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| Arthropoda:  Insecta   TABANIDAE (Contact)     Please
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              Most adult "horseflies" are bloodsuckers,
  with females of most species feeding during the day.  The larvae are mostly aquatic
  or semi aquatic, feeding on various kinds of animals occurring in the medium
  in which they develop.  Over 4320
  species have been identified in about 135 genera.  One preferred food is Tipulidae larvae and other groups
  inhabiting the banks of ponds and streams. 
  Earthworms and snails are also attacked.  Tabanus stigma F.
  is known to develop in drying seaweed in Puerto Rico, the larvae feeding on
  sand fly larvae.  Davis (1919)
  recorded several species of Tabanus
  as predaceous on Scarabaeidae grubs. 
  The eggs of most species are laid in large masses on foliage
  overhanging water or on stones or other nearby objects.  With some species they are found in a
  single compact layer, the eggs placed vertically, side by side; while in
  others they are several layers deep (Clausen 1940/62)   Brachycera = "short antennae" includes larger flies with
  large eyes.        Tabanidae. -- <Habits>; <Adults> & <Juveniles> -- The horse
  flies and deer flies
  are vicious biters, and they inject toxic saliva into their hosts. The larvae
  are aquatic and predaceous.  The
  adults may spread diseases such as Tularemia, Loiasis
  and Anthrax.     Importance          Primarily
  important species are in the genera Tabanus,
  Haematopota and Chrysops (See Distinctions).  Service (2008) noted that they might
  vector Anthrax, Tularemia,
  Loa Loa in Africa and even Lyme
  Disease.  They are
  especially important pests of domestic animals in their ability to transmit
  bacteria, protozoa viruses and filarial worms.  Tabanids are also a problem because of their painful bites,
  which can result in allergic responses. 
  Images of important species created from collection specimens
  include:  Apatolestes sp., Atylotus sp.,  Chrysops sp., 
  Diachlorus sp.,  Esenbeckia sp.,  Goniops sp., Haematopota sp.,  Silvius sp.,  Stenotabanus sp.,  Stonemyia sp.,  Tabanus sp.          A critically
  important disease is Loiasis that can be vectored to
  humans by tabanids.  It is found
  mostly en the equatorial rainforests of Central Africa.  Service (2008) listed Chrysops silaceus and C. dimidiatus as primary vectors, but C. distinctipennis and C. longicornis have some importance in
  other parts of Africa.   Behavior          Adult flies
  feed on sweet substances in the environment, but females also attack mammals
  and humans.  Some also attack
  birds.  Females lay eggs were the
  larvae are able to survive, such as damp or aquatic sites.  The waterproof eggs are glued in a
  secluded fashion on the bottom of leaves, stones and rocks.  Hatching can occur from four days to two
  weeks depending on temperature and varying with different species.  The larvae complete their
  development in damp sites of standing water, which can last up to two years
  even in tropical environments.  Tabanus and Haematopota
  species are also predaceous or cannibalistic (Service 2008).  Larvae that are carnivorous inject venom
  into the prey and adults can cause pain when they bite humans.  Chrysops
  larvae are mostly scavengers.  Before
  the onset of pupation the larvae will move to drier habitats adjacent to
  their larval sites.          Most species
  females feed during the day in full sunlight, but some are also active only
  at twilight.  Hosts are found by sight
  and olfactory stimuli.  They are all
  strong fliers, which allow them to fly several miles or kilometers.  Their habitats are primarily in and around
  forested areas.  Chrysops species are especially abundant in wooded marshes and
  swamps, but they can range to open fields. 
  Generally adults remain outdoors although a few African species may
  enter dwellings.  The abundance of
  adults is influenced by the season in all areas where they occur.  In areas with a rainy season the start of
  rains will trigger activity.   Control          The Tabanidae are extremely difficult to
  control, especially in areas where aquatic habitats cannot be practically
  reduced, such as swamps and lakes. 
