(Diptera: Bibionidae) in Dominican Amber
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Distribution and Population Dynamics of the Asian Cockroach
DISTRIBUTION AND POPULATION DYNAMICS OF THE ASIAN COCKROACH (BLATTELLA ASAHINIA MIZUKUBO) IN SOUTHERN ALABAMA AND GEORGIA Except where reference is made to the work of others, the work described in this thesis is my own or was done in collaboration with my advisory committee. This thesis does not include proprietary or classified information. ___________________________________ Edward Todd Snoddy Certificate of Approval: ___________________________ ___________________________ Micky D. Eubanks Arthur G. Appel, Chair Associate Professor Professor Entomology and Plant Pathology Entomology and Plant Pathology ___________________________ ___________________________ Xing Ping Hu George T. Flowers Associate Professor Interim Dean Entomology and Plant Pathology Graduate School DISTRIBUTION AND POPULATION DYNAMICS OF THE ASIAN COCKROACH (BLATTELLA ASAHINIA MIZUKUBO) IN SOUTHERN ALABAMA AND GEORGIA Edward Todd Snoddy A Thesis Submitted to the Graduate Faculty of Auburn University in Partial Fulfillment of the Requirements for the Degree of Master of Science Auburn, Alabama May 10, 2007 DISTRIBUTION AND POPULATION DYNAMICS OF THE ASIAN COCKROACH (BLATTELLA ASAHINIA MIZUKUBO) IN SOUTHERN ALABAMA AND GEORGIA Edward Todd Snoddy Permission is granted to Auburn University to make copies of this thesis at its discretion, upon request of individuals or institutions and at their expense. The author reserves all publication rights. _______________________ Signature of Author _______________________ Date of Graduation iii VITA Edward Todd Snoddy was born in Auburn, Alabama on February 28, 1964 to Dr. Edward Lewis Snoddy and Lucy Mae Snoddy. He graduated Sheffield High School, Sheffield, Alabama in 1981. He attended Alexander Junior College from 1981 to 1983 at which time he transferred to Auburn University. He married Tracy Smith of Uchee, Alabama in 1984. -
Lovebug Plecia Nearcticahardy (Insecta: Diptera: Bibionidae)1 H
EENY 47 Lovebug Plecia nearcticaHardy (Insecta: Diptera: Bibionidae)1 H. A. Denmark, F. W. Mead, and T. R. Fasulo2 Introduction University of Florida entomologists introduced this species into Florida. However, Buschman (1976) documented the The lovebug, Plecia nearctica Hardy, is a bibionid fly species progressive movement of this fly species around the Gulf that motorists may encounter as a serious nuisance when Coast into Florida. Research was conducted by University traveling in southern states. It was first described by Hardy of Florida and US Department of Agriculture entomologists (1940) from Galveston, Texas. At that time he reported it to only after the lovebug was well established in Florida. be widely spread, but more common in Texas and Louisiana than other Gulf Coast states. Figure 1. Swarm of lovebugs, Plecia nearctica Hardy, on flowers. Credits: James Castner, UF/IFAS Figure 2. Adult lovebugs, Plecia nearctica Hardy, swarm on a building. Credits: Debra Young, used with permission Within Florida, this fly was first collected in 1949 in Escambia County, the westernmost county of the Florida panhandle. Today, it is found throughout Florida. With numerous variations, it is a widely held myth that 1. This document is EENY 47, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date August 1998. Revised April 2015. Reviewed February 2021. Visit the EDIS website at https://edis.ifas.ufl.edu for the lastest version of this publication. This document is also available on the Featured Creatures website at http://entnemdept.ifas.ufl.edu/creatures/. 2. H. A. Denmark, courtesy professor; F. -
