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Although parasites represent a substantial part of marine communities' biomass and diversity, their influence on ecosystem functioning, especially via the modification of host behaviour, remains largely unknown. Here, we explored the effects of the bopyrid ectoparasite Gyge branchialis on the engineering activities of the thalassinid crustacean Upogebia pusilla and the cascading effects on intertidal ecosystem processes (e.g. sediment bioturbation) and functions (e.g. nutrient regeneration).Laboratory experiments revealed that the overall activity level of parasitized mud shrimp is reduced by a factor 3.3 due to a decrease in time allocated to burrowing and ventilating activities (by factors 1.9 and 2.9, respectively).Decrease in activity level led to strong reductions of bioturbation rates and biogeochemical fluxes at the sediment–water interface.Given the world‐wide distribution of mud shrimp and their key role in biogeochemical processes, parasite‐mediated alteration of their engineering behaviour has undoubtedly broad ecological impacts on marine coastal systems functioning.Our results illustrate further the need to consider host–parasite interactions (including trait‐mediated indirect effects) when assessing the contribution of species to ecosystem properties, functions and services. [ABSTRACT FROM AUTHOR]

We investigate where bottom‐up and top‐down control regulates ecological communities as a mechanism linking ecological gradients to the geography of consumer abundance and biomass. We use standardized surveys of 54 North American grasslands to test alternate hypotheses predicting 100‐fold shifts in the biomass of four common grassland arthropod taxa—Auchenorrhyncha, sucking herbivores, Acrididae, chewing herbivores, Tettigoniidae, omnivores, and Araneae, predators.Bottom‐up models predict that consumer biomass tracks plant quantity (e.g. productivity and standing biomass) and quality (nutrient content) and that ectotherm access to food increases with temperature. Each of the focal trophic groups responded differently to these drivers: the biomass of sucking herbivores and omnivores increased with plant biomass; that of chewing herbivores tracked plant quality; and predator biomass did not depend on plant quality, plant quantity or temperature.The Exploitation Ecosystem Hypothesis is a top‐down hypothesis that predicts a shift from resource limitation of herbivores when plant production is low, to predator limitation when plant production is high. In grasslands where spider biomass was low, herbivore biomass increased with plant biomass, whereas bottom‐up structuring was not evident when spiders were abundant. Furthermore, neither predator biomass nor trophic position (via stable isotope analysis) increased with plant biomass, suggesting predators themselves are top‐down limited.Stable isotope analysis revealed that trophic position of the chewing herbivore and omnivore increased significantly with plant biomass, suggesting these groups increased scavenging and meat consumption in grasslands with higher carbohydrate availability.Taken together, our snapshot sampling documents gradients of food web structure across 54 grasslands, consistent with multiple hypotheses of bottom‐up and top‐down regulation. [ABSTRACT FROM AUTHOR]

Considerable emphasis has been placed recently on the importance of incorporating non‐trophic effects into our understanding of ecological networks. Interaction modifications are well‐established as generating strong non‐trophic impacts by modulating the strength of interspecific interactions.For simplicity and comparison with direct interactions within a network context, the consequences of interaction modifications have often been described as direct pairwise interactions. The consequences of this assumption have not been examined in non‐equilibrium settings where unexpected consequences of interaction modifications are most likely.To test the distinct dynamic nature of these "higher‐order" effects, we directly compare, using dynamic simulations, the robustness to extinctions under perturbation of systems where interaction modifications are either explicitly modelled or represented by corresponding equivalent pairwise non‐trophic interactions.Full, multi‐species representations of interaction modifications resulted in a greater robustness to extinctions compared to equivalent pairwise effects. Explanations for this increased stability despite apparent greater dynamic complexity can be found in additional routes for dynamic feedbacks. Furthermore, interaction modifications changed the relative vulnerability of species to extinction from those trophically connected close to the perturbed species towards those receiving a large number of modifications.Future empirical and theoretical research into non‐trophic effects should distinguish interaction modifications from direct pairwise effects in order to maximize information about the system dynamics. Interaction modifications have the potential to shift expectations of species vulnerability based exclusively on trophic networks. [ABSTRACT FROM AUTHOR]

Theory suggests that non‐trophic interactions can be a major mechanism behind community stability and persistence, but community‐level empirical data are scarce, particularly for effects on species interactions mediated through changes in the physical environment.Here, we explored how ecosystem engineering effects can feed back to the engineer, not only modulating the engineer's population density (node modulation) but also affecting its interactions with other species (link modulation).Gall induction can be viewed as ecosystem engineering since galls serve as habitat for other species. In a community‐level field experiment, we generated treatments with reduced or elevated ecosystem engineering by removing or adding post‐emergence galls to different plots of their host plant in the Brazilian Cerrado. We tested the effect of post‐emergence galls on the galler, as well as on the galler–parasitoid and galler—aphid interactions.The manipulation of post‐emergence galls had little effect on the galler—abundance and survivorship were not affected, and gall volume changed only slightly—but modified interactions involving the galler, parasitoid wasps and inquiline aphids. Aphid inquilines negatively affected density‐dependent parasitism rates (interaction modification) likely by killing parasitised galling larvae. Post‐emergence galls interfered with aphid inquilinism—likely by the provision of alternative habitat for aphids—and thus interfered with the negative effect of aphids on parasitism (modification of an interaction modification).This work is one of the few studies to demonstrate experimentally the role played by environment‐mediated interaction modification at a community level in the field. Moreover, by manipulating a species' ecosystem engineering effect (post‐emergence galls) instead of the species itself, we demonstrate the novel result that populations can be regulated by non‐trophic effects initiated by their own activities that alter their interaction with other species. This reveals that indirect interactions mediated via the environment offer new pathways of feedback loops for population regulation. Our results indicate that interaction modification has the potential to be a key regulatory mechanism underlying interaction variation in nature, and play a major role in community structure, dynamics and stability. [ABSTRACT FROM AUTHOR]