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Alternative mating strategy
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Alternative mating strategy
An alternative mating strategy is a strategy used by male or female animals, often with distinct phenotypes, that differs from the prevailing mating strategy of their sex. Such strategies are diverse and variable both across and within species. Animal sexual behaviour and mate choice directly affect social structure and relationships in many different mating systems, whether monogamous, polygamous, polyandrous, or polygynous. Though males and females in a given population typically employ a predominant reproductive strategy based on the overarching mating system, individuals of the same sex often use different mating strategies. The most common alternative mating strategy is a sneaker morph. Among some reptiles, frogs and fish, large, territorial males compete for females, while small males may use sneaking tactics to mate without being noticed. Ray-finned fish express the most alternative mating strategies of any clade, including satellites that help territorial males, "pirate" males that demonstrate territorial tendencies but periodically attack other parental males for spawning access, and female mimics.
Alternative mating strategies have been observed among both male and female animals. Most typically, alternative strategies are adopted in the face of competition within a sex, especially in species that mate multiply. In these scenarios, some individuals adopt very different mating strategies to achieve reproductive success. The result over time is a variety of evolutionarily stable strategies and phenotypes, consisting of both conventional individuals and unconventional individuals who mate through alternative means. Successful strategies are maintained through sexual selection. The coexistence of alternative and traditional mating strategies can maximize the average fitness of the sex in question and be evolutionarily stable for a population. However, the utilization of alternative mating strategies may oscillate as a result of varying reproductive conditions, such as the availability of potential mates. Under changing circumstances, the existence of a variety of strategies allows individuals to choose the conditional behaviour that maximizes their fitness.
Conventional and alternative mating behaviours arise through sexual selection. More specifically, varying levels of reproductive success select for phenotypes and strategies that maximize an animal's chance of obtaining a mate. As a result, certain animals successfully use a conventional mating strategy while others employing this strategy fail to obtain mates. Over time, phenotypic variance arises both between and within the sexes, with males exhibiting greater diversity in phenotype. The resulting variance in male fitness creates a niche in which alternative strategies may develop, such as sneaking to obtain a mate. The alternative behaviours persist as part of this polymorphism, or variety of phenotypes, because the average fitness of unconventional males equals the average reproductive success of conventional males.
Alternative behaviours are maintained through frequency-dependent selection because of their equal fitness benefits and functional equivalence. Under frequency-dependent selection, the fitness of a given phenotype is determined by its frequency relative to other phenotypes within a population. Similarly, negative frequency-dependent selection describes a scenario in which rarer phenotypes experience greater fitness. Given that the utilization of alternative mating strategies has been shown to fluctuate over time, it has been suggested that frequency or negative frequency-dependent selection is the mechanism through which alternative mating strategies are maintained in animal populations.
A second proposed model for the maintenance of alternative mating behaviours is status-dependent selection. This describes a conditional strategy in which the fitness of alternative phenotypes depend on the status, or competitive ability, of an individual. Status includes environmental and genetic factors as well as age and size, and determines the level of fitness that may be obtained from a given phenotype. As shown in Figure 1, the fitness benefits of a given phenotype vary based on whether an individual is of high or low status. In a case where two phenotypes and strategies are possible, such as mate guarding or sneaking, there is an intermediate point of intersection where the fitness gained from these alternative behaviours is equivalent. At this point (s), the fitness gained from these strategies is equal, and the particular strategy employed at a given time depends on an individual's status. A low status individual below the switch point obtains higher fitness with phenotype B, while an individual of high status above the switch point benefits from higher fitness with phenotype A. Such a model shows how individuals of lesser status or competitive ability may maximize their fitness by exhibiting an alternative phenotype. In this manner, these selective forces maintain the phenotypic diversity observed among animals with respect to mating behaviour, though strategies utilized depends on a variety of circumstances.
Most of the organisms in question do not have the cognitive capacity to "strategize" in a logical sense. Here, a strategy is an underlying rule for making decisions about a certain behaviour. A strategy provides an organism with a set of tactics that are adaptive in various circumstances. A tactic is an action taken to achieve a specific goal.
Organisms within a population may not always have the same strategy, and different strategies may offer individuals either a range of tactical options or just one tactic. Furthermore, given strategy may be considered Mendelian, developmental, conditional, or a combination of the above. A Mendelian strategy depends on a genetically determined phenotypic difference, such as body size. This is the case in marine isopods, described below. Developmentally driven strategies are associated with phenotypic differences caused by varying conditions during the course of development that affect body size or overall adult health. Individuals may have a conditional behaviour strategy that depends not on the genetic or developmental impact on one's life circumstance, but on external factors. These may include the number of available mates, or the number of nearby competitors and their employed tactics. Some mating strategies are impacted by multiple factors, so these categorizations of Mendelian, developmental, and conditional are not mutually exclusive. They simply offer ways to think about alternative mating strategies and their root causes.
In any case, the mating strategies employed by organisms in various situations ultimately depend on the strength of selection acting to maintain or eliminate certain reproductive strategies. If sexual selection strongly favors one mating strategy over a potential alternative, individuals not conforming to the successful strategy fail to reproduce.
