Exploratory behaviour plays an important role in most animals for gathering information about their environment. If it constitutes an adaptation to different environmental conditions exploratory behaviour should differ between species. This has been tested with several hypotheses. Sixty‐one parrot species (Psittacidae) from eight tribes with different diets and habitat preferences were investigated in aviaries. Two tests were carried out. First, a novel object (wooden ring) in the familiar aviary was presented on two test days in the exploration test. Latencies until first contact with the object and the duration of exploration were recorded. Secondly, in the neophobia test, novel objects were placed beside the feeding dish and latencies until first food intake were recorded. The exploration and neophobia data were related to 12 (13) ecological variables using multiple regression analyses. Phylogenetic relationships were considered. Species that inhabit complex habitats, such as forest edges, or that feed on buds or species from islands showed the shortest latencies in the exploration test. In contrast, long latencies were related to a diet including a great amount of seeds and/or flowers. The longest duration of exploration occurred in species eating nuts or originating from islands, whereas short durations were related to feeding on seeds. Neophobia was positively related to a diet consisting of insects, and negatively to a diet of leaves. There was no relationship between measures of exploration and neophobia. Exploration and neophobia seem to be tightly related to the ecology of a species.

Summary 1.Dispersal is one of the key ecological parameters but it is very difficult to quantify directly. As a consequence, empirical studies often ignore dispersal or use indirect measures. 2. Ringing data have previously been used to estimate the natal dispersal distances of 47 British passerine bird species. This provides an excellent opportunity to examine the potential of various indirect measures to predict natal dispersal distances in British birds. 3. We use a phylogenetic comparative framework and single-and multipredictor models including ecomorphological, behavioural or ecological traits to predict natal dispersal distance. 4. A multipredictor model that includes Kipp's distance (a measure of wing tip length), bill depth and tail graduation explains 45% of the interspecific variation in natal dispersal distance. These morphological characters all relate to aerodynamics with stronger flyers dispersing further. 5. However, an index of migration is a strong (but less informative) correlate of dispersal distance and Kipp's distance and bill depth are strong correlates of migration. Thus, we cannot disentangle whether these ecomorphological traits influence dispersal distance directly or whether the relationship between ecomorphology and dispersal is mediated through migratory behaviour. 6. Notwithstanding uncertainties regarding the causal links between dispersal distance and wing morphology, we suggest that two ecomorphological traits, Kipp's distance and bill depth, may provide a useful surrogate.

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Although elaborate bird song provides one of the prime examples of a trait that evolved under sexual selection, it is still unclear whether females judge the quality of males by attributes of their song and whether these song features honestly signal a male's genetic quality. We measured the ability of male dusky warblers Phylloscopus fuscatus to maintain a high sound amplitude during singing, which probably reflects an individual's physiological limitations. This new measure of singing performance was correlated with male longevity and with extra-pair paternity, indicating that females who copulated with better singers obtained 'good genes' for their offspring. Our findings are consistent with the idea that females assess male quality by subtle differences in their performance during the production of notes, rather than by the quantity or versatility of song. In addition, observations on territorial conflicts indicate that attractive males invest less in competition over territories because they can reproduce via extra-pair paternity.

A multivariate analysis of data from a wide range of avian species revealed that migratory distance was related to a high aspect ratio, long and pointed wings and well‐developed distal wing segments. Migration also appeared to set limits on the development of the hind limb and on the wing muscles not involved in forward flight. Among Sylvia warblers it is shown that habitat use and migration may constrain each other.

The wintering strategies of Pied Flycatchers Ficedula hypoleuca and Willow Warblers Phylloscopus trochilus in their West African winter quarters were compared. Pied Flycatchers arrived early in the season (September) and stayed in the study area throughout the winter. They were territorial and showed a high return rate. Intraspecific relationships were mostly expressed by territorial behaviour. Interspecific relations seemed to be unimportant. Willow Warblers arrived relatively late (November) and were absent from the area for some weeks in January and February, a behaviour which was interpreted as itinerancy. Willow Warblers were non‐territorial and never returned to a site. Willow Warblers usually moved through the area in monospecific or mixed‐species flocks. Habitat and microhabitat choice of these species were similar but in feeding ecology they differed by the higher diversity of feeding substrates and feeding techniques of Pied Flycatchers. The differences in the winter strategies are explained by the ability of Pied Flycatchers to defend a territory because of their diversity in foraging behaviour, whereas Willow Warblers are more specialized and are therefore forced to be more mobile to find their patchily distributed food.

Birds have brains that are comparable in size to those of mammals. However, variation in relative avian brain size is greater in birds. Thus, birds are ideal subjects for comparative studies on the ecological and behavioral influences on the evolution of the brain and its components. Previous studies of ecological or behavioral correlates in relative brain size were mainly based on gross comparisons between higher taxa or focussed on the relationships between the sizes of specific brain structures and the complexity of different tasks.Here we examine variation in dimensions of the braincase, relative overall brain size and size of its components, in reference to one general ecological and behavioral task: migration. We used data from three lineages of closely related species (14 Acrocephalines, 17 Sylvia and 49 parulid warblers). Within each group, species vary in their migratory tendencies. We found that species migrating long distances have lower skulls and smaller forebrains than resident species. We discuss four hypotheses that could explain smaller forebrain sizes, and suggest relevant taxa to use in comparative analyses to examine each of these hypotheses: -Brain size is energetically constrained. Contrasts can be made not only between migrants and residents, but also between birds in habitats with high and low levels of available food. -Brain size is developmentally constrained; birds with short growing periods should have smaller forebrains. Comparisons need to be made between birds living in habitats with long and short breeding seasons. -Bill adaptations for foraging constrain braincase dimensions. Further analyses would need to be done on groups with high variation in bill dimensions and foraging modes. -Birds with small brains have to migrate to compensate for low behavioral flexibility. Contrasts between members of families containing tropical residents and migrants need to be made.We also raise the question of whether only those parts of the brain are reduced that are most dispensable and whether brain size reduction limits foraging skills and social competence.

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