Indoor Flies and Their Control Michael Merchant*
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Curriculum Vitae
CURRICULUM VITAE M. Lee Goff Home Address: 45-187 Namoku St. Kaneohe, Hawaii 96744 Telephone (808) 235-0926 Cell (808) 497-9110 email: [email protected] Date of Birth: 19 Jan. 1944 Place of Birth: Glendale California Military Status: U.S. Army, 2 years active duty 1966-68 Education: University of Hawaii at Manoa; B.S. in Zoology 1966 California State University, Long Beach; M.S. in Biology 1974 University of Hawaii at Manoa; Ph.D. in Entomology 1977 Professional Experience: 1964 - 1966. Department of Entomology, B.P. Bishop Museum, Honolulu. Research Assistant (Diptera Section). 1968 - 1971. Department of Entomology, B.P. Bishop Museum, Honolulu. Research Assistant (Acarology Section). 1971 -1971. International Biological Program, Hawaii Volcanoes National Park. Site Manager for IBP field station. 1971 - 1974. Department of Biology, California State University, Long Beach. Teaching Assistant and Research Assistant. 1974 - 1974. Kaiser Hospital, Harbor City,California. Clinical Laboratory Assistant (Parasitology and Regional Endocrinology Laboratory). 1974 - 1977. Department of Entomology, University of Hawaii at Manoa, Honolulu. Teaching Assistant. 1977 - 1983. Department of Entomology, B.P. Bishop Museum, Honolulu. Acarologist. 1983 - 2001. Department of Entomology, University of Hawaii at Manoa, Honolulu. Professor of Entomology. 1977 - present. Curatorial responsibility for National Chigger Collection of U.S. National Museum of Natural History/Smithsonian Institution. 1986 -1992. Editorial Board, Bulletin of the Society of Vector Ecologists. 1986 - present. Department of the Medical Examiner, City & County of Honolulu. Consultant in forensic entomology. 1986 - 1993. State of Hawaii, Natural Area Reserves System Commission. Commissioner and Chair of Commission. 1989 – 2006 Editorial Board, International Journal of Acarology. 1992 - present. -
Insects Commonly Mistaken for Mosquitoes
Mosquito Proboscis (Figure 1) THE MOSQUITO LIFE CYCLE ABOUT CONTRA COSTA INSECTS Mosquitoes have four distinct developmental stages: MOSQUITO & VECTOR egg, larva, pupa and adult. The average time a mosquito takes to go from egg to adult is five to CONTROL DISTRICT COMMONLY Photo by Sean McCann by Photo seven days. Mosquitoes require water to complete Protecting Public Health Since 1927 their life cycle. Prevent mosquitoes from breeding by Early in the 1900s, Northern California suffered MISTAKEN FOR eliminating or managing standing water. through epidemics of encephalitis and malaria, and severe outbreaks of saltwater mosquitoes. At times, MOSQUITOES EGG RAFT parts of Contra Costa County were considered Most mosquitoes lay egg rafts uninhabitable resulting in the closure of waterfront that float on the water. Each areas and schools during peak mosquito seasons. raft contains up to 200 eggs. Recreational areas were abandoned and Realtors had trouble selling homes. The general economy Within a few days the eggs suffered. As a result, residents established the Contra hatch into larvae. Mosquito Costa Mosquito Abatement District which began egg rafts are the size of a grain service in 1927. of rice. Today, the Contra Costa Mosquito and Vector LARVA Control District continues to protect public health The larva or ÒwigglerÓ comes with environmentally sound techniques, reliable and to the surface to breathe efficient services, as well as programs to combat Contra Costa County is home to 23 species of through a tube called a emerging diseases, all while preserving and/or mosquitoes. There are also several types of insects siphon and feeds on bacteria enhancing the environment. -
Diptera: Psychodidae) of Northern Thailand, with a Revision of the World Species of the Genus Neotelmatoscopus Tonnoir (Psychodinae: Telmatoscopini)" (2005)
