Arthropod Pests of Equines
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Ancient Roaches Further Exemplify 'No Land Return' in Aquatic Insects
Gondwana Research 68 (2019) 22–33 Contents lists available at ScienceDirect Gondwana Research journal homepage: www.elsevier.com/locate/gr Ancient roaches further exemplify ‘no land return’ in aquatic insects Peter Vršanský a,b,c,d,1, Hemen Sendi e,⁎,1, Danil Aristov d,f,1, Günter Bechly g,PatrickMüllerh, Sieghard Ellenberger i, Dany Azar j,k, Kyoichiro Ueda l, Peter Barna c,ThierryGarciam a Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia b Slovak Academy of Sciences, Institute of Physics, Research Center for Quantum Information, Dúbravská cesta 9, Bratislava 84511, Slovakia c Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, P.O. BOX 106, 840 05 Bratislava, Slovakia d Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya 123, 117868 Moscow, Russia e Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava 84215, Slovakia f Cherepovets State University, Cherepovets 162600, Russia g Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, D-70191 Stuttgart, Germany h Friedhofstraße 9, 66894 Käshofen, Germany i Bodelschwinghstraße 13, 34119 Kassel, Germany j State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, PR China k Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, PO Box 26110217, Fanar - Matn, Lebanon l Kitakyushu Museum, Japan m River Bigal Conservation Project, Avenida Rafael Andrade y clotario Vargas, 220450 Loreto, Orellana, Ecuador article info abstract Article history: Among insects, 236 families in 18 of 44 orders independently invaded water. We report living amphibiotic cock- Received 13 July 2018 roaches from tropical streams of UNESCO BR Sumaco, Ecuador. -
Evolutionary History of Stomach Bot Flies in the Light of Mitogenomics
Evolutionary history of stomach bot flies in the light of mitogenomics Yan, Liping; Pape, Thomas; Elgar, Mark A.; Gao, Yunyun; Zhang, Dong Published in: Systematic Entomology DOI: 10.1111/syen.12356 Publication date: 2019 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Yan, L., Pape, T., Elgar, M. A., Gao, Y., & Zhang, D. (2019). Evolutionary history of stomach bot flies in the light of mitogenomics. Systematic Entomology, 44(4), 797-809. https://doi.org/10.1111/syen.12356 Download date: 28. Sep. 2021 Systematic Entomology (2019), 44, 797–809 DOI: 10.1111/syen.12356 Evolutionary history of stomach bot flies in the light of mitogenomics LIPING YAN1, THOMAS PAPE2 , MARK A. ELGAR3, YUNYUN GAO1 andDONG ZHANG1 1School of Nature Conservation, Beijing Forestry University, Beijing, China, 2Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark and 3School of BioSciences, University of Melbourne, Melbourne, Australia Abstract. Stomach bot flies (Calyptratae: Oestridae, Gasterophilinae) are obligate endoparasitoids of Proboscidea (i.e. elephants), Rhinocerotidae (i.e. rhinos) and Equidae (i.e. horses and zebras, etc.), with their larvae developing in the digestive tract of hosts with very strong host specificity. They represent an extremely unusual diver- sity among dipteran, or even insect parasites in general, and therefore provide sig- nificant insights into the evolution of parasitism. The phylogeny of stomach botflies was reconstructed -
Pest Management News
Pest Management News Dr. John D. Hopkins, Associate Professor and Extension Entomologist – Coeditor Dr. Kelly M. Loftin, Professor and Extension Entomologist – Coeditor Contributors Dr. Becky McPeake, Professor and Wildlife Extension Specialist Sherrie E. Smith, Plant Pathology Instructor, Plant Health Clinic Diagnostician Letter #6 October 31, 2017 ________________________________________________________________________________ Stopping Occasional Arthropod Invaders John D. Hopkins When the weather begins to change in the fall and things get cooler, arthropod pests like the multi-colored Asian lady beetle, the boxelder bug, crickets, various stinkbugs, or spiders are just some of the pest problems that homeowners may have to deal with. The first thing most people think of when trying to prevent a pest problem is WHAT INSECTICIDE DO I SPRAY? However, there are other measures that should be taken that will help prevent these pests from entering your home and may even eliminate the need for an insecticide application. Pest proofing your home is the BEST way to prevent unwanted invaders at this time or any other time of year. Your goal is to prevent pest entry and eliminate conditions that are conducive to pest infestation. Here are the ABC’s of pest proofing your home: A. Ensure that screens on doors and windows are properly installed and maintained. If you don't have screen doors on your home, install them. Any damaged screens should be repaired or replaced. Fine mesh screening will prevent all but the tiniest insects from entering your home. B. Doors should seal properly. If air can pass through or light can be seen through cracks around doors then insects or spiders can get in. -
