Termites are instantly recognizable mound-builders and house-eaters: their complex social lifestyles have made them incredibly successful throughout the tropics. Although known as ‘white ants’, they are not ants and their relationships with other insects remain unclear. Our molecular phylogenetic analyses, the most comprehensive yet attempted, show that termites are social cockroaches, no longer meriting being classified as a separate order (Isoptera) from the cockroaches (Blattodea). Instead, we propose that they should be treated as a family (Termitidae) of cockroaches. It is surprising to find that a group of wood-feeding cockroaches has evolved full sociality, as other ecologically dominant fully social insects (e.g. ants, social bees and social wasps) have evolved from solitary predatory wasps.

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Data are presented which confirm previous findings that syrnpatric mimicry complexes dominated by unpalatable Neotropical ithomiine butterflies (Nymphalidae: Ithomiinae) are vertically stratified by height of flight. Flight height of ithomiine species is positively correlated with the height of their larval host-plants. Thus members of a mimicry complex utilize hostplants of similar heights. Non-mimetic British woodland butterflies also show a positive relationship between flight height and host-plant height, which suggests that the relationship is independent of mimicry. I propose that female butterflies fly at heights which maximize the probability of encountering their larval host-plants, and that males fly at similar heights to females in order to maximize the probability of encountering potential mates. Female butterflies probably encounter plants of similar heights to their larval hosts more frequently than they encounter plants of other heights. I suggest that butterlly species may therefore be more likely to make host shifts to plant species of a similar height to their current hostplants. Finally, I discuss how the relationship between flight height and height of larval hostplants, coupled with microhabitat-dependent selection on colour pattern, could lead to the evolution in sympatry of vertically stratiied mimicry complexes. 0 1997 The Iinnean Socirty of London ADDITIONAL KEY WORDS-behaviourecologyevolutionhost shifts -Lepidoptera

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Prevailing methods of measuring diet breadth of phytophagous insects are not consistent between studies and generally rely on counts of a variety of higher plant taxa (e.g. genera, families, orders). Results derived from them can be inconsistent if different taxonomic levels are used between studies. In any case, such indices do not include information from the whole branching structure of the host plant phylogeny, and do not address the fact that higher taxa are not necessarily phylogenetically equivalent. Here we present novel phylogeny-based methods which address these shortcomings. Although a previously proposed index (the Phylogenetic Diversity index) may be employed, it cannot be used to measure diets of strictly monophagous insects (i.e. those which utilise a single host species). We therefore introduce a modification of this index (the Root Phylogenetic Diversity index) which may be applied to all diets. In addition, we propose a Clade Dispersion index as a branch-length-independent measure of the degree to which hosts are scattered across the host phylogeny. We describe how these indices could be employed in studies of insect diet breadth and discuss potential problems which may be encountered in their use.

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Host‐plant data for North American and Australian butterflies were used to test the hypothesis that larval diet breadth increases with decreasing resource predictability (where the latter was estimated by host‐plant growth‐form/duration). For each region in turn we compared the diet breadths of butterflies which utilise herbaceous host‐plants with those of species having woody hosts. For North America alone we also compared the diet breadths of species having annual hosts with those utilising perennial hosts, and the diets of species having herbaceous‐annual hosts with those using woody‐perennial hosts. Studies of diet breadth may be biased by the host taxonomic level which contributes most to the diet index used. For example, the results of analyses which employ indices based on numbers of families of hosts utilised may differ from those using indices based on counts of host species or genera. To investigate this potential problem we performed cross‐species analyses where diet breadth was defined in turn as the number of host species, genera, or families eaten. We found that using different taxonomic levels did give inconsistent results. To avoid this we employed phylogenetic diet breadth indices in comparative analyses of Independent Contrasts. The former incorporate information from the whole of the host‐plant phylogeny, whilst the comparative method eliminates any confounding effects of butterfly phylogeny. The results indicated that there is a phylogenetic component to butterfly diet breadth. They also largely differed from those of the cross‐species investigations, although there were similarities (i.e. results differed between regions and varied according to whether the whole fauna or just endemics were investigated). Our results suggested that in both regions, non‐endemics which feed on herbaceous plants have wider diet breadths than non‐endemics which utilise woody hosts. However, we found no consistent evidence that the diet breadths of endemics increase with decreasing resource predictability (as estimated here).