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Lake-dwelling fish that form species pairs/flocks characterized by body size divergence are important model systems for speciation research. Although several sources of divergent selection have been identified in these systems, their importance for driving the speciation process remains elusive. A major problem is that in retrospect, we cannot distinguish selection pressures that initiated divergence from those acting later in the process. To address this issue, we studied the initial stages of speciation in European whitefish (Coregonus lavaretus) using data from 358 populations of varying age (26-10,000 years). We find that whitefish speciation is driven by a large-growing predator, the northern pike (Esox lucius). Pike initiates divergence by causing a largely plastic differentiation into benthic giants and pelagic dwarfs: ecotypes that will subsequently develop partial reproductive isolation and heritable differences in gill raker number. Using an eco-evolutionary model, we demonstrate how pike's habitat specificity and large gape size are critical for imposing a between-habitat trade-off, causing prey to mature in a safer place or at a safer size. Thereby, we propose a novel mechanism for how predators may cause dwarf/giant speciation in lake-dwelling fish species.

Sustainable yields that are at least 80% of the maximum sustainable yield are sometimes referred to as "pretty good yields" (PGY). The range of PGY harvesting strategies is generally broad and thus leaves room to account for additional objectives besides high yield. Here, we analyze stage-dependent harvesting strategies that realize PGY with conservation as a second objective. We show that (1) PGY harvesting strategies can give large conservation benefits and (2) equal harvesting rates of juveniles and adults is often a good strategy. These conclusions are based on trade-off curves between yield and four measures of conservation that form in two established population models, one age-structured model and one stage-structured model, when considering different harvesting rates of juveniles and adults. These conclusions hold for a broad range of parameter settings, although our investigation of robustness also reveals that (3) predictions of the age-structured model are more sensitive to variations in parameter values than those of the stage-structured model. Finally, we find that (4) measures of stability that are often quite difficult to assess in the field (e.g., basic reproduction ratio and resilience) are systematically negatively correlated with impacts on biomass and size structure, so that these later quantities can provide integrative signals to detect possible collapses.

With increasing fishing pressures having brought several stocks to the brink of collapse, there is a need for developing efficient harvesting methods that account for factors beyond merely yield or profit. We consider the dynamics and management of a stage-structured fish stock. Our work is based on a consumer-resource model which De Roos et al. (in Theor. Popul. Biol. 73, 47-62, 2008) have derived as an approximation of a physiologically-structured counterpart. First, we rigorously prove the existence of steady states in both models, that the models share the same steady states, and that there exists at most one positive steady state. Furthermore, we carry out numerical investigations which suggest that a steady state is globally stable if it is locally stable. Second, we consider multiobjective harvesting strategies which account for yield, profit, and the recovery potential of the fish stock. The recovery potential is a measure of how quickly a fish stock can recover from a major disturbance and serves as an indication of the extinction risk associated with a harvesting strategy. Our analysis reveals that a small reduction in yield or profit allows for a disproportional increase in recovery potential. We also show that there exists a harvesting strategy with yield close to the maximum sustainable yield (MSY) and profit close to that associated with the maximum economic yield (MEY). In offering a good compromise between MSY and MEY, we believe that this harvesting strategy is preferable in most instances. Third, we consider the impact of harvesting on population size structure and analytically determine the most and least harmful harvesting strategies. We conclude that the most harmful harvesting strategy consists of harvesting both adults and juveniles, while harvesting only adults is the least harmful strategy. Finally, we find that a high percentage of juvenile biomass indicates elevated extinction risk and might therefore serve as an early-warning signal of impending stock collapse.

There are concerns that anthropogenic harvesting may cause phenotypic adaptive changes in exploited wild populations, in particular maturation at a smaller size and younger age. In this paper, we study the evolutionarily stable size at maturation of prey subjected to size-selective harvesting in a simple predator-prey model, taking into account three recognized life-history costs of early maturation, namely reduced fecundity, reduced growth, and increased mortality. Our analysis shows that harvesting large individuals favors maturation at smaller size compared to the unharvested system, independent of life-history tradeoff and the predator's prey-size preference. In general, however, the evolutionarily stable maturation size can either increase or decrease relative to the unharvested system, depending on the harvesting regime, the life-history tradeoff, and the predator's preferred size of prey. Furthermore, we examine how the predator population size changes in response to adaptive change in size at maturation of the prey. Surprisingly, in some situations, we find that the evolutionarily stable maturation size under harvesting is associated with an increased predator population size. This occurs, in particular, when early maturation trades off with growth rate. In total, we determine the evolutionarily stable size at maturation and associated predator population size for a total of forty-five different combinations of tradeoff, harvest regime, and predated size class.

R. S. Strichartz proposes a discrete definition of Besov spaces on self-similar fractals having a regular harmonic structure. In this paper, we characterize some of these Holder-Zygmund and Besov-Lipschitz functions on nested fractals by means of the magnitude of the coefficients of the expansion of a function in a continuous piecewise harmonic base.

R. S. Strichartz proposes a discrete definition of Besov spaces on self-similar fractals having a regular harmonic structure. In this paper, we characterize some of these Hölder-Zygmund and Besov-Lipschitz functions on nested fractals by means of the magnitude of the coefficients of the expansion of a function in a continuous piecewise harmonic base.