. ochra— ceuS Boheman, L. furcatus Olivier, L. rubicundus Zoubkoff, L. angustatus (Fabricius), L. punctiventris Boheman, L. fasciculatus Boheman, L. bardanae (Fabricius), L. sp. n. pr. korbi Petri, and L. scolopax Boheman deposited eggs in the main stem. Lixusfiliformis (Fabricius), L. cardui Olivier, and L. korbi Petri oviposited in the main stem and lateral branch of their host plants. L. circum— cinctus Boheman laid eggs on both stem and petiole, whereas L. siculus Boheman, L. farinifer Reitter, L. cylindrus (Fabricius), and L. sp. n. pr. furcatus Olivier used the petioles, a new ecological niche for the genus Lixus. The unique species L. obesus Petri selected the seed capsule for laying eggs and completing its generation. Levent Giiltekin, Ataturk University, Faculty ofAgriculture, Plant Protection Department, 25240, Erzurum—Turkey; E—mail: lgul@atauni. edu. tr Received 24 March 2005, accepted 29 August 2006 1. Introduction cies, size constraint could play an important role in oviposition and larval development (Eber et al. The superfamily Curculionoidea, which contains 1999). A study of the different species of endo- more than 50,000 described species, is the richest phagous stem borers on thistles showed niche organisms known (O’Brien & Wibmer 1978). -
An Investigation to the Subfamily of Lixinae from Khorasan Junoubi and Razavi Provinces of Iran (Coleoptera: Curculionidae)
_____________Mun. Ent. Zool. Vol. 5, No. 2, June 2010__________ 559 AN INVESTIGATION TO THE SUBFAMILY OF LIXINAE FROM KHORASAN JUNOUBI AND RAZAVI PROVINCES OF IRAN (COLEOPTERA: CURCULIONIDAE) Mehdi Modarres Awal* and Fahimeh Hossein Pour* * Department of Plant Protection, College of Agriculture, Ferdowsi University of Mashhad, IRAN. Email: [email protected] [Moderres Awal, M. & Hossein Pour, F. 2010. An investigation to the subfamily Lixinae from Khorasan Junoubi and Razavi provinces of Iran (Coleoptera: Curculionidae). Munis Entomology & Zoology, 5 (2): 559-562] ABSTRACT: During 2006-2008 subfamily of Lixinae was surveyed in North eastern and east provinces of Iran. In total, 27 species belonging to 15 genera were determined. Among them three species including of Larinus sericatus (Boheman, 1834), Bangasternus provincialis (Fairmaire, 1863) and Conorhynchus verucundus (Faust, 1883) are new record for Iran fauna. KEY WORDS: Curculionidae, Lixinae, Khorasan, Iran, new records. Khorasan is the widest region in Iran (with total area 315686 Km²) that is divided in three provinces concern Khorasan Junoubi, Razavi and Shomali. This area surrounded by Turkmenistan and Afghanistan, also linked with four provinces include Kerman, Balouchestan, Yazd and Semnan. Curculionidae is currently the largest family of insects in the world with at least 3600 genera and 41000 species. Lixinae is a subfamily of true weevils, included three tribes Cleonini, Lixini and Rhinocyllini. Main characteristic of this subfamily include tarsal claws are fused at the base, and labial palps are short and telescoping. In addition, their body is elongated shape as for some other weevils, tibiae bear and uncus on its distal end and the rostrum is forwardly directed (Boothe et al., 1990). -
Natural History Studies for the Preliminary Evaluation of Larinus Filiformis (Coleoptera: Curculionidae) As a Prospective Biolog
POPULATION ECOLOGY Natural History Studies for the Preliminary Evaluation of Larinus filiformis (Coleoptera: Curculionidae) as a Prospective Biological Control Agent of Yellow Starthistle 1 2 3 4 L. GU¨ LTEKIN, M. CRISTOFARO, C. TRONCI, AND L. SMITH Faculty of Agriculture, Plant Protection Department, Atatu¨ rk University, 25240 TR Erzurum, Turkey Environ. Entomol. 37(5): 1185Ð1199 (2008) ABSTRACT We studied the life history, geographic distribution, behavior, and ecology of Larinus filiformis Petri (Coleoptera: Curculionidae) in its native range to determine whether it is worthy of further evaluation as a classical biological control agent of yellow starthistle, Centaurea solstitialis (Asteraceae: Cardueae). Larinus filiformis occurs in Armenia, Azerbaijan, Turkey, and Bulgaria and has been reared only from C. solstitialis. At Þeld sites in central and eastern Turkey, adults were well synchronized with the plant, being active from mid-May to late July and ovipositing in capitula (ßowerheads) of C. solstitialis from mid-June to mid-July. Larvae destroy all the seeds in a capitulum. The insect is univoltine in Turkey, and adults hibernate from mid-September to mid-May. In the spring, before adults begin ovipositing, they feed on the immature ßower buds of C. solstitialis, causing them to die. The weevil destroyed 25Ð75% of capitula at natural Þeld sites, depending on the sample date. Preliminary host speciÞcity experiments on adult feeding indicate that the weevil seems to be restricted to a relatively small number of plants within the Cardueae. Approximately 57% of larvae or pupae collected late in the summer were parasitized by hymenopterans [Bracon urinator, B. tshitsherini (Braconidae) and Exeristes roborator (Ichneumonidae), Aprostocetus sp. -
Gaskin 262373.Pdf
