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Synopsis As species move into new environments through founder events, their phenotypes may diverge from native populations. Identifying the drivers underlying such variation, and the constraints on the adaptive potential of this variation, is essential for understanding how organisms respond to new or rapidly changing habitats. Such phenotypic divergence may be especially evident in populations introduced to new environments via human-assisted transport or populations in dramatically altered environments such as cities. Sexually dimorphic species beg the additional questions of how these new environments may influence sexes differently and how dimorphism may shape the range of potential responses. The repeated translocation, establishment, and spread of wall lizards (Podarcis spp.) from native European populations to new locations in North America provide an excellent natural experiment to explore how phenotypes may differ after establishment in a new environment. Here, we quantify body shape and the multivariate morphological phenotype (incorporating limb dimensions and head length) of common wall lizards (P. muralis) and Italian wall lizards (P. siculus) in replicated North American introductions. In both species, males are larger and have larger head length and limb dimensions than females across all sampled groups. Sexual dimorphism in the multivariate morphological phenotype was of similar magnitude when comparing native and introduced populations for both species, though the trajectory angles in multivariate trait space differed in P. siculus. When comparing introduced lizards from contemporary and historically collected museum specimens, we identified differences of similar magnitude but in different trajectories between sexes in P. siculus, and differences in both magnitude and direction of sexual dimorphism in P. muralis. These idiosyncratic patterns in phenotypic trajectories provide insight to the potential array of processes generating phenotypic variation within species at the intersection of invasion biology and urban evolution. 

Urbanization drastically transforms landscapes, resulting in fragmentation, degradation, and the loss of local biodiversity. Yet, urban environments also offer opportunities to observe rapid evolutionary change in wild populations that survive and even thrive in these novel habitats. In many ways, cities represent replicated “natural experiments” in which geographically separated populations adaptively respond to similar selection pressures over rapid evolutionary timescales. Little is known, however, about the genetic basis of adaptive phenotypic differentiation in urban populations nor the extent to which phenotypic parallelism is reflected at the genomic level with signatures of parallel selection. Here, we analyzed the genomic underpinnings of parallel urban-associated phenotypic change in Anolis cristatellus , a small-bodied neotropical lizard found abundantly in both urbanized and forested environments. We show that phenotypic parallelism in response to parallel urban environmental change is underlain by genomic parallelism and identify candidate loci across the Anolis genome associated with this adaptive morphological divergence. Our findings point to polygenic selection on standing genetic variation as a key process to effectuate rapid morphological adaptation. Identified candidate loci represent several functions associated with skeletomuscular development, morphology, and human disease. Taken together, these results shed light on the genomic basis of complex morphological adaptations, provide insight into the role of contingency and determinism in adaptation to novel environments, and underscore the value of urban environments to address fundamental evolutionary questions. 

Abstract Urban evolutionary ecology is inherently interdisciplinary. Moreover, it is a field with global significance. However, bringing researchers and resources together across fields and countries is challenging. Therefore, an online collaborative research hub, where common methods and best practices are shared among scientists from diverse geographic, ethnic, and career backgrounds would make research focused on urban evolutionary ecology more inclusive. Here, we describe a freely available online research hub for toolkits that facilitate global research in urban evolutionary ecology. We provide rationales and descriptions of toolkits for: (1) decolonizing urban evolutionary ecology; (2) identifying and fostering international collaborative partnerships; (3) common methods and freely‐available datasets for trait mapping across cities; (4) common methods and freely‐available datasets for cross‐city evolutionary ecology experiments; and (5) best practices and freely available resources for public outreach and communication of research findings in urban evolutionary ecology. We outline how the toolkits can be accessed, archived, and modified over time in order to sustain long‐term global research that will advance our understanding of urban evolutionary ecology. 

Abstract Human activity drastically transforms landscapes, generating novel habitats to which species must adaptively respond. Consequently, urbanization is increasingly recognized as a driver of phenotypic change. The structural environment of urban habitats presents a replicated natural experiment to examine trait–environment relationships and phenotypic variation related to locomotion. We use geometric morphometrics to examine claw morphology of five species of Anolis lizards in urban and forest habitats. We find that urban lizards undergo a shift in claw shape in the same direction but varying magnitude across species. Urban claws are overall taller, less curved, less pointed and shorter in length than those of forest lizards. These differences may enable more effective attachment or reduce interference with toepad function on smooth anthropogenic substrates. We also find an increase in shape disparity, a measurement of variation, in urban populations, suggesting relaxed selection or niche expansion rather than directional selection. This study expands our understanding of the relatively understudied trait of claw morphology and adds to a growing number of studies demonstrating phenotypic changes in urban lizards. The consistency in the direction of the shape changes we observed supports the intriguing possibility that urban environments may lead to predictable convergent adaptive change.