Polygynandry is a mating system in which both males and females have multiple mating partners during a breeding season. [1] In sexually reproducing diploid animals, different mating strategies are employed by males and females, because the cost of gamete production is lower for males than it is for females. [2] The different mating tactics employed by males and females are thought to be the outcome of stochastic reproductive conflicts both ecologically and socially. [2]
Reproductive conflicts in animal societies may arise because individuals are not genetically identical and have different optimal strategies for maximizing their fitness; and often it is found that reproductive conflicts generally arise due to dominance hierarchy in which all or a major part of reproduction is monopolized by only one individual. In the wasp Polistes carolina , the dominant queen amongst female wasps is determined by whoever arrives at the nest first rather than the largest foundress, who is expected to be the best at fighting (wasp). In a study of the bird Prunella collaris , the close proximity and sharing of ranges on the mountain tops of the French Pyrenees led to a polygynandrous mating system, where two to four males would mate with a range of two to four females within the same vicinity.
Polygynandry is another way to describe a multi-male and multi-female polygamous mating system. When females have multiple mating partners, it is known as polyandry, and when males have multiple mating partners, it is known as polygyny. Each sex has potential benefits in being promiscuous; females, especially those with genetically 'inferior' social partners, have the chance to increase the genetic quality of their offspring, [3] while males are able to fertilize the eggs of many other mates. [1] Essentially, the ideal mating behavior for males is to be promiscuous rather than monogamous (when they only have one mating partner), because this leads to multiple offspring, and these males monopolize their female partners by physically preventing them from copulating with other males. [2] On the other hand, females benefit through polyandry, as they have more sired offspring. [3]
Oftentimes females mate voluntarily with more than one male. Mating with several males reduces the risk of females having unfertilized eggs because one male may not have enough sperm to fertilize all her eggs. [1] In dark-eyed juncos, a female mates with more than one male because oftentimes, her social partner is of lower genetic quality than other potential sperm donors. [3] The females voluntarily mate with other males besides their mate because she sees the potential to improve her offspring viability and sexual attractiveness. [3] [1] Females may also mate with several males for genetic benefits such as genetic diversity among her offspring due to the variety of sperm available to her. [1] In song birds, extra-pair matings occur because females are able to sneak away from their home territories to solicit to other males. [1] When female song birds seek extra-male partners, they sexually select males with colorful plumage more elaborate than those of their social partner. [1] Studies show that female song birds that have less plumage partners most actively seek extra-pair matings, [1] furthermore males with the most developed traits—such as longer tails or brighter plumage survive better. Thus, when female song birds have multiple mating partners, they are increasing the genetic quality of their offspring.
To a female, multiple mating means an increase number of young that a female can produce, and oftentimes this also means an increase number of young they have to take care of. [1] In order to ensure the safety and wellbeing of her offspring, females may have multiple mating partners in order to gain more resources from males for herself and her offspring. [1] In dark-eyed juncos, dunnocks, and Galapagos hawks, mating with multiple males increases the amount of care a female can gain for her offspring. [3] [1] Oftentimes multiple mates allow females to have more sired offspring and the paternity of the offspring typically falls outside of the biological parents—meaning a different male may look after another male's offspring. [3]
Males can potentially fertilize eggs at a much faster rate than females can produce them, meaning a male can best increase his reproductive success by finding and fertilizing as many different females as possible. [1] In Drosophila melanogaster , the reproductive success of males increased with the number of matings, but for females there was no direct relationship with number of mates and number of offspring produced. [1] When males have multiple mating partners, they sometimes have to share parentage of the offspring, reducing the genetic value of the offspring to him and thus reduces the relative benefit of staying to help. [1] When paternity is shared between multiple males, males are expected to be less likely to stay in order to help the female care for the offspring because there is little benefit in staying to help raise the other offspring when there are other males present. [1]
Although males are able to increase their reproductive success faster than females by being able to fertilize eggs faster than females can produce them, males also at a disadvantage when it comes to mating because of sexual selection. Females usually choose males that are 'charming' and those who display sexual ornaments. [1] In a study of long-tailed widowbirds, males with longer tails were sexually selected over those with shorter and less impressive tails. [1] In birds such as the red-collared widowbird, males who display their sexual ornament during courtship are generally paired up faster and attract more females than males who display shorter tails during courtship. [1] Males are often sexually selected based on their physical characteristics and what they have to 'offer', for example, male peacocks with flamboyant colored tails are sexually selected over those with dull and less elaborate tails. [1] Sexual