Larval-derived nutritional reserves are essential in shaping insects' adult fitness. Early larval instars of many Lepidopteran species are often sessile, and the conditions experienced by these larvae are often highly dependent on the mother's oviposition choice. Later larval stages are more mobile and therefore can choose their food whenever alternatives are available. We tested how feeding on a drought-exposed host plant impacts life history in an insect herbivore, and whether the observed responses depended on developmental stage. We used drought to alter host plant quality of the ribwort plantain, Plantago lanceolata , and assessed whether host plant preference of postdiapause larvae and adult females increased their own or their offspring's performance, respectively, in the Glanville fritillary butterfly, Melitaea cinxia . Larval response to drought-exposed host plants varied with developmental stage: early larval stages (prediapause) had decreased survival and body mass on drought-exposed plants, while later larval stages (postdiapause) developed faster, weighed more and had a higher growth rate on the drought-exposed plants. Postdiapause larvae also showed a preference for drought-exposed host plants, i.e. those that increased their performance, but only when fed on well-watered host plants. Adult females, on the other hand, showed an oviposition preference for well-watered plants, hence matching the performance of their prediapause but not their postdiapause offspring. Our results highlight how variation in environmental conditions generates stage-specific responses in insects. Individuals fine-tune their own or their offspring's diet by behavioural adjustments when variation in host plant quality is available.

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Elevation gradients impose large differences in abiotic and biotic conditions over short distances, in turn, likely driving differences in gene expression more than would genetic variation per se, as natural selection and drift are less likely to fix alleles at such a narrow spatial scale. As elevation increases, the pressure exerted on plants by herbivores and on arthropod herbivores by predators decreases, and organisms spanning the elevation gradient are thus expected to show lower levels of defence at high elevation. The alternative hypothesis, based on the optimal defence theory, is that defence allocation should be higher in low-resource habitats such as those at high elevation, due to higher costs associated with tissue replacement. In this study, we analyse variation with elevation in (i) defence compound content in the plant Lotus corniculatus and (ii) gene expression associated with defence against predators in the specific phytophagous moth, Zygaena filipendulae. Both species produce cyanogenic glycosides (CNglcs) such as lotaustralin and linamarin as defence mechanisms, with the moth, in addition, being able to sequester CNglcs from its host plant. Specifically, we tested the assumption that the defence-associated phenotype in plants and the gene expression in the insect herbivore should covary between low- and high-elevation environments. We found that L. corniculatus accumulated more CNglcs at high elevation, a result in agreement with the optimal defence theory. By contrast, we found that the levels of expression in the defence genes of Z. filipendulae larvae were not related to the CNglc content of their host plant. Overall, expression levels were not correlated with elevation either, with the exception of the UGT33A1 gene, which showed a marginally significant trend towards higher expression at high elevation when using a simple statistical framework. These results suggest that the defence phenotype of plants against herbivores, and subsequent herbivore sequestration machineries and de novo production, are based on a complex network of interactions.

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