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| DIPTERA, Nemestrinidae --  <Images> & <Juveniles>     This is a rare family of Diptera, several
  species of which are known to parasitize larvae of Coleoptera and a few are
  internally parasitic on locusts.   Biology & Behavior  Handlirsch (1882, 1883) and Brauer (1883, 1884) gave early
  accounts of the host preferences of the family on Hirmoneura obscura
  Meig., parasitic on Amphimallus solstitialis L. (= Rhizotrogus sp.) pupae.  Riley (1883a, 1884) elaborated on their
  observations.  Hirmoneura obscura
  adults are present in the field during July and early August, when females
  are frequently observed laying eggs in abandoned burrows of Anthaxia quadripunctata L., and probably of other coleopterous borers, in
  broken branches, spruce poles, etc., from which bark had been removed.  The parasitoid seems closely associated
  with spruce, and adults could be found abundant only at the borders of spruce
  forests where fallen trees or branches were common, or in fields bordered by
  fences made of spruce.  No oviposition
  was observed in hosts in living trees. 
  During oviposition the female parasitoid inserts her abdomen tip
  deeply into the exit hole of the beetle and lays a mass of eggs.   After hatching, young larvae make their way to the surface of the
  branch or pole, assume an erect position and are thought to then be blown
  away by wind.  Riley (1883a, 1884)
  hinted that they might be carried into the soil by adult host beetles, but
  Clausen (1940) thought this improbable, for the normal movements of the
  beetles would not bring them into contact with the young larvae and in any
  case just carrying them into the soil would not be advantageous to
  establishing contact with a pupa or grub that was in a vulnerable stage for
  attack.  Brauer (1883, 1884) found
  parasitization of Amphimallus pupae
  to be highest within 3 m. of the spruce fence and that it decreased rapidly
  with an increase in distance away.   Second instar larvae are found in living host pupae during June
  and 3rd instar soon thereafter.  The
  host beetle is fully formed and its integument heavily chitinized before it
  dies.  The parasitoid is oriented in
  the same way as the host.  After the
  fluid contents are completely consumed, it makes a large hole in the venter
  of the thoracic region and eventually pupates alongside the host remains or partly
  extruded from the opening (Clausen 1940/1962).  It is thought that the mature larva persists until the
  following season, because some individuals that had emerged from host pupae
  during June did not pupate by August. 
  In the field, the pupae work their way to the soil surface just before
  they emerge as adult flies.  The pupal
  shells were observed in large numbers in the field, each standing upright
  with its posterior end held in the burrow by the caudal fork and spines.   Brauer (1883, 1884) concluded that the life cycle of Hirmoneura must cover two years just
  as its host.  Beetles lay their eggs
  in late summer, with larval and pupal stages being completed by autumn of the
  following year.  Newly formed adults
  hibernate in their pupal cells and then appear in the field in June of the
  2nd year.  Hirmoneura eggs hatch in July and early August.  At this time no beetle pupae are
  available, and thus they wait until the following May or June to
  develop.  If the protracted larval
  diapause is normal, the 2-year cycle is obligatory; for larval development is
  not completed until the season following oviposition, and the second winter
  is then passed in the mature larval or pupal stage (Clausen 1940/1962).   Brauer tried to determine how and when 1st instar larvae reach
  their hosts.  He noted that the in the
  case of Anthrax sp. the 1st instar
  larva enters the Agrotis larva and
  then awaits its pupation before completing its own development.  Also, Mantispa
  hibernates in the first stage and then searches for the spider egg masses the
  following spring.  First instar larvae
  of Hirmoneura were found to be very
  long-lived, and Handlirsch (1882, 1883) found one that remained alive without
  food from August 17th to October 29th. 
  This suggests the possibility of living overwinter in the free
  condition, yet Clausen (1940) thought it more probable that they enter the
  more mature beetle larvae during autumn, remaining inactive until after host
  pupation in late springtime.   In South America, Hirmoneura
  exotica Wied. lays its eggs in the
  tunnels of wood boring bees (Brauer 1883, 1884).  Spencer (1931, 1932) observed the manner of oviposition of Parasymmictus clausus O.S. (= Rhynchocephalus
  sackeni Will.).  Females inserted their ovipositors in
  holes and cracks of telegraph poles in which no borers of any kind were present.  They remained in that position for an hour
  or more.  Circumstantial evidence
  suggests that larvae of cerambycid borers of genera Asemum and Xylotrechus
  are probable hosts.  Stuardo (1935)
  found females of H. articulata Ph. to oviposit principally
  during late morning and early afternoon. 
  They were attracted only to poles or posts lacking bark, and the
  ovipositor was inserted deeply into the crevices.  While for one or more hours in that position, a female may lay
  a mass of eggs exceeding 100.   The behavior of lateral larval stages of two species that are
  solitary internal parasitoids of locusts in South Africa (Potgieter 1929),
  suggest that mature larvae of Symmictus
  costatus Loew are on the ground
  surface in association with Locusta
  vardalina Wlk. nighttime resting
  areas.  An examination of living
  parasitized locusts showed that the partly grown parasitoid larva fed only on
  body fluids, with little injury to the host. 
  This was judged by the normal oviposition and development of the
  female locust eggs. The Symmictus
  larva leaves the dead host when mature, and burrows into the soil to 2.5-50.0
  cm.  Pupation takes place soon
  thereafter if conditions are favorable, and the fly emerges ca. 14 days
  later.  However, mature larvae are
  able to adapt themselves to adverse conditions by entering diapause
  (Potgieter 1929).  Diapause may
  persist for 3.5 years, but normally the cycle is requires ca. one year
  (Potgieter 1929).   Trichopsidea ostracea Westw. in Australia is parasitic
  in adults of the plague grasshopper, Chortoicetes
  terminifera Wlk.  Noble (1936) and Fuller (1938) published
  notes on the immature stages.  Larvae
  are solitary, being found in the abdomen. 
  This parasitoid leaves the host while it is still alive, which differs
  from Symmictus.  The prepupal stage in soil extends over
  several months, and the pupal stage lasts 3 weeks.  Field parasitization was ca. 5%.   For detailed descriptions of immature stages of Nemestrinidae
  please see (Clausen 1940/1962).     References:   Please refer to  <biology.ref.htm>, [Additional references
  may be found at:  MELVYL
  Library]     |