selection of males by females also leads to male-male competition. Unlike females who invest a lot prior to mating, males do not invest as much when generating their sperm, however this increases competition amongst males for female investment. High mating competition also means a greater variance in male success—the best competitors will have better success in mating than those who fail to mate. The best competitors will less likely be inclined to care for their offspring upon mating because they have the ability to produce offspring elsewhere. Males with the greatest size, strength, or best developed weapons achieve the greatest mating success. In other cases, males may have a higher reproductive success if they have better access to resources than other competitors. [1] For instance, female hanging flies mate with a male only if he provides a large insect for her to eat during copulation and North American bullfrogs protect ponds and small lakes where females come to lay their eggs. [1]
The various mating tactics are found in a broad number of taxa. In amphibians such as Salamandrina perspicillata , multiple paternity is a consequence of females mating with multiple males. [4] As of now, all species in the suborder Salamandroidea have shown to employ polyandrous mating strategies by females. [4] In a study of a population of Salamandrina perspicillata, multiple paternity occurs as a pervasive reproductive strategy under natural conditions and it is seen that in these species, when males mated with two females, they sired offspring who were inversely related with their genetic similarity to the female. [4] Females in this species practiced polygynandry in order to increase genetic variability among her offspring by choosing mates that were genetically different from themselves. [4] Unlike other studies of polygynandry where the females had multiple mating partners in order to gain resources from the male, in the study of Salamandrina perspicillata, multiple paternity did not provide a genetic indirect benefit to the offspring. [4] This, resulted in a cost/benefit mechanism in which the gained benefit of multiple mating counterbalanced the negative effect of the number of mates on offspring heterozygosity. [4] Females choosing mates that are genetically different from themselves were also seen in Ichthyosaura alpestris and Lissotriton vulgaris , where in a two-male mating system, the less-related males were preferred by the females. [4] And like the case of Salamandrina perspicillata, there were no indirect genetic benefits gained from having multiple mating partners.
In Ammothea hilgendorfi , a sea spider species, fertilization occurs as a female transfers her eggs to a male who holds them with ovigers, a specialized pair of legs and fertilizes the eggs externally. [5] The males glue the eggs into clusters and carries the eggs on his ovigers until they hatch. [5] The personal cost to males for providing a prolonged care for the young is seen to be a significant parental investment because parental assurance is thought to be substantial for post-zygotic investment. [5] A high level of paternity assurance is Ammothea hilgendorfi, suggests that reduced foraging ability, increased predation risk, and lower mobility exist. [5] An experimental study of Ammothea hilgendorfi showed that although males mate with multiple females, males do not mix egg batches from different dams. [5] The eggs held in clusters by a male hatched in a close time frame, indicating that males mated with different females within a short time span. [5]
Multiple mating by female pycnogonids are possible since a recently mated female often retains unused mature eggs in one or more femora, which allows her to mate with additional partners. In species with external fertilization and male parental care, females are able to distribute her clutch amongst different males and by doing so the female increases the likelihood that at least some of her offspring will receive indirect genetic benefits and/or extensive parental care from a quality provider. [6]
The reproductive females of social Hymenoptera—wasps, bees, and ants—mate with multiple partners. These females are called queens, to distinguish them from the non-reprodutive females that tend the colony and do not mate.
A honey bee queen ideally mates with about a dozen drones (males) in her nuptial flight. The sperm of matings are stored in a special reservoir, called the spermatheca, for the life of the queen—which can be several years.
Although promiscuity is said to benefit both males and females, there has not yet been sufficient data to support the fact that promiscuity benefits females. In a study of dark-eyed juncos, the offspring produced by extra-pair males were neither better nor worse than the offspring of their male social partners. [3] However, the study of dark-eyed juncos did reveal more sired offspring in promiscuous females than monogamous females. In a study of female water striders, the results showed that multiple matings can become costly to the female—especially since a lot of time and energy is invested in producing an egg. [7] Not only were extra matings costly, but there was no support for any genetic benefits from having multiple mating partners. [7] Instead, the results from the experiment showed that egg production and egg hatching success were the highest when the number of partners were kept at a minimum. [7]
On the other hand, studies have shown that males have had a higher reproductive success than females when they were polygynandrous. [2] When compared to female chimpanzees, male chimpanzees had a better ratio of number of matings and number of offspring produced. Not only did studies show a higher reproductive success, but Columbian ground squirrels exhibited a significant male-biased sexual size and body mass, suggesting male-male competition. [2] Male-male competition means sexual dimorphism amongst the males and this means females are able to sexually select males based on the sexual ornaments they display.
