475 research outputs found

    The Evolution of Dispersal in Reserve Networks

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    Optimal Investment to Enable Evolutionary Rescue

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    'Evolutionary rescue' is the potential for evolution to enable population persistence in a changing environment. Even with eventual rescue, evolutionary time lags can cause the population size to temporarily fall below a threshold susceptible to extinction. To reduce extinction risk given human-driven global change, conservation management can enhance populations through actions such as captive breeding. To quantify the optimal timing of, and indicators for engaging in, investment in temporary enhancement to enable evolutionary rescue, we construct a model of coupled demographic-genetic dynamics given a moving optimum. We assume 'decelerating change', as might be relevant to climate change, where the rate of environmental change initially exceeds a rate where evolutionary rescue is possible, but eventually slows. We analyze the optimal control path of an intervention to avoid the population size falling below a threshold susceptible to extinction, minimizing costs. We find that the optimal path of intervention initially increases as the population declines, then declines and ceases when the population growth rate becomes positive, which lags the stabilization in environmental change. In other words, the optimal strategy involves increasing investment even in the face of a declining population, and positive population growth could serve as a signal to end the intervention. In addition, a greater carrying capacity relative to the initial population size decreases the optimal intervention. Therefore, a one-time action to increase carrying capacity, such as habitat restoration, can reduce the amount and duration of longer-term investment in population enhancement, even if the population is initially lower than and declining away from the new carrying capacity

    Quantifying the balance between bycatch and predator or competitor release for nontarget species

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    If a species is bycatch in a fishery targeted at its competitor or predator, it experiences both direct anthropogenic mortality and indirect positive effects through species interactions. If the species involved interact strongly, the release from competition or predation can counteract or exceed the negative effects of bycatch. We used a set of two- and three-species community modules to analyze the relative importance of species interactions when modeling the overall effect of harvest with bycatch on a nontarget species. To measure the trade-off between direct mortality and indirect positive effects, we developed a "bycatch transition point" metric to determine, for different scenarios, what levels of bycatch shift overall harvest impact from positive to negative. Under strong direct competition with a targeted competitor, release from competition due to harvest leads to a net increase in abundance even under moderate levels of bycatch. For a three-species model with a shared obligate predator, the release from apparent competition exceeds direct competitive release and outweighs the decrease from bycatch mortality under a wide range of parameters. Therefore, in communities where a shared predator forms a strong link between the target and nontarget species, the effects of indirect interactions on populations can be larger than those of direct interactions. The bycatch transition point metric can be used for tightly linked species to evaluate the relative strengths of positive indirect effects and negative anthropogenic impacts such as bycatch, habitat degradation, and introduction of invasive species

    Partitioning colony size variation into growth and partial mortality

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    We thank the Australian Research Council for fellowship and research support. M.A.D. is funded by a Leverhulme Fellowship and by the John Templeton Foundation grant no. 60501.Body size is a trait that broadly influences the demography and ecology of organisms. In unitary organisms, body size tends to increase with age. In modular organisms, body size can either increase or decrease with age, with size changes being the net difference between modules added through growth and modules lost through partial mortality. Rates of colony extension are independent of body size, but net growth is allometric, suggesting a significant role of size-dependent mortality. In this study, we develop a generalizable model of partitioned growth and partial mortality and apply it to data from 11 species of reef-building coral. We show that corals generally grow at constant radial increments that are size independent, and that partial mortality acts more strongly on small colonies. We also show a clear life-history trade-off between growth and partial mortality that is governed by growth form. This decomposition of net growth can provide mechanistic insights into the relative demographic effects of the intrinsic factors (e.g. acquisition of food and life-history strategy), which tend to affect growth, and extrinsic factors (e.g. physical damage, and predation), which tend to affect mortality.PostprintPostprintPeer reviewe

    When is dispersal for dispersal? Unifying marine and terrestrial perspectives

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    Recent syntheses on the evolutionary causes of dispersal have focused on dispersal as a direct adaptation, but many traits that influence dispersal have other functions, raising the question: when is dispersal 'for' dispersal? We review and critically evaluate the ecological causes of selection on traits that give rise to dispersal in marine and terrestrial organisms. In the sea, passive dispersal is relatively easy and specific morphological, behavioural, and physiological adaptations for dispersal are rare. Instead, there may often be selection to limit dispersal. On land, dispersal is relatively difficult without specific adaptations, which are relatively common. Although selection for dispersal is expected in both systems and traits leading to dispersal are often linked to fitness, systems may differ in the extent to which dispersal in nature arises from direct selection for dispersal or as a by-product of selection on traits with other functions. Our analysis highlights incompleteness of theories that assume a simple and direct relationship between dispersal and fitness, not just insofar as they ignore a vast array of taxa in the marine realm, but also because they may be missing critically important effects of traits influencing dispersal in all realms
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