2019 Entomology Program Highlights
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Cerambycidae of Tennessee
Cerambycidae of Tennessee! Disteniinae: Disteniini! Parandrinae: Parandriini! Closed circles represent previously published county records, museum specimen records, and specimens examined. Open circles are county records reported in Jamerson (1973) for which a specimen could not be located. Future collections are needed to substantiate these accounts. Fig. 2. Elytrimitatrix (Elytrimitatrix) undata (F.)! Fig. 3. Neandra brunnea (F.)! Prioninae: Macrotomini! Prioninae: Meroscheliscini! Fig. 4. Archodontes melanoplus melanoplus (L.)! Fig. 5. Mallodon dasystomus dasystomus Say! Fig. 6. Tragosoma harrisii (LeConte)! Prioninae: Prionini! Fig. 7. Derobrachus brevicollis Audinet-Serville! Fig. 8. Orthosoma brunneum (Forster)! Fig. 9. Prionus (Neopolyarthron) imbricornis (L.)! Prioninae! : Solenopterini! Fig. 10. Prionus (Prionus) laticollis (Drury) ! Fig. 11. Prionus (Prionus) pocularis Dalman ! Fig. 12. Sphenosethus taslei (Buquet) ! Necydalinae: Necydalini! Spondylidinae: Asemini! Fig. 13. Necydalis melitta (Say)! Fig. 14. Arhopalus foveicollis (Haldeman)! Fig. 15. Arhopalus rusticus obsoletus (Randall)! ! ! Suppl. Figs. 2-15. Tennessee county collection localities for longhorned beetle (Cerambycidae) species: Disteniinae, Parandrinae, Prioninae, Necydalinae, Spondylinae: Asemini (in part). ! Spondylidinae: Asemini (ctd.)! Fig. 16. Asemum striatum (L.)! Fig. 17. Tetropium schwarzianum Casey! Fig. 18. Atimia confusa confusa (Say)! ! Spondylidinae: Saphanini! Lepturinae: Desmocerini! Lepturinae: Encyclopini! Fig. 19. Michthisoma heterodoxum LeConte -
5 Chemical Ecology of Cerambycids
5 Chemical Ecology of Cerambycids Jocelyn G. Millar University of California Riverside, California Lawrence M. Hanks University of Illinois at Urbana-Champaign Urbana, Illinois CONTENTS 5.1 Introduction .................................................................................................................................. 161 5.2 Use of Pheromones in Cerambycid Reproduction ....................................................................... 162 5.3 Volatile Pheromones from the Various Subfamilies .................................................................... 173 5.3.1 Subfamily Cerambycinae ................................................................................................ 173 5.3.2 Subfamily Lamiinae ........................................................................................................ 176 5.3.3 Subfamily Spondylidinae ................................................................................................ 178 5.3.4 Subfamily Prioninae ........................................................................................................ 178 5.3.5 Subfamily Lepturinae ...................................................................................................... 179 5.4 Contact Pheromones ..................................................................................................................... 179 5.5 Trail Pheromones ......................................................................................................................... 182 5.6 Mechanisms for -
Species Richness and Phenology of Cerambycid Beetles in Urban Forest Fragments of Northern Delaware
ECOLOGY AND POPULATION BIOLOGY Species Richness and Phenology of Cerambycid Beetles in Urban Forest Fragments of Northern Delaware 1 1,2 3 4 5 K. HANDLEY, J. HOUGH-GOLDSTEIN, L. M. HANKS, J. G. MILLAR, AND V. D’AMICO Ann. Entomol. Soc. Am. 1–12 (2015); DOI: 10.1093/aesa/sav005 ABSTRACT Cerambycid beetles are abundant and diverse in forests, but much about their host rela- tionships and adult behavior remains unknown. Generic blends of synthetic pheromones were used as lures in traps, to assess the species richness, and phenology of cerambycids in forest fragments in north- ern Delaware. More than 15,000 cerambycid beetles of 69 species were trapped over 2 yr. Activity periods were similar to those found in previous studies, but many species were active 1–3 wk earlier in 2012 than in 2013, probably owing to warmer spring temperatures that year. In 2012, the blends were tested with and without ethanol, a host plant volatile produced by stressed