Overall, studies have shown that polygynandry benefits males more than it benefits females. When polygynandry is observed in different species, males most often have the upper hand—meaning males benefit more from polygynandry than do females. Females generally seek multiple mating partners in order to increase benefits for their offspring, whether it be by gaining physical resources for their offspring or by providing their offspring with healthier genes that are fit for survival. [3] On the other hand, in most cases males generally have multiple mating partners in order to obtain as much offspring as they can during their lifespan and they are able to achieve this easier than females because in most cases, males are not parentally involved in caring and raising their offspring. [2]
Sperm competition is the competitive process between spermatozoa of two or more different males to fertilize the same egg during sexual reproduction. Competition can occur when females have multiple potential mating partners. Greater choice and variety of mates increases a female's chance to produce more viable offspring. However, multiple mates for a female means each individual male has decreased chances of producing offspring. Sperm competition is an evolutionary pressure on males, and has led to the development of adaptations to increase male's chance of reproductive success. Sperm competition results in a sexual conflict between males and females. Males have evolved several defensive tactics including: mate-guarding, mating plugs, and releasing toxic seminal substances to reduce female re-mating tendencies to cope with sperm competition. Offensive tactics of sperm competition involve direct interference by one male on the reproductive success of another male, for instance by physically removing another male's sperm prior to mating with a female. For an example, see Gryllus bimaculatus.
Parental investment, in evolutionary biology and evolutionary psychology, is any parental expenditure that benefits offspring. Parental investment may be performed by both males and females, females alone or males alone. Care can be provided at any stage of the offspring's life, from pre-natal to post-natal.
Monogamous pairing in animals refers to the natural history of mating systems in which species pair bond to raise offspring. This is associated, usually implicitly, with sexual monogamy.
Sexual conflict or sexual antagonism occurs when the two sexes have conflicting optimal fitness strategies concerning reproduction, particularly over the mode and frequency of mating, potentially leading to an evolutionary arms race between males and females. In one example, males may benefit from multiple matings, while multiple matings may harm or endanger females, due to the anatomical differences of that species. Sexual conflict underlies the evolutionary distinction between male and female.
Extra-pair copulation (EPC) is a mating behaviour in monogamous species. Monogamy is the practice of having only one sexual partner at any one time, forming a long-term bond and combining efforts to raise offspring together; mating outside this pairing is extra-pair copulation. Across the animal kingdom, extra-pair copulation is common in monogamous species, and only a very few pair-bonded species are thought to be exclusively sexually monogamous. EPC in the animal kingdom has mostly been studied in birds and mammals. Possible benefits of EPC can be investigated within non-human species, such as birds.
Mate choice is one of the primary mechanisms under which evolution can occur. It is characterized by a "selective response by animals to particular stimuli" which can be observed as behavior. In other words, before an animal engages with a potential mate, they first evaluate various aspects of that mate which are indicative of quality—such as the resources or phenotypes they have—and evaluate whether or not those particular trait(s) are somehow beneficial to them. The evaluation will then incur a response of some sort.
The sexy son hypothesis in evolutionary biology and sexual selection, proposed by Patrick J. Weatherhead and Raleigh J. Robertson of Queen's University in Kingston, Ontario in 1979, states that a female's ideal mate choice among potential mates is one whose genes will produce males with the best chance of reproductive success. This implies that other benefits the father can offer the mother or offspring are less relevant than they may appear, including his capacity as a parental caregiver, territory and any nuptial gifts. Fisher's principle means that the sex ratio is always near 1:1 between males and females, yet what matters most are her "sexy sons'" future breeding successes, more likely if they have a promiscuous father, in creating large numbers of offspring carrying copies of her genes. This sexual selection hypothesis has been researched in species such as the European pied flycatcher.
Parental care is a behavioural and evolutionary strategy adopted by some animals, involving a parental investment being made to the evolutionary fitness of offspring. Patterns of parental care are widespread and highly diverse across the animal kingdom. There is great variation in different animal groups in terms of how parents care for offspring, and the amount of resources invested by parents. For example, there may be considerable variation in the amount of care invested by each sex, where females may invest more in some species, males invest more in others, or investment may be shared equally. Numerous hypotheses have been proposed to describe this variation and patterns in parental care that exist between the sexes, as well as among species.
The ocoee salamander is a species of salamander in the family Plethodontidae. This salamander has a variety of colors and patterns, and got its name from Tennessee state wildflower. Its natural habitats are temperate forests, rivers, intermittent rivers, freshwater springs and wet rocks in mountainous areas of the Southeastern United States. It was first described by Nicholls in 1949. They are territorial and feed on small invertebrates. It is widely distributed in the southeastern United States and is listed as "Least Concern" by the International Union for Conservation of Nature.
Mate desertion occurs when one or both parents abandon their current offspring, and thereby reduce or stop providing parental care. Often, by deserting, a parent attempts to increase breeding opportunities by seeking out another mate. This form of mating strategy behavior is exhibited in insects, birds and mammals. Typically, males are more likely to desert, but both males and females have been observed to practice mate desertion.
Bateman's principle, in evolutionary biology, is that in most species, variability in reproductive success is greater in males than in females. It was first proposed by Angus John Bateman (1919–1996), an English geneticist. Bateman suggested that, since males are capable of producing millions of sperm cells with little effort, while females invest much higher levels of energy in order to nurture a relatively small number of eggs, the female plays a significantly larger role in their offspring's reproductive success. Bateman's paradigm thus views females as the limiting factor of parental investment, over which males will compete in order to copulate successfully.
Polygyny is a mating system in which one male lives and mates with multiple females but each female only mates with a single male. Systems where several females mate with several males are defined either as promiscuity or polygynandry. Lek mating is frequently regarded as a form of polygyny, because one male mates with many females, but lek-based mating systems differ in that the male has no attachment to the females with whom he mates, and that mating females lack attachment to one another.
Sexual selection in insects is about how sexual selection functions in insects. The males of some species have evolved exaggerated adornments and mechanisms for self-defense. These traits play a role in increasing male reproductive expectations by triggering male-male competition or influencing the female mate choice, and can be thought of as functioning on three different levels: individuals, colonies, and populations within an area.
Sexual selection in amphibians involves sexual selection processes in amphibians, including frogs, salamanders and newts. Prolonged breeders, the majority of frog species, have breeding seasons at regular intervals where male-male competition occurs with males arriving at the waters edge first in large number and producing a wide range of vocalizations, with variations in depth of calls the speed of calls and other complex behaviours to attract mates. The fittest males will have the deepest croaks and the best territories, with females making their mate choices at least partly based on the males depth of croaking. This has led to sexual dimorphism, with females being larger than males in 90% of species, males in 10% and males fighting for groups of females.
Polyandry in fishes is a mating system where females mate with multiple males within one mating season. This type of mating exists in a variety of animal species. Polyandry has been found in both oviparous and viviparous bony fishes and sharks. General examples of polyandry occur in fish species, such as green swordtails and Trinidadian guppies. Specific types of polyandry have also been classified, such as classical polyandry in pipefish cooperative polyandry in cichlids and convenience polyandry in sharks.
In biology, paternal care is parental investment provided by a male to his own offspring. It is a complex social behaviour in vertebrates associated with animal mating systems, life history traits, and ecology. Paternal care may be provided in concert with the mother or, more rarely, by the male alone.
Cryptic female choice is a form of mate choice which occurs both in pre and post copulatory circumstances when females in certain species use physical or chemical mechanisms to control a male's success of fertilizing their ova or ovum; i.e. by selecting whether sperm are successful in fertilizing their eggs or not. It occurs in internally-fertilizing species and involves differential use of sperm by females when sperm are available in the reproductive tract.
Inbreeding avoidance, or the inbreeding avoidance hypothesis, is a concept in evolutionary biology that refers to the prevention of the deleterious effects of inbreeding. Animals only rarely exhibit inbreeding avoidance. The inbreeding avoidance hypothesis posits that certain mechanisms develop within a species, or within a given population of a species, as a result of assortative mating and natural and sexual selection, in order to prevent breeding among related individuals. Although inbreeding may impose certain evolutionary costs, inbreeding avoidance, which limits the number of potential mates for a given individual, can inflict opportunity costs. Therefore, a balance exists between inbreeding and inbreeding avoidance. This balance determines whether inbreeding mechanisms develop and the specific nature of such mechanisms.
In behavioral ecology, polyandry is a class of mating system where one female mates with several males in a breeding season. Polyandry is often compared to the polygyny system based on the cost and benefits incurred by members of each sex. Polygyny is where one male mates with several females in a breeding season . A common example of polyandrous mating can be found in the field cricket of the invertebrate order Orthoptera. Polyandrous behavior is also prominent in many other insect species, including the red flour beetle and the species of spider Stegodyphus lineatus. Polyandry also occurs in some primates such as marmosets, mammal groups, the marsupial genus' Antechinus and bandicoots, around 1% of all bird species, such as jacanas and dunnocks, insects such as honeybees, and fish such as pipefish.
Parental care refers to the level of investment provided by the mother and the father to ensure development and survival of their offspring. In most birds, parents invest profoundly in their offspring as a mutual effort, making a majority of them socially monogamous for the duration of the breeding season. This happens regardless of whether there is a paternal uncertainty.