Biological Control 58 (2011) 1–21 Contents lists available at ScienceDirect Biological Control journal homepage: www.elsevier.com/locate/ybcon Review Applying molecular-based approaches to classical biological control of weeds ⇑ John F. Gaskin a, , Marie-Claude Bon b, Matthew J.W. Cock c, Massimo Cristofaro d, Alessio De Biase e, Rose De Clerck-Floate f, Carol A. Ellison g, Hariet L. Hinz c, Ruth A. Hufbauer h, Mic H. Julien i, René Sforza b a USDA Agricultural Research Service, 1500 N. Central Avenue, Sidney, MT 59270, USA b European Biological Control Laboratories, USDA Agricultural Research Service, Campus International de Baillarguet, 34980 Montferrier le Lez, France c CABI Europe – Switzerland, Rue des Grillons 1, CH-2800 Delémont, Switzerland d ENEA Casaccia, UTAGRI-ECO (BBCA), Via Anguillarese 301, Rome 00123, Italy e Department of Biology and Biotechnologies ‘‘Charles Darwin’’, University of Rome ‘‘La Sapienza’’, Viale dell’Università 32, I-00185 Rome, Italy f Agriculture and Agri-Food Canada, Lethbridge Research Centre, 5403 1 Ave S, Lethbridge, Alberta, Canada T1J 4B1 g CABI Europe – UK, Bakeham Lane, Egham, Surrey, TW209TY, United Kingdom h Department of Bioagricultural Sciences and Pest Management and Graduate Degree Program in Ecology, Colorado State University, Fort Collins, CO 80523, USA i CSIRO Ecosystem Sciences, Ecosciences Precinct, 41 Boggo Road, Dutton Park, Qld 4102, Australia article info abstract Article history: The use of molecular techniques is rapidly growing as the tools have become more diverse and powerful, Received 14 October 2010 more widely available, and easier to implement. Molecular analyses are able to elucidate information Accepted 30 March 2011 about target weeds that is critical to improving control success, such as taxonomic clarification, evidence Available online 5 April 2011 of hybridization and cryptic species, better development of test plant lists, population structure and ori- gin of invasions. -
Tech Series 7 (.Pdf, 511.91KB)
CRC for Australian Weed Management #7 Technical Series Improving the selection, testing and evaluation of weed biological control agents Technical Series #7 • Improving the selection, testing and evaluation of weed biological control agents the selection, testing and evaluation of weed biological control Series #7 • Improving Technical Editors: H. Spafford Jacob and D.T. Briese CRC for Australian Weed Management #7 Technical Series Improving the selection, testing and evaluation of weed biological control agents Proceedings of the CRC for Australian Weed Management Biological Control of Weeds Symposium and Workshop September 13, 2002 University of Western Australia Perth, Western Australia Editors: H. Spafford Jacob and D.T. Briese Improving the selection, testing and evaluation of weed biological control agents the selection, testing and evaluation of weed biological control Improving CRC for Australian Weed Management Technical Series no. 7 April 2003 Copyright © CRC for Australian Weed Management 2003 This book is copyright. Except as permitted under the Australian Copyright Act 1968 (Commonwealth) and subsequent amendments, no part of this publication my be reproduced, stored or transmitted in any form or by any means, electronic or otherwise, without the specific written permission of the copyright owner. Enquiries and additional copies: CRC for Australian Weed Management, Waite Campus, University of Adelaide, PMB 1, Glen Osmond, SA 5064, Australia Telephone: (61) (08) 8303 6590 Fax: (61) (08) 8303 7311 Email: [email protected] -
Cleonis Pigra (Scopoli, 1763) (Coleoptera: Curculionidae: Lixinae): Morphological Re-Description of the Immature Stages, Keys, Tribal Comparisons and Biology
insects Article Cleonis pigra (Scopoli, 1763) (Coleoptera: Curculionidae: Lixinae): Morphological Re-Description of the Immature Stages, Keys, Tribal Comparisons and Biology Jiˇrí Skuhrovec 1,* , Semyon Volovnik 2, Rafał Gosik 3, Robert Stejskal 4 and Filip Trnka 5 1 Group Function of Invertebrate and Plant Biodiversity in Agro-Ecosystems, Crop Research Institute, Drnovská 507, CZ-161 06 Praha 6 Ruzynˇe,Czech Republic 2 Independent Researcher, 72311 Melitopol, Ukraine; [email protected] 3 Department of Zoology and Plant Protection, Maria Curie-Skłodowska University, Akademicka 19, 20-033 Lublin, Poland; [email protected] 4 Administration of Podyji National Park, Na Vyhlídce 5, CZ-669 02 Znojmo, Czech Republic; [email protected] 5 Department of Ecology & Environmental Sciences, Faculty of Science, Palacký University Olomouc, Šlechtitel ˚u27, CZ-783 71 Olomouc, Czech Republic; fi[email protected] * Correspondence: [email protected]; Tel.: +420-702087694 Received: 19 August 2019; Accepted: 24 September 2019; Published: 30 September 2019 Abstract: Mature larvae and pupae of Cleonis pigra (Scopoli, 1763) (Curculionidae: Lixinae: Cleonini) are morphologically described in detail for the first time and compared with known larvae and pupae of other Cleonini species. The results of measurements and characteristics most typical for larvae and pupae of Cleonini are newly extracted and critically discussed, along with some records given previously. Keys for the determination of selected Cleonini species based on their larval and pupal characteristics are attached. Dyar’s law was used for the estimation of a number of larval instars of C. pigra. Descriptions of habitats, adult behavior, host plants, life cycle, and biotic interactions are reported here. Adults and larvae feed on plants from the Asteraceae family only (genera Carduus, Cirsium, Centaurea, and Onopordum).