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Impact of Imidacloprid and Horticultural Oil on Nonâ•Fitarget
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Masters Theses Graduate School 8-2007 Impact of Imidacloprid and Horticultural Oil on Non–target Phytophagous and Transient Canopy Insects Associated with Eastern Hemlock, Tsuga canadensis (L.) Carrieré, in the Southern Appalachians Carla Irene Dilling University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_gradthes Part of the Entomology Commons Recommended Citation Dilling, Carla Irene, "Impact of Imidacloprid and Horticultural Oil on Non–target Phytophagous and Transient Canopy Insects Associated with Eastern Hemlock, Tsuga canadensis (L.) Carrieré, in the Southern Appalachians. " Master's Thesis, University of Tennessee, 2007. https://trace.tennessee.edu/utk_gradthes/120 This Thesis is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Masters Theses by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a thesis written by Carla Irene Dilling entitled "Impact of Imidacloprid and Horticultural Oil on Non–target Phytophagous and Transient Canopy Insects Associated with Eastern Hemlock, Tsuga canadensis (L.) Carrieré, in the Southern Appalachians." I have examined the final electronic copy of this thesis for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Master of Science, with a major in Entomology and Plant Pathology. Paris L. Lambdin, Major Professor We have read this thesis and recommend its acceptance: Jerome Grant, Nathan Sanders, James Rhea, Nicole Labbé Accepted for the Council: Carolyn R. -
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. -
Tachinidae, Tachinid Flies
Beneficial Insects Class Insecta, Insects Order Diptera, Flies, gnats, and midges Diptera means “two wings,” and true flies bear only one pair of functional wings. Flies are one of the largest insect groups, with approximately 35 families that contain predatory or parasitic species. All flies have piercing/sucking/sponging mouthparts. Tachinid flies Family Tachinidae Description and life history: This is a large and important family, with up to 1300 native parasitoid species in North America and additional introduced species to help control foreign pests. These flies vary in color, size, and shape but most resemble houseflies. Adults are usually gray, black, or striped, and hairy. Adults lay eggs on plants to be consumed by hosts, or they glue eggs to the outside of hosts, so the maggots can burrow into the host. Rarely will tachinids insert eggs into host bodies. Tachinid flies develop rapidly within their host and pupate in 4–14 days. By the time they emerge, they have killed their host. Many species have several generations a year, although some are limited by hosts with a single annual generation. Prey species: Most tachinid flies attack caterpillars and adult and larval beetles, although others specialize on Tachinid fly adult. (327) sawfly larvae, true bugs, grasshoppers, or other insects. Photo: John Davidson Lydella thompsoni is a parasitoid of European corn borer, Voria ruralis attacks cabbage looper caterpillars, Myiopharus doryphorae attacks Colorado potato beetle larvae, and Istocheta aldrichi parasitizes adult Japanese beetles. Although these are very important natural en- emies, none is available commercially. IPM of Midwest Landscapes 263. -
Ohara\Catalogues\World Genera\Tach
WORLD GENERA OF THE TACHINIDAE (DIPTERA) AND THEIR REGIONAL OCCURRENCE by James E. O’Hara1 23 February 2005 Version 1.0 ________________________ 1 Invertebrate Biodiversity, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario, Canada, K1A 0C6. E-mail: [email protected]. TABLE OF CONTENTS Click on a page number to go to the page indicated Foreword ............................................................................................................................... 2 Biogeographic summary ....................................................................................................... 3 Acknowledgements ............................................................................................................... 3 Table of genera and their regional occurrence ...................................................................... 4 References ........................................................................................................................... 66 Select a letter to go directly to corresponding genus in list of world genera A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z FOREWORD The following table is a listing of the tachinid genera of the world with their regional occurrence. It was compiled from the generic names and distributions given in the most recent regional catalogues, as listed here, and brought up-to-date using information from subsequently published papers. Regional catalogues Nearctic Region O’Hara & Wood (2004) Neotropical -
