| File:
  <aphidiid.htm>                          [For educational purposes
  only]        Glossary           
  <Principal Natural Enemy Groups>             <Citations>             <Home> | 
 
 
| COLEOPTERA, Anthribidae. --  <Images> & <Juveniles>     Description & Statistics   Clausen (1940) noted that neither of the above
  researchers observed actual oviposition, although Yano assumed that the eggs
  were placed on or in the vicinity of the host scales and that the young
  larvae later penetrated the egg chamber. 
  Silvestri believed that they were laid beneath the margin of the scale
  and into the chamber by means of the extensible ovipositor.  Clausen (1940) observed oviposition of B. niveovariegatus
  in both field and laboratory, in E.
  pela and several species of Kermes. 
  The feeding habit of the female was found to have an intimate
  relationship with oviposition.  The
  female breaks the hardened integument of the host scale and feeds on the body
  contents, after which she reverses her position, thrusts the ovipositor into
  the wound and through the thin ventral body wall, and places her egg within
  the egg chamber.  The beetle egg is
  usually found adhering to the body wall of the host at the point of
  penetration of the beetle's ovipositor. 
  The feeding wound is quite large, but it often heals over and normal
  oviposition by the scale is possible, though a large number die from their
  injuries.   Young beetle larvae feed only on the eggs.  Later, after the host female dies, they
  feed extensively on body tissues also. 
  When hosts are killed by injury associated with feeding of the female
  beetle, the larva may develop largely as a scavenger rather than an egg
  predator.   Only a single B.
  niveovariegatus develops in a
  host, even though the latter may be quite large and have sufficient eggs to
  bring several beetles to maturity. 
  Therefore, the degree of control exercised is not as high as the
  50-70% of scales attacked wound indicate (Clausen 1940/1962).  In B.
  niveovariegatus and B. fasciatus,
  there is thought to be only a single annual generation, at least on the above
  single-brooded hosts.  Adults emerge
  late in June, persist in that stage through winter and appear for oviposition
  the following April-May.   This is a small family of “fungus weevils” that
  is unique by having a broad beak.  The
  larvae of some species reside in 
  woody fungi while others occur in corn and wheat smut, and some in
  dead wood.  Adults are found under old
  bark or on dead twigs  (Headstrom
  1977, White 1983).   Some members of the genus Brachytarsus (= Anthribus) have been reared from
  lecaniine Coccidae.  Yano (1915) first
  reported on the predaceous behavior and life history of B. niveovariegatus
  Roel. attacking the Chinese wax scale, Ericerus
  pela Chev. in Japan.  During May-June ca. 50% of female scales
  contained mature Brachytarsus
  larvae, pupae or adults in the egg chamber. 
  Adults emerged during late June, and the remains of host scales were
  conspicuous because of the large, circular emergence holes on the dorsum.  Silvestri (1919b) found B. fasciatus
  Foerst. common as a natural enemy of Eulecanium
  coryli in south Europe, where a
  maximum parasitization of 50% of scales occurred.  Oviposition is mainly in April when a considerable number of
  eggs are present beneath host scales and the beetle egg is apparently laid among
  them.  Female beetles feed on the body
  fluids of the host scales and also on the eggs.  The larvae are confined to the cavity underneath the individual
  host scale and are dependent on the eggs found there for food.  Therefore, the relationship is identical
  with that of the chalcidoid Scutellista
  cyanea Motsch. and its host Saissetia oleae Bern.  The
  larva is weevil-like and robust, with the legs being represented by small
  conical protuberances.  The cycle from
  egg to adult is around 2 months. 
  Adults appear in June and persist without oviposition until hosts of
  the proper stage become available the following spring.  Brachytarsus
  nebulosus Foerst. is also a
  natural enemy of several other species of lecaniine Coccidae in Europe (Prell
  1925).             Anthribidae
  Billberg, 1820 [placed on the Official List of Family-Group Names in Zoology
  by ICZN (1994: 72), with the endorsement that it and other family-group names
  based on Anthribus Geoffroy,
  1762 are to be given precedence over those based on Choragus Kirby, 1819] [source: ICZN
  (1994: 72)]              Type
  genus: Anthribus Geoffroy, 1762
  [source: ICZN (1994: 72)] [stem = Anthrib-]
     Synonyms            
  Choragidae Kirby, 1819 [placed on the Official List of Family-Group
  Names in Zoology by ICZN (1994: 72), with the endorsement that it and other
  family-group names based on Choragus
  Kirby, 1819 are not to be given priority over those based on Anthribus Geoffroy, 1762] [source: ICZN
  (1994: 72)] [subfamily] Type genus: Choragus
  Kirby, 1819 [source: ICZN (1994: 72)] [stem = Chorag-]     References:  
  Please refer to  <biology.ref.htm>,
  [Additional references may
  be found at:  MELVYL Library ]   Headstrom,
  R.  1977.  The Beetles of America. 
  A. S. Barnes & Co. London & NY.  488 p.   White,
  R. E.  1983.  A Field Guide to the Beetles of North America.  Houghton Mifflin Co., Boston.  368 p.   |