Gut microbial communities (microbiomes) profoundly shape the ecology and evolution of multicellular life. Interactions between host and microbiome appear to be reciprocal, and ecological theory is now being applied to better understand how hosts and their microbiome influence each other. However, some ecological processes that underlie reciprocal host–microbiome interactions may be obscured by the current convention of highly controlled transplantation experiments. Although these approaches have yielded invaluable insights, there is a need for a broader array of approaches to fully understand host–microbiome reciprocity. Using a directed review, we surveyed the breadth of ecological reality in the current literature on gut microbiome transplants with non-human recipients. For 55 studies, we categorized nine key experimental conditions that impact the ecological reality (EcoReality) of the transplant, including host taxon match and donor environment. Using these categories, we rated the EcoReality of each transplant. Encouragingly, the breadth of EcoReality has increased over time, but some components of EcoReality are still relatively unexplored, including recipient host environment and microbiome state. The conceptual framework we develop here maps the landscape of possible EcoReality to highlight where fundamental ecological processes can be considered in future transplant experiments.
Nature's variability plays a major role in maintenance of biodiversity. As global change is altering variability, understanding how key food web structures maintain stability in the face of variation becomes critical. Surprisingly, little research has been undertaken to mechanistically understand how key food web structures are expected to operate in a noisy world and what this means for stability. Omnivory, for example, has been historically well studied but largely from a static perspective. Recent empirical evidence suggests that the strength of omnivory varies in response to changing conditions in ways that may be fundamental to stability. In the present article, we extend existing omnivory theory to predict how omnivory responds to variation and to show that dynamic omnivory responses are indeed a potent stabilizing structure in the face of variation. We end by synthesizing empirical examples within this framework, demonstrating the ubiquity of the theoretical mechanisms proposed across ecosystem types, spatial scales, and taxa.
The world is astoundingly variable, and individuals to whole communities must respond to variability to survive. One example of nature's variability is the massive fluctuations in spruce budworm (Choristoneura fumiferana Clemens, Lepidoptera: Tortricidae) populations that occur over 35 years. We examined how the parasitoid community altered its parasitism of budworm and other caterpillar species in response to these fluctuations. Budworm and other caterpillar species were sampled from balsam fir in three plots for 14 years in Atlantic Canada, and then reared to identify any emerging parasitoids. We found that the parasitoid community showed a simple linear, indiscriminate response (i.e., no preference, where densities purely dictated parasitism rates) to changes in budworm densities relative to other caterpillar species on balsam fir. We also observed strong changes in topology and distributions of interaction strengths between the parasitoids, budworm and other caterpillar species as budworm densities fluctuated. Our study contributes to the suggestion that hardwood trees are a critical part of the budworm-parasitoid food web, where parasitoids attack other caterpillar species on hardwood trees when budworm populations are low. Taken together, our study shows that a parasitoid community collectively alters species interactions in response to variable budworm densities, fundamentally shifting food web pathways.
Gut microbial communities (microbiomes) profoundly shape the ecology and evolution of multicellular life. Interactions between host and microbiome appear to be reciprocal, and ecological theory is now being applied to better understand how hosts and their microbiome influence each other. However, some ecological processes that underlie reciprocal host-microbiome interactions may be obscured by the current convention of highly-controlled transplantation experiments. Although these approaches have yielded invaluable insights, there is a need for a broader array of approaches to fully understand host-microbiome reciprocity. Using a directed review, we surveyed the breadth of ecological reality in the current literature on gut microbiome transplants with non-human recipients. For 55 studies, we categorized 9 key experimental conditions that impact the ecological reality (EcoReality) of the transplant, including host taxon match and donor environment. Using these categories, we rated the EcoReality of each transplant. Encouragingly, the breadth of EcoReality has increased over time, but some components of EcoReality are still relatively unexplored, including recipient host environment and microbiome state. The conceptual framework we develop here maps the landscape of possible EcoReality to highlight where fundamental ecological processes can be considered in future transplant experiments.
Movement between host plants during the growing season is a common behaviour among insect herbivores, although the mechanisms promoting these movements are poorly understood for many systems. Two possible reasons why insect herbivores relocate include compensating for host plant quantity and/or quality changes and the avoidance of natural enemies. The Arctic caterpillar (Gynaephora groenlandica (Wocke); Lepidoptera: Lymantriidae) moves several metres each day, feeds on its patchily distributed host plant, Arctic willow (Salix arctica Pallas; Salicaceae), and has two main natural enemies, the parasitoids Exorista thula Wood (Diptera: Tachinidae) and Hyposoter diechmanni (Nielsen) (Hymenoptera: Ichneumonidae). We physically moved caterpillars between Arctic willows and restricted other caterpillar individuals each to a single willow throughout the active period of Arctic caterpillars. We found that growth rate, herbivory rate, and the proportion of available leaf fascicles eaten were higher for experimentally moved caterpillars. Parasitoid abundances were low and did not differ between experimentally moved and stationary caterpillars. Taken together, our study addresses the bottom–up and top–down controls on insect herbivore movement during the short duration of the growing season in the Arctic. Our results suggest that caterpillars are likely moving to new willow shrubs to access high quality resources.
The loss of biodiversity is altering the structure of ecological networks; however, we are currently in a poor position to predict how these altered communities will affect the evolution of remaining populations. Theory on fitness landscapes provides a framework for predicting how selection alters the evolutionary trajectory and adaptive potential of populations, but often treats the network of interacting populations as a “black box.” Here, we integrate ecological networks and fitness landscapes to examine how changes in food‐web structure shape phenotypic evolution. We conducted a field experiment that removed a guild of larval parasitoids that imposed direct and indirect selection pressures on an insect herbivore. We then measured herbivore survival as a function of three key phenotypic traits to estimate directional, quadratic, and correlational selection gradients in each treatment. We used these selection gradients to characterize the slope and curvature of the fitness landscape to understand the direct and indirect effects of consumer loss on phenotypic evolution. We found that the number of traits under directional selection increased with the removal of larval parasitoids, indicating evolution was more constrained toward a specific combination of traits. Similarly, we found that the removal of larval parasitoids altered the curvature of the fitness landscape in such a way that tended to decrease the evolvability of the traits we measured in the next generation. Our results suggest that the loss of trophic interactions can impose greater constraints on phenotypic evolution. This indicates that the simplification of ecological communities may constrain the adaptive potential of remaining populations to future environmental change.
Uncovering the fundamental properties of ecological stability is a central question in theoretical biology since its inception at the turn of the century. Here, motivated by simple modular theory (e.g., population models to few species models), we review the role of interactions strength and lags on dynamics and stability. Specifically, we argue that modular theory consistently finds that lags combined with high growth rates or strong interaction strengths underly all forms of instability in ecological models. To fully explore this relationship, we first need to understand the role of both explicit lags—using lagged versions of classical models, such as the lagged logistic population model, as well as the more subtle role of implicit lags that arise in all biological models of growth. Given this, and the realization that nature is replete with lags (e.g., age structure, stage structure, predator-prey, reproductive lags, recycling lags), it becomes important to understand how lags, both implicit and explicit, interact. With an eye towards correcting the frequently overlooked role of lags on stability we review existing mathematical examples that argue lags can combine to drive instability (lag excitation) or inhibit the expression of instability by cancelling each other out effectively (lag cancellation). We suggest that further understanding the role of lags and how they interact within whole webs and ecosystems remains an important research area for the future.
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