trees. Of cerambycid species trapped in sufficient numbers for statistical analysis, ethanol synergized pheromone trap catches for seven species, but had no effect on attraction to pheromone for six species. One species was attracted only by ethanol. The generic pheromone blend, especially when combined with ethanol, was an effective tool for assessing the species richness and adult phenology of many cerambycid species, including nocturnal, crepuscular, and cryptic species that are otherwise difficult to find. KEY WORDS Cerambycidae, attractant, phenology, forest fragmentation Cerambycid beetles can be serious pests of forest trees long as those in Europe, almost half of the forests in the and wood products (Speight 1989, Solomon 1995). -
Coleoptera: Cerambycidae)
PHEROMONE CHEMISTRY AND REPRODUCTIVE ISOLATION IN THE SUBFAMILY LAMIINAE (COLEOPTERA: CERAMBYCIDAE) BY LINNEA R. MEIER DISSERTATION Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology in the Graduate College of the University of Illinois at Urbana-Champaign, 2018 Urbana, Illinois Doctoral Committee: Professor Lawrence M. Hanks, Chair, Director of Research Professor May R. Berenbaum Professor Andrew V. Suarez Associate Professor Brian F. Allan ABSTRACT Research on the chemical ecology of cerambycid beetles has revealed that the pheromone chemistry of related species is often highly conserved. Sympatric species often share pheromone components, even having identical attractant pheromones. For example, many cerambycines native to different continents use pheromones composed of hydroxyalkanones and related alkanediols. Avoidance mechanisms of interspecific attraction in cerambycines that share pheromone components include segregation by seasonal and diel phenology and synergism and antagonism by minor pheromone components. Less is known about the pheromone chemistry of cerambycid species in the largest subfamily, the Lamiinae. As with the cerambycines, all known pheromones of lamiines are male-produced aggregation-sex pheromones, and pheromone chemistry has been conserved across continents. Lamiine pheromones identified to date are based on either hydroxyethers or terpenoids. The purpose of my dissertation research is to broaden the current understanding of pheromone chemistry in lamiines and to elucidate chemical mechanisms of reproductive isolation among sympatric species that share pheromone components. In Chapter 1, I summarize what is known about the pheromone chemistry of cerambycids, with emphasis on the subfamily Lamiinae. In Chapter 2, I identify the pheromone composition for two species of lamiines common in East-Central Illinois. -
Predator to Prey to Poop: Bats As Microbial Hosts and Insectivorous Hunters
Predator to Prey to Poop: Bats as Microbial Hosts and Insectivorous Hunters A Thesis SUBMITTED TO THE FACULTY OF THE UNIVERSITY OF MINNESOTA BY Miranda Galey IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE Dr. Ron Moen, Dr. Jessica R. Sieber September 2020 Copyright © Miranda Galey 2020 Abstract Bat fecal samples are a rich source of ecological data for bat biologists, entomologists, and microbiologists. Feces collected from individual bats can be used to profile the gut microbiome using microbial DNA and to understand bat foraging strategies using arthropod DNA. We used eDNA collected from bat fecal samples to better understand bats as predators in the context of their unique gut physiology. We used high through- put sequencing of the COI gene and 16S rRNA gene to determine the diet composition and gut microbiome composition of three bat species in Minnesota: Eptesicus fuscus, Myotis lucifugus and M. septentrionalis. In our analysis of insect prey, we found that E. fuscus consistently foraged for a higher diversity of beetle species compared to other insects. We found that the proportional frequency of tympanate samples from M. septentrionalis and M. lucifugus was similar, while M. septentrionalis consistently preyed more often upon non-flying species. We used the same set of COI sequences to determine presence of pest species, rare species, and insects not previously observed in Minnesota. We were able to combine precise arthropod identification and the for- aging areas of individually sampled bats to observe possible range expansion of some insects. The taxonomic composition of the bat gut microbiome in all three species was found to be consistent with the composition of a mammalian small intestine. -
