| File: <braconid.htm>                                           
  [For educational purposes only]       
  Glossary            <Principal Natural Enemy Groups >             <Citations>             <Home> | 
 
| HYMENOPTERA, Braconidae (Kirby 1837) -
  (Ichneumonoidea). <Images-1> & <Images-2>
  & <Images-3>  &   <Juveniles>     Description & Statistics             Braconidae. -- All species
  of the braconids are parasitic on other insects.  They sting the host and thereby paralyze it.             There are more than 1850 North
  American species most of which are beneficial. The adults are all fairly
  small rarely exceeding 16 mm in long.  Many are stout-bodied than the ichneumons, and the abdomen is
  about as long as the head and the thorax combined.  They are similar to ichneumonids by lacking a costal cell, but
  they differ by not having more than one recurrent vein.  Many species are valued as natural
  controls of pest insects.              Braconids and ichneumonids have
  similar habits, but unlike the ichneumonids many pupate in silken cocoons on
  the outside of the body of their hosts, while others spin silken cocoons
  entirely apart from the host. 
  Polyembryony occurs in a few species, primarily in the genus Macrocentrus,
  each egg of M. grandis Goidanich, a parasitoid of the European
  corn borer, develops into from 16 to 24 larvae.             This is a family of parasitoid
  wasps and one of the richest families of insects. Between 50,000 and 150,000
  species exist worldwide. The species are grouped into about 45 subfamilies
  and 1,000 genera, some important ones being: Ademon, Aphanta, Asobara,
  Bracon hebetor, Cenocoelius, Chaenusa, Chorebidea,
  Chorebidella, Chorebus, Cotesia, Dacnusa, Microgaster,
  Opius, Parapanteles, Phaenocarpa, Psenobolus.             The morphological variation among
  braconids is notable. Braconids are often black-brown (sometimes with reddish
  markings), though some species exhibit striking coloration and pattern, being
  parts of Müllerian mimicry complexes. They have one or no recurrent veins,
  unlike other members of the Ichneumonoidea which usually have two. Wing
  venation patterns are also divergent to apparent randomness. The antennae
  have 16 segments or more; the hind trochanters have 2 segments.             Females often have long
  ovipositors, an organ that largely varies intraspecifically. This variation
  is closely related to the host species upon which the wasp deposits its egg.
  Species that parasitize microlepidoptera, for instance, have longer
  ovipositors, presumably to reach the caterpillar through layers of plant
  tissue. Some wasps also have long ovipositors because of caterpillar defense
  mechanisms such as spines or hairs.             Most species are primary
  parasitoids (both external and internal) on other insects, especially upon
  the larval stages of Coleoptera, Diptera, and Lepidoptera, but also some
  hemimetabolous insects like aphids, Heteroptera or Embiidina. Most species
  kill their hosts, though some cause the hosts to become sterile and less
  active. Endoparasitoid species often display elaborate physiological
  adaptations to enhance larval survival within host, such as the co-option of
  endosymbiotic viruses for compromising host immune defenses. These
  polydnaviruses are often used by the wasps instead of a venom cocktail. The
  DNA of the wasp actually contains portions that are the templates for the
  components of the viral particles and they are assembled in an organ in the
  female's abdomen known as the calyx.[1] A 2009
  study has traced the origins of these templates to a 100-million-year-old
  viral infection whose alterations to its host DNA provided the necessary
  basis for these virus-like "templates."             These viruses suppress the immune
  system and allow the parasitoid to grow inside the host undetected. The exact
  function and evolutionary history of these viruses are unknown. It is a
  little surprising to consider that sequences of polydnavirus genes show the
  possibility that venom-like proteins are expressed inside the host
  caterpillar. It appears that through evolutionary history the wasps have so
  highly modified these viruses that they appear unlike any other known viruses
  today. Because of this highly modified system of host immunosuppression it is
  not surprising that there is a high level of parasitoid-host specificity. It
  is this specificity that makes Braconids a very powerful and important
  biological control agent.             Parasitism on adult insects
  (particularly on Hemiptera and Coleoptera) is also observed. Members of two
  subfamilies (Mesostoinae and Doryctinae) are known to form galls on
  plants.  Both syncitial and
  holoblastic cleavage are present, even in closely related taxa.             Larvae can be found on hosts as
  diverse as aphids, bark beetles, and foliage-feeding caterpillars. Many
  species are egg-larval parasitoids; hence they are often utilized as
  biological pest control agents, especially against aphids.   Natural History             The family dates from early
  Cretaceous (provided that Eobracon is properly assigned to this
  family). It underwent extensive diversification from mid or late Cretaceous
  to early Tertiary, correlating with the radiation of flowering plants and
  associated herbivores, the Braconidae is traditionally divided into more than
  40 subfamilies. These fall to two major groups, informally called the
  cyclostomes and non-cyclostomes. In cyclostome braconids, the labrum and the
  lower part of the clypeus are concave with respect to the upper clypeus and
  the dorsal margin of the mandibles. These groups may be clades that diverged
  early in the evolution of braconids.             The species Microplitis
  croceipes possesses an extremely accurate sense of smell and can be
  trained for use in narcotics and explosives detection.   --------------------------------------------   References:   Please refer to  <biology.ref.htm>, [Additional references may be found
  at: MELVYL Library]   Basinger, G.  1938.  The orange tortrix.  Hilgardia 11:  661-63.   Brown.  1946.  Canad. Ent. 78: 
  121-29.   Chiri, A. A. & E. F. Legner.  1982.  Host-searching kairomones alter behavior
  of Chelonus sp. nr. curvimaculatus, a hymenopterous parasite
  of the pink bollworm, Pectinophora gossypiella (Saunders).  Environ. Ent. 11:  452-55.   Chiri, A. A. & E. F. Legner. 
