A New Dipteran Parasitoid of Rose Sawfly from Turkey
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Tachinid Times Issue 29
Walking in the Footsteps of American Frontiersman Daniel Boone The Tachinid Times Issue 29 Exploring Chile Curious case of Girschneria Kentucky tachinids Progress in Iran Tussling with New Zealand February 2016 Table of Contents ARTICLES Update on New Zealand Tachinidae 4 by F.-R. Schnitzler Teratological specimens and the curious case of Girschneria Townsend 7 by J.E. O’Hara Interim report on the project to study the tachinid fauna of Khuzestan, Iran 11 by E. Gilasian, J. Ziegler and M. Parchami-Araghi Tachinidae of the Red River Gorge area of eastern Kentucky 13 by J.E. O’Hara and J.O. Stireman III Landscape dynamics of tachinid parasitoids 18 by D.J. Inclán Tachinid collecting in temperate South America. 20 Expeditions of the World Tachinidae Project. Part III: Chile by J.O. Stireman III, J.E. O’Hara, P. Cerretti and D.J. Inclán 41 Tachinid Photo 42 Tachinid Bibliography 47 Mailing List 51 Original Cartoon 2 The Tachinid Times Issue 29, 2016 The Tachinid Times February 2016, Issue 29 INSTRUCTIONS TO AUTHORS Chief Editor JAMES E. O’HARA This newsletter accepts submissions on all aspects of tach- InDesign Editor SHANNON J. HENDERSON inid biology and systematics. It is intentionally maintained as a non-peer-reviewed publication so as not to relinquish its status as Staff JUST US a venue for those who wish to share information about tachinids in an informal medium. All submissions are subjected to careful ISSN 1925-3435 (Print) editing and some are (informally) reviewed if the content is thought to need another opinion. Some submissions are rejected because ISSN 1925-3443 (Online) they are poorly prepared, not well illustrated, or excruciatingly bor- ing. -
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(S): Diego J
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(s): Diego J. Inclan and John O. Stireman, III Source: Annals of the Entomological Society of America, 104(2):287-296. Published By: Entomological Society of America https://doi.org/10.1603/AN10047 URL: http://www.bioone.org/doi/full/10.1603/AN10047 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. CONSERVATION BIOLOGY AND BIODIVERSITY Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States 1 DIEGO J. INCLAN AND JOHN O. STIREMAN, III Department of Biological Sciences, 3640 Colonel Glenn Highway, 235A, BH, Wright State University, Dayton, OH 45435 Ann. Entomol. Soc. Am. 104(2): 287Ð296 (2011); DOI: 10.1603/AN10047 ABSTRACT Although tachinids are one of the most diverse families of Diptera and represent the largest group of nonhymenopteran parasitoids, their local diversity and distribution patterns of most species in the family are poorly known. -
Scientific Notes 365
Scientific Notes 365 FENNAH, R. G. 1942. The citrus pests investigation in the Windward and Leeward Is- lands, British West Indies 1937-1942. Agr. Advisory Dept., Imp. Coll. Tropical Agr. Trinidad, British West Indies. pp. 1-67. JONES, T. H. 1915. The sugar-cane weevil root-borer (Diaprepes sprengleri Linn.) In- sular Exp. Stn. (Rio Piedras, P. R.) Bull. 14: 1-9, 11. SCHROEDER, W. J. 1981. Attraction, mating, and oviposition behavior in field popula- tions of Diaprepes abbreviatus on citrus. Environ. Entomol. 10: 898-900. WOLCOTT, G. N. 1933. Otiorhynchids oviposit between paper. J. Econ. Entomol. 26: 1172. WOLCOTT, G. N. 1936. The life history of Diaprepes abbreviatus at Rio Piedras, Puerto Rico. J. Agr. Univ. Puerto Rico 20: 883-914. WOODRUFF, R. E. 1964. A Puerto Rican weevil new to the United States (Coleoptera: Curculionidae). Fla. Dept. Agr., Div. Plant Ind., Entomol. Circ. 30: 1-2. WOODRUFF, R. E. 1968. The present status of a West Indian weevil Diaprepes abbre- viatus (L.) in Florida (Coleoptera: Curculionidae). Fla. Dept. Agr., Div. Plant Ind., Entomol. Circ. 77: 1-4. ♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦♦ PARASITISM OF EASTERN LUBBER GRASSHOPPER BY ANISIA SEROTINA (DIPTERA: TACHINIDAE) IN FLORIDA MAGGIE A. LAMB, DANIEL J. OTTO AND DOUGLAS W. WHITMAN* Behavior, Ecology, Evolution, and Systematics Section Department of Biological Sciences, Illinois State University Normal, IL 61790-4120 The eastern lubber grasshopper, Romalea microptera Beauvois (= guttata; see Otte 1995) is a large romaleid grasshopper (adults = 2-12 g) that occurs sporadically throughout the southeastern USA, but in relatively high densities in the Everglades- Big Cypress area of south Florida (Rehn & Grant 1959, 1961). -
