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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. -
Molecular Detection of Culicoides Spp. and Culicoides Imicola, The
Molecular detection of Culicoides spp. and Culicoides imicola, the principal vector of bluetongue (BT) and African horse sickness (AHS) in Africa and Europe Catherine Cêtre-Sossah, Thierry Baldet, Jean-Claude Delécolle, Bruno Mathieu, Aurélie Perrin, Colette Grillet, Emmanuel Albina To cite this version: Catherine Cêtre-Sossah, Thierry Baldet, Jean-Claude Delécolle, Bruno Mathieu, Aurélie Perrin, et al.. Molecular detection of Culicoides spp. and Culicoides imicola, the principal vector of bluetongue (BT) and African horse sickness (AHS) in Africa and Europe. Veterinary Research, BioMed Central, 2004, 35 (3), pp.325-337. 10.1051/vetres:2004015. hal-00902785 HAL Id: hal-00902785 https://hal.archives-ouvertes.fr/hal-00902785 Submitted on 1 Jan 2004 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Vet. Res. 35 (2004) 325–337 325 © INRA, EDP Sciences, 2004 DOI: 10.1051/vetres:2004015 Original article Molecular detection of Culicoides spp. and Culicoides imicola, the principal vector of bluetongue (BT) and African horse sickness (AHS) in Africa and Europe -
The Stalk-Eyed Fly As a Model for Aggression – Is There a Conserved Role for 5-HT Between Vertebrates and Invertebrates? Andrew N
© 2020. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2020) 223, jeb132159. doi:10.1242/jeb.132159 COMMENTARY The stalk-eyed fly as a model for aggression – is there a conserved role for 5-HT between vertebrates and invertebrates? Andrew N. Bubak1, Michael J. Watt2, Jazmine D. W. Yaeger3, Kenneth J. Renner3 and John G. Swallow4,* ABSTRACT Takahashi et al., 2012). In stalk-eyed flies, 5-HT appears to mediate Serotonin (5-HT) has largely been accepted to be inhibitory to appropriate behavioral responses upon perception of aggressive vertebrate aggression, whereas an opposing stimulatory role has signals (Bubak et al., 2014a). been proposed for invertebrates. Herein, we argue that critical gaps in 5-HT, 5-HT receptor structure and function, and the 5-HT our understanding of the nuanced role of 5-HT in invertebrate systems transporter (SERT), which removes 5-HT from the synaptic cleft to drove this conclusion prematurely, and that emerging data suggest a terminate 5-HT signaling (Fig. 1), are phylogenetically conserved previously unrecognized level of phylogenetic conservation with (Blenau and Baumann, 2001; Martin and Krantz, 2014). Despite this, respect to neurochemical mechanisms regulating the expression of 5-HT appears to play generally opposing roles in the generation of the aggressive behaviors. This is especially apparent when considering the complex behaviors associated with aggression in invertebrates and interplay among factors governing 5-HT activity, many of which share vertebrates (see Table S1). However, we propose that this seemingly functional homology across taxa. We discuss recent findings using contrasting role of 5-HT may be an overly simplistic generalization. -
Insects in Cretaceous and Cenozoic Amber of Eurasia and North America
Insects in Cretaceous and Cenozoic Amber of Eurasia and North America Schmalhausen Institute of Zoology, National Academy of Sciences of Ukraine, ul. Bogdana Khmel’nitskogo 15, Kiev, 01601 Ukraine email: [email protected] Edited by E. E. Perkovsky ISSN 00310301, Paleontological Journal, 2016, Vol. 50, No. 9, p. 935. © Pleiades Publishing, Ltd., 2016. Preface DOI: 10.1134/S0031030116090100 The amber is wellknown as a source of the most Eocene ambers. However, based on paleobotanical valuable, otherwise inaccessible information on the data, confirmed by new paleoentomological data, it is biota and conditions in the past. The interest in study dated Middle Eocene. Detailed discussions of dating ing Mesozoic and Paleogene ambers has recently and relationships of Sakhalinian ants is provided in the sharply increased throughout the world. The studies first paper of the present volume, in which the earliest included in this volume concern Coleoptera, ant of the subfamily Myrmicinae is described from Hymenoptera, and Diptera from the Cretaceous, the Sakhalinian amber and assigned to an extant Eocene, and