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The recent growth of research on animal personality could provide new insights into our understanding of sociality and the structure of animal groups. Although simple assays of the type commonly used to study animal personality have been shown to correlate with social aggressiveness in some bird species, conflicting empirical results do not yet make it clear when such assays, typically using isolated individuals, predict behaviour within social groups. We measured aggressiveness in groups of a very gregarious species, the common waxbill (Estrilda astrild), and performed five commonly used behavioural assays on the same individuals: tonic immobility, mirror test, novel object test, open-field test and a variant of the latter in an enriched environment. We found that larger individuals were more dominant and that differences in aggressiveness were repeatable. None of the traditional behavioural assays were related to aggressiveness or dominance. Standard personality assays may fail to capture individual differences relevant to predict social behaviour, and we discuss biological and methodological explanations for these results, such as social behaviour being in part an emergent property of groups rather than an intrinsic property of individuals, or gregarious species being particularly sensitive to the conditions of standard personality assays that test individuals alone.Ethology 121 (2015) 84-93

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The forces shaping female plumage color have long been debated but remain unresolved. Females may benefit from conspicuous colors but are also expected to suffer costs. Predation is one potential cost, but few studies have explicitly investigated the relationship between predation risk and coloration. The fairy-wrens show pronounced variation in female coloration and reside in a wide variety of habitats across Australasia. Species with more conspicuous females are found in denser habitats, suggesting that conspicuousness in open habitat increases vulnerability to predators. To test this, we measured attack rates on 3-D-printed models mimicking conspicuously colored males and females and dull females in eight different fairy-wren habitats across Australia. Attack rates were higher in open habitats and at higher latitudes. Contrary to our predictions, dull female models were attacked at similar rates to the conspicuous models. Further, the probability of attack in open habitats increased more for both types of female models than for the conspicuous male model. Across models, the degree of contrast (chromatic and achromatic) to environmental backgrounds was unrelated to predation rate. These findings do not support the long-standing hypothesis that conspicuous plumage, in isolation, is costly due to increased attraction of predators. Our results indicate that conspicuousness interacts with other factors in driving the evolution of plumage coloration.

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Selection due to social interactions comprises competition over matings (sexual selection stricto sensu) plus other forms of social competition and cooperation. Sexual selection explains sex differences in ornamentation and in various other phenotypes, but does not easily explain cases where those phenotypes are similar in males and females. Understanding such similarities requires knowing how phenotypes influence nonsexual social interactions as well, which can be very important in gregarious animals, but whose role for phenotypic evolution has been overlooked. For example, 'mate choice' experiments often found preferences for ornamentation, but have not assessed whether those are strictly sexual or are general social preferences. Using choice experiments with a gregarious and mutually ornamented finch, the common waxbill (Estrilda astrild), we show that preferences for ornamentation in the opposite-sex also extend to same-sex interactions. Waxbills discriminated between opposite-and same-sex individuals, but most preferences for colour traits were similar when interacting with either sex. Similar preferences in sexual and nonsexual associations may be widespread in nature, either as social adaptations or as by-product of mate preferences. In either case, such preferences may set the stage for the evolution of mutual ornamentation and of various other similarities between the sexes.

Avian plumage colouration is one of the most impressive displays in nature and is frequently used as sexual signal. There is now considerable evidence that females consistently prefer males with the most elaborated colour displays. Bird colour vision expands into the ultraviolet (UV) range, which prompted several studies to test the importance of UV in mate choice, revealing that females are affected by the UV light component. These studies were mostly performed on structural plumage, whereas carotenoid-based plumage was rarely considered, although it also has a typical reflection peak in the UV. Our study tested the female choice over male yellow colouration, and whether it is influenced by UV removal, in the European serin (Serinus serinus ), a sexually dichromatic cardueline finch, with males showing a conspicuous carotenoid-based yellow plumage. We shows that females preferred yellower males and that male attractiveness was lost when the UV colouration was blocked, with either of the UVblocking techniques used. The results of our study indicate that the UV component of carotenoid colouration is important in the female mate assessment in serins and highlights the importance of considering colour perception in avian mate choice.

Coevolutionary interactions between avian brood parasites and their hosts often lead to the evolution of discrimination and rejection of parasite eggs or chicks by hosts based on visual cues, and the evolution of visual mimicry of host eggs or chicks by brood parasites. Hosts may also base rejection of brood parasite nestlings on vocal cues, which would in turn select for mimicry of host begging calls in brood parasite chicks. In cuckoos that exploit multiple hosts with different begging calls, call structure may be plastic, allowing nestlings to modify their calls to match those of their various hosts, or fixed, in which case we would predict either imperfect mimicry or divergence of the species into host-specific lineages. In our study of the little bronze-cuckoo Chalcites minutillus and its primary host, the large-billed gerygone Gerygone magnirostris, we tested whether: (a) hosts use nestling vocalisations as a cue to discriminate cuckoo chicks; (b) cuckoo nestlings mimic the host begging calls throughout the nestling period; and (c) the cuckoo begging calls are plastic, thereby facilitating mimicry of the calls of different hosts. We found that the begging calls of little bronze-cuckoos are most similar to their gerygone hosts shortly after hatching (when rejection by hosts typically occurs) but become less similar as cuckoo chicks get older. Begging call structure may be used as a cue for rejection by hosts, and these results are consistent with gerygone defences selecting for age-specific vocal mimicry in cuckoo chicks. We found no evidence that little bronze-cuckoo begging calls were plastic.