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Summary1. Quantitative genetic analysis of variation in host-use ability was performed in an extremely polyphagous species -the Gypsy Moth. Various life-history traits were investigated by applying a split-family two-environment experimental design, where 30 full-sibling families were reared on oak and Locust Tree leaves. 2. Feeding on Locust Tree leaves decreased preadult viability, prolonged development time, decreased pupal mass both in males and females, and decreased reproductive effort in females. 3. The majority of broad-sense heritabilities did not change across host plants. 4. Significant expression of genetic variation in diet breadth was observed for development time and pupal mass both in males and females, but not for female reproductive effort traits. The heritabilities of plasticities were, on average, lower than heritabilities of the traits themselves. 5. The majority of genetic correlations between the host plants were significantly positive. The only trade-off was found between reciprocal value of reproductive index and the average mass of a fertilized egg within oak. This means that selection for the decrease in relative reproductive investment (under starvation during gradation) will be followed by laying larger eggs. Given that the Gypsy Moth has a cyclic population dynamics, this negative genetic correlation could have a role in maintaining genetic variability in this species.

The pattern of adaptation with regard to life history traits and traits thought to be important in feeding habits of caterpillars in two populations of the gypsy moth (Lymantria dispar L.; Lepidoptera: Lymantriidae) originating from the locust tree (Robinia pseudoacacia; Fabaceae) and oak (Quercus petrea; Fagaceae) forests were investigated in the laboratory. The Robinia population has experienced unsuitable locust tree leaves as an exclusive food resource for more than 40 years. Since Quercus species are the principal host plants of the gypsy moth, the specific objectives of this study have been to measure the extent of differentiation between ancestral and derived populations in several life history traits (egg‐to‐adult viability, duration of larval and pupal stages, and pupal weight) and nutritional indices – relative growth rate (RGR), relative consumption rate (RCR), assimilation efficiency (AD), gross growth efficiency (ECI), and net growth efficiency (ECD). Significant differences between the Quercus and Robinia populations were detected in pupal duration, RGR, RCR, and AD. The presence of a significant population × host interaction in traits such as preadult viability, duration of pupal stage, RGR, and ECI suggests that adaptation of the gypsy moth to the unsuitable host might be ongoing. Using a full‐sib design, we screened for genetic variation in life history traits within both populations, and examined the genetic correlations of performance across oak and locust leaves within both populations. The genetic variances for analyzed life history traits were lower under conditions that are commonly encountered in nature. Our data show that positive cross‐host genetic correlations preponderate within both populations.

The effects of parental and offspring diet on larval growth, food consumption and utilization, and activities of three digestive enzymes (a-amylase, trypsin, leucine aminopeptidase) were examined in extremely polyphagous insect, the gypsy moth (Lymantria dispar). In parental generation, gypsy moth larvae were reared on oak (Quercus cerris) leaves as optimal host or beech (Fagus silvatica) leaves which contains flavonoids and alkaloids. In offspring generation, after molting into the 4 th instar, they were either switched from oak to beech or remained on oak leaves. Decreased growth and food utilization efficiency, increased assimilation efficiency and activities of a-amylase and trypsin were recorded in larvae switched to beech leaves. Significant parental effects were demonstrated for fourth instar duration, weight of fifth instar larvae and specific activity of leucine aminopeptidase. Physiological, ecological and evolutionary context of the obtained results were stressed in the present paper.

The neurohormones are the master regulators of all life processes in insects and they create a strategy of stress protecting events. Neurohormones are synthesized mainly in insect brain neurosecretory neurons. Various stressors of different intensity cause specific changes which influence on neurosecretory neurons activity and synthesis of neurohormones (biogene amines, ecdysiotropins, ecdysiostatins, allatoregulatory neurohormones, adipokinetic neurohormones, etc.). Biogene amines in insects may function as neurohormones controlling carbohydrate and lipid metabolism as the primary response of the insects to the effect of stressors. Intermediary metabolism in insects is mainly regulated by adipokinetic hormones which supply organism by energy especially in extreme conditions. Stress induces changes in release of ecdysioregulatory and allatoregulatory neurohormones and modificates ecdysones and juvenile hormones synthesis in prothoracic gland and corpora allata. The involvement of hormones of an ecdysteroid or JH type in response to stress creates the danger of an untimely induction of morphogenetic process in target cells. Limiting the quantity of secreted hormones and shortening the period when target cells are sensitive to morphogenetic stimuli removes this danger