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. Phratora vitellinae L. and Chrysomela tremulae F. (Chrysomelinae, Coleoptera) feed on Salix or Populus spp. (Salicaceae). Their larvae, as well as the larvae of other chrysomelines feeding on Salicaceae, secrete salicylaldehyde. In this study, we demonstrate that salicylaldehyde is derived from salicin, a phenylglucoside present in the leaves of the host plant. The concentration of salicylaldehyde in the secretion is positively correlated with the amount of salicin in the food of the larvae. The transformation of salicin into salicylaldehyde occurs in the defence glands since the β‐glucosidase activity is 4 times higher in their glands than in the gut. The larvae recover most of the glucose that results from the hydrolysis of salicin. For generalist predators, such as ants, salicylaldehyde is a more potent deterrent than saligenin or salicin.

We reared larvae of three generalist insect species on plants occurring in their habitats. Individuals of each species were kept either on mixed diets, or on each plant species separately. We measured food plant preference in the mixed-diet group and compared insect performance on single plants to the performance on the mixed diet. For all three insect species, food choice within the mixed-diet groups was non-random and delivered the best overall performance, thus ful®lling the criteria for self-selected diets. When a single diet was as good as the mixed diet for one particular aspect of performance (Adenostyles alliariae and Petasites albus for Miramella alpina; A. alliariae for Callimorpha dominula), it was never the most preferred food plant in the mixed-diet treatment. Whether the bene®t achieved by mixing diets is due to nutrient complementation or toxin dilution, we argue that there is no easy way to distinguish between the two hypotheses on the basis of consumption and performance measurements, as has previously been proposed. From the interpretation of utilisation plots, the ANCOVA equivalent of nutritional indices, we were able to gain insight into where in the sequence from ingestion to growth (preingestive, predigestive or postdigestive) single diets caused di erences from mixed diets. The elements of this control system which were in¯uenced by single diets varied considerably, both within and between insect species. No food plant was toxic or deterrent to all experimental insect species; a food plant that caused consumption e ects (preingestive) for one insect species could be dealt with metabolically (postdigestive) by another; di erent food plants could cause behavioural e ects (preingestive), metabolic e ects (postdigestive), or a combination of both e ects, all within the same insect species. However, one generality did emerge: once a food was ingested, further growth-relevant e ects occurred metabolically (postdigestive) rather than via di erential egestion (digestibility).

Insect‐plant interactions have played a prominent role in investigating phylogenetic constraints in the evolution of ecological traits. The patterns of host association among specialized insects have often been described as highly conservative, yet not all specialized herbivorous insect lineages display the same degree of fidelity to their host plants. In this paper, we present an estimate of the evolutionary history of the leaf beetle genus Oreina. This genus displays an amazing flexibility in several aspects of its ecology and life history: (1) host plant switches in Oreina occurred between plant families or distantly related tribes within families and thereby to more distantly related plants than in several model systems that have contributed to the idea of parallel cladogenesis; (2) all species of the genus are chemically defended, but within the genus a transition between autogenous production of defensive toxins and sequestration of secondary plant compounds has occurred; and (3) reproductive strategies in the genus range from oviparity to viviparity including all intermediates that could allow the gradual evolution of viviparity. Cladistic analysis of 18 allozyme loci found two most parsimonious trees that differ only in the branching of one species. According to this phylogeny estimate, Oreina species were originally associated with Asteraceae, with an inclusion of Apiaceae in the diet of one oligophagous species and an independent switch to Apiaceae in a derived clade. The original mode of defense appears to be the autogenous production of cardenolides as previously postulated; the additional sequestration of pyrrolizidine alkaloids could have either originated at the base of the genus or have arisen three times independently in all species that switched to plants containing these compounds. Viviparity apparently evolved twice in the genus, once without matrotrophy, through a retention of the eggs inside the female's oviducts, and once in combination with matrotrophy. We hypothesize that the combination of autogenous defense and a life history that involves mobile externally feeding larvae allowed these beetles to switch host plants more readily than has been reported for highly conservative systems.

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