| Mortality factor | Importance | Mortality | Density dependence | Causes |
| Unfulfilled fecundity | Major | 70-86% | Yes for larval crowding | Mainly weather, host plant, larval density |
| Infertility | Insignificant | <1% | No | |
| Inviability | Minor | 2-4% | No | Weather |
| Egg predation/parasitism | Minor | 4-10% | Delayed density dependence for Trichogramma spp. | Predatory bugs, Anystis baccarum, Trichogramma spp. |
| Predation and losses of young larvae | Major | 48-94% | Imperfect
density dependence |
Spiders, earwigs, predatory bugs, Anystis baccarum, emigration, weather, birds |
| Larval
parasitism, all species Dolichogenidea tasmanica |
Unknown in NZ* |
23-55% 20-50% |
Species-dependent Not clear for this species* |
Complex of parasitoids, the most abundant in New Zealand being Dolichogenidea tasmanica |
| Nucleopolyhedrosis virus | Insignificant | <1% | Yes | |
| Larval/pupal parasitism | Minor | <5% in orchards | Unknown | Pales spp. and complex of introduced parasitoids. |
| Migration | Major | Highly probable | High populations on nearby host plants causing immigration into low resident density in orchards | |
| * Studies in Australia indicate that none of the parasitoids of lightbrown apple moth there are major mortality factors affecting population density. Some parasitoids show density dependence but are not major mortality factors.. | ||||