Molecular Detection of Theileria and Babesia in a Diversity of Stomoxyini
Original Article Molecular Detection of Theileria and Babesia in a Diversity of Stomoxyini Flies (Diptera: Muscidae) from Khao Yai National Park, Thailand Tanasak Changbunjong1,2* Sivapong Sungpradit1 Oraphan Kanthasaewee2 Poonyapat Sedwisai2 Siriporn Tangsudjai2 Jiraporn Ruangsittichai3 Abstract Blood protozoan species of the genera Theileria and Babesia are known to infect both domestic and wild animals. This study was carried out to detect Theileria and Babesia DNA in Stomoxyini flies collected in Khao Yai National Park, Thailand. A total of 110 Stomoxyini flies including 6 species, Stomoxys calcitrans, Stomoxys indicus, Stomoxys pullus, Stomoxys uruma, Haematobosca sanguinolenta and Haematostoma austeni, were examined by amplification against the 18S rRNA gene of the Theileria/Babesia species and then the PCR products were sequenced for species identification by comparison with published sequences from the GenBank database. Ten (9.1%) out of 110 samples were positive against the 18S rRNA gene of the Theileria/Babesia species. For sequence analysis, 7 samples (6.4%) were identified as Theileria sp. and showed high identity (99%) with Theileria sp. (JQ751279) and T. cervi (HQ184406 and HQ184411), while 3 samples (2.7%) were identified as Babesia canis vogeli and showed 100% identity with reported sequences of B. canis vogeli (AB083374 and HM590440). Phylogenetic relationships among the sequenced samples showed that the Theileria sp. appeared in the same group as T. cervi, while B. canis vogeli appeared in a distinct group. This study -
The Black Flies of Maine
THE BLACK FLIES OF MAINE L.S. Bauer and J. Granett Department of Entomology University of Maine at Orono, Orono, ME 04469 Maine Life Sciences and Agriculture Experiment Station Technical Bulletin 95 May 1979 LS-\ F.\PFRi\ii-Nr Si \IION TK HNK \I BUI I HIN 9? ACKNOWLEDGMENTS We wish to thank Dr. Ivan McDaniel for his involvement in the USDA-funding of this project. We thank him for his assistance at the beginning of this project in loaning us literature, equipment, and giving us pointers on taxonomy. He also aided the second author on a number of collection trips and identified a number of collection specimens. We thank Edward R. Bauer, Lt. Lewis R. Boobar, Mr. Thomas Haskins. Ms. Leslie Schimmel, Mr. James Eckler, and Mr. Jan Nyrop for assistance in field collections, sorting, and identifications. Mr. Ber- nie May made the electrophoretic identifications. This project was supported by grant funds from the United States Department of Agriculture under CSRS agreement No. 616-15-94 and Regional Project NE 118, Hatch funds, and the Maine Towns of Brad ford, Brownville. East Millinocket, Enfield, Lincoln, Millinocket. Milo, Old Town. Orono. and Maine counties of Penobscot and Piscataquis, and the State of Maine. The electrophoretic work was supported in part by a faculty research grant from the University of Maine at Orono. INTRODUCTION Black flies have been long-time residents of Maine and cause exten sive nuisance problems for people, domestic animals, and wildlife. The black fly problem has no simple solution because of the multitude of species present, the diverse and ecologically sensitive habitats in which they are found, and the problems inherent in measuring the extent of the damage they cause. -
(Mallophaga: Trichodectidae) from the Introduced Fallow Deer to the Columbian Black-Tailed Deer in California
J. Med. Ent. Vol. 13, no. 2: 169-173 10 September 1976 TRANSFER OF BOVICOLA TIBIALIS (PIAGET) (MALLOPHAGA: TRICHODECTIDAE) FROM THE INTRODUCED FALLOW DEER TO THE COLUMBIAN BLACK-TAILED DEER IN CALIFORNIA By Dale R. Westrom1, Bernard C. Nelson24 and Guy E. Connolly3 Abstract: Bovicola tibialis (Piaget), a louse parasite of the known in the family Boopidae that was not found European Fallow Deer, was found infesting 3 Columbian exclusively on marsupials. In 1971 Clay described Downloaded from https://academic.oup.com/jme/article/13/2/169/2219257 by guest on 28 September 2021 Black-tailed Deer at Hopland Field Station, Mendocino Co., California. In 19(55, Fallow Deer were introduced onto the a new genus and species of boopid from the avian Station and were kept in an experimental pasture with Black- host Casuarius casuarius sclaterii Salvadori, indicating tailed Deer. Transfer of lice presumably occurred by direct that an interclass transfer of lice had occurred. contact