Diapausing larvae of Aphidoletes aphidimyza (Diptera: Cecidomyiidae) had relatively low supercooling points (SCP) ranging from -19.0 to -26.4°C. None of the specimens that froze at this temperature survived. A high survival rate (up to 87%) at -10°C for 10 days was observed in supercooled larvae. Such features are characteristic for insects that use a chill-tolerance strategy of cold hardiness. However, the cocoons formed by the diapausing larvae were penetrable by external ice crystals and the larvae showed a relatively high survival rate (23 - 34%) at -10°C for 10 days also in the frozen state caused by inoculation by external ice at high subzero temperatures. Such a duality with respect to cold hardiness strategies seems to be ecologically relevant to overwintering in soil habitats where there may be unpredictable contact with external ice.
Larvae of Aphidoletes aphidimyza (Rondani) (Diptera: Cecidomyiidae) secrete an oviposition-deterring pheromone (ODP). In choice tests, females of A. aphidimyza laid significantly fewer eggs on Vicia faba L. plants infested with Aphis fabae Scopoli (Homoptera: Aphidoidea) that were previously exposed to conspecific third-instar larvae or a water extract of their ODP.
A. aphidimyza females also laid fewer eggs on aphid-infested plants that were previously exposed to unfed first-instar larvae of Chrysopa oculata Say, Chrysopa perla (L.) or Chrysoperla carnea (Stephens) (Neuroptera: Chrysopidae), or second-instar larvae of Coccinella septempunctata L. (Coleoptera: Coccinellidae). However, the response to traces of C. carnea larvae was very weak.
Determination of embryonic stages is an important prerequisite for the long-term cryopreservation of eggs and embryos of the predatory gall midge Aphidoletes aphidimyza. This paper describes the embryonic development of this insect based on light microscopy. Gall midge embryogenesis lasts, on average, 102 h at 17°C and 144 h at 15°C. Living embryos can be quickly separated into ten stages that are clearly defined by specific morphological markers. The necessity for selecting definite embryonic stages for cryobiological storage is discussed.