Masthead Logo Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1-1-2005 A review of the moth flies D( iptera: Psychodidae) of northern Thailand, with a revision of the world species of the genus Neotelmatoscopus Tonnoir (Psychodinae: Telmatoscopini) Gregory Russel Curler Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Recommended Citation Curler, Gregory Russel, "A review of the moth flies (Diptera: Psychodidae) of northern Thailand, with a revision of the world species of the genus Neotelmatoscopus Tonnoir (Psychodinae: Telmatoscopini)" (2005). Retrospective Theses and Dissertations. 18903. https://lib.dr.iastate.edu/rtd/18903 This Thesis is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. A review of the moth flies (Diptera: Psychodidae) of northern Thailand, with a revision of the world species of the genus Neotelmatoscopus Tonnoir (Psychodinae: Telmatoscopini) by Gregory Russel Curler A thesis submitted to the graduate faculty in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Major: Entomology Program of Study Committee: Gregory W. Courtney (Major Professor) Lynn G. Clark Marlin E. Rice Iowa State University Ames, Iowa 2005 Copyright © Gregory Russel Curler, 2005. All rights reserved. 11 Graduate College Iowa State University This is to certify that the master's thesis of Gregory Russel Curler has met the thesis requirements of Iowa State University Signatures have been redacted for privacy Ill TABLE OF CONTENTS LIST OF FIGURES .............................. -
IV. Sandflies and Midges - Psychodidae and Ceratopogonidae
IV. Sandflies and Midges - Psychodidae and Ceratopogonidae 1. PARASITES RICKETTSIAE Grubyella ochoterenai Culicoides phlebotomus (exposed adults died, exhibiting Ricksettia sp. fungal outgrowths) (Ciferri, 1929). Phlebotomus vexator (in gonads) (Hertig, 1936). Penicillium glaucum P. papatasii (killed larvae in the laboratory) (Zotov, 1930). BACTERIA PROTOZOA Bacteria Ceratopogonidae (larvae) 1 (Mayer, 1934). (1) MASTIGOPHORA Culicoides nubeculosus (in fat body of larvae) (Lawson, 1951). Crithidia sp. C. nubeculosus (Steinhaus, 1946). P. baghdadis (Adler & Theodor, 1929). Pseudomonas sp. Herpetomonas phlebotomi Culicoides salinarius (Becker, 1958). P. minutus (10% incidence in India) (Mackie, 1914; Patton, 1919). Spirochaeta phlebotomi (= Treponema phlebotomi) P. minutus (in gut) (Shortt, 1925). P. perniciosus (in gut) (Pringault, 1921a). P. papatasii (in gut) (Mackie, 1914). (2) SPOROZOA FUNGI (a) GREGARINIDA Aspergillus sp. Lankesteria ? Phlebotomus spp. (young larvae may become entangled P. papatasii (no pathological damage) (Missiroli, 1932). in mycelium; spores germinate in larval intestine, the mycelium invading muscles of thoracic area and causing Monocystis mackiei death; this fungus is highly pathogenic in laboratory P. argentipes (25 % in nature) (Shortt & Swaminath, cultures) (Hertig & Johnson, 1961). 1927). P. papatasii (Missiroli, 1929b). Entomophthora papatasii P. papatasii (Marett, 1915). (b) HAEMOSPORIDIIDA E. phlebotomnus Haemoproteus canachites P. papatasii (Adler & Theodor, 1929). Culicoides sphagnumensis (Fallis & Bennett, -
FLY Infographicv2
FIGHT THE FLY Did you know there are 200 known species of flies in North America? These flies are not only a nuisance but can also spread diseases. They tarnish your hard-earned reputation by damaging your customer loyalty and bottom line. Use the information below to understand the threats of flies, identify the pests and learn how to help prevent them. The Threats of Flies Food Contaminators: Disease Spreaders: Fast Breeders: Flies oen find their food in Flies can transmit pathogens Some species of female decaying organic matter such that cause E. coli, Salmonella flies lay up to 1,000 eggs as animal feces. They are poor and shingles. They are also in their lives, and fly fliers, and can leave fecal known to carry diseases that larvae develop into adults particles on clean food and can cause food poisoning or in about 7-10 days. preparation surfaces when respiratory infections. they land. Did You Know? A fly can carry potentially = twice as many pathogens as a cockroach. Common Flies in Commercial Establishments House Fly Drain Fly Fruit Fly Musca domestica Family Psychodidae Drosophila spp. Blow Fly Phorid Fly Fungus Gnat Family Calliphoridae Family Phoridae Lycoriella spp. Did You Know? In a recent survey, 75% of respondents listed flies as one of three most commonly 75% encountered pests.* Prevention Measures InspectionInspection : Exclusion Sanitation CWorkheck withfor s iag pestns of fly Seal cracks, gaps Use cleaning solutions acmanagementtivity around food and holes in doors, that decompose professional to identify windows and walls organic materials from preparation areas, conducive conditions with caulk or weather drains and high-use andsto rfindage theare asources, load ofin g stripping. -
Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico
insects Article Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico Guadalupe Amancio 1 , Armando Aguirre-Jaimes 1, Vicente Hernández-Ortiz 1,* , Roger Guevara 2 and Mauricio Quesada 3,4 1 Red de Interacciones Multitróficas, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 2 Red de Biologia Evolutiva, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 3 Laboratorio Nacional de Análisis y Síntesis Ecológica, Escuela Nacional de Estudios Superiores Unidad Morelia, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico 4 Instituto de Investigaciones en Ecosistemas y Sustentabilidad, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico * Correspondence: [email protected] Received: 20 June 2019; Accepted: 9 August 2019; Published: 15 August 2019 Abstract: Insect-aroid interaction studies have focused largely on pollination systems; however, few report trophic interactions with other herbivores. This study features the endophagous insect community in reproductive aroid structures of a tropical rainforest of Mexico, and the shifting that occurs along an altitudinal gradient and among different hosts. In three sites of the Los Tuxtlas Biosphere Reserve in Mexico, we surveyed eight aroid species over a yearly cycle. The insects found were reared in the laboratory, quantified and identified. Data were analyzed through species interaction networks. We recorded 34 endophagous species from 21 families belonging to four insect orders. The community was highly specialized at both network and species levels. Along the altitudinal gradient, there was a reduction in richness and a high turnover of species, while the assemblage among hosts was also highly specific, with different dominant species. -
Diptera) of Finland
A peer-reviewed open-access journal ZooKeys 441: 37–46Checklist (2014) of the familes Chaoboridae, Dixidae, Thaumaleidae, Psychodidae... 37 doi: 10.3897/zookeys.441.7532 CHECKLIST www.zookeys.org Launched to accelerate biodiversity research Checklist of the familes Chaoboridae, Dixidae, Thaumaleidae, Psychodidae and Ptychopteridae (Diptera) of Finland Jukka Salmela1, Lauri Paasivirta2, Gunnar M. Kvifte3 1 Metsähallitus, Natural Heritage Services, P.O. Box 8016, FI-96101 Rovaniemi, Finland 2 Ruuhikosken- katu 17 B 5, 24240 Salo, Finland 3 Department of Limnology, University of Kassel, Heinrich-Plett-Str. 40, 34132 Kassel-Oberzwehren, Germany Corresponding author: Jukka Salmela ([email protected]) Academic editor: J. Kahanpää | Received 17 March 2014 | Accepted 22 May 2014 | Published 19 September 2014 http://zoobank.org/87CA3FF8-F041-48E7-8981-40A10BACC998 Citation: Salmela J, Paasivirta L, Kvifte GM (2014) Checklist of the familes Chaoboridae, Dixidae, Thaumaleidae, Psychodidae and Ptychopteridae (Diptera) of Finland. In: Kahanpää J, Salmela J (Eds) Checklist of the Diptera of Finland. ZooKeys 441: 37–46. doi: 10.3897/zookeys.441.7532 Abstract A checklist of the families Chaoboridae, Dixidae, Thaumaleidae, Psychodidae and Ptychopteridae (Diptera) recorded from Finland is given. Four species, Dixella dyari Garret, 1924 (Dixidae), Threticus tridactilis (Kincaid, 1899), Panimerus albifacies (Tonnoir, 1919) and P. przhiboroi Wagner, 2005 (Psychodidae) are reported for the first time from Finland. Keywords Finland, Diptera, species list, biodiversity, faunistics Introduction Psychodidae or moth flies are an intermediately diverse family of nematocerous flies, comprising over 3000 species world-wide (Pape et al. 2011). Its taxonomy is still very unstable, and multiple conflicting classifications exist (Duckhouse 1987, Vaillant 1990, Ježek and van Harten 2005). -
Diptera: Drosophilidae)
