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| Arthropoda:  Insecta   RHAGIONIDAE (Contact)   Please
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   The two genera, Lampromyia
  and Vermileo have been
  thoroughly studied in Europe.  Vermileo vermileo L. was investigated very early in the history of
  entomology by DeReaumur (1753) and Degeer (1776).  Larvae of this and species of similar behavior are called
  "worm lions" to distinguish them from ant lions of the Neuroptera,
  with which they have some similarity. 
  Larvae construct pits in the dust and sand at the bases of cliffs and
  other similar locations.  These pits
  are conically shaped, and the Vermileo
  larva lies on its dorsum at the bottom of the pit where it encircles any
  suitable prey that falls within reach, dragging it underneath the sand.  Ants are one of the principal foods.  The behavior of V. comstocki
  Wheeler was discussed by Wheeler (1930). 
  This species inhabits glacial silt and dust in the mountains of
  western North America.  Eggs are laid
  in masses of 50 or more, adhering together in rows in the dust or silt.  They hatch in ca. 8 days.  Young larvae are gregarious, but later
  instars are solitary.  The larva lies
  in the inverted position in the pit, with its anterior end across the bottom.  Prey consists principally of a common ant
  species, Formica fusca L.  Engle (1929) reported on behavior in Lampromyia sericea
  Westw. and Wheeler (1930) on several species of Lampromyia.  Larvae
  of African L. pallida Macq. differs in behavior from
  others of the genus and from Vermileo
  by holding its body in a vertical position, with the anterior end coiled at
  the bottom of the pit where it awaits its prey.     Species of the genus Chrysopilus
  that have been studied are quite different in their larval habits and host
  preferences from those previously discussed. 
  Chrysopilus nubeculus Macq. is predaceous in the egg
  capsules of Algerian locusts, and C.
  ferruginosus Wied. lives in
  decaying plant roots or tissues in the East Indies and Philippines.  The latter species is a predator on the
  larvae of the banana weevil, Cosmopolites
  sordidus Germ., and the
  sugarcane beetle borer, Rhobdocnemis
  obscura Bsd..  it was introduced into several areas in
  efforts at biological control. 
  Froggatt (1928) reported that the eggs were deposited in clusters of
  16-60 in the borer holes in slightly decayed stem tissue.  Young larvae found in decaying stems that
  contained no weevil larvae were believed to be phytophagous.   In North America Atherix
  variegata Wlk. is an aquatic
  species of considerable abundance. 
  Large egg masses and the remains of many flies have found on the
  underside of a Connecticut bridge by Britton (1936).  The largest of the masses covered an area
  of ca. 50 sq-ft., and was at least one-half inch deep.  Eggs hatch in ca. 6 days, and young larvae
  drop into water, where they feed on various soft bodied insects and other
  organisms.  Some species of Symphoromyia also have aquatic larvae
  (Clausen 1940/62).   = = = = = = = = = = = = = = = = = = = =   Key References:  
    <medvet.ref.htm>    <Hexapoda>   Bezzi, M.  Bezzi, M. 
  1928. Diptera Brachycera and Athericera of the Fiji
  Islands based on material in the British Museum.  Brit. Mus. Nat. Hist.       London. viii + 220 pp. Kerr, P. H.  2010. Phylogeny and
  classification of Rhagionidae, with implications for Tabanomorpha (Diptera:
  Brachycera). Zootaxa 2592: 1–133. Leonard, M. D.  1930. A revision of the Dipterous family Rhagionidae
  (Leptidae) in the United States and Canada, Memoirs Am. Ent. Soc. 7:1–      181. Lindner, E.  1924–1925.  Rhagionidae in Die Fliegen der Paläarktischen Region 4 (20)
  1–49. Malloch, J. R.  1932. 
  Rhagionidae, Therevidae. British Museum (Natural History). Dept. of
  Entomology [eds] Diptera of Patagonia and      South Chile, based mainly on material
  in the British Museum (Natural History). Part V. Fascicle 3.-Rhagionidae
  (Leptidae), Therevidae,       Scenopinidae, Mydaidae, Asilidae,
  Lonchopteridae, pp. 199–293. Matheson, R. 1950.  Medical Entomology.  Comstock Publ. Co, Inc.  610 p. Nagatomi, A. & K. Soroida.  1985. The structure of the
  mouthparts of the orthorrhaphous Brachycera (Diptera) with special reference
  to       blood-sucking. Beitr. Ent. 35(2): 263–368,
  480. Nagatomi, A.  1982.  The genera of Rhagionidae (Diptera). J. Nat. Hist. 16:
  31–70. 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. Stuckenberg, B.  1960. Diptera (Brachycera):
  Rhagionidae, Keys to genera and species. So.Afr. Anim. Life 7: 216–308. Stuckenberg, B.  1965. The Rhagionidae of
  Madagascar (Diptera), Keys to genera and species.  Ann.Natal Mus. 18:89–170.   | 
 
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