Host Volatile Percepts of Two Sympatric Longhorned Beetles, Anoplophora Chinensis and Anoplophora Glabripennis
SUNY College of Environmental Science and Forestry Digital Commons @ ESF Dissertations and Theses Spring 4-1-2020 Host Volatile Percepts of Two Sympatric Longhorned Beetles, Anoplophora Chinensis and Anoplophora Glabripennis Laura Hansen SUNY College of Environmental Science and Forestry, [email protected] Follow this and additional works at: https://digitalcommons.esf.edu/etds Part of the Environmental Monitoring Commons Recommended Citation Hansen, Laura, "Host Volatile Percepts of Two Sympatric Longhorned Beetles, Anoplophora Chinensis and Anoplophora Glabripennis" (2020). Dissertations and Theses. 153. https://digitalcommons.esf.edu/etds/153 This Open Access Dissertation is brought to you for free and open access by Digital Commons @ ESF. It has been accepted for inclusion in Dissertations and Theses by an authorized administrator of Digital Commons @ ESF. For more information, please contact [email protected], [email protected]. HOST VOLATILE PERCEPTS OF TWO SYMPATRIC LONGHORNED BEETLES, ANOPLOPHORA CHINENSIS AND ANOPLOPHORA GLABRIPENNIS by Laura Hansen A dissertation submitted in partial fulfillment of the requirements for the Doctor of Philosophy Degree State University of New York College of Environmental Science and Forestry Syracuse, New York April 2020 Department of Environmental and Forest Biology Approved by: Stephen Teale, Major Professor Mary Collins, Chair, Examining Committee Melissa Fierke, Department Chair S. Scott Shannon, The Graduate School ©2020 Copyright L.E. Hansen All rights reserved ACKNOWLEDGMENTS I would like to thank my major professor. Steve is a constant source of encouragement and guidance. It is impossible to meet with him without being impressed by his immense expertise and experience in every topic related to my project – from entomology to statistics to chemical analysis. -
Blends of Pheromones, with and Without Host Plant Volatiles, Can Attract Multiple Species of Cerambycid Beetles Simultaneously
Blends of pheromones, with and without host plant volatiles, can attract multiple species of cerambycid beetles simultaneously Hanks, L. M.,1* J. A. Mongold-Diers,1 T. H. Atkinson,2 M. K. Fierke,3 M. D. Ginzel,4 E. E. Graham,5† T. M. Poland,6 A. B. Richards,7 M. L. Richardson,8 and J. G. Millar9 1Department of Entomology, University of Illinois at Urbana-Champaign, Urbana, IL 61801 2University of Texas Collection, Lake Austin Center, Austin, TX 78703 3Department of Environmental and Forest Biology, State University of New York, Syracuse, NY 13210 4Department of Entomology, Purdue University, West Lafayette, IN 47907 5Department of Entomology, Michigan State University, East Lansing MI 48824 6USDA Forest Service, Lansing, MI 48910 7Aquatic Bioassessment Laboratory, California State University, Chico, CA 95929 8College of Agriculture, Urban Sustainability, and Environmental Sciences, University of the District of Columbia, Washington, DC 20008 9Department of Entomology, University of California, Riverside, CA 92521 Supplementary material Table S1. Taxonomy of cerambycid beetles, and numbers of specimens trapped during two field experiments conducted at study sites in the various areas of the USA presented in Table 1. Taxonomy NY MI IN FL TX CA Total CERAMBYCIDAE Cerambycinae Agallissini Zagymnus clerinus (LeConte) 1 1 Anaglyptini Cyrtophorus verrucosus (Olivier) 33 3 125 161 Bothriospilini Knulliana c. cincta (Drury) 2 2 Callichromatini Plinthocoelium s. suaveolens (L.) 1 1 Callidiini Phymatodes aereus (Newman) 22 20 42 Phymatodes amoenus (Say) 12 382 394 Phymatodes dimidiatus (Kirby) 22 22 Phymatodes grandis Casey 1 1 Phymatodes nitidus LeConte 6 6 Phymatodes testaceus (L.) 21 1 6 28 Phymatodes varius (F.) 8 8 Physocnemum brevilineum (Say) 1 1 Clytini Clytoleptus albofasciatus (Laporte & Gory) 1 1 Clytus marginicollis Laporte & Gory 1 1 Clytus ruricola (Olivier) 85 2 11 98 Megacyllene caryae (Gahan) 1 134 135 Neoclytus a. -
Butterflies of North America