between the 2 species of deer as they congregated at a feeder within the pasture, and subsequent transfers among Most examples of secondary infestation given by Black-tailed Deer accounted for the infestations reported herein. the above authors indicate that these occurred As no males were found among the 18,148 specimens collected, naturally. We conclude that lice, in like manner we suggest that parthenogenetic. reproduction occurs in B. to free-living animals, have the opportunities and tibialis. abilities to colonize new habitats. Colonizing species Although lice of the order Mallophaga are of lice are subject to the same hazards that free- usually considered extremely host-specific ecto- living colonizers face when entering into new areas parasites of birds and mammals, examples exist and habitats. -
DNA Barcoding Distinguishes Pest Species of the Black Fly Genus <I
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 11-2013 DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae) I. M. Confitti University of Toronto K. P. Pruess University of Nebraska-Lincoln A. Cywinska Ingenomics, Inc. T. O. Powers University of Nebraska-Lincoln D. C. Currie University of Toronto and Royal Ontario Museum, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/entomologyfacpub Part of the Entomology Commons Confitti, I. M.; Pruess, K. P.; Cywinska, A.; Powers, T. O.; and Currie, D. C., "DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae)" (2013). Faculty Publications: Department of Entomology. 616. http://digitalcommons.unl.edu/entomologyfacpub/616 This Article is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications: Department of Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. MOLECULAR BIOLOGY/GENOMICS DNA Barcoding Distinguishes Pest Species of the Black Fly Genus Cnephia (Diptera: Simuliidae) 1,2 3 4 5 1,2,6 I. M. CONFLITTI, K. P. PRUESS, A. CYWINSKA, T. O. POWERS, AND D. C. CURRIE J. Med. Entomol. 50(6): 1250Ð1260 (2013); DOI: http://dx.doi.org/10.1603/ME13063 ABSTRACT Accurate species identiÞcation is essential for cost-effective pest control strategies. We tested the utility of COI barcodes for identifying members of the black ßy genus Cnephia Enderlein (Diptera: Simuliidae). Our efforts focus on four Nearctic Cnephia speciesÑCnephia dacotensis (Dyar & Shannon), Cnephia eremities Shewell, Cnephia ornithophilia (Davies, Peterson & Wood), and Cnephia pecuarum (Riley)Ñthe latter two being current or potential targets of biological control programs. -
Introduction to Arthropod Groups What Is Entomology?
Entomology 340 Introduction to Arthropod Groups What is Entomology? The study of insects (and their near relatives). Species Diversity PLANTS INSECTS OTHER ANIMALS OTHER ARTHROPODS How many kinds of insects are there in the world? • 1,000,0001,000,000 speciesspecies knownknown Possibly 3,000,000 unidentified species Insects & Relatives 100,000 species in N America 1,000 in a typical backyard Mostly beneficial or harmless Pollination Food for birds and fish Produce honey, wax, shellac, silk Less than 3% are pests Destroy food crops, ornamentals Attack humans and pets Transmit disease Classification of Japanese Beetle Kingdom Animalia Phylum Arthropoda Class Insecta Order Coleoptera Family Scarabaeidae Genus Popillia Species japonica Arthropoda (jointed foot) Arachnida -Spiders, Ticks, Mites, Scorpions Xiphosura -Horseshoe crabs Crustacea -Sowbugs, Pillbugs, Crabs, Shrimp Diplopoda - Millipedes Chilopoda - Centipedes Symphyla - Symphylans Insecta - Insects Shared Characteristics of Phylum Arthropoda - Segmented bodies are arranged into regions, called tagmata (in insects = head, thorax, abdomen). - Paired appendages (e.g., legs, antennae) are jointed. - Posess chitinous exoskeletion that must be shed during growth. - Have bilateral symmetry. - Nervous system is ventral (belly) and the circulatory system is open and dorsal (back). Arthropod Groups Mouthpart characteristics are divided arthropods into two large groups •Chelicerates (Scissors-like) •Mandibulates (Pliers-like) Arthropod Groups Chelicerate Arachnida -Spiders, -
Blister Beetles in Alfalfa Circular 536 Revised by Jane Breen Pierce1
