How innovations such as vision, flight and pregnancy evolve is a central question in evolutionary biology. Examination of transitional (intermediate) forms of these traits can help address this question, but these intermediate phenotypes are very rare in extant species. Here we explore the biology and evolution of transitional forms of pregnancy that are midway between the ancestral state of oviparity (egg‐laying) and the derived state, viviparity (live birth). Transitional forms of pregnancy occur in only three vertebrates, all of which are lizard species that also display intraspecific variation in reproductive phenotype. In these lizards (Lerista bougainvillii, Saiphos equalis, and Zootoca vivipara), geographic variation of three reproductive forms occurs within a single species: oviparity, viviparity, and a transitional form of pregnancy. This phenomenon offers the valuable prospect of watching ‘evolution in action’. In these species, it is possible to conduct comparative research using different reproductive forms that are not confounded by speciation, and are of relatively recent origin. We identify major proximate and ultimate questions that can be addressed in these species, and the genetic and genomic tools that can help us understand how transitional forms of pregnancy are produced, despite predicted fitness costs. We argue that these taxa represent an excellent prospect for understanding the major evolutionary shift between egg‐laying and live birth, which is a fundamental innovation in the history of animals.
Human commensal species are thought to depend so closely on resources provided by humans that they are effectively ‘natives' of urban environments. However, while their adaptations to urban existence are well understood, their ecology and habitat choices have not been closely examined. This study investigated the habitat preferences of the archetypal commensal species, the invasive black rat Rattus rattus, at the urban–bushland interface in Sydney, Australia, and modelled the results using isodar analysis. Unexpectedly, we found evidence that rats perceived bushland as a more resource‐rich habitat compared to urban areas, resulting in higher rat abundance in bushland areas. Resultant spillover of commensal species into native vegetation may pose acute ecological risks in the future, yet management of commensal pests remains focused on urban areas. Ultimately, these findings highlight the complex nature of commensal ecology, suggesting that adaptation to human coexistence does not necessarily lead to a preference for human‐modified landscapes. We suggest that inter‐specific interactions with competitors, or the lack thereof, likely modulate the habitat preferences of commensals.
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