Prevailing theories about animal foraging behaviours and the food webs they occupy offer divergent predictions about whether seasonally limited food availability promotes dietary diversification or specialization. Emphasis on how animals compete for food predominates in work on the foraging ecology of large mammalian herbivores, whereas emphasis on how the diversity of available foods generally constrains dietary opportunity predominates work on entire food webs. Reconciling predictions about what promotes dietary diversification is challenging because species’ different body sizes and mobilities modulate how they seek and compete for resources—the mechanistic bases of common predictions may not pertain to all species equally. We evaluated predictions about five large-herbivore species that differ in body size and mobility in Yellowstone National Park using GPS tracking and dietary DNA. The data illuminated remarkably strong and significant correlations between body size and five key indicators of diet seasonality ( R2 = 0.71–0.80). Compared to smaller species, bison and elk showed muted diet seasonality and maintained access to more unique foods when winter conditions constrained food availability. Evidence from GPS collars revealed size-based differences in species’ seasonal movements and habitat-use patterns, suggesting that better accounting for the allometry of foraging behaviours may help reconcile disparate ideas about the ecological drivers of seasonal diet switching.
Environmental change, such as increased rates of urbanization, can induce shifts in phenotypic plasticity with some individuals adapting to city life while others are displaced. A key trait that can facilitate adaptation is the degree at which animals respond to stress. This stress response has a heritable component and exhibits intra- and inter-individual variation. However, the mechanisms behind this variability and whether they might be responsible for adaptation to different environments are not known. Variation in DNA methylation can be a potential mechanism that mediates environmental effects on the stress response. We used an inter- and intra-environmental cross-foster experiment to analyze the contribution of DNA methylation to early-life phenotypic variation. We found that at hatching, urban house wren ( Troglodytes aedon ) offspring had increased methylation as compared to their rural counterparts, and observed plasticity in methylation as offspring aged, indicating developmental effects of the rearing environment on methylation. Differential methylation analyses showed that cellular respiration genes were differentially expressed at hatching and behavioral and metabolism genes were differentially expressed at fledgling. Lastly, hyper-methylation of a single gene ( CNTNAP2 ) is associated with increased glucocorticoid levels. These differential methylation patterns linked to a specific physiological phenotype suggest that DNA methylation may be a mechanism by which individuals adapt to novel environments. Characterizing genetic and environmental influences on methylation is critical for understanding the role of epigenetic mechanisms in evolutionary adaptation.
Cleistogamy is a mating system in which plants produce some proportion of closed, autonomously self-pollinating flowers. Cleistogamous flowers differ from chasmogamous flowers, which are open flowers capable of outcrossing. Both dimorphic cleistogamy (cleistogamous and chasmogamous flowers produced on the same plant) and complete cleistogamy occur. Cleistogamy has been hypothesized to be a bet hedging strategy for reducing risk in the face of unpredictable pollinator availability. However, conflicting results across species and challenges connecting theory to data have prevented researchers from proving that cleistogamy is bet hedging. To test the bet hedging hypothesis, we investigated the distribution of over 400 cleistogamous species through biogeographical analyses. We find that cleistogamy is more prevalent in cooler, more variable environments. Additionally, we find that among cleistogamous species, complete cleistogamy is more likely to occur in warmer, more stable, tropical and subtropical environments. We hypothesize that the difference in distribution between complete and dimorphic cleistogamy may be driven by the opposing forces of selection to increase cleistogamy proportion and extinction risk, which we test using a heuristic Markov transition model. We conclude that the distribution of cleistogamy suggests that the strategy has evolved in variable environments, consistent with expectations for bet hedging.