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  1. Abstract Integral projection models (IPMs) are widely used for studying continuously size‐structured populations. IPMs require a growth sub‐model that describes the probability of future size conditional on current size and any covariates. Most IPM studies assume that this distribution is Gaussian, despite calls for non‐Gaussian models that accommodate skewness and excess kurtosis. We provide a general workflow for accommodating non‐Gaussian growth patterns while retaining important covariates and random effects. Our approach emphasizes visual diagnostics from pilot Gaussian models and quantile‐based metrics of skewness and kurtosis that guide selection of a non‐Gaussian alternative, if necessary. Across six case studies, skewness and excess kurtosis were common features of growth data, and non‐Gaussian models consistently generated simulated data that were more consistent with real data than pilot Gaussian models. However, effects of “improved” growth modeling on IPM results were moderate to weak and differed in direction or magnitude between different outputs from the same model. Using tools not available when IPMs were first developed, it is now possible to fit non‐Gaussian models to growth data without sacrificing ecological complexity. Doing so, as guided by careful interrogation of the data, will result in models that better represent the populations for which they are intended. 
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  2. Abstract Species' persistence in increasingly variable climates will depend on resilience against the fitness costs of environmental stochasticity. Most organisms host microbiota that shield against stressors. Here, we test the hypothesis that, by limiting exposure to temporally variable stressors, microbial symbionts reduce hosts' demographic variance. We parameterized stochastic population models using data from a 14‐year symbiont‐removal experiment including seven grass species that hostEpichloëfungal endophytes. Results provide novel evidence that symbiotic benefits arise not only through improved mean fitness, but also through dampened inter‐annual variance. Hosts with “fast” life‐history traits benefited most from symbiont‐mediated demographic buffering. Under current climate conditions, contributions of demographic buffering were modest compared to benefits to mean fitness. However, simulations of increased stochasticity amplified benefits of demographic buffering and made it the more important pathway of host–symbiont mutualism. Microbial‐mediated variance buffering is likely an important, yet cryptic, mechanism of resilience in an increasingly variable world. 
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  3. Abstract Understanding mechanisms that generate range limits is central to knowing why species are found where they are and how they will respond to environmental change. There is growing awareness that biotic interactions play an important role in generating range limits. However, current theory and data overwhelmingly focus on abiotic drivers and antagonistic interactions. Here we explore the effect that mutualists have on their partner's range limits: the geographic “footprint” of mutualism. This footprint arises from two general processes: modification of a partner's niche through environment‐dependent fitness effects and, for a subset of mutualisms, dispersal opportunities that lead suitable habitats to be filled. We developed a conceptual framework that organizes different footprints of mutualism and the underlying mechanisms that shape them, and evaluated supporting empirical evidence from the primary literature. In the available literature, we found that the fitness benefits and dispersal opportunities provided by mutualism can extend species' ranges; conversely, the absence of mutualism can constrain species from otherwise suitable regions of their range. Most studies found that the footprint of mutualism is driven by changes in the frequency of mutualist partners from range core to range edge, whereas fewer found changes in interaction outcomes, the diversity of partners, or varying sensitivities of fitness to the effects of mutualists. We discuss these findings with respect to specialization, dependence, and intimacy of mutualism. Much remains unknown about the geographic footprint of mutualisms, leaving fruitful areas for future work. A particularly important future direction is to explore the role of mutualism during range shifts under global change, including the promotion of shifts at leading edges and persistence at trailing edges. 
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  4. Global climate change has triggered an urgent need for predicting the reorganization of Earth’s biodiversity. For dioecious species (those with separate sexes), it is unclear how commonly unique climate sensitivities of females and males could influence projections for species-level responses to climate change. We developed demographic models of range limitation, parameterized from geographically distributed common garden experiments, with females and males of a dioecious grass species (Poa arachnifera) throughout and beyond its range in the south-central U.S. We contrasted predictions of a standard female-dominant model with those of a two-sex model that accounts for feedbacks between sex ratio and vital rates. Both model versions predict that future climate change will induce a poleward shift of niche suitability beyond current northern limits. However, the magnitude of the poleward shift was underestimated by the female-dominant model because females have broader temperature tolerance than males but become mate-limited under female-biased sex ratios, which are forecasted to become more common under future climate. Our results illustrate how explicitly accounting for both sexes can enhance population viability forecasts and conservation planning for dioecious species in response to climate change. 
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    Free, publicly-accessible full text available May 27, 2026
  5. Species' distributions and abundances are shifting in response to climate change. Most species harbor microbial symbionts that have the potential to influence these responses. Mutualistic microbial symbionts may provide resilience to environmental change by protecting their hosts from increasing stress. However, environmental change that disrupts these interactions may lead to declines in hosts or symbionts. Microbes preserved within herbarium specimens offer a unique opportunity to quantify changes in microbial symbiosis across broad temporal and spatial scales. We asked how the prevalence of seed-transmitted fungal symbionts of grasses (Epichloe endophytes), which can protect hosts from abiotic stress, have changed over time in response to climate change, and how these changes vary across host species' ranges. Specifically, we analyzed 2,346 herbarium specimens of three grass host species collected over the last two centuries (1824 -- 2019) for the presence or absence of endophyte symbiosis, and evaluated spatial and temporal trends in endophyte prevalence. We found that endophytes increased in prevalence over the last two centuries from ca. 25% prevalence to ca. 75% prevalence, on average, across three host species. We also found that changes in prevalence were associated with observed changes in seasonal climate drivers; notably increasing precipitation corresponding to each host species' peak growing season and changes in off-peak season variability in precipitation. Our analysis performed favorably in an out-of-sample predictive test with contemporary data, however we identified greater local-scale variability in endophyte prevalence in contemporary data compared to historic data, suggesting that model fusion may be an important step moving forward. Our results provide novel evidence for a cryptic biological response to climate change that may contribute to the resilience of host-microbe symbiosis through context-dependent benefits that confer a fitness advantage to symbiotic hosts under environmental change. 
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