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Dispersal is a key process in community assembly but is often considered separately from downstream assembly processes (e.g., competition, herbivory). However, dispersal varies by species and can interact with other assembly processes through establishment as species enter communities. Here, we sought to distinguish the role of dispersal in community assembly and its interaction with two biotic assembly processes: competition and herbivory. We used a tallgrass prairie restoration experiment that manipulated the competitive and herbivore environments while allowing for natural dispersal and establishment from a diverse regional species pool into areas of low diversity. Dispersal, competition, and herbivory all influenced local communities. By tracking the spread of four target species across the plots, we found interspecific and intraspecific differences in establishment patterns, with herbivores influencing the number of individuals present and the distances species moved. At the community level, only dispersal and competition significantly influenced alpha diversity, but all three processes additively influenced community composition. There was also evidence of herbivore-competition and herbivore-colonization trade-offs in our experiment. Some species that could tolerate herbivory were less likely to establish in competitive environments, while others that could tolerate herbivory were more likely to disperse greater distances. More work is needed to understand the contexts under which dispersal variation affects community assembly and its synergy with other processes.

Substantial intra‐specific trait variation exists within plant communities, and in theory this variation could influence community dynamics. Although recent research has focused on intra‐specific variation in traits themselves, it is the influence of this variation on plant performance that makes intra‐specific trait variation relevant to ecological dynamics within or among species. Understanding the links between trait and performance variation, and the role of traits in mediating relationships among multiple components of performance, is critical for assessing the importance of intra‐specific trait variation for community dynamics. Seed size is thought to affect aspects of plant performance including fecundity, seedling growth, dispersal and tolerance of natural enemies. For two tropical tree species, we assessed how seed size was related to performance variation within each species and determined whether intra‐specific trait variation mediates intra‐specific performance tradeoffs. We used field seed rain collection to characterize size‐dependent outcomes of dispersal, sowed seeds of known size in soil collected near or far from conspecifics to characterize susceptibility to soil pathogens, and monitored growth of seedlings from seeds of known size. We found that intra‐specific seed size variation caused intra‐specific performance variation. The degree of trait‐based performance variation was consistently smaller than the degree of trait variation, and seed size influenced different components of performance for each species. One species exhibited a tradeoff in which small seeds had a fecundity advantage (more seedlings per unit reproductive mass) but produced smaller seedlings, whereas the other species exhibited a tradeoff in which small seeds dispersed to areas of low conspecific density but were less tolerant of density‐responsive natural enemies. Our results indicate that a single trait can influence multiple components of performance and can mediate different tradeoffs in co‐occurring species. Complex and heterogeneous effects of a single trait in multidimensional niche space may favour inter‐specific niche differentiation and coexistence.

Current understanding of mutualistic networks is grounded largely in data on interaction frequency, yet mutualistic network dynamics are also shaped by interaction quality—the functional outcomes of individual interactions on reproduction and survival. The difficulty of obtaining data on functional outcomes has resulted in limited understanding of functional variation among a network's pairwise species interactions, of the study designs that are necessary to capture major sources of functional variation, and of predictors of functional variation that may allow generalization across networks. In this community‐scale study, we targeted a key functional outcome in plant–frugivore networks: the impact of frugivore gut passage on seed germination. We used captive frugivore feeding trials and germination experiments in an island ecosystem, attaining species‐level coverage across all extant native frugivores and the plants they consume to (a) assess sources of functional variation, (b) separate effects of pulp removal from those of scarification via gut passage, and (c) test trait‐based correlates of gut passage effect sizes. We found antagonistic seed predation effects of a frugivore previously assumed to be a seed disperser, highlighting the need to consider functional outcomes rather than interaction frequency alone. The other frugivores each exhibited similar impacts for individual plant species, with benefits primarily caused by pulp removal rather than scarification, supporting the use of animal functional groups in this context. In contrast, plant species varied widely in impacts of gut passage on germination. Species with smaller seeds and more frugivore partners had larger benefits of gut passage, showing promise for network metrics and functional traits to predict functional variation among plants. Synthesis. Combining network and demographic approaches, we assessed the degree and sources of variation in a key functional outcome of plant–frugivore interactions across an entire network. Using a detailed study design, our work shows how simpler study designs can capture primary sources of functional variation and that functional traits and network metrics may allow generalization across networks. Efficiently measuring and generalizing sources of functional variation within mutualistic networks will strengthen our ability to model network dynamics and predict mutualist responses to global change.