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Alternative mating strategy
An alternative mating strategy is a strategy used by male or female animals, often with distinct phenotypes, that differs from the prevailing mating strategy of their sex. Such strategies are diverse and variable both across and within species. Animal sexual behaviour and mate choice directly affect social structure and relationships in many different mating systems, whether monogamous, polygamous, polyandrous, or polygynous. Though males and females in a given population typically employ a predominant reproductive strategy based on the overarching mating system, individuals of the same sex often use different mating strategies. The most common alternative mating strategy is a sneaker morph. Among some reptiles, frogs and fish, large, territorial males compete for females, while small males may use sneaking tactics to mate without being noticed. Ray-finned fish express the most alternative mating strategies of any clade, including satellites that help territorial males, "pirate" males that demonstrate territorial tendencies but periodically attack other parental males for spawning access, and female mimics.
Alternative mating strategies have been observed among both male and female animals. Most typically, alternative strategies are adopted in the face of competition within a sex, especially in species that mate multiply. In these scenarios, some individuals adopt very different mating strategies to achieve reproductive success. The result over time is a variety of evolutionarily stable strategies and phenotypes, consisting of both conventional individuals and unconventional individuals who mate through alternative means. Successful strategies are maintained through sexual selection. The coexistence of alternative and traditional mating strategies can maximize the average fitness of the sex in question and be evolutionarily stable for a population. However, the utilization of alternative mating strategies may oscillate as a result of varying reproductive conditions, such as the availability of potential mates. Under changing circumstances, the existence of a variety of strategies allows individuals to choose the conditional behaviour that maximizes their fitness.
Conventional and alternative mating behaviours arise through sexual selection. More specifically, varying levels of reproductive success select for phenotypes and strategies that maximize an animal's chance of obtaining a mate. As a result, certain animals successfully use a conventional mating strategy while others employing this strategy fail to obtain mates. Over time, phenotypic variance arises both between and within the sexes, with males exhibiting greater diversity in phenotype. The resulting variance in male fitness creates a niche in which alternative strategies may develop, such as sneaking to obtain a mate. The alternative behaviours persist as part of this polymorphism, or variety of phenotypes, because the average fitness of unconventional males equals the average reproductive success of conventional males.
Alternative behaviours are maintained through frequency-dependent selection because of their equal fitness benefits and functional equivalence. Under frequency-dependent selection, the fitness of a given phenotype is determined by its frequency relative to other phenotypes within a population. Similarly, negative frequency-dependent selection describes a scenario in which rarer phenotypes experience greater fitness. Given that the utilization of alternative mating strategies has been shown to fluctuate over time, it has been suggested that frequency or negative frequency-dependent selection is the mechanism through which alternative mating strategies are maintained in animal populations.
A second proposed model for the maintenance of alternative mating behaviours is status-dependent selection. This describes a conditional strategy in which the fitness of alternative phenotypes depend on the status, or competitive ability, of an individual. Status includes environmental and genetic factors as well as age and size, and determines the level of fitness that may be obtained from a given phenotype. As shown in Figure 1, the fitness benefits of a given phenotype vary based on whether an individual is of high or low status. In a case where two phenotypes and strategies are possible, such as mate guarding or sneaking, there is an intermediate point of intersection where the fitness gained from these alternative behaviours is equivalent. At this point (s), the fitness gained from these strategies is equal, and the particular strategy employed at a given time depends on an individual's status. A low status individual below the switch point obtains higher fitness with phenotype B, while an individual of high status above the switch point benefits from higher fitness with phenotype A. Such a model shows how individuals of lesser status or competitive ability may maximize their fitness by exhibiting an alternative phenotype. In this manner, these selective forces maintain the phenotypic diversity observed among animals with respect to mating behaviour, though strategies utilized depends on a variety of circumstances.
Most of the organisms in question do not have the cognitive capacity to "strategize" in a logical sense. Here, a strategy is an underlying rule for making decisions about a certain behaviour. A strategy provides an organism with a set of tactics that are adaptive in various circumstances. A tactic is an action taken to achieve a specific goal.
Organisms within a population may not always have the same strategy, and different strategies may offer individuals either a range of tactical options or just one tactic. Furthermore, given strategy may be considered Mendelian, developmental, conditional, or a combination of the above. A Mendelian strategy depends on a genetically determined phenotypic difference, such as body size. This is the case in marine isopods, described below. Developmentally driven strategies are associated with phenotypic differences caused by varying conditions during the course of development that affect body size or overall adult health. Individuals may have a conditional behaviour strategy that depends not on the genetic or developmental impact on one's life circumstance, but on external factors. These may include the number of available mates, or the number of nearby competitors and their employed tactics. Some mating strategies are impacted by multiple factors, so these categorizations of Mendelian, developmental, and conditional are not mutually exclusive. They simply offer ways to think about alternative mating strategies and their root causes.
In any case, the mating strategies employed by organisms in various situations ultimately depend on the strength of selection acting to maintain or eliminate certain reproductive strategies. If sexual selection strongly favors one mating strategy over a potential alternative, individuals not conforming to the successful strategy fail to reproduce.