  1983.  Field applications of
  host-searching kairomones to enhance parasitization of the pink bollworm
  (Lepidoptera: Gelechiidae).  J. Econ. Ent. 76:  254-255.   Chiri, A. A. & E. F. Legner.  1986.  Response of three Chelonus (Hymenoptera: Braconidae) species to kairomones in
  scales of six Lepidoptera.  Canad.
  Ent. 118:  329-33.   Crossman.  1922.  USDA Bull 1028:  1-25.   Davis.  1944.  USDA Tech. Bull. 871:  1-19.   Fallis.  1942.  Canad. J. Res. Sect. D., Zool. Sci.
  20:  13-19.   Faure. 
  1926.  Contrib. a l'étude de la
  Piéride du Chon.  Univ Lyon.  p. 41-52.   Fulton.  1940.  Ann. Ent. Soc. Amer. 33:  240.   Gilmore.  1938.  J. Econ. Ent. 31:  712-15.   Hamilton.  1935.  Ent. Mon. Mag. 71:  262-70   Khandage, V. S., K. P. Pokhadkar & L. M. Nair.  1980. 
  Studies on the efficacy of Trichogramma
  brasiliensis A.  egg parasite and Apanteles angaleti M.
  larval parasite in controlling cotton bollworms.  Andhra Agr. J. 27: 
  41-2.   Legner, E. F. & S. N. Thompson.  1977.  Effects of the
  parental host on host selection, reproductive potential, survival and
  fecundity of the egg-larval parasitoid, Chelonus
  sp. near curvimaculatus Cameron,
  reared on Pectinophora gossypiella (Saunders) and Phthorimaea operculella (Zeller).  Entomophaga 22:  75-84.   Leius, G.  1960.  Canad. Ent. 92:  371-75.   Marsh, P.  1971. 
  Ann. Ent. Soc. Amer. 119: 
  33-78.   Michelbacher & Smith.  1943.  Factors limiting the alfalfa
  butterfly.  Hilgarida 15(4):  369-91.   Muesebeck & Dohanian.  1917. 
  USDA Agr. Bull 1487:  1-34.   Muesebeck.  1918.  J. Agr. Res.
  17:  191-206.   Narayanan, E. S., B. R. Subha Rao &
  G. A. Gangrade.  1956.  beitr. Ent. 261-70.   Narayanan, E. S., B. R. Subba Rao &
  T. S. Thontadarya.  1962.  Effect of
  temperature and humidity on the rate of development of the immature stages of
  Apanteles angaleti Muesebeck (Br., Hym.). 
  Proc. Nanth. Inst. Sci. India B-28:  156-63.   Telenga, N. A.  1952.  Origin and Evolution of Parasitism in
  Hymenoptera Parasitica and Development of their Fauna in U.S.S.R.  St. Publ. 
  109 p.   Tothill.  1927.  Canad. Dept. Agr. Tech. Bull.
  (n.s.)3:  76-88.   van Achterberg, C.  1976.  Tijdschr. Ent. 119:  33-78.   Worth, C. B.  1939.  Obseervations on parasitism and
  superparasitism (Lepid.: Sphingidae; Hymen.:Braconidae, Chalcididae).  Ent. News 50:  137-41.   Zwölfer, H.  1964.  Notes on the parasites of Swammerdamia lutarea Hw. and S. caessella. Hb. (Lep. Hyponomentidae)
  in Central Europe.  Tech. Bull.
  Commonw. Inst. Biol. Contr. 4: 
  121-46.   |