For organisms living in unpredictable environments, timing important life‐history events is challenging. One way to deal with uncertainty is to spread the emergence of offspring across multiple years via dormancy. However, timing of emergence is not only important among years, but also within each growing season. Here, we study the evolutionary interactions between germination strategies that deal with among‐ and within‐season uncertainty. We use a modelling approach that considers among‐season dormancy and within‐season germination phenology of annual plants as potentially independent traits and study their separate and joint evolution in a variable environment. We find that higher among‐season dormancy selects for earlier germination within the growing season. Furthermore, our results indicate that more unpredictable natural environments can counter‐intuitively select for less risk‐spreading within the season. Furthermore, strong priority effects select for earlier within‐season germination phenology which in turn increases the need for bet hedging through among‐season dormancy.

Almost all animal species undergo metamorphosis, even though empirical data show that this life-history strategy evolved only a few times. Why is metamorphosis so widespread, and why has it evolved? Here we study the evolution of metamorphosis by using a fully size-structured population model in conjunction with the adaptivedynamics approach. We assume that individuals compete for two food sources; one of these, the primary food source, is available to individuals of all sizes. The secondary food source is available only to large individuals. Without metamorphosis, unresolvable tensions arise for species faced with the opportunity of specializing on such a secondary food source. We show that metamorphosis can evolve as a way to resolve these tensions, such that small individuals specialize on the primary food source while large individuals specialize on the secondary food source. We find, however, that metamorphosis evolves only when the supply rate of the secondary food source exceeds a high threshold. Individuals postpone metamorphosis when the ecological conditions under which metamorphosis originally evolved deteriorate but will often not abandon this life-history strategy, even if it causes population extinction through evolutionary trapping. In summary, our results show that metamorphosis is not easy to evolve but that, once evolved, it is hard to lose. These findings can explain the widespread occurrence of metamorphosis in the animal kingdom despite its few evolutionary origins.

In haplodiploids, (1) alleles spend twice as many generations in females as in males, (2) males are never heterozygous and therefore express recessive alleles, and (3) males sire daughters, but no sons. Intralocus sexual conflict therefore operates differently in haplodiploids than in diploids, and shares strong similarities with loci on X (or Z) chromosomes. The common co-occurrence of all three features makes it difficult to pinpoint their respective roles. However, they do not always co-occur in nature, and missing cases can be additionally studied with hypothetical life cycles. We model sexually antagonistic alleles in eight different sex determination systems, and find that arguments (1) and (2) promote invasion and fixation of female-beneficial and male-beneficial alleles, respectively; (2) also improves prospects for polymorphism. Argument (3) harms the invasion prospects of sexually antagonistic alleles (irrespective of which sex benefits), but promotes fixation should invasion nevertheless occur. Disentangling the features helps to evaluate the validity of previous verbal arguments and yields better informed predictions about intralocus sexual conflict under different sex determination systems, including hitherto undiscovered ones.

Many free-living animal species, including the majority of fish, insects, and amphibians, change their food and habitat during their life. Even though these ontogenetic changes in niche are common, it is not well understood which ecological conditions have favored the evolution of these shifts. Using an adaptive dynamics approach, we show that it is evolutionarily advantageous to switch to an alternative food source in the course of ontogeny when this results in a higher intake rate for the switching consumers. Individuals are, however, not able to specialize on this new food source when this negatively affects the performance early in life on the original food source. Selection on these early life stages is so strong that in species with a complete diet shift, evolution results in large juveniles and adults that are maladapted to the alternative food source while their offspring are specialized on the original food source when young. These outcomes suggest strong selection to decouple the different life stages, such that they can maximize their performance on different food sources independently from each other. Metamorphosis could be a way to decouple the different life stages and therefore evolve in species that feed on multiple food sources during their life.

Ontogenetic diet shifts, where individuals change their resource use during development, are the rule rather than the exception in the animal world. Here, we aim to understand how such changes in diet during development affect the conditions for an adaptive radiation in the presence of ecological opportunity. We use a size-structured consumer–resource model and the adaptive dynamics approach to study the ecological conditions for speciation. We assume that small individuals all feed on a shared resource. Large individuals, on the other hand, have access to multiple food sources on which they can specialize. We find that competition among small individuals can hinder an adaptive radiation to unfold, despite plenty of ecological opportunity for large individuals. When small individuals experience strong competition for food, they grow slowly and only a few individuals are recruited to the larger size classes. Hence, competition for food among large individuals is weak and there is therefore no disruptive selection. In addition, initial conditions determine if an adaptive radiation occurs or not. A consumer population initially dominated by small individuals will not radiate. On the other hand, a population initially dominated by large individuals may undergo adaptive radiation and diversify into multiple species.

Although metamorphosis is widespread in the animal kingdom, several species have evolved life‐cycle modifications to avoid complete metamorphosis. Some species, for example, many salamanders and newts, have deleted the adult stage via a process called paedomorphosis. Others, for example, some frog species and marine invertebrates, no longer have a distinct larval stage and reach maturation via direct development. Here we study which ecological conditions can lead to the loss of metamorphosis via the evolution of direct development. To do so, we use size‐structured consumer‐resource models in conjunction with the adaptive‐dynamics approach. In case the larval habitat deteriorates, individuals will produce larger offspring and in concert accelerate metamorphosis. Although this leads to the evolutionary transition from metamorphosis to direct development when the adult habitat is highly favorable, the population will go extinct in case the adult habitat does not provide sufficient food to escape metamorphosis. With a phylogenetic approach we furthermore show that among amphibians the transition of metamorphosis to direct development is indeed, in line with model predictions, conditional on and preceded by the evolution of larger egg sizes.

Summary 1.Coexistence of predators that share the same prey is common. This is still the case in sizestructured predator communities where predators consume prey species of different sizes (interspecific prey responses) or consume different size classes of the same species of prey (intraspecific prey responses). 2. A mechanism has recently been proposed to explain coexistence between predators that differ in size but share the same prey species, emergent facilitation, which is dependent on strong intraspecific responses from one or more prey species. Under emergent facilitation, predators can depend on each other for invasion, persistence or success in a size-structured prey community. 3. Experimental evidence for intraspecific size-structured responses in prey populations remains rare, and further questions remain about direct interactions between predators that could prevent or limit any positive effects between predators [e.g. intraguild predation (IGP)]. 4. Here, we provide a community-wide experiment on emergent facilitation including natural predators. We investigate both the direct interactions between two predators that differ in body size (fish vs. invertebrate predator), and the indirect interaction between them via their shared prey community (zooplankton). 5. Our evidence supports the most likely expectation of interactions between differently sized predators that IGP rates are high, and interspecific interactions in the shared prey community dominate the response to predation (i.e. predator-mediated competition). The question of whether emergent facilitation occurs frequently in nature requires more empirical and theoretical attention, specifically to address the likelihood that its pre-conditions may co-occur with high rates of IGP.

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