Alien and Invasive Species of Harmful Insects in Bosnia and Herzegovina
Alien and invasive species of harmful insects in Bosnia and Herzegovina Mirza Dautbašić1,*, Osman Mujezinović1 1 Faculty of Forestry University in Sarajevo, Chair of Forest Protection, Urban Greenery and Wildlife and Hunting. Zagrebačka 20, 71000 Sarajevo * Corresponding author: [email protected] Abstract: An alien species – animal, plant or micro-organism – is one that has been introduced as a result of human activity to an area it could not have reached on its own. In cases where the foreign species expands in its new habitat, causing environmental and economic damage, then it is classified as invasive. The maturity of foreign species in the new area may also be influenced by climate changes. The detrimental effect of alien species is reflected in the reduction of biodiversity as well as plant vitality. A large number of alien species of insects are not harmful to plants in new habitats, but there are also those that cause catastrophic consequences to a significant extent. The aim of this paper is to present an overview of newly discovered species of insects in Bosnia and Herzegovina. The research area, for this work included forest and urban ecosystems in the territory of Bosnia and Herzegovina. For the purposes of this paper, an overview of the species found is provided: /HSWRJORVVXVRFFLGHQWDOLV Heidemann; (Hemiptera: Coreidae) - The western conifer seed bug, found at two sites in Central Bosnia, in 2013 and 2015; $UJHEHUEHULGLVSchrank; (Hymenoptera: Argidae) - The berberis sawfly, recorded in one locality (Central Bosnia), in 2015; -
Phylogenetic Relationships of Tachinid Flies in Subfamily Exoristinae Tachinidae: Diptera) Based on 28S Rdna and Elongation Factor-1A
Systematic Entomology *2002) 27,409±435 Phylogenetic relationships of tachinid flies in subfamily Exoristinae Tachinidae: Diptera) based on 28S rDNA and elongation factor-1a JOHN O. STIREMAN III Department of Ecology and Evolutionary Biology,University of Arizona,Tucson,U.S.A. Abstract. The phylogenetic relationships within the largest subfamily of Tachi- nidae,Exoristinae,were explored using nucleotide sequences of two genes *EF-1 a and 28S rDNA). A total of fifty-five and forty-three taxa were represented in the analyses for each gene,respectively,representing forty-three genera. Neighbour joining,parsimony and maximum likelihood inference methods were employed to reconstruct phylogenetic relationships in separate analyses of each gene,and parsimony was used to analyse the combined dataset. Although certain taxa were highly mobile,phylogenetic reconstructions generally supported recent clas- sification schemes based on reproductive habits and genitalia. Generally,the monophyly of Tachinidae and Exoristinae was supported. Tribes Winthemiini, Exoristini and Blondeliini were repeatedly constructed as monophyletic groups, with the former two clades often occupying a basal position among Exoristinae. Goniini and Eryciini generally clustered together as a derived clade within Exoristinae; however,they were never reconstructed as two distinct clades. These results suggest that the possession of unembryonated eggs is plesiomorphic within the subfamily and that there may have been multiple transitions between micro- type and macrotype egg forms. Introduction 1987; Williams et al.,1990; Eggleton & Belshaw,1993), and the wide variety of mechanisms by which they attack Tachinidae is generally regarded as a relatively recent, them *O'Hara,1985). These oviposition strategies include actively radiating clade of parasitic flies *Crosskey,1976). -