Zootaxa 1069: 1–32 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1069 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) Molecular systematics and geographical distribution of the Drosophila longicornis species complex (Diptera: Drosophilidae) DEODORO C. S. G. OLIVEIRA1, 2, PATRICK M. O’GRADY1, 3, WILLIAM J. ETGES4, WILLIAM B. HEED5 & ROB DeSALLE1 1Division of Invertebrate Zoology, American Museum of Natural History, New York, NY, USA; email: [email protected] 2Department of Biology, University of Rochester, Rochester, NY, USA; email: [email protected] 3Department of Biology, University of Vermont, VT, USA; email: [email protected] 4Department of Biological Sciences, University of Arkansas, Fayetteville, AR, USA; email: [email protected] 5Department of Ecology and Evolutionary Biology, The University of Arizona, Tucson, AZ, USA; email: [email protected] Abstract Here we examine the phylogenetic relationships of eleven species previously hypothesized to be members of the Drosophila longicornis complex (repleta group, mulleri subgroup) using combined analyses of four mitochondrial genes. This complex, as currently redefined, is composed of the longicornis cluster (D. longicornis, D. pachuca, D. propachuca, and D. mainlandi), the ritae cluster (D. desertorum, D. mathisi, and D. ritae), and several miscellaneous species (D. hamatofila, D. hexastigma, D. spenceri, and an undescribed species “from Sonora”). A maximum likelihood inference also includes the huckinsi cluster (D. huckinsi and D. huichole) as the most distant members in the longicornis complex, a condition not recovered using maximum parsimony. We were unable to diagnose species in the triad of sibling species D. longicornis, D. pachuca, and D. propachuca using rapidly evolving mitochondrial DNA data, and we discuss possible species concept conflict for this triad. -
Refuse Containers As a Source of Flies in Honolulu and Nearby Communities
Vol. XVII, No. 3, August, 1961 477 Refuse Containers as a Source of Flies in Honolulu and Nearby Communities Donald P. Wilton DIVISION OF SANITATION HAWAII STATE DEPARTMENT OF HEALTH HONOLULU, HAWAII {Submitted for publication December, I960) The garbage can has long been recognized as an important site of domestic fly production. Quarterman et al. (1949) found garbage cans second only to the city dump as a source of flies in Savannah, Georgia. They reported fly breeding in or under 60 per cent of the containers examined. Fifty per cent of the infested media detected by Schoof et al. (1954) in fly breeding surveys conducted in Charleston, West Virginia were garbage. A similar situation was found by Siverly and Schoof (1955) in Phoenix, Arizona. Kilpatrick and Bogue (1956) demonstrated fly emergence from ground surfaces under and near garbage cans at Mission and Pharr, Texas. As an illustration of the significance of garbage as a breeding medium for domestic flies, it was stated by Siverly and Schoof (1955) that as many as 70,000 flies have been produced by one cubic foot of this material. Campbell and Black (i960) reporting on an investigation of prepupal migration of fly larvae from refuse containers in Concord, California recommended twice-a- week refuse collection during hot weather. They suggested that this would remove refuse before any significant migration (and hence, any significant fly production) could occur. Often, however, routine refuse collection fails to remove all the material in the can. As pointed out by Quarterman et al. (1949), a sludge-like deposit which is not dislodged when the container is upended frequently builds up in the bottoms of neglected cans. -
Flesh Flies (Diptera: Sarcophagidae) of Sandy and Marshy Habitats of the Polish Baltic Coast
© Entomologica Fennica. 30 March 2009 Flesh flies (Diptera: Sarcophagidae) of sandy and marshy habitats of the Polish Baltic coast Elibieta Kaczorowska Kaczorowska, E. 2009: Flesh flies (Diptera: Sarcophagidae) of sandy and marshy habitats of the Polish Baltic coast. — Entomol. Fennica 20: 61—64. The results ofa seven-year study on flesh flies (Diptera: Sarcophagidae) in sandy and marshy habitats ofthe Polish Baltic coast are presented. During this research, carried out in 20 localities, 25 species of Sarcophagidae were collected, ofwhich 24 were new for the study areas. Based on these results, flesh fly abundance and trophic groups are described. E. Kaczorowska, Department ofInvertebrate Zoology, University ofGdansk, Al. Marszalka Pilsadskiego 46, 81—3 78 Gdynia, Poland; E—mail.