Miocene amber of the Taimyr Peninsula, genus. The earliest pedogenetic gall midge of the Sakhalin Island, Baltic Region, Ukraine, and Mexico. tribe Heteropezini from the Sakhalinian amber is Yantardakh is the most important Upper Creta also described here. ceous insect locality in northern Asia, which was dis The Late Eocene Baltic amber is investigated better covered by an expedition of the Paleontological Insti than any other; nevertheless, more than half of its tute of the Academy of Sciences of the USSR fauna remains undescribed; the contemporaneous (at present, Borissiak Paleontological Institute, Rus fauna from the Rovno amber is investigated to a con sian Academy of Sciences: PIN) in 1970 and addition siderably lesser degree. -
Syrphid Flies
Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory Ent-200-18PR February 2019 Beneficial Predators: Syrphid Flies Steven Price, Carbon Co. Extension • Ron Patterson, University of Idaho, Bonneville Co. Extension DESCRIPTION What you should know Eggs are oblong, white or grey with a lace-like pattern • Syrphid flies are common residents in agricultural on the surface, and measure around 1/16 inch long. areas, gardens, and home landscapes providing They are laid singly on plants often near dense colonies pollination services. of prey which are located by females by olfactory, • Larvae of syrphid flies are important beneficial visual, and tactile cues. predators of soft-bodied pests providing naturally Larvae can be found living among their prey, although occurring pest control. are sometimes misidentified as pests, such as sawfly • Syrphid flies cannot be purchased commercially larvae, slugs, alfalfa weevil larvae, or different kinds of but populations can be conserved by reducing caterpillars (Table 1). Syrphid fly larvae have a tapered broad-spectrum pesticide use. anterior which lacks an external head capsule. The flattened rear has two small breathing holes (spiracles). Larvae are semi-translucent, often being striped or Syrphid (pronounced ‘sir-fid’) flies, also known as hover mottled in shades of white, green, tan, or brown with flies or flower flies, commonly occur in field crops, additional small bumps or spikes (Fig. 1). Being 1/16 inch orchards, gardens and home landscapes. They are long upon hatching, they are typically less than 1/2 inch members of the Syrphidae family. They are “true flies” long once they are full-sized. -
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. -
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. -
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. -
Austroconops Wirth and Lee, a Lower Cretaceous Genus of Biting Midges
PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK, NY 10024 Number 3449, 67 pp., 26 ®gures, 6 tables August 23, 2004 Austroconops Wirth and Lee, a Lower Cretaceous Genus of Biting Midges Yet Living in Western Australia: a New Species, First Description of the Immatures and Discussion of Their Biology and Phylogeny (Diptera: Ceratopogonidae) ART BORKENT1 AND DOUGLAS A. CRAIG2 ABSTRACT The eggs and all four larval instars of Austroconops mcmillani Wirth and Lee and A. annettae Borkent, new species, are described. The pupa of A. mcmillani is also described. Life cycles and details of behavior of each life stage are reported, including feeding by the aquatic larvae on microscopic organisms in very wet soil/detritus, larval locomotion, female adult biting habits on humans and kangaroos, and male adult swarming. Austroconops an- nettae Borkent, new species, is attributed to the ®rst author. Cladistic analysis shows that the two extant Austroconops Wirth and Lee species are sister species. Increasingly older fossil species of Austroconops represent increasingly earlier line- ages. Among extant lineages, Austroconops is the sister group of Leptoconops Skuse, and together they form the sister group of all other Ceratopogonidae. Dasyhelea Kieffer is the sister group of Forcipomyia Meigen 1 Atrichopogon Kieffer, and together they form the sister group of the Ceratopogoninae. Forcipomyia has no synapomorphies and may be paraphyletic in relation to Atrichopogon. Austroconops is morphologically conservative (possesses many plesiomorphic features) in each life stage and this allows for interpretation of a number of features within Ceratopogonidae and other Culicomorpha. A new interpretation of Cretaceous fossil lineages shows that Austroconops, Leptoconops, Minyohelea Borkent, Jordanoconops 1 Royal British Columbia Museum, American Museum of Natural History, and Instituto Nacional de Biodiversidad. -