Living with Lovebugs1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. ENY-840 Living With Lovebugs1 Norman C. Leppla2 The "lovebug," Plecia nearctica Hardy (Diptera: suborder Nematocera. Flies in the other suborder, Bibionidae), is a seasonally abundant member of a Brachycera, have five or fewer antennal segments. generally unnoticed family of small flies related to Some families of Nematocera contain pests of gnats and mosquitoes. The males are about 1/4 inch agriculture and vectors of pathogens that cause and the females 1/3 inch in length, both entirely black human and animal diseases, e.g., sand flies except for red on top of their thoraxes (middle insect (Psychodidae), mosquitoes (Culicidae), biting body segment). Other common names for this insect midges (Ceratopogonidae), black flies (Simuliidae), include March flies, double-headed bugs, honeymoon fungus gnats (Mycetophilidae) and gall midges flies, united bugs and some expletives that are not (Cecidomyiidae). Bibionids have antennae with repeatable. Lovebugs characteristically appear in seven to 12 segments and ocelli (simple eyes) on their excessive abundance throughout Florida as heads (Figure 2 A, a,o). Their wings each have an male-female pairs for only a few weeks every undivided medial cell, a costal vein (front of wing) April-May and August-September (IPM Florida that ends at or before the wing tip, a large anal area 2006). Although they exist over the entire state and two basal cells (Figure 2 E, mc, c, a, bc). All during these months, they can reach outbreak levels members of the genus Plecia have an upper branch to in some areas and be absent in others. -
Ecological Consequences Artificial Night Lighting
Rich Longcore ECOLOGY Advance praise for Ecological Consequences of Artificial Night Lighting E c Ecological Consequences “As a kid, I spent many a night under streetlamps looking for toads and bugs, or o l simply watching the bats. The two dozen experts who wrote this text still do. This o of isis aa definitive,definitive, readable,readable, comprehensivecomprehensive reviewreview ofof howhow artificialartificial nightnight lightinglighting affectsaffects g animals and plants. The reader learns about possible and definite effects of i animals and plants. The reader learns about possible and definite effects of c Artificial Night Lighting photopollution, illustrated with important examples of how to mitigate these effects a on species ranging from sea turtles to moths. Each section is introduced by a l delightful vignette that sends you rushing back to your own nighttime adventures, C be they chasing fireflies or grabbing frogs.” o n —JOHN M. MARZLUFF,, DenmanDenman ProfessorProfessor ofof SustainableSustainable ResourceResource Sciences,Sciences, s College of Forest Resources, University of Washington e q “This book is that rare phenomenon, one that provides us with a unique, relevant, and u seminal contribution to our knowledge, examining the physiological, behavioral, e n reproductive, community,community, and other ecological effectseffects of light pollution. It will c enhance our ability to mitigate this ominous envirenvironmentalonmental alteration thrthroughough mormoree e conscious and effective design of the built environment.” -
Evolution and Classification of Bibionidae (Diptera: Bibionomorpha)
AN ABSTRACT OF THE DISSERTATION OF Scott J. Fitzgerald for the degree of Doctor of Philosophy in Entomology presented on 3 June, 2004. Title: Evolution and Classification of Bibionidae (Diptera: Bibionomorpha). Abstract approved: Signature redacted forprivacy. p 1ff Darlene D. Judd The family Bibionidae has a worldwide distribution and includes approximately 700 species in eight extant genera. Recent studies have not produced compelling evidence supporting Bibionidae as a monophyletic group or identified the sister group to bibionids. Therefore, the purpose of this study is to examine the classification and evolution of the family Bibionidae in a cladistic framework. The study has four primary objectives: 1) test the monophyly of the family; 2) determine the sister group of Bibionidae; 3) examine generic and subfamilial relationships within the family; and 4) provide a taxonomic revision of the extant and fossil genera of Bibionidae. Cladistic methodology was employed and 212 morphological characters were developed from all life stages (adult, pupa, larva, and egg). Characters were coded as binary or multistate and considered equally weighted and unordered. A heuristic search with a multiple random taxon addition sequence was used and Bremer support values are provided to show relative branch support. A strict consensus of 43 equal-length trees of 1,106 steps indicates that the family Bibionidae is monophyletic and is sister group to Pachyneuridae. All bibionid genera are supported as monophyletic except for Bibio and Bibiodes (monophyly of the latter genus was not examined because only one exemplar was included). Results indicate that the subfamilies Hesperininae and Bibioninae are monophyletic and Pleciinae is paraphyletic. -