‘ saline@ocean. aniv.gda.pl, telephone: 0048 58 5236642 Received 1 1 December 200 7, accepted 19 March 2008 1. Introduction menoptera, while others are predators or para- sitoids on insects and snails (Povolny & Verves Sarcophagidae is a species-rich family, distri- 1997). Therefore, flesh flies occur in various buted worldwide and comprising over 2500 de- kinds of biotopes, including coastal marshy and scribed species. At present more than 150 species sandy habitats. On the Polish Baltic coast, species of flesh flies are known from central Europe of Sarcophagidae have been found in low abun- (Povolny & Verves 1997) and 129 from Poland. dance, and only one species, Sarcophaga (Myo— The Polish fauna of Sarcophagidae is relatively rlzina) nigriventris Meigen, has so far been re- well known, but the state of knowledge about corded (Draber—Monko 1973). Szadziewski these flies is uneven for particular regions of the (1983), carrying out research on Diptera ofthe sa- country. -
Volume 2, Chapter 12-19: Terrestrial Insects: Holometabola-Diptera
Glime, J. M. 2017. Terrestrial Insects: Holometabola – Diptera Nematocera 2. In: Glime, J. M. Bryophyte Ecology. Volume 2. 12-19-1 Interactions. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. eBook last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 12-19 TERRESTRIAL INSECTS: HOLOMETABOLA – DIPTERA NEMATOCERA 2 TABLE OF CONTENTS Cecidomyiidae – Gall Midges ........................................................................................................................ 12-19-2 Mycetophilidae – Fungus Gnats ..................................................................................................................... 12-19-3 Sciaridae – Dark-winged Fungus Gnats ......................................................................................................... 12-19-4 Ceratopogonidae – Biting Midges .................................................................................................................. 12-19-6 Chironomidae – Midges ................................................................................................................................. 12-19-9 Belgica .................................................................................................................................................. 12-19-14 Culicidae – Mosquitoes ................................................................................................................................ 12-19-15 Simuliidae – Blackflies -
Trapping Drosophila Repleta (Diptera: Drosophilidae) Using Color and Volatiles B
Trapping Drosophila repleta (Diptera: Drosophilidae) using color and volatiles B. A. Hottel1,*, J. L. Spencer1 and S. T. Ratcliffe3 Abstract Color and volatile stimulus preferences of Drosophila repleta (Patterson) Diptera: Drosophilidae), a nuisance pest of swine and poultry facilities, were tested using sticky card and bottle traps. Attractions to red, yellow, blue, orange, green, purple, black, grey and a white-on-black contrast treatment were tested in the laboratory. Drosophila repleta preferred red over yellow and white but not over blue. Other than showing preferences over the white con- trol, D. repleta was not observed to have preferences between other colors and shade combinations. Pinot Noir red wine, apple cider vinegar, and wet swine feed were used in volatile preference field trials. Red wine was more attractiveD. to repleta than the other volatiles tested, but there were no dif- ferences in response to combinations of a red wine volatile lure and various colors. Odor was found to play the primary role in attracting D. repleta. Key Words: Drosophila repleta; color preference; volatile preference; trapping Resumen Se evaluaron las preferencias de estímulo de volátiles y color de Drosophila repleta (Patterson) (Diptera: Drosophilidae), una plaga molesta en las instalaciones porcinas y avícolas, utilzando trampas de tarjetas pegajosas y de botella. Su atracción a los tratamientos de color rojo, amarillo, azul, anaranjado, verde, morado, negro, gris y un contraste de blanco sobre negro fue probado en el laboratorio. Drosophila repleta preferio el rojo mas que el amarillo y el blanco, pero no sobre el azul. Aparte de mostrar una preferencia por el control de color blanco, no se observó que D.