No Slide Title
Tachinidae: The “other” parasitoids Diego Inclán University of Padova Outline • Briefly (re-) introduce parasitoids & the parasitoid lifestyle • Quick survey of dipteran parasitoids • Introduce you to tachinid flies • major groups • oviposition strategies • host associations • host range… • Discuss role of tachinids in biological control Parasite vs. parasitoid Parasite Life cycle of a parasitoid Alien (1979) Life cycle of a parasitoid Parasite vs. parasitoid Parasite Parasitoid does not kill the host kill its host Insects life cycles Life cycle of a parasitoid Some facts about parasitoids • Parasitoids are diverse (15-25% of all insect species) • Hosts of parasitoids = virtually all terrestrial insects • Parasitoids are among the dominant natural enemies of phytophagous insects (e.g., crop pests) • Offer model systems for understanding community structure, coevolution & evolutionary diversification Distribution/frequency of parasitoids among insect orders Primary groups of parasitoids Diptera (flies) ca. 20% of parasitoids Hymenoptera (wasps) ca. 70% of parasitoids Described Family Primary hosts Diptera parasitoid sp Sciomyzidae 200? Gastropods: (snails/slugs) Nemestrinidae 300 Orth.: Acrididae Bombyliidae 5000 primarily Hym., Col., Dip. Pipunculidae 1000 Hom.:Auchenorrycha Conopidae 800 Hym:Aculeata Lep., Orth., Hom., Col., Sarcophagidae 1250? Gastropoda + others Lep., Hym., Col., Hem., Tachinidae > 8500 Dip., + many others Pyrgotidae 350 Col:Scarabaeidae Acroceridae 500 Arach.:Aranea Hym., Dip., Col., Lep., Phoridae 400?? Isop.,Diplopoda -
Functional Diversity of Tachinid Parasitoids in Managed Boreal Forests
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/339676824 Functional diversity of tachinid parasitoids in managed boreal forests Article · March 2020 CITATIONS READS 0 65 1 author: Antonio Rodríguez Olmo Swedish University of Agricultural Sciences 8 PUBLICATIONS 84 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Conservation of ecosystem services in Fennoscandian managed Boreal forests View project Short term effects of intensive forest fertilization on biodiversity View project All content following this page was uploaded by Antonio Rodríguez Olmo on 04 March 2020. The user has requested enhancement of the downloaded file. functional diversity of tachinid parasitoids in managed boreal forests by Antonio Rodríguez Department of Wildlife, Fish and Environmental Studies, Swedish University of Agricultural Sciences (SLU), SE-90183 Umeå, Sweden. E-mail: [email protected] Intensive forest management is characterized by clear-cut harvesting, artificial regeneration, short rota- tion cycles, and fire suppression. This management poses a threat to forest multi-functionality and biodiversity, leading to forest simplification and reducing the provision of ecosystem services other than the steady supply of wood for fuel, pulp and timber (Bengtsson et al. 2000, Puettmann et al. 2009). Although negative effects of in- tensive forestry are widely acknowledged for saproxylic species diversity (species dependent on dead or decay- ing wood, Niemelä 1997), much less is known about its effects on other groups.There is especially a dearth of information about the effect of intensive forest management on insect parasitoid diversity and function, despite their staggering diversity (Heraty 2009), and their key role on the maintenance of forest biological control (Per- alta et al. -
Tachinid Collecting in Southwest New Mexico and Arizona During the 2007 NADS Field Meeting