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, -
(Neuroptera) from the Upper Cenomanian Nizhnyaya Agapa Amber, Northern Siberia
Cretaceous Research 93 (2019) 107e113 Contents lists available at ScienceDirect Cretaceous Research journal homepage: www.elsevier.com/locate/CretRes Short communication New Coniopterygidae (Neuroptera) from the upper Cenomanian Nizhnyaya Agapa amber, northern Siberia * Vladimir N. Makarkin a, Evgeny E. Perkovsky b, a Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok, 690022, Russia b Schmalhausen Institute of Zoology, National Academy of Sciences of Ukraine, ul. Bogdana Khmel'nitskogo 15, Kiev, 01601, Ukraine article info abstract Article history: Libanoconis siberica sp. nov. and two specimens of uncertain affinities (Neuroptera: Coniopterygidae) are Received 28 April 2018 described from the Upper Cretaceous (upper Cenomanian) Nizhnyaya Agapa amber, northern Siberia. Received in revised form The new species is distinguished from L. fadiacra (Whalley, 1980) by the position of the crossvein 3r-m 9 August 2018 being at a right angle to both RP1 and the anterior trace of M in both wings. The validity of the genus Accepted in revised form 11 September Libanoconis is discussed. It easily differs from all other Aleuropteryginae by a set of plesiomorphic 2018 Available online 15 September 2018 character states. The climatic conditions at high latitudes in the late Cenomanian were favourable enough for this tropical genus, hitherto known from the Gondwanan Lebanese amber. Therefore, the Keywords: record of a species of Libanoconis in northern Siberia is highly likely. © Neuroptera 2018 Elsevier Ltd. All rights reserved. Coniopterygidae Aleuropteryginae Cenomanian Nizhnyaya Agapa amber 1. Introduction 2. Material and methods The small-sized neuropteran family Coniopterygidae comprises This study is based on three specimens originally embedded in ca. -
Diptera: Nematocera) of the Piedmont of the Yungas Forests of Tucuma´N: Ecology and Distribution
Ceratopogonidae (Diptera: Nematocera) of the piedmont of the Yungas forests of Tucuma´n: ecology and distribution Jose´ Manuel Direni Mancini1,2, Cecilia Adriana Veggiani-Aybar1, Ana Denise Fuenzalida1,3, Mercedes Sara Lizarralde de Grosso1 and Marı´a Gabriela Quintana1,2,3 1 Facultad de Ciencias Naturales e Instituto Miguel Lillo, Universidad Nacional de Tucuma´n, Instituto Superior de Entomologı´a “Dr. Abraham Willink”, San Miguel de Tucuma´n, Tucuma´n, Argentina 2 Consejo Nacional de Investigaciones Cientı´ficas y Te´cnicas, San Miguel de Tucuma´n, Tucuma´n, Argentina 3 Instituto Nacional de Medicina Tropical, Puerto Iguazu´ , Misiones, Argentina ABSTRACT Within the Ceratopogonidae family, many genera transmit numerous diseases to humans and animals, while others are important pollinators of tropical crops. In the Yungas ecoregion of Argentina, previous systematic and ecological research on Ceratopogonidae focused on Culicoides, since they are the main transmitters of mansonelliasis in northwestern Argentina; however, few studies included the genera Forcipomyia, Dasyhelea, Atrichopogon, Alluaudomyia, Echinohelea, and Bezzia. Therefore, the objective of this study was to determine the presence and abundance of Ceratopogonidae in this region, their association with meteorological variables, and their variation in areas disturbed by human activity. Monthly collection of specimens was performed from July 2008 to July 2009 using CDC miniature light traps deployed for two consecutive days. A total of 360 specimens were collected, being the most abundant Dasyhelea genus (48.06%) followed by Forcipomyia (26.94%) and Atrichopogon (13.61%). Bivariate analyses showed significant differences in the abundance of the genera at different sampling sites and climatic Submitted 15 July 2016 Accepted 4 October 2016 conditions, with the summer season and El Corralito site showing the greatest Published 17 November 2016 abundance of specimens.