Timothy Alexander Mousseau
TIMOTHY ALEXANDER MOUSSEAU Curriculum Vitae – January 2020 Office Address University of South Carolina, Department of Biological Sciences, Columbia, SC 29208 USA PROFESSIONAL EXPERIENCE 2002- Professor of Biological Sciences 2019-20 SURA/NASA Visiting Scientist, Kennedy Space Center 2016-17 Visiting Professor (part-time), Chubu University (Nagoya, Japan) 2014-15 Visiting Professor (part-time), Chubu University (Nagoya, Japan) 2010-11 Associate Vice President for Research and Graduate Education 2010-11 Dean of the Graduate School 2006-10 Associate Dean for Research and Graduate Education, College of Arts and Sciences, USC 1999-2000 Visiting Professor, Université of Pierre et Marie Curie (Paris VI) 1998-2001 Chair, Graduate Program in Ecology, Evolution and Organismal Biology 1997-1998 Program Director, National Science Foundation (NSF)(Population Biology) 1996-1997 Chair, Graduate Program in Ecology, Evolution and Organismal Biology 1996-2008 Professor of Entomology (Adjunct), Clemson University 1996-2002 Associate Professor, USC 1991-1996 Assistant Professor, USC EDUCATION PDF University of California, Davis (1988-90), NSERC Postdoctoral Fellow Ph.D. McGill University (1988), Biology M.Sc. University of Toronto (1983), Zoology B.Sc.(Hons) University of Ottawa (1980), Biology (Cum Laude) B.Sc. University of Ottawa (1979), Biology Curriculum Vita – Timothy Mousseau HONORS AND AWARDS • Fellow, Royal Geographical Society (2020-) • Fellow, American Association for the Advancement of Sciences (2008-) • Fellow, American Council of Learned Societies -
Mcguire Center News, Vol
McGuire Center Florida Museum of Natural History April, 2008 Issue 2 UF University of Florida News In this issue: •Florida Entomological Center’s Exhibits: Society honors McGuires •Moths of Paynes Prairie Cast the Nets Broadly, but Aim High •Center in the News •Collection Donations The McGuire Center for Lepidoptera and electron microscope. •New Owl Butterfly Biodiversity is a place that truly illustrates Outside the Rainforest, the live exhibit •Grants and Awards the popular saying: “It takes all kinds to continues in the form of a recently added make the world.” Florida Wildflower and Butterfly Garden. •The Butterfly From scientists, obsessed with the number Not only butterflies, but frogs, lizards, Conservation Initiative of setae, the shape of the uncus, or the and birds are at home here. One resident, •Seminars, Visiting position of androconia (go Google it, if you a perfectly harmless black racer snake, is Scientists, and Meetings want!), to educators and horticulturalists, we often seen sunning itself in this garden. are all housed under the same roof (though Indoors, there is the world’s largest •Museum’s Expeditions a few are under a screen, which does not museum exhibit on butterfly and moth •Recent Publications keep out sun or rain). Different as we might diversity. The Wall of Wings tells at one •Where is Bob? be, we are all united by the same purpose, glance the story of diversity and beauty, •ButterflyFest the purpose of changing the future. which is epitomized by the Lepidoptera. •Butterfliesofamerica.com One might say that the future is not yet It also tells a story of the passion that here, but unfortunately that is only partially people have for butterflies, which is often true. -
Norman C. Leppla Professor
