The gut microbiomes of Channel Island foxes and island spotted skunks exhibit fine-scale differentiation across host species and island populations.

California's Channel Islands are home to two endemic mammalian carnivores: island foxes (Urocyon littoralis) and island spotted skunks (Spilogale gracilis amphiala). Although it is rare for two insular terrestrial carnivores to coexist, these known competitors persist on both Santa Cruz Island and Santa Rosa Island. We hypothesized that examination of their gut microbial communities would provide insight into the factors that enable this coexistence, as microbial symbionts often reflect host evolutionary history and contemporary ecology. Using rectal swabs collected from island foxes and island spotted skunks sampled across both islands, we generated 16S rRNA amplicon sequencing data to characterize their gut microbiomes. While island foxes and island spotted skunks both harbored the core mammalian microbiome, host species explained the largest proportion of variation in the dataset. We further identified intraspecific variation between island populations, with greater differentiation observed between more specialist island spotted skunk populations compared to more generalist island fox populations. This pattern may reflect differences in resource utilization following fine-scale niche differentiation. It may further reflect evolutionary differences regarding the timing of intraspecific separation. Considered together, this study contributes to the growing catalog of wildlife microbiome studies, with important implications for understanding how eco-evolutionary processes enable the coexistence of terrestrial carnivores-and their microbiomes-in island environments.

Interspecific Asymmetries in Behavioral Plasticity Drive Seasonal Patterns of Temporal Niche Partitioning in an Island Carnivore Community.

Animals vary considerably in the amount of behavioral plasticity they exhibit in daily activity timing and temporal niche switching. It is not well understood how environmental factors drive changes in temporal activity or how interspecific differences in the plasticity of activity timing ultimately manifest in free-living animals. Here, we investigated the temporal structure and organization of activity patterns of two insular mammalian carnivores living in sympatry, the island fox (Urocyon littoralis) and island spotted skunk (Spilogale gracilis amphiala). Using collar-mounted accelerometers, we assessed the plasticity of behavioral activity rhythms in foxes and skunks by investigating how environmental factors drive the distribution of locomotor activity across the day and year, and subsequently examined the dynamics of temporal niche overlap between the two species. We documented that foxes express phenotypic plasticity in daily activity timing across the year, ranging from nocturnal to diurnal to crepuscular rhythms depending on the individual and time of year. Most notably, foxes increased the proportion of daytime activity as seasonal temperatures decreased. Overall, activity patterns of foxes were consistent with the circadian thermoenergetics hypothesis, which posits that animals that switch their patterns of activity do so to coincide with the most energetically favorable time of day. In contrast to foxes, skunks exhibited little behavioral plasticity, appearing strictly nocturnal across the year. While the duration of skunk activity bouts increased with the duration of night, timing of activity onset and offset extended into daytime hours during summer when the duration of darkness was shortest. Analysis of temporal niche overlap between foxes and skunks suggested that niche overlap was highest during summer and lowest during winter and was dictated primarily by temporal niche switching in foxes, rather than skunks. Collectively, our results highlight how interspecific asymmetries in behavioral plasticity drive dynamic patterns of temporal niche overlap within an island carnivore community.