Initial offspring size is a fundamental component of absolute growth rate, where large offspring will reach a given adult body size faster than smaller offspring. Yet, our knowledge regarding the coevolution between offspring and adult size is limited. In time-constrained environments, organisms need to reproduce at a high rate and reach a reproductive size quickly. To rapidly attain a large adult body size, we hypothesize that, in seasonal habitats, large species are bound to having a large initial size, and consequently, the evolution of egg size will be tightly matched to that of body size, compared to less time-limited systems. We tested this hypothesis in killifishes, and found a significantly steeper allometric relationship between egg and body sizes in annual, compared to nonannual species. We also found higher rates of evolution of egg and body size in annual compared to nonannual species. Our results suggest that time-constrained environments impose strong selection on rapidly reaching a species-specific body size, and reproduce at a high rate, which in turn imposes constraints on the evolution of egg sizes. In combination, these distinct selection pressures result in different relationships between egg and body size among species in time-constrained versus permanent habitats.

Adaptive radiations have proven important for understanding the mechanisms and processes underlying biological diversity. The convergence of form and function, as well as admixture and adaptive introgression, are common in adaptive radiations.However, distinguishing between these two scenarios remains a challenge for evolutionary research. The Midas cichlid species complex (Amphilophus spp.) is a prime example of adaptive radiation, with phenotypic diversification occurring at various stages of genetic differentiation. One species, A. labiatus, has large fleshy lips, is associated with rocky lake substrates, and occurs patchily within Lakes Nicaragua and Managua. By contrast, the similar, but thin-lipped, congener, A. citrinellus, is more common and widespread. We investigated the evolutionary history of the large-lipped form, specifically regarding whether the trait has evolved independently in both lakes from ancestral thin-lipped populations, or via dispersal and/or admixture events.We collected samples from distinct locations in both lakes, and assessed differences in morphology and ecology. Using RAD-seq, we genotyped thousands of SNPs to measure population structure and divergence, demographic history, and admixture.We found significant between-species differences in ecology and morphology, local intraspecific differences in body shape and trophic traits, but only limited intraspecific variation in lip shape. Despite clear ecological differences, our genomic approach

Colour polymorphisms are a striking example of phenotypic diversity, yet the sources of selection that allow different morphs to persist within populations remain poorly understood. In particular, despite the importance of aggression in mediating social dominance, few studies have considered how heterospecific aggression might contribute to the maintenance or divergence of different colour morphs. To redress this gap, we carried out a field-based study in a Nicaraguan crater lake to investigate patterns of heterospecific aggression directed by the cichlid fish, Hypsophrys nicaraguensis, towards colour polymorphic cichlids in the genus Amphilophus. We found that H. nicaraguensis was the most frequent territorial neighbour of the colour polymorphic A. sagittae. Furthermore, when manipulating territorial intrusions using models, H. nicaraguensis were more aggressive towards the gold than dark colour morph of the sympatric Amphilophus species, including A. sagittae. Such a pattern of heterospecific aggression should be costly to the gold colour morph, potentially accounting for its lower than expected frequency and, more generally, highlighting the importance of considering heterospecific aggression in the context of morph frequencies and coexistence in the wild.

Metabolic rate is considered to determine the energetic investment placed into life-history traits, regulating the speed of an organism’s life-cycle and forming the so called “pace-of-life”. However, how metabolic rate and life-history traits co-evolve remains unclear. For instance, the energetic demands of life-history traits, including the number of energy allocation trade-offs, is unlikely to remain constant over ontogeny. Therefore, the predicted coevolution between metabolic rate and life-history could be specific to particular ontogenetic stages, rather than a stable property of an organism. Here, we test the ontogenetic dependency of the coevolution between metabolic rate and the pace of life-history, under strictly standardized conditions using 30 species of killifish, which are either annual species adapted to ephemeral pools or non-annual species inhabiting more permanent waterbodies. Standard metabolic rates were estimated at three ontogenetic stages, together with relevant life-history traits, i.e. growth (juveniles), maturity (young adults), and reproductive rate (reproductive adults). Life-history traits largely followed predicted pace-of-life patterns, with overall faster/higher rates in annual species. The divergences in life-history traits across species tended to increase over ontogeny, being smallest during juvenile growth and largest in reproductive adults. However, associations between life-history strategy and metabolic rate followed a reversed pattern, being strongest in juveniles, but lowest in reproductive adults. Our results are concordant with the number of energetic trade-offs increasing over ontogeny, which results in a stronger covariation between physiology and life-history traits earlier in ontogeny.