Vertebrate frugivores enhance tropical forest regeneration by dispersing seeds into degraded areas. However, the importance of individual species as dispersers may vary within a community. Management and restoration would benefit from understanding which species are critical in moving native seeds into degraded habitats. We compared habitat composition of bird start and end locations for movement intervals based on mean gut passage times for the avian frugivore community on the island of Saipan. The proportion of movement intervals that began in intact, native forest varied among species, with Golden White-eyes having the highest proportion. However, this species tended to remain in intact forest and only rarely crossed into degraded habitats. Bridled White-eyes and Mariana Fruit Doves exhibited slightly higher rates of crossing from intact forest to degraded habitats, suggesting an ability to disperse native seeds to degraded areas. White-throated Ground Doves were never recorded crossing from intact forest to degraded habitats. Despite having a low proportion of movement intervals beginning in intact forest, Micronesian Starlings showed a higher proportion and absolute number of movements from intact forest to degraded habitats, due to their propensity to move frequently, across long distances, and across habitat types. In this species-poor frugivore network, seed dispersal into degraded habitats appears highly dependent on one species within the community. Regeneration of degraded lands may be severely hindered if this key disperser is lost.

Following defaunation, the loss of interactions with mutualists such as pollinators or seed dispersers may be compensated through increased interactions with remaining mutualists, ameliorating the negative cascading impacts on biodiversity. Alternatively, remaining mutualists may respond to altered competition by reducing the breadth or intensity of their interactions, exacerbating negative impacts on biodiversity. Despite the importance of these responses for our understanding of the dynamics of mutualistic networks and their response to global change, the mechanism and magnitude of interaction compensation within real mutualistic networks remains largely unknown. We examined differences in mutualistic interactions between frugivores and fruiting plants in two island ecosystems possessing an intact or disrupted seed dispersal network. We determined how changes in the abundance and behavior of remaining seed dispersers either increased mutualistic interactions (contributing to “interaction compensation”) or decreased interactions (causing an “interaction deficit”) in the disrupted network. We found a “rich-get-richer” response in the disrupted network, where remaining frugivores favored the plant species with highest interaction frequency, a dynamic that worsened the interaction deficit among plant species with low interaction frequency. Only one of five plant species experienced compensation and the other four had significant interaction deficits, with interaction frequencies 56-95% lower in the disrupted network. These results do not provide support for the strong compensating mechanisms assumed in theoretical network models, suggesting that existing network models underestimate the prevalence of cascading mutualism disruption after defaunation. This work supports a mutualist biodiversity-ecosystem functioning relationship, highlighting the importance of mutualist diversity for sustaining diverse and resilient ecosystems. This article is protected by copyright. All rights reserved.

Understanding the influence of environmental variability on population dynamics is a fundamental goal of ecology. Theory suggests that, for populations in variable environments, temporal correlations between demographic vital rates (e.g., growth, survival, reproduction) can increase (if positive) or decrease (if negative) the variability of year-to-year population growth. Because this variability generally decreases long-term population viability, vital rate correlations may importantly affect population dynamics in stochastic environments. Despite long-standing theoretical interest, it is unclear whether vital rate correlations are common in nature, whether their directions are predominantly negative or positive, and whether they are of sufficient magnitude to warrant broad consideration in studies of stochastic population dynamics. We used long-term demographic data for three perennial plant species, hierarchical Bayesian parameterization of population projection models, and stochastic simulations to address the following questions: (1) What are the sign, magnitude, and uncertainty of temporal correlations between vital rates? (2) How do specific pairwise correlations affect the year-to-year variability of population growth? (3) Does the net effect of all vital rate correlations increase or decrease year-to-year variability? (4) What is the net effect of vital rate correlations on the long-term stochastic population growth rate (λS)? We found only four moderate to strong correlations, both positive and negative in sign, across all species and vital rate pairs; otherwise, correlations were generally weak in magnitude and variable in sign. The net effect of vital rate correlations ranged from a slight decrease to an increase in the year-to-year variability of population growth, with average changes in variance ranging from -1% to +22%. However, vital rate correlations caused virtually no change in the estimates of λS (mean effects ranging from -0.01% to +0.17%). Therefore, the proportional changes in the variance of population growth caused by demographic correlations were too small on an absolute scale to importantly affect population growth and viability. We conclude that in our three focal populations and perhaps more generally, vital rate correlations have little effect on stochastic population dynamics. This may be good news for population ecologists, because estimating vital rate correlations and incorporating them into population models can be data-intensive and technically challenging. This article is protected by copyright. All rights reserved.

Interspecific interactions are important structuring forces in ecological communities. Interactions can be disturbed when species are lost from a community. When interactions result in fitness gains for at least one participating organism, that organism may experience reduced fitness as a result of interaction disturbance. However, many species exhibit traits that enable individuals to persist and reproduce in spite of such disruptions, resulting in resilience to interaction disturbance. Such traits can result in interaction generalization, phenotypic and behavioral plasticity, and adaptive capacity. We discuss examples of these traits and use case studies to illustrate how restoration practitioners can use a trait-based approach to examine species of concern, identify traits that are associated with interspecific interactions and are relevant to resilience, and target such traits in restoration. Restoration activities that bolster interaction resilience could include, for example, reintroducing or supporting specific functional groups or managing abiotic conditions to reduce interaction dependence by at-risk species (e.g. providing structural complexity offering shelter and cover). Resilience may also be an important consideration in species selection for restoration. Establishment of resilient species, able to persist after interaction disturbance, may be essential to restoring to a functioning ecological community. Once such species are present, they could help support more specialized species that lack resilience traits, such as many species of concern. Understanding the conditions under which processes linked to resilience may enable species to persist and communities to reform following interaction disturbance is a key application of community ecology to ecological restoration.

