Dq. Zhang et al., ULTRASTRUCTURE OF MICROPLITIS-CROCEIPES (CRESSON) (BRACONIDAE, HYMENOPTERA) TERATOCYTES, International journal of insect morphology & embryology, 23(3), 1994, pp. 173-187
The developing embryo of the braconid, Microplitis croceipes (Braconid
ae : Hymenoptera), is encased in an extraembryonic serosal membrane. H
atching of the parasitoid within the larva of its habitual host, Helio
this virescens (Noctuidae Lepidoptera), is initiated about 40 hr after
oviposition when held at 25 +/- 2-degrees-C. At this time, the monola
yered serosal membrane begins to dissociate into individual cells (ter
atocytes). After dissociation, teratocytes become dispersed in the hem
olymph of the host. The average number of teratocytes released from ea
ch parasitoid embryo is 914 +/- 43. Teratocytes average 14.1 +/- 2.4 m
um in diameter when first released, and reach a maximum average diamet
er of 68.1 +/- 4.6 mum 6 days after liberation. Newly released teratoc
ytes have ovoid nuclei, simple mitochondria and a limited number of pr
ofiles of the endoplasmic reticulum, all of which indicate relative me
tabolic inactivity. The ramified nuclei, extensive endoplasmic reticul
um, polymorphic mitochondria and accumulation of glycogen granules and
lipid droplets observed in older teratocytes provide circumstantial e
vidence that protein synthesis is occurring. Within hours after dissoc
iation, microvilli begin to cover the surface of the teratocytes. Anat
omical deformation (blebs) that occurred on some older (8-day-old) ter
atocytes probably resulted from enlargement or expansion of microvilli
.