Blister Beetles in Alfalfa Circular 536 Revised by Jane Breen Pierce1 Cooperative Extension Service • College of Agricultural, Consumer and Environmental Sciences This publication provides information on the veterinary Table 1. Estimated Number of Beetles for a Lethal and agronomic importance, distinguishing features, (1 mg/kg) Dose of Cantharidin biology, distribution, and control of blister beetles. Beetle Horse Weight (lb) Recommendations for the purchase and use of alfalfa Cantharidin hay by horse owners and other livestock owners are Content (mg) 275 550 1,000 also provided. 1 125 250 455 2 63 125 244 3 41 83 161 VETERINARY SIGNIFICANCE OF BLISTER BEETLES 4 31 63 122 The common name for blister beetles comes from the 5 25 50 97 irritating reaction the beetle’s body fluids cause on ani- Adapted from Campinera et al. (1985) mal skin or delicate membranes. These fluids contain cantharidin, a potent blistering agent that is present in varying amounts in most blister beetle species. Fluids are blistering of the mouth, esophagus, stomach, and blad- released when the beetle is crushed or handled roughly. der. Death can occur 24 hours after a heavy dose. Cantharidin is a stable chemical and a long-term health Laboratory studies have been conducted to determine threat to nearly all livestock (particularly horses) that are the amount of cantharidin contained in various species fed contaminated hay. Storing infested hay does not sig- of blister beetles. Reports on beetles in several genera nificantly reduce the amount of cantharidin in the hay. indicate cantharidin content varying from 1 to 11.3% Research reports indicate cantharidin toxosis can be of their dry weight. -
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, -
Phylum Arthropod Silvia Rondon, and Mary Corp, OSU Extension Entomologist and Agronomist, Respectively Hermiston Research and Extension Center, Hermiston, Oregon
Phylum Arthropod Silvia Rondon, and Mary Corp, OSU Extension Entomologist and Agronomist, respectively Hermiston Research and Extension Center, Hermiston, Oregon Member of the Phyllum Arthropoda can be found in the seas, in fresh water, on land, or even flying freely; a group with amazing differences of structure, and so abundant that all the other animals taken together are less than 1/6 as many as the arthropods. Well-known members of this group are the Kingdom lobsters, crayfish and crabs; scorpions, spiders, mites, ticks, Phylum Phylum Phylum Class the centipedes and millipedes; and last, but not least, the Order most abundant of all, the insects. Family Genus The Phylum Arthropods consist of the following Species classes: arachnids, chilopods, diplopods, crustaceans and hexapods (insects). All arthropods possess: • Exoskeleton. A hard protective covering around the outside of the body (divided by sutures into plates called sclerites). An insect's exoskeleton (integument) serves as a protective covering over the body, but also as a surface for muscle attachment, a water-tight barrier against desiccation, and a sensory interface with the environment. It is a multi-layered structure with four functional regions: epicuticle (top layer), procuticle, epidermis, and basement membrane. • Segmented body • Jointed limbs and jointed mouthparts that allow extensive specialization • Bilateral symmetry, whereby a central line can divide the body Insect molting or removing its into two identical halves, left and right exoesqueleton • Ventral nerve -
Phthiraptera: Trichodectidae): Occurrence of an Exotic Chewing Louse on Cervids in North America
SAMPLING,DISTRIBUTION,DISPERSAL Bovicola tibialis (Phthiraptera: Trichodectidae): Occurrence of an Exotic Chewing Louse on Cervids in North America JAMES W. MERTINS,1 JACK A. MORTENSON,2,3 JEFFREY A. BERNATOWICZ,4 5 AND P. BRIGGS HALL J. Med. Entomol. 48(1): 1Ð12 (2011); DOI: 10.1603/ME10057 ABSTRACT Through a recent (2003Ð2007) survey of ectoparasites on hoofed mammals in western North America, a literature review, and examination of archived museum specimens, we found that the exotic deer-chewing louse, Bovicola tibialis (Piaget), is a long-term, widespread resident in the region. The earliest known collection was from Salt Spring Island, Canada, in 1941. We found these lice on the typical host, that is, introduced European fallow deer (Dama dama L.), and on Asian chital (Axis axis [Erxleben]), native Columbian black-tailed deer (Odocoileus hemionus columbianus [Ri- chardson]), and Rocky Mountain mule deer (O. h. hemionus [RaÞnesque]) ϫ black-tailed deer hybrids. Chital and the hybrid deer are new host records. All identiÞed hosts were known to be or probably were exposed to fallow deer. Geographic records include southwestern British Columbia, Canada; Marin and Mendocino Counties, California; Deschutes, Lincoln, and Linn Counties, Oregon; Yakima and Kittitas Counties, Washington; Curry County, New Mexico; and circumstantially, at least, Kerr County, Texas. All but the Canadian and Mendocino County records are new. Bovicola tibialis displays a number of noteworthy similarities to another exotic deer-chewing louse already established in the region, that is, Damalinia (Cervicola) sp., which is associated with a severe hair-loss syndrome in black-tailed deer. We discuss longstanding problems with proper identiÞcation of B.