92 research outputs found

    Mate choice in a changing world

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    Human activities by altering environmental conditions are influencing the mate choice of animals. This is by impacts on: (i) the production and expression of traits evaluated by mate choosers; (ii) the transmission of information about potential mates to choosers; (iii) the reception and processing of the information by choosers; and (iv) the final mate choice. Here, I first discuss how these four stages of the mate-choice process can be altered by environmental change, and how these alterations, in turn, can influence individuals, populations, and communities. Much evidence exists for human-induced environmental changes influencing mate choice, but the consequences for the fitness of courters and choosers are less well known, and even less is known about the impact on population dynamics, species interactions and community composition. More evidence exists for altered mate-choice systems influencing interspecific matings and thereby community composition and biodiversity. I then consider whether plastic adjustments and evolutionary changes can rescue adaptive mate-choice systems, and reflect on the possibility of non-adaptive mate-choice systems becoming less maladaptive under environmental change. Much evidence exists for plastic adjustments of mate-choice systems, but whether these are adaptive is seldom known, as is the contribution of genetic changes. Finally, I contemplate the possibility of mate-choice systems rescuing populations from decline in changing environments. I explain how this is context dependent with both positive and negative outcomes possible. In summary, while much evidence exists for human-induced environmental changes influencing mate-choice systems, less is known about the consequences for ecological and evolutionary processes. Considering the importance that mate choice plays in determining individual fitness and population viability, the effects of environmental change on mate-choice systems should be considered in studies on the ecological and evolutionary consequences of human disturbances to habitats.Peer reviewe

    Mechanisms behind bottom-up effects : eutrophication increases fecundity by shortening the interspawning interval in stickleback

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    Anthropogenic eutrophication is altering aquatic environments by promoting primary production. This influences the population dynamics of consumers through bottom-up effects, but the underlying mechanisms and pathways are not always clear. To evaluate and mitigate effects of eutrophication on ecological communities, more research is needed on the underlying factors. Here we show that anthropogenic eutrophication increases population fecundity in the threespine stickleback (Gasterosteus aculeatus) by increasing the number of times females reproduce-lifetime fecundity-rather than instantaneous fecundity. When we exposed females to nutrient-enriched waters with enhanced algal growth, their interspawning interval shortened but the size of their egg clutches, or the size of their eggs, did not change. The shortening of the interspawning interval was probably caused by higher food intake, as algae growth promotes the growth of preferred prey populations. Enhanced female lifetime fecundity could increase offspring production and, hence, influence population dynamics. In support of this, earlier studies show that more offspring are emerging in habitats with denser algae growth. Thus, our results stress the importance of considering lifetime fecundity, in addition to instantaneous fecundity, when investigating the impact of human-induced eutrophication on population processes. At a broader level, our results highlight the importance of following individuals over longer time spans when evaluating the pathways and processes through which environmental changes influence individual fitness and population processes.Peer reviewe

    Do algae blooms dilute the risk of trematode infections in threespine sticklebacks?

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    Human-induced growth of macro-algae is often assumed to increase trematode infections in fishes by increasing the abundance and condition of the parasite’s intermediate host – snails – as this can boost the release of trematode larvae, cercariae, from the intermediate hosts. However, macro-algae can also impose barriers to the transmission of cercariae and reduce infections. We investigated whether an increased growth of filamentous algae affects the transmission of Diplostomum pseudospathaceum cercariae to the threespine stickleback Gasterosteus aculeatus, a common fish in eutrophied shallow waters. We exposed sticklebacks to trematode cercariae in the absence and presence of artificial filamentous algae, and recorded effects on the proportion of sticklebacks infected and the number of encysted metacercariae per fish. No significant effect of artificial algae on cercariae transmission was detected. However, the body size and the sex of the sticklebacks were strongly correlated with the number of encysted metacercariae per infected fish, with females and larger individuals being more infected. We discuss different factors that could have caused the difference in parasite transmission, including sex-related differences in body size and behaviour of sticklebacks.Peer reviewe

    Reproduction under predation risk and the trade-off between current and future reproduction in the threespine stickleback

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    An increasing number of studies show that animals adjust their reproductive e¡ort to the risk of predation. However, to maximize lifetime reproductive success this adjustment should depend on the animals' current and future reproductive potential. Here I tested this hypothesis by allowing threespine stickleback males (Gasterosteus aculeatus), differing in current and future mating probabilities, to reproduce in pools in both the presence and absence of predators. As expected, males adjusted their reproductive effort to the risk of predation. Fewer males bred, and all males developed less nuptial coloration in the presence of predators. However, males with a low current mating probability took less risk than males with a higher mating probability, whereas all males increased risk taking when future reproductive opportunities decreased. The results thus support the hypothesis that males are able to assess both the risk of predation and their current versus future mating probability, and adjust their reproductive decisions accordingly. The study further suggests that predation risk may have less effect on sexual selection than previously assumed, as the males which refrained from reproducing in the presence of predators were mainly males with a low mating probability

    Male-male competition facilitates female choice in sticklebacks

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    In many species, secondary sexual characteristics are used in both male-male competition and in attracting females. This suggests that social control of deception could contribute to the maintenance of honest sexual signalling. In the three-spined stickleback Gasterosteus aculeatus, male red breeding coloration plays a dual role in sexual selection by functioning as both a threat signal in male-male competition and as a cue for female choice. To investigate whether male competition determines the level of signalling, the expression of red coloration and courtship activity were recorded both before and after male interactions. The results show that male competition influences signal expression by increasing the difference between males in signalling level. This in turn facilitates female choice and induces a preference for dominant males. Since a preference for dominant males may benefit females both directly and indirectly in this species with exclusively paternal care, male-male competition seems to increase the honesty of signalling and, thus, facilitates female choice in relation to male quality. This may increase the intensity of sexual selection and promote the evolution of breeding aggregations

    Plasticity in a changing world: Behavioural responses to human perturbations

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    Most insect species are affected by Human Induced Rapid Environmental Changes (HIREC). Multiple responses to HIREC are observed in insects, such as modifications of their morphology, physiology, behavioural strategies or phenology. Most of the responses involve phenotypic plasticity rather than genetic evolution. Here, we review the involvement of behavioural plasticity in foraging, reproduction, habitat choice and dispersal; and how behavioural plasticity modifies social behaviour and inter-specific interactions. Although important, behavioural plasticity is rarely sufficient to cope with HIREC. An increasing number of studies find species to respond maladaptively or insufficiently to various anthropogenic disturbances, and less often is large degree of plasticity linked to success.Peer reviewe

    Changes in expression and honesty of sexual signalling over the reproductive lifetime of sticklebacks

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    Fitness costs of signalling are essential in order for reliable sexual signalling to prevail when the interests of the sexes con£ict. This means that signalling can be subjected to a life history trade-o¡ between present and future signalling e¡ort. Here, I show that three-spined stickleback males (Gasterosteus aculeatus), who have a single breeding season during which they breed repeatedly, change their red nuptial coloration over the season depending on their body size at the start of breeding. Large males that completed several breeding cycles increased their red coloration over the season, whereas small males, who completed only a few cycles, did not. The increase in coloration was accompanied by an increase in parental success when males were energy constrained, but not when they had access to an unlimited food supply. Red coloration was thus an honest signal of male parental ability despite changes in signal expression when both signalling and parental care were costly and the investments in them changed simultaneously over the reproductive lifetime. However, the honesty of the signal varied over a lifetime. At the penultimate cycle, bright males cannibalized some of their eggs, probably to increase survival to the last cycle, whereas males cared for their o¡spring independent of coloration at the ultimate cycle
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