Insects of Western North America 4. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. Part 3 Chapter 1 Survey of Spiders (Arachnida, Araneae) of Fort Sill, Comanche Co., Oklahoma Chapter 2 Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. III. Arachnida: Ixodidae, Scorpiones, Hexapoda: Ephemeroptera, Hemiptera, Homoptera, Coleoptera, Neuroptera, Trichoptera, Lepidoptera, and Diptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University 1 Cover Photo Credits: The Black and Yellow Argiope, Argiope aurantia Lucas, (Photo by P.E. Cushing), a robber fly Efferia texana (Banks) (Photo by C. Riley Nelson). ISBN 1084-8819 Information about the availability of this publication and others in the series may be obtained from Managing Editor, C.P. Gillette Museum of Arthropod Ddiversity, Department of Bbioagricultural Sciences and Pest Management, Colorado State University, Ft. Collins, CO 80523-1177 2 Insects of Western North America 4. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. III Edited by Paul A. Opler Chapter 1 Survey of Spiders (Arachnida, Araneae) of Fort Sill, Comanche Co., Oklahoma by Paula E. Cushing and Maren Francis Department of Zoology, Denver Museum of Nature and Science Denver, Colorado 80205 Chapter 2 Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. III. Arachnida: Ixodidae, Scorpiones, Hexapoda: Ephemeroptera, Hemiptera, Homoptera, Coleoptera, Neuroptera, Trichoptera, Lepidoptera, and Diptera by Boris C. Kondratieff, Jason P. Schmidt, Paul A. Opler, and Matthew C. Garhart C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 January 2005 Contributions of the C.P. -
Food Webs 18 (2019) E00112
Food Webs 18 (2019) e00112 Contents lists available at ScienceDirect Food Webs journal homepage: www.journals.elsevier.com/food-webs Trophic interactions among dead-wood-dependent forest arthropods in the southern Appalachian Mountains, USA R.C. Garrick a,⁎, D.K. Reppel a, J.T. Morgan a, S. Burgess a, C. Hyseni a, R.J. Worthington a, M.D. Ulyshen b a Department of Biology, University of Mississippi, Oxford, MS 38677, USA b USDA Forest Service, Southern Research Station, Athens, GA 30602, USA article info abstract Article history: Food webs based on dead organic matter have received relatively little research attention. Here we focus dead- Received 8 June 2018 wood-dependent (saproxylic) arthropod communities—an overlooked component of forest biodiversity that Received in revised form 16 November 2018 contributes to decomposition of fallen trees and nutrient cycling. First, we summarized information on factors Accepted 11 December 2018 that impact saproxylic arthropod biodiversity via a descriptive mini-review of the literature, given that the struc- ture of food webs should be contingent upon local community composition, species richness, and/or species Keywords: fi Appalachian Mountains abundances within and among neighboring rotting logs. Next, we coupled intensive eldwork with molecular fi Dead wood approaches to taxonomic identi cation of saproxylic arthropods sampled from rotting logs in the southern Appa- Food web lachian Mountains, and synthesized information on their feeding ecology, in order to infer trophic interactions. Mitochondrial DNA Our mini-review highlighted major influences of local-scale (site-specific) factors affecting biodiversity, and by Molecular taxonomic assignment extension, food web structure; a pronounced publication bias toward saproxylic beetles from evergreen forests Saproxylic in Europe was also evident. -
Asian Longhorned Beetle (Coleoptera: Cerambycidae), an Introduced Pest of Maple and Other Hardwood Trees in North America and Europe P
Journal of Integrated Pest Management PROFILES Asian Longhorned Beetle (Coleoptera: Cerambycidae), an Introduced Pest of Maple and Other Hardwood Trees in North America and Europe P. S. Meng,1 K. Hoover,1 and M. A. Keena2,3 1Department of Entomology and Center for Chemical Ecology, The Pennsylvania State University, 501 ASI Bldg., University Park, PA 16802. 2U.S. Forest Service, Northern Research Station, 51 Mill Pond Rd., Hamden, CT 06514. 