Wright State University CORE Scholar Biological Sciences Faculty Publications Biological Sciences 2-2008 Tachinid Collecting in Southwest New Mexico and Arizona during the 2007 NADS Field Meeting John O. Stireman III Wright State University - Main Campus, [email protected] Follow this and additional works at: https://corescholar.libraries.wright.edu/biology Part of the Biology Commons, Ecology and Evolutionary Biology Commons, Entomology Commons, and the Systems Biology Commons Repository Citation Stireman, J. O. (2008). Tachinid Collecting in Southwest New Mexico and Arizona during the 2007 NADS Field Meeting. The Tachinid Times (21), 14-16. https://corescholar.libraries.wright.edu/biology/404 This Article is brought to you for free and open access by the Biological Sciences at CORE Scholar. It has been accepted for inclusion in Biological Sciences Faculty Publications by an authorized administrator of CORE Scholar. For more information, please contact [email protected]. The Tachinid Times part of Florida’s natural heritage, its native bromeliads. some of the rarer species on that particular hilltop. Once this goal has been achieved, a program for repop- Identifications were made with generic and species ulating devastated areas with small plants grown from seed keys and descriptions from the literature (see O’Hara and specifically collected from a number of hard-hit areas can Wood 2004) with particular reliance on Monty Wood’s begin. (1987) key to Nearctic genera. Specimens were also com- pared to previously identified material in my collection. Tachinid collecting in southwest New Mexico and These identifications should be considered preliminary as Arizona during the 2007 NADS field meeting (by J.O. -
Hellenic Plant Protection Journal
Volume 1, Issue 2, July 2008 ISSN 1791-3691 Hellenic Plant Protection Journal A semiannual scientifi c publication of the BENAKIBEB PHYTOPATHOLOGICAL INSTITUTE The Hellenic Plant Protection Journal (ISSN 1791-3691) is the new scientifi c publication of the Benaki Phytopathological Institute replacing the Annals of the Benaki Phytopathologi- cal Institute (ISSN 1790-1480) which had been published since 1935. Starting from January 2008, the Benaki Phytopathological Institute is publishing the Hel- lenic Plant Protection Journal semiannually, in January and July each year, and accepts for publication any work related to plant protection in the Mediterranean region regardless of where it was conducted. All aspects of plant protection referring to plant pathogens, pests, weeds (identifi cation, biology, control), pesticides and relevant environmental is- sues are topics covered by the journal. Articles in the form of either a complete research paper or a short communication (in- cluding new records) may be submitted. Instructions on how to prepare the manuscript are provided in the fi rst issue of the year. Manuscripts should be submitted in electronic form either by e-mail at [email protected] or by post on a disk addressed to the Editorial Board, Benaki Phytopathological Institute, 8 St. Delta str., GR-145 61 Kifi ssia (Athens), Greece. Only original articles are considered and published after successful completion Hellenic Plant Protection Journal Hellenic Plant of a review procedure by two competent referees. EDITORIAL BOARD Editor: Dr C.N. Giannopolitis (Weed Science Department, B.P.I.) Associate editors: Dr K. Elena (Phytopathology Department, B.P.I.) Dr K. Machera (Pesticides Control & Phytopharmacy Department, BPI) Dr A.N. -
Rosa and Integrated Pest Control Measures B. K
Proceedings of Online International Conference on Technological Developments in Systematic Research (ICTDSR-2020) Organized by Novateur Publications, Pune, Maharashtra, India International Journal of Innovations in Engineering Research and Technology [IJIERT] ISSN: 2394-3696, Website: ijiert.org, August 14th, 2020. RHSA AND ,17EGRATED PEST CONTROL MEASURES B. K. Mukhammadiev, TSAU, Ph.D., Associate Professor N. A. Khasilava, TSAU 1st year student e-mail: [email protected] Abstract: This article provides information on the value of the medicinal Rhsa plant in the national economy and pharmaceuticals, its botanical definition and its main harmful organisms and measures to combat them. It is noted that mainly in the wild rose contains the main harmful organisms, such as Rhagoletis alternata, Celypha rosaceana, 0acrosiphum rosae /., :rge ochropus, Tetranychus urticae. Keywords: sawfly, pink, pharmaceuticals, medicinal, chemical, fruit, flower, bud, acaricide, pyrethroid, organophosphorus INTRODUCTION On global scale, special attention