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). -
Japanese Beetle Popillia Japonica Japanese Beetle Damages Plants in Two Distinct Ways
Japanese Beetle Popillia japonica Japanese beetle damages plants in two distinct ways Japanese beetle adults chew on leaves and flowers of many plants White grubs prune the roots, producing drought stress symptoms Flowers are often a favored plant part targeted by adult Japanese beetles Issue of unusual concern with Japanese beetle Overlap of adult feeding on flowers – and use of those flowers by pollinators Uber-host Plants Favored by Japanese Beetle Adults in CO • Roses** • Littleleaf Linden* • Virginia Creeper* • Silver lace** Damage to Virginia creeper Damage to linden Other Plants Commonly Grown in CO that are Highly Favored by Japanese Beetle Ornamentals Food Crops • Hollyhock* • Beans (green, edamame) • Gaura** • Basil • Rose-of-Sharon** • Raspberry* • Crabapple • Grape • Japanese maple • Peking cotoneaster • * JB populations overlap with flowering • ** JB populations overlap >alot< with flowering Japanese beetle traps are excellent for detecting presence of the insect in an area 9 Proposed Project for 2019 Repeat/Expand the 2008 Japanese beetle survey to establish the present situation in eastern Colorado 10 Should we now consider trying to introduce natural enemies of Japanese beetle into Colorado? Yes! Natural Enemies of Japanese Beetle Exist Elsewhere in the US • Paenibacillus popilliae (Milky spore) –Bacterium • Istocheta aldrichi* –Tachinid fly • Tiphia species* –Parasitic wasps • Ovavesicula popilliae* –Microsporidium (fungus) * Species involved in Colorado Japanese Beetle Biological Control Program Natural Enemies of Japanese Beetle for Potential Introduction into Colorado? Ovavesicula popilliae – a microsporidian disease of Japanese beetle larvae Ovavesicula infection of Malphighian tubules of Japanese beetle larva Main observed effects from infection – reduced fecundity, reduced winter survival The Malpighian tubules of insects filter wastes from the blood, functioning somewhat like what the kidney does in humans Heavy O. -
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 -
Specialization in Plant–Pollinator Networks
Villalobos et al. BMC Ecol (2019) 19:34 https://doi.org/10.1186/s12898-019-0250-z BMC Ecology RESEARCH ARTICLE Open Access Specialization in plant–pollinator networks: insights from local-scale interactions in Glenbow Ranch Provincial Park in Alberta, Canada Soraya Villalobos1* , José Manuel Sevenello‑Montagner2 and Jana C. Vamosi1 Abstract Background: The occurrence and frequency of plant–pollinator interactions are acknowledged to be a function of multiple factors, including the spatio‑temporal distribution of species. The study of pollination specialization by exam‑ ining network properties and more recently incorporating predictors of pairwise interactions is emerging as a useful framework, yet integrated datasets combining network structure, habitat disturbance, and phylogenetic information are still scarce. Results: We found that plant–pollinator interactions in a grassland ecosystem in the foothills of the Rocky Mountains are not randomly distributed and that high levels of reciprocal specialization are generated by biological constraints, such as foral symmetry, pollinator size and pollinator sociality, because these traits lead to morphological or pheno‑ logical mismatching between interacting species. We also detected that landscape degradation was associated with diferences in the network topology, but the interaction webs still maintained a consistently higher number of recip‑ rocal specialization cases than expected. Evidence for the reciprocal evolutionary dependence in visitors (e.g., related pollinators visiting related plants) were weak in this study system, however we identifed key species joining clustered units. Conclusions: Our results indicate that the conserved links with keystone species may provide the foundation for generating local reciprocal specialization. From the general topology of the networks, plant–pollinators interactions in sites with disturbance consisted of generalized nodes connecting modules (i.e., hub and numerous connectors). -
Benton County Prairie Species Habitat Conservation Plan