Norman C. Leppla Professor Contact University of Florida Entomology and Nematology Dept. Building 970, Natural Area Dr. (Steinmetz Hall) Gainesville, FL 32611 Email: [email protected] Phone: (352) 392-2484 (50% Research, 45% Extension, 5% Teaching) Education B.S., Arizona State University (Zoology), 1968 M.S., Arizona State University (Zoology), 1970 Ph.D., University of Arizona (Entomology/ Biological Sciences), 1972 Relevant Employment History Professor and IPM Coordinator (2001-present), University of Florida. Professor (1999-2001), University of Florida. Professor and Center Director (1997-1998), University of Florida. Associate Director (1995-1996), USDA, APHIS, National Biological Control Institute. Chief (1992-1994), USDA, APHIS, Plant Protection and Quarantine, Methods Development. Director (1989-1992), USDA, APHIS, Science and Technology, Methods Development. Research Leader (1988-1989), USDA, ARS, Biological Control of Pests Research Lab. Research Entomologist (1972 - 1988), USDA, ARS, Insect Attractants, Behavior, and Basic Biology Research Laboratory. Faculty Position Description Conduct integrated pest management (IPM) and biological control research, extension and education Identify, develop and implement new pest management technologies in collaboration with public and private organizations Establish partnerships among international, national, state and private sector organizations to resolve technical problems in implementing IPM and biological control Develop entrepreneurial initiatives that advance IPM and biological control, -
Biography of D. Elmo Hardy (1914-2002)1
D. Elmo Hardy Memorial Volume. Contributions to the Systematics 1 and Evolution of Diptera. Edited by N.L. Evenhuis & K.Y. Kaneshiro. Bishop Museum Bulletin in Entomology 12: 1–11 (2004). Biography of D. Elmo Hardy (1914-2002)1 NEAL L. EVENHUIS J. Linsley Gressitt Center for Entomological Research, Bishop Museum, 1525 Bernice Street, Honolulu, Hawai‘i 96817-2704, USA; email: [email protected] Introduction D. Elmo Hardy, “Elmo” to all who knew him personally, was one of the last polymaths in Diptera systematics. His knowledge of Diptera families spanned the order from Nematocera (specializing in Bibionidae), through to the Brachycera (specializing in the families Pipunculidae, Drosophilidae, and Tephritidae). He expanded his knowledge of the systematics to many other Diptera families through his monumental efforts in producing 5 volumes of Diptera for the “Insects of Hawaii” series where he described 581 species in no less than 20 families in the 30 years it took to conduct that research and produce those volumes. He coordinated the cataloging of the Diptera of the Oriental Region in the 1970s, the first and only comprehensive catalog from that region. He helped start the Hawaiian Drosophila project in 1963 which, with the help of numerous collaborators, increased the systematic and genetic knowledge of and stimulated world interest in a group of flies that exhibits one of the most explosive speciation and adaptive radiations of any animal on Earth—the genus Drosophila having upwards of 800 species known only from a tiny group of volcanic islands in the middle of the Pacific. In his almost 70 years of work on flies, he described 1,867 species in 34 dif- ferent families of Diptera. -
Lovebug Plecia Nearctica Hardy (Insecta: Diptera: Bibionidae)1 H
EENY 47 Lovebug Plecia nearctica Hardy (Insecta: Diptera: Bibionidae)1 H. A. Denmark, F. W. Mead, and T. R. Fasulo2 Introduction into Florida. However, Buschman (1976) documented the progressive movement of this fly species around the Gulf The lovebug, Plecia nearctica Hardy, is a bibionid fly species Coast into Florida. Research was conducted by University that motorists may encounter as a serious nuisance when of Florida and US Department of Agriculture entomologists traveling in southern states. It was first described by Hardy only after the lovebug was well established in Florida. (1940) from Galveston, Texas. At that time he reported it to be widely spread, but more common in Texas and Louisiana than other Gulf Coast states. Figure 1. Swarm of lovebugs, Plecia nearctica Hardy, on flowers. Figure 2. Adult lovebugs, Plecia nearctica Hardy, swarm on a building. Credits: James Castner, UF/IFAS Credits: Debra Young, used with permission Within Florida, this fly was first collected in 1949 in Classification Escambia County, the westernmost county of the Florida panhandle. Today, it is found throughout Florida. With Thompson (1975) reported over 200 species in the genus numerous variations, it is a widely held myth that Uni- Plecia. However, there are only two species of Plecia in versity of Florida entomologists introduced this species the US—Plecia nearctica and Plecia americana Hardy. Their ranges are similar, but Plecia americana extends 1. This document is EENY 47, one of a series of the Department of Entomology and Nematology, UF/IFAS Extension. Original publication date August 1998. Revised April 2015. Reviewed April 2018. Visit the EDIS website at http://edis.ifas.ufl.edu. -
