An emerging hypothesis of animal personality posits that animals choose the habitat that best fits their personality, and that the match between habitat and personality can facilitate population differentiation, and eventually speciation. However, behavioural plasticity and the adjustment of behaviours to new environments have been a classical explanation for such matching patterns. Using a population of dunnocks (), we empirically tested whether personality or behavioural plasticity is responsible for the non-random distribution of shy and bold individuals in a heterogeneous environment. We found evidence for bold individuals settling in areas with high human disturbance, but also that birds became bolder with increasing age. Importantly, personality primarily determines the distribution of individuals, and behavioural adjustment over time contributes very little to the observed patterns. We cannot, however, exclude a possibility of very early behavioural plasticity (a type of developmental plasticity) shaping what we refer to as 'personality'. Nonetheless, our findings highlight the role personality plays in shaping population structure, lending support to the theory of personality-mediated speciation. Moreover, personality-matching habitat choice has important implications for population management and conservation.
Summary Consistent individual differences in hormone levels and metabolic rates have been proposed to be potential state variables underlying consistent individual differences in behaviour (i.e. animal personality). However, it remains unclear whether either one alone or both of these potential state variables could be an underlying driver of animal personality. We address this question using meta‐analyses of published data from bird species. We hypothesized that state variables that mediate individual differences in behaviour would display similar or higher repeatability estimates than behavioural traits. To test this hypothesis, we quantified repeatability estimates of hormone levels, metabolic rates and behavioural traits. We found moderate to high mean repeatability estimates for both metabolic rates and behavioural traits, but low repeatability estimates for hormone levels. These findings indicate that metabolic rates likely represent an important mechanism for generating adaptive personality differences in behaviour. We also show that: (i) for hormones and behaviour, repeatability decreased with increasing interval time between two measurements; (ii) males and females differed in repeatability for behavioural traits; (iii) stress‐induced hormone levels were more repeatable than baseline levels. Future studies are now required to determine the direction of the association between metabolic rates and behavioural traits. At the same time, these studies should try to investigate which of the proposed mechanisms is responsible for the relationship between state variable and state‐dependent behaviour. In addition, we encourage researchers to report the coefficient of variation for between‐individual variance (CVB) along with repeatability estimates because these two indices carry different information. We discuss how CVB may better facilitate future comparative studies, including meta‐analyses. A http://onlinelibrary.wiley.com/doi/10.1111/1365-2435.12779/suppinfo is available for this article.
Quantifying the variation in behaviour-related genes within and between populations provides insight into how evolutionary processes shape consistent behavioural traits (i.e. personality). Deliberate introductions of non-native species offer opportunities to investigate how such genes differ between native and introduced populations and how polymorphisms in the genes are related to variation in behaviour. Here, we compared the genetic variation of the two 'personality' genes, DRD4 and SERT, between a native (United Kingdom, UK) and an introduced (New Zealand, NZ) population of dunnocks, Prunella modularis. The NZ population showed a significantly lower number of single nucleotide polymorphisms (SNPs) compared to the UK population. Standardized F'st estimates of the personality genes and neutral microsatellites indicate that selection (anthropogenic and natural) probably occurred during and post the introduction event. Notably, the largest genetic differentiation was found in the intronic regions of the genes. In the NZ population, we also examined the association between polymorphisms in DRD4 and SERT and two highly repeatable behavioural traits: flight-initiation distance and mating status (promiscuous females and cobreeding males). We found 38 significant associations (for different allele effect models) between the two behavioural traits and the studied genes. Further, 22 of the tested associations showed antagonistic allele effects for males and females. Our findings illustrate how introduction events and accompanying ecological changes could influence the genetic diversity of behaviour-related genes.
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