Seed dispersal sets the stage for the suite of biotic and abiotic interactions that determine the fate of individual seeds. In this review, we first focus on how dispersal influences the ‘seedscape’, or the combination of abiotic and biotic factors that affect the probability of recruitment once a seed has reached its final location. We review recent papers that examine the effect of different dispersal vectors on (1) the quality of the habitat in which a seed lands; (2) the distance seeds are dispersed from the parent tree; and (3) the density and composition of plants within the neighborhood of a seed following deposition. Next, we explore methods used to scale these processes up to the level of populations. We highlight demographic models that integrate across multiple life history stages and predict the impact of dispersal in variable environments on population growth. We also review studies that analyze existing spatial patterns of trees within large forest plots and use various strategies to infer the processes that led to those patterns. We continue to scale up from populations to communities, and discuss approaches that have been taken to understand how dispersal may affect diversity and abundance in the community. We then turn to human disturbances and discuss the implications of frugivore defaunation for plant communities. We finish by highlighting several areas of research that are particularly promising for future directions of study.

Humans are the dominant ecological and evolutionary force on the planet today, transforming habitats, polluting environments, changing climates, introducing new species, and causing other species to decline in number or go extinct. Th ese worrying anthropogenic impacts, collectively termed global change, are often viewed as a confounding factor to minimize in basic studies and a problem to resolve or quantify in applied studies. However, these ‘ accidental experiments ’ also represent opportunities to gain fundamental insight into ecological and evolutionary processes, especially when they result in perturbations that are large or long in duration and diffi cult or unethical to impose experimentally. We demonstrate this by describing important fundamental insights already gained from studies which utilize global change factors as accidental experiments. In doing so, we highlight why accidental experiments are sometimes more likely to yield insights than traditional approaches. Next, we argue that emerging environmental problems can provide even more opportunities for scientifi c discovery in the future, and provide both examples and guidelines for moving forward. We recommend 1) a greater fl ow of information between basic and applied subfi elds of ecology and evolution to identify emerging opportunities; 2) considering the advantages of the ‘ accidental experiment ’ approach relative to more traditional approaches; and 3) planning for the challenges inherent to uncontrolled accidental experiments. We emphasize that we do not view the accidental experiments provided by global change as replacements for scientifi c studies quantifying the magnitude of anthropogenic impacts or outlining strategies for mitigating impacts. Instead, we believe that accidental experiments are uniquely situated to provide insights into evolutionary and ecological processes that ultimately allow us to better predict and manage change on our human-dominated planet.

The effects of premating light regimes on sexual reproduction and the production of spherical cells in Chloromonas sp.-D, a unicellular green snow alga, were studied using cross-mating strains 582C and 582D isolated from snowpacks associated with mixed hardwood-softwood forests in Whetstone Gulf State Park, Tughill Plateau, NY. Two preacclimation regimes were used, Vita-Lite as controls (530-700 nm peak) and blue light as experimentals (430-460 nm peak) prior to the mating experiments. In blue light, an increase in the number of matings and spherical cells (spheres) produced in the life cycle was observed as the photoperiod increased. This implies that longer photoperiods of blue light are more optimal for sexual reproduction in Chloromonas sp.-D than shorter ones. Under Vita-Lite, there was a significant increase in the number of matings and spheres with the extended 20 : 4 photoperiod compared with the shorter 14 : 10 photoperiod. Under blue light, significantly more matings and spheres occurred than under Vita-Lite using the same irradiance level of 95 μmol photons m -2 s -1 (photosynthetically active radiation [PAR] of 400-700 nm) for the 14: 10 and 20: 4 photoperiods. The results of these experiments suggest that Chloromonas sp.-D. known only from the Tughill Plateau, NY, is not reproducing optimally at this site where it grows and reproduces under an approximate 14: 10 photoperiod in early April. However, in the upper 10 cm of snow in the Tughill Plateau, a blue light irradiance level of 95 μmol photons m 2 s -1 occurs, which is optimal for this species. When these conditions are combined with a 14: 10 photoperiod, the Tughill Plateau appears to be sub-optimal for mating and production of spherical cells. Since Chloromonas sp.-D does not appear to have a dependence on a dark cycle, this would allow it to expand its geographical distribution. It may reproduce more optimally under blue light (95 μmol photons m -2 s -1 ) with an extended photoperiod (>20:4 h, light:dark) in high latitude field sites such as Lake Bienville, Quebec, in eastern North America where other species of Chloromonas are known in snow associated with coniferous forests.