Luring and Trapping Love Bugs, Plecia Nearctica (Diptera: Bibionidae), Using Various Food Attractants
Luring and Trapping Love Bugs, Plecia nearctica (Diptera: Bibionidae), Using Various Food Attractants Hanson, M., Diaz, E., Pellacani, J., Armbrister, S., Mohiuddin, H. Edited by Thai Vu Texas A&M University—College Station Abstract: It’s no secret that food left outside will attract various species of nuisance insects. What becomes an even bigger problem is when there are swarms of hundreds to thousands of insects already out and about during their mating flight. This is the case in a certain nuisance species called the Love Bug, or Plecia nearctica (D.E. Hardy) (Diptera: Bibionidae). They are abundant some times of the year in Texas and other areas in the South. This experiment was conducted in order to see if specific food sources could be used as a valid trapping method to lure this species. Five food samples were used to test the attraction of the love bug. These samples were salt water, Coca-Cola, pineapples, apple cider vinegar, and peaches. Salt water was set as the control. The fruit samples were chosen because they reflect what may be found in nature. Coca-Cola was chosen because it is a common drink that insects may encounter in urban areas. The love bugs would be attracted to the Coca-Cola the most because it has the highest sugar content. The purpose of this study was to determine what substance best attracts these nuisance species in order to trap them and prevent them from multiplying, and therefore prevent them from surfacing in large numbers. These samples were then placed outside in containers for four days. -
True Flies (Insecta: Diptera) from The
Earth and Environmental Science Transactions of the Royal Society of Edinburgh, 1–60, 2019 True flies (Insecta: Diptera) from the late Eocene insect limestone (Bembridge Marls) of the Isle of Wight, England, UK Wiesław KRZEMIN´ SKI1*, Vladimir BLAGODEROV2, Dany AZAR3, Elena LUKASHEVICH4, Ryszard SZADZIEWSKI5, Sonja WEDMANN6, Andre´ NEL7, Franc¸ois-Marie COLLOMB7, Alain WALLER7 and David B. NICHOLSON8 1 Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Ul. Sławkowska 17, 31-016 Krako´w, Poland. Email: [email protected] 2 Department of Natural Sciences, National Museums Scotland, Chambers St., Edinburgh EH1 1JF, UK. 3 Department of Biology, Faculty of Sciences II, Lebanese University, Fanar – Matn, P. O. box 26110217, Lebanon. 4 Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya Str. 123, 117868 Moscow, Russia. 5 Department of Invertebrate Zoology, University of Gdan´sk, Pilsudskiego 46, 81-378 Gdynia, Poland. 6 Senckenberg Research Institute and Museum, Research station Grube Messel, Markstraße 35, D-64409 Messel, Germany. 7 CNRS UMR 5202, Muse´um National d’Histoire Naturelle, CP 50, Entomologie, 45 rue Buffon, F-75005, Paris, France. 8 School of Earth and Environmental Sciences, University of Portsmouth, Burnaby Road, Portsmouth PO1 3QL, UK. *Corresponding author. ABSTRACT: The Diptera fauna from the late Eocene of the Isle of Wight (Bembridge Marls) is studied including redescriptions of formerly described material. The fauna includes the following taxa: Anisopodidae – one species; Bibionidae – 11 species; Ceratopogonidae – one described and two unidentified species; Chironomidae – undetermined species of three subfamilies; Culicidae – four species; Cylindrotomidae – one species; Dixidae – one species; Keroplatidae – one described and four unidentified species; Limoniidae – 31 species; Mycetophilidae – 14 species; Psychodidae – two species; Scatopsidae – two species; Sciaridae – three species; Simuliidae – an unnamed species; Tipulidae – nine species.