3Corresponding author, e-mail: [email protected]. J. Integ. Pest Mngmt. (2015) 6(1): 4; DOI: 10.1093/jipm/pmv003 The use of trade, firm, or corporation names in this publication is for the information and convenience of the reader. Such use does not constitute an official en- dorsement or approval by the U.S. Department of Agriculture or the Forest Service of any product or service to the exclusion of others that may be suitable. ABSTRACT. The Asian longhorned beetle, Anoplophora glabripennis (Motschulsky), threatens urban and forest hardwood trees both where introduced and in parts of its native range. Native to Asia, this beetle has hitchhiked several times in infested wood packaging used in international trade, and has established breeding populations in five U.S. states, Canada, and at least 11 countries in Europe. It has a broad host range for a cerambycid that attacks living trees, but in the introduced ranges it prefers maples. Identification, classifi- cation, and life history of this insect are reviewed here. Eradication is the goal where it has been introduced, which requires detection of infested trees using several approaches, including ground and tree-climbing surveys. -
Chromosome Numbers of Coleoptera*
CHROMOSOME NUMBERS OF COLEOPTERA* STANLEY G. SMITH Forest Insect Laboratory, Sault Ste. Marie, Ontario Received 7.vi.52 THE present is a complete list of the chromosome numbers of Coleoptera. That in Makino's (I95I) An Atlas of the Chromosome Numbers in Animals is replete with errors : not in the numbers themselves -almost without exception, these have been faithfully recorded from the originals-but in the spelling of the specific, generic, and family names, as well as in the nomenclature and systematic disposition of many of the species. f Considering the difficulties with which Makino was faced, the coverage of the literature is good, perhaps no more than I4 determinations by nine authors being omitted. I had earlier intended to compile a list of some I6o chromosome determinations, which I have made as time permitted during the course of the past eight years, together with others that have appeared in print, and to publish them as a supplement bringing those given by Harvey (Igi6 and Ig2o) up to date, but it now appears that a complete revision of Makino's list is warranted. It is perhaps note worthy that II families find themselves represented for the first time and that the total of cytologically known Coleoptera now reaches 340. According to Makino's tabulation, this number is surpassed among Insecta only in the Orthoptera and Heteroptera but in no other animal group, and constitutes approximately IO per cent. of the species of animals whose chromosome numbers have been recorded. The distribution of species, genera, subfamilies, and families by haploid number of autosomes and by sex-chromosome type is given graphically in fig. -
Newsletter of the Michigan Entomological Society
Newsletter of the Michigan Entomological Society Volume 57, Numbers 1 & 2 June 2012 Inside this Issue: 58th Annual MES Meeting: June 22-23, 2012 Martinoptera ... 2-3 David C. Houghton, MES President-Elect Little Bug, a Poem ... 3 Department of Biology, Hillsdale College, 33 East College Street, Hillsdale, MI 49242 Email: [email protected] Experiences with Tabanids ... 4 MES Governing Board Minutes The 2012 MES annual conference will take place on 22-23 June at the G.H. Gordon ... 4 - 5 Biological Station and Rockwell Lake Lodge (http://www.therockwelllakelodge.com), lo- Michigan Butterflies & Skippers cated in Lake County approximately 25 miles Under New Management ... 5 southeast of Cadillac. This is the largest pri- vate college biological station in Michigan, Collecting Gray Petaltails ... 6 - 7 combining an active research station with a functioning resort and conference center. The Michigan Odonata Atlas ... 7 The property features a 50-acre lake with good fishing. There are kayaks, canoes, and other boats available for attendees to use free of charge. The property also contains Michigan Mosquitoes ... 8 - 9 a small creek, upland forest, meadows, and various types of wetland habitats. There are also several miles of interpretive hiking trails. Insect collecting is encouraged. Trapping Cerambycids ... 10 - 11 Elegant rooms for 1–2 people at the Lodge are available at $79.00 per night (which includes breakfast). Beds in the cabins are available for $15.00 per night. Meals can Hemlock Woolly Adelgid in MI 12 also be purchased in any combination from the Lodge. All lodging options include free Wi-Fi. Registration details were mailed to all members and can be found on the MES Restoring Savanna Ecosystems 13 website.