| File: <chama1.ima.htm>        [For educational purposes only]       Terminology       Glossary    <Principal Natural
  Enemy Groups >  <Citations> | 
 
| Immature Stages
  of Chamaemyidae            Detailed information on immature stages of Chamaemyidae
  (= Ochthiphilidae) is being acquired. 
  However, Martelli (1908) studied Filippia
  oleae Costa in Italy. He
  found that the entire contents of the host=s egg sac was consumed by a single
  larva, and the cycle from egg to adult covered 30 days.  He reported 4-5 generations per year.             A Leucopis
  species was studied by Cherian (1933). 
  This is a predator of aphids in India.  The egg is 0.36 mm long, white and ribbed longitudinally.  The 1st instar larva lacks integumentary
  hairs, while the mature form has several fleshy processes on each body
  segment.  The posterior spiracles of
  all instars are borne on stalked processes, which are most pronounced on the
  mature larva and the puparium.  Before
  pupation, the larva exudes a large quantity of mucilaginous material which
  darkens quickly and firmly attaches the puparium to the substratum.  The egg, larval, and pupal stages cover
  2-4, 4-5 and 5-7 days, respectively.             Please CLICK on picture to view details:                In Leucopis bella
  Lw. And L. griseola Fall in North America,
  Maple (Clausen 1940) found the eggs to measure ca. 0.5 by 0.16 mm, with the
  anterior end somewhat pointed.  They
  are pearly white with the surface bearing longitudinal ridges.  They are laid singly among the egg mass or
  colonies of the host and hatch in 3-4 days. 
  There are 3 larval instars in L.
  bella.  The first is white in color, later
  becoming reddish, broadest in the abdominal region and bluntly rounded
  posteriorly, and it tapers considerably toward the head.  The integument is bare.  The posterior spiracles are simple and
  borne on prominent conical processes, and the anterior spiracles are
  minute.  The 3rd instar larva (Fig.
  192A) is 5.0 mm long and clothed only with minute setae.  The posterior spiracles (Fig. 192C) are
  borne on long and almost cylindrical processes, which are widely separated,
  diverging and directed dorsad.  Each
  spiracle consists of 3 curved finger-like projections, each of which bears an
  opening at the apex.  The larva of L. griseola differs from L.
  bella by possessing small
  fleshy spines on all body segments.             In both species the number of molts varies at times,
  seemingly due to temperature variations. 
  Some individuals have only 2 larval instars rather than the usual 3.             Pupation occurs among the host egg masses.  An incomplete cocoon is spun, which is
  composed of a network of coarse threads. 
  The puparium (Fig. 192D) is dull reddish-brown in color and
  indistinctly segmented except for the anterior region (Clausen 1940).  The stalked caudal spiracles of the mature
  larva persist unchanged, and there are no protruding prothoracic pupal
  cornicles.             Malloch (1921) described the puparia of several
  predatory species from Illinois.  The
  puparium of L. orbitalis Malloch has minute
  4-branched anterior spiracles, and the caudal pair are borne on short, stout
  stalks lying closely adherent to the substratum on which the puparium is
  formed.  In Leucopomyia pulvinariae
  Malloch, the posterior spiracles are very small and sessile, differing in
  this respect from those described for other species of this family.  Most species have the ventral side of the
  puparium somewhat flattened, and in some the dorsum is depressed (Clausen
  1940).   References:   Please refer to  <biology.ref.htm>,
  [Additional references may be
  found at: MELVYL Library ]   |