BENTON COUNTY PRAIRIE SPECIES HABITAT CONSERVATION PLAN DECEMBER 2010 For more information, please contact: Benton County Natural Areas & Parks Department 360 SW Avery Ave. Corvallis, Oregon 97333-1192 Phone: 541.766.6871 - Fax: 541.766.6891 http://www.co.benton.or.us/parks/hcp This document was prepared for Benton County by staff at the Institute for Applied Ecology: Tom Kaye Carolyn Menke Michelle Michaud Rachel Schwindt Lori Wisehart The Institute for Applied Ecology is a non-profit 501(c)(3) organization whose mission is to conserve native ecosystems through restoration, research, and education. P.O. Box 2855 Corvallis, OR 97339-2855 (541) 753-3099 www.appliedeco.org Suggested Citation: Benton County. 2010. Prairie Species Habitat Conservation Plan. 160 pp plus appendices. www.co.benton.or.us/parks/hcp Front cover photos, top to bottom: Kincaid’s lupine, photo by Tom Kaye Nelson’s checkermallow, photo by Tom Kaye Fender’s blue butterfly, photo by Cheryl Schultz Peacock larkspur, photo by Lori Wisehart Bradshaw’s lomatium, photo by Tom Kaye Taylor’s checkerspot, photo by Dana Ross Willamette daisy, photo by Tom Kaye Benton County Prairie Species HCP Preamble The Benton County Prairie Species Habitat Conservation Plan (HCP) was initiated to bring Benton County’s activities on its own lands into compliance with the Federal and State Endangered Species Acts. Federal law requires a non-federal landowner who wishes to conduct activities that may harm (“take”) threatened or endangered wildlife on their land to obtain an incidental take permit from the U.S. Fish and Wildlife Service. State law requires a non-federal public landowner who wishes to conduct activities that may harm threatened or endangered plants to obtain a permit from the Oregon Department of Agriculture. -
Japanese Beetles This Year Again Proposes for a Dramatic Increase in the Populations of Japanese Beetles
Japanese Beetles This year again proposes for a dramatic increase in the populations of Japanese beetles. These beetles can be very damaging in both their adult and larval stage. Beetles are approximately 3/4" long, and are easily distinguished by their blue/green//brown/silver color, which is shiny and makes them look like they are made out of metal. Typically they are unlike anything you are used to seeing. The most damaging and expensive injury caused by Japanese beetle is by its larval stage feeding on the roots of turf grass. Browning turf, in spotted areas, which can be pulled up in clumps is a sure sign. The less concerning, but most noticeable, damage occurs to the leaves of many different species of plants. Leaves will be eaten, with only the leaf veins remaining (looks similar to lace). Trees can be treated with a foliar application, which will only be effective for only a few days, an injected systemic insecticide, or by soil applied insecticide. The truly effective, and least costly, way to treat for beetles is not to treat the tree at all, but to eliminate them in the larval stage (in the soil). The beetles lay eggs in the soil, which over-winter and mature as grubs, which feed on grass and other roots. A turf grub control treatment in early to mid May will reduce and control the adult populations. It is very difficult to fully eliminate the beetles as they may reside in your neighbors turf as well. The solution is to take this information to your neighbors and institute a cooperative plan to treat the turf, and/or otherwise manage the pest in the spring. -
August, 2009 ======Enjoy the Rest of the Summer, and I Hope to See You August 7-10 at the Minor Orders Blitz at Schoodic Point
============================================================================================= Vol. 13, No. 3 August, 2009 =========================================================================================== Enjoy the rest of the summer, and I hope to see you August 7-10 at the Minor Orders Blitz at Schoodic Point. * * * * * Last Chance for Minor Order Blitz! (with dates for 2010 and 2011 Blitzes) The Acadia BioBlitz on August 7-10, for Minor Insect Orders (full details in the May issue of The Maine Entomologist and on our web site), is about full. BUT if you have a last- minute change of heart (or just procrastinated), and want to attend and participate, please contact Melissa Rice ASAP at Acadia Partners for Science and Learning, at 207-288-1326 or [email protected] . Writing is not one of my favorite activities and certainly not in the summer. But here I am, presenting some words of wisdom for the Summer of Rain, 2009. Collecting has been tough; it has to be squeezed in between rain - not just showers - but rain and cool weather. Planned days off, free afternoons, and weekend trips all are getting rained out this year. Collecting insects is more difficult and not as much fun in the wet. Last weekend I was at my camp in T4 R7 WELS and the storm clouds cleared off just before sunset. As dusk deepened we sat by the pond and watched the thousands of insects skittering across the water while the bats swooped across the water scooping up their prey. What surprised all of us was the lack of A veritable army of workers in the lab at last year's Bug Blitz mosquitoes.