Organismal appearances are shaped by selection from both biotic and abiotic drivers. For example, Gloger’s rule describes the pervasive pattern that more pigmented populations are found in more humid areas. However, species may also converge on nearly identical colours and patterns in sympatry, often to avoid predation by mimicking noxious species. Here we leverage a massive global citizen-science database to determine how biotic and abiotic factors act in concert to shape plumage in the world’s 230 species of woodpeckers. We find that habitat and climate profoundly influence woodpecker plumage, and we recover support for the generality of Gloger’s rule. However, many species exhibit remarkable convergence explained neither by these factors nor by shared ancestry. Instead, this convergence is associated with geographic overlap between species, suggesting occasional strong selection for interspecific mimicry.

Although communicative complexity is often predicted to correlate with social complexity in animal societies, few studies have employed large-scale comparative analyses to test whether socially complex species have more complex systems of communication. I tested this social complexity hypothesis in birds (Class: Aves) using the large amount of natural history information that describes both vocal repertoire and social system in these species. To do so, I marshalled data from primary and secondary records of avian vocal repertoires ( = 253), and for each of the species in the dataset I recorded the reported repertoire size and associated species information. Using phylogenetic comparative methods, I found that cooperative breeding was a strong and repeatable predictor of vocal repertoire size, while other social variables, e.g. group size and group stability, had little or no influence on repertoire size. Importantly, repertoire sizes expanded concurrently with the evolution of cooperative breeding, suggesting a direct link between these two traits. Cooperatively breeding species devoted significantly more of their repertoire to contact calls and alarm calls. Overall, these results therefore lend support to the hypothesis that social complexity via behavioural coordination leads to increases in vocal complexity.

Animals produce a wide array of sounds with highly variable acoustic structures. It is possible to understand the causes and consequences of this variation across taxa with phylogenetic comparative analyses. Acoustic and evolutionary analyses are rapidly increasing in sophistication such that choosing appropriate acoustic and evolutionary approaches is increasingly difficult. However, the correct choice of analysis can have profound effects on output and evolutionary inferences. Here, we identify and address some of the challenges for this growing field by providing a roadmap for quantifying and comparing sound in a phylogenetic context for researchers with a broad range of scientific backgrounds. Sound, as a continuous, multidimensional trait can be particularly challenging to measure because it can be hard to identify variables that can be compared across taxa and it is also no small feat to process and analyse the resulting high‐dimensional acoustic data using approaches that are appropriate for subsequent evolutionary analysis. Additionally, terminological inconsistencies and the role of learning in the development of acoustic traits need to be considered. Phylogenetic comparative analyses also have their own sets of caveats to consider. We provide a set of recommendations for delimiting acoustic signals into discrete, comparable acoustic units. We also present a three‐stage workflow for extracting relevant acoustic data, including options for multivariate analyses and dimensionality reduction that is compatible with phylogenetic comparative analysis. We then summarize available phylogenetic comparative approaches and how they have been used in comparative bioacoustics, and address the limitations of comparative analyses with behavioural data. Lastly, we recommend how to apply these methods to acoustic data across a range of study systems. In this way, we provide an integrated framework to aid in quantitative analysis of cross‐taxa variation in animal sounds for comparative phylogenetic analysis. In addition, we advocate the standardization of acoustic terminology across disciplines and taxa, adoption of automated methods for acoustic feature extraction, and establishment of strong data archival practices for acoustic recordings and data analyses. Combining such practices with our proposed workflow will greatly advance the reproducibility, biological interpretation, and longevity of comparative bioacoustic studies.

Understanding the emergence and persistence of convergent phenotypes is the subject of considerable debate. Species may converge on nearly identical phenotypes for a variety of reasons, including occupying similar environments, exhibiting similar foraging ecologies, and for signalling reasons such as mimicry. Interspecific social dominance mimicry (ISDM) is a hypothesis that states that socially subordinate species evolve a phenotype mimicking a dominant species so as to accrue resources and avoid aggression. A recently proposed test case for this phenomenon asserts that downy woodpeckers, Picoides pubescens, evolved mimetic plumage to avoid attacks from hairy woodpeckers, Picoides villosus. We examined this claim with a large behavioural data set collected by citizen scientists. We employed phylogenetic methods and simulations to test whether downy woodpeckers avoid aggression, and whether downy woodpeckers are more dominant than expected based on body mass. Contrary to the expectations of ISDM, we found that downy woodpeckers were markedly more often the target of hairy woodpecker attacks than expected based on their relative abundances. Our empirical data thus offers no support for the strict ISDM hypothesis as an explanation for downy-hairy woodpecker plumage convergence. However, downy woodpeckers are slightly more dominant than expected based on their body mass, albeit not significantly so. Our data therefore lend weight to previous suggestions that the benefits of mimicry potentially accrue from third-party species mistaking the mimic for the model, rather than the model mistaking the mimic for another model.

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The major evolutionary transitions often result in reorganization of biological systems, and a component of such reorganization is that individuals within the system specialize on performing certain tasks, resulting in a division of labor. Although the traditional benefit of division of labor is thought to be a gain in work efficiency, one alternative benefit of specialization is avoiding temporal delays associated with switching tasks. While models have demonstrated that costs of task switching can drive the evolution of division of labor, little empirical support exists for this hypothesis. We tested whether there were task-switching costs in Temnothorax rugatulus. We recorded the behavior of every individual in 44 colonies and used this dataset to identify each instance where an individual performed a task, spent time in the interval (i.e., inactive, wandering inside, and self-grooming), and then performed a task again. We compared the interval time where an individual switched task type between that first and second bout of work to instances where an individual performed the same type of work in both bouts. In certain cases, we find that the interval time was significantly shorter if individuals repeated the same task. We find this time cost for switching to a new behavior in all active worker groups, that is, independently of worker specialization. These results suggest that task-switching costs may select for behavioral specialization.

Communal nests often provide benefits, such as protection from predators and refuge from extreme temperatures, to the inhabitants of the nest. The benefits returned to individuals performing nest construction may not scale linearly with the amount of nest construction performed. If the returns on nest construction are non-linear, then recent theoretical studies suggest that selection for reproductive competition may destabilise the cooperative behaviours that maintain the communal nest. To investigate these questions, we measured the thermal benefits provided by sociable weaver (Philetairus socius) nests, and how those benefits scale at multiple nest sizes, including the point where zero investment in nest building returns no benefits. We find that the average temperature buffering provided by nest chambers is correlated with distance to the edge of the nest and that the benefits provided by nest construction are asymptotic. This suggests that cooperative nest construction will maintained at a lower level than if the benefits were linear.