The ability to assess the threat posed by competitors, and to respond appropriately, is important for reducing the costs of aggression. In this respect, aggression directed toward heterospecifics is often just as significant as aggression among conspecifics. This is especially true for cichlid fish that share breeding grounds with heterospecifics. Indeed, cichlids are known to differentiate not only between conspecifics that pose different levels of threat but also between heterospecific territorial intruders by directing more aggression toward nonbreeding individuals. To assess whether the ability to make such distinctions could be based on color cues alone, we carried out a field study in which we experimentally presented Amphilophus sagittae cichlid pairs with model intruders of a sympatric congener, Amphilophus xiloaensis, in breeding versus nonbreeding coloration. Consistent with our prediction, we found that A. sagittae exhibited more aggression toward A. xiloaensis models of the latter color type. The results are, to our knowledge, the first to show that territory holders can, based on coloration alone, assess variation among individuals of a species other than their own in the threat posed to offspring survival.

The evolution and maintenance of colour polymorphisms remains a topic of considerable research interest. One key mechanism thought to contribute to the coexistence of different colour morphs is a bias in how conspicuous they are to visual predators. Although individuals of many species camouflage themselves against their background to avoid predation, differently coloured individuals within a species may vary in their capacity to do so. However, to date, very few studies have explicitly investigated the ability of different colour morphs to plastically adjust their colouration to match their background. The red devil (Amphilophus labiatus) is a Neotropical cichlid fish with a stable colour polymorphism, with the gold morph being genetically dominant and having a myriad of documented advantages over the dark morph. However, gold individuals are much rarer, which may be related to their heightened conspicuousness to would-be predators. Here, we tested the ability of differently coloured individuals to phenotypically adjust the shade of their body colour and patterns to match their background. In particular, we filmed dark, gold and mottled (a transitioning phase from dark to gold) individuals under an identical set-up on light vs. dark-coloured substrates. We found that, in contrast to individuals of the dark morph, gold and mottled individuals were less capable of matching their body colouration to their background. As a result, gold individuals appeared to be more conspicuous. These results suggest that a difference in background matching ability could play an important role in the maintenance of colour polymorphisms.

Sex ratios can differ from an expected equal proportion of males and females, carrying substantial implications for our understanding of how mating systems evolve. Typically, macro-evolutionary studies have been conducted without assessing how deviations from an equal sex ratio could be explained by sex-biased mortality or dispersal. Our understanding of sex ratio evolution independent of these confounds, in addition to any putative links between skewed sex ratios and other factors (e.g. life history), therefore remains largely unexplored. Here, we conducted an exploratory study investigating differences in sex ratios across closely related species while controlling for extrinsic mortality. We also tested two factors, non-overlapping/overlapping generations and the social environment, which have both been hypothesised to affect sex ratios. Specifically, we raised 15 species of killifish, which have either overlapping or discrete generations, under both solitary and social treatments. We found substantial divergences in sex ratios across closely related species, which exhibited both male and female biases. In conjunction with a low phylogenetic signal, our results suggest that sex ratios can evolve rapidly in this group. However, we found no evidence that overlapping generations or the social environment affected sex biases, suggesting that other factors drive the rapid evolution of sex ratios in killifishes.

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