is paid to the protection of territories where medicinal plants grow. There are 10-12 thousand species of medicinal plants in the world, chemical- pharmacological and medicinal properties of more than 100 plant species have been studied. There are 577 species of medicinal plants in Uzbekistan. Currently, the area of rosa plantations and the amount of raw materials extracted from them are increasing in the world. However, due to the fact that rosa is affected by various pests and diseases at different stages of development, not only its large yield is lost, but also the quality and quantity of medicinal substances in it is sharply reduced. General Description of rosa: Rosa is a shrub that includes more than 3000 species belonging to about 100 genera, including grasses, shrubs, shrubs and trees. -
Hymenoptera: Symphyta: Argidae) from South Korea with Key to Species of the Subfamily Arginae
Journal of Asia-Pacific Biodiversity 9 (2016) 183e193 HOSTED BY Contents lists available at ScienceDirect Journal of Asia-Pacific Biodiversity journal homepage: http://www.elsevier.com/locate/japb Original article Three new species of the genus Arge (Hymenoptera: Symphyta: Argidae) from South Korea with key to species of the subfamily Arginae Jin-Kyung Choi a, Su-Bin Lee a, Meicai Wei b, Jong-Wook Lee a,* a Department of Life Sciences, Yeungnam University, Gyeongsan, South Korea b Key Laboratory of Cultivation and Protection for Non-Wood Forest Trees (Central South University of Forestry and Technology), Ministry of Education, Changsha, China article info abstract Article history: Three new species, Arge koreana Wei & Lee sp. nov. from South Korea, Arge pseudorejecta Wei & Lee sp. Received 20 January 2016 nov., and Arge shengi Wei & Lee sp. nov. from South Korea and China are described. Keys to known genera Received in revised form of Argidae and known species of Arginae from South Korea are provided. 11 February 2016 Copyright Ó 2016, National Science Museum of Korea (NSMK) and Korea National Arboretum (KNA). Accepted 15 February 2016 Production and hosting by Elsevier. This is an open access article under the CC BY-NC-ND license (http:// Available online 24 February 2016 creativecommons.org/licenses/by-nc-nd/4.0/). Keywords: Arginae China key Korea Introduction Takeuchi 1927, 1939; Doi 1938; Kim 1957, 1963, 1970; Togashi 1973, 1990, 1997; Zombori 1974, 1978; Paek et al 2010; Shinohara Taeger et al (2010) listed 58 genera and 913 valid species and et al 2009; Shinohara et al 2012). -
VC55 Species Number
VC55 Species Number: 135 Last updated: 3rd Feb 2018 Species Common Records Last Seen Arge berberidis Berberis Sawfly 16 2017 Arge cyanocrocea Bramble Sawfly 30 2017 Arge melanochra none 2 2016 Arge ochropus Rose Sawfly 15 2017 Arge pagana Large Rose Sawfly 19 2017 Arge ustulata none 8 2017 Calameuta filiformis Reed Stem Borer 3 2015 Cephus nigrinus none 1 2017 Cephus pygmeus Wheat Stem Borer 6 2017 Cephus spinipes none 2 2017 Hartigia xanthostoma none 1 2014 Abia sericea Scabious/Club-horned Sawfly 6 2017 Cimbex connatus Large Alder Sawfly 4 2017 Cimbex femoratus Birch Sawfly 8 2017 Trichiosoma lucorum 1 1990 Trichiosoma tibiale Hawthorn Sawfly 2 1999 Zaraea fasciata 2 2017 Diprion similis Imported Pine Sawfly 2 2014 Diprion pini 1 2017 Pamphilius betulae 2 2017 Sirex noctilio 1 1980 Urocerus gigas Giant Woodwasp 25 2017 Allantus cinctus Curled Rose Sawfly 6 2014 Allantus cingulatus 2 2014 Allantus calceatus 1 2015 Ametastegia carpini Geranium Sawfly 3 2017 Ametastegia glabrata 1 2014 Apethymus filiformis 1 2014 Athalia bicolor 1 2014 Athalia circularis 5 2017 Athalia cordata 11 2017 Athalia liberta 2 2016 Athalia rosae Turnip Sawfly 31 2017 Athalia scutellariae Skullcap Sawfly 7 2017 Blennocampa pusilla 3 1996 Blennocampa phyllocolpa 7 2017 Caliroa annulipes Oak Slug Sawfly 2 2014 Caliroa cerasi Pear Slug Sawfly 4 2015 Eutomostethus ephippium 8 2017 Eutomostethus luteiventris 1 2014 Halidamia affinis 2 2013 Monophadnus pallescens 1 2011 Periclista albida 1 2010 Periclista lineolata Oak Sawfly 4 2016 Phymatocera aterrima Solomon's Seal