  Nevertheless,  control measures
  have involved draining swampland where the flies breed.  Insecticidal control is also plagued by
  the development of resistance and difficulties in locating principal breeding
  areas.  Service (2008) noted that some
  control could be achieved with attractant traps for adults and the use of
  repellents.   = = = = = = = = = = = = = = = = = = = =   Key References:     <medvet.ref.htm>    <Hexapoda>   Anderson, J. F.  1985. 
  The control of horse flies and deer flies (Diptera: Tabanidae).  Myia 3: 
  547-98. Anthony, D. W.  1962. 
  Tabanids as disease vectors. IN: Biological Transmission of Disease
  Agents.  Academic Press, NY. p.
  93-107. Braga da Rosa; Gustavo
  A.  2006. Predation
  of hill topping horse-flies (Tabanidae) by birds in Brazil.  Ornitologia Neotropical. 17:
  619–622. Cheke, R. A., J. Mas & J. F. Chainey.  2003.  Potential vectors of Ioiasis and other tabanids on the island
  of Bioko, Equatorial Guinea.        Med. Vet. Ent. 17:  221-3. Chippaux, J. P., B. Bouchite, M. Demanov, I. Morlais
  & G. LeGoff.  2000.  Density and dispersal of the Loiasis vector Chrysops dimidiata in      southern Cameroon.  Med. & Vet. Ent. 14:  339-44.  Eaton,
  Eric R.; Kaufman, Kenn (2007). "Deer
  flies and horse flies". Kaufman Field Guide to Insects of North
  America.  Hillstar Editions.
  p. 284.  Egri, A.; Blaho, M.; Kriska, G.;
  Farkas, R.; Gyurkovszky, M.; Akesson, S.; Horvath, G.  2012. "Polarotactic tabanids find
  striped patterns with       brightness and/or polarization
  modulation least attractive: An advantage of zebra stripes". Journal of
  Experimental Biology. 215 (5): 736. Foil, L. D.  1989. 
  Tabanids as vectors of disease agents.  Parasitology Today 5: 
  88-95. Matheson, R. 1950.  Medical Entomology.  Comstock Publ. Co, Inc.  610 p. Middlekauff, Woodrow Wilson; Lane,
  Robert S. 1980. Adult & Immature Tabanidae (Diptera) of California.  University of California Press.       pp. 1–2. Noireau, F., A. Nzoulani, D. Sinda & A. Itoua.  1990.  Transmission indices of Loa
  loa in the Chaillu Mountains, Congo.  Amer. J. Trop. Med.       43: 
  382-8. Padgett, J.J.; Jacobsen, K.H. (2008).
  "Loiasis: African eye worm". Transactions of the Royal Society of
  Tropical Medicine and Hygiene.       102 (10): 983–9. Quercia, O.; Emiliani, F.; Foschi, F.G.; Stefanini,
  G.F.  The wasp-horsefly
  syncrome.  European Annals of Allergy
  and Clinical Immunology.       40 (3): 61–63 Service, M.  2008. 
  Medical Entomology For Students. 
  Cambridge Univ. Press.  289 p Legner, E. F.  1995.  Biological control of Diptera of medical and veterinary
  importance.  J. Vector Ecology 20(1):
  59-120. Legner, E. F.  2000. 
  Biological control of aquatic Diptera.  p. 847-870. 
  Contributions to a Manual of Palaearctic Diptera,        Vol. 1, Science  Herald, Budapest.  978 p. Thomson, M. C., V. Obsomer & J. Kamgno et
  al.  2004.  Mapping the distribution of Loa
  loa in Cameroon in support of the African Programme        for Onchocerciasis Control.  Filaria J. 3: 7.    Wilkerson,
  R.C.; Butler, J.F.; Pechuman, L.L. (1985). "Swarming, hovering &
  mating behavior of male horse flies & deer flies (Diptera:     
  Tabanidae)". Myia. 3: 515–546   | 
 
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