Ата-аналық инвестиция теориясы

Parental expenditure (e. g. time, energy, resources) that benefits offspring

Parental investment, in evolutionary biology and evolutionary psychology, is any parental expenditure (e. g. time, energy, resources) that benefits offspring. Parental investment may be performed by both males and females (biparental care), females alone (exclusive maternal care) or males alone (exclusive paternal care). Care can be provided at any stage of the offspring's life, from pre natal (e. g. egg guarding and incubation in birds, and placental nourishment in mammals) to post natal (e. g. food provisioning and protection of offspring). Parental investment theory, a term coined by Robert Trivers in 1972, predicts that the sex that invests more in its offspring will be more selective when choosing a mate, and the less investing sex will have intra sexual competition for access to mates. This theory has been influential in explaining sex differences in sexual selection and mate preferences, throughout the animal kingdom and in humans. This introduced the concept of natural selection to the world, as well as related theories such as sexual selection. For the first time, evolutionary theory was used to explain why females are "coy" and males are "ardent" and compete with each other for females' attention. In 1930, Ronald Fisher wrote The Genetical Theory of Natural Selection, in which he introduced the modern concept of parental investment, introduced the sexy son hypothesis, and introduced Fisher's principle. In 1948, Angus John Bateman published an influential study of fruit flies in which he concluded that because female gametes are more costly to produce than male gametes, the reproductive success of females was limited by the ability to produce ovum, and the reproductive success of males was limited by access to females. In 1972, Trivers continued this line of thinking with his proposal of parental investment theory, which describes how parental investment affects sexual behavior. He concludes that the sex that has higher parental investment will be more selective when choosing a mate, and the sex with lower investment will compete intra sexually for mating opportunities.

Parental investment theory is a branch of life history theory. The earliest consideration of parental investment is given by Ronald Fisher in his 1930 book The Genetical Theory of Natural Selection, wherein Fisher argued that parental expenditure on both sexes of offspring should be equal. Clutton Brock expanded the concept of parental investment to include costs to any other component of parental fitness. Male dunnocks tend to not discriminate between their own young and those of another male in polyandrous or polygynandrous systems. They increase their own reproductive success through feeding the offspring in relation to their own access to the female throughout the mating period, which is generally a good predictor of paternity. This indiscriminative parental care by males is also observed in redlip blennies. In some insects, male parental investment is given in the form of a nuptial gift. For instance, ornate moth females receive a spermatophore containing nutrients, sperm and defensive toxins from the male during copulation. This gift, which can account for up to 10% of the male's body mass, constitutes the total parental investment the male provides. In some species, such as humans and many birds, the offspring are altricial and unable to fend for themselves for an extended period of time after birth. In these species, males invest more in their offspring than do the male parents of precocial species, since reproductive success would otherwise suffer. The benefits of parental investment to the offspring are large and are associated with the effects on condition, growth, survival, and ultimately on reproductive success of the offspring. For example, in the cichlid fish Tropheus moorii, a female has very high parental investment in her young because she mouthbroods the young and while mouthbrooding, all nourishment she takes in goes to feed the young and she effectively starves herself. In doing this, her young are larger, heavier, and faster than they would have been without it. These benefits are very advantageous since it lowers their risk of being eaten by predators and size is usually the determining factor in conflicts over resources. However, such benefits can come at the cost of parent's ability to reproduce in the future e. g., through increased risk of injury when defending offspring against predators, loss of mating opportunities whilst rearing offspring, and an increase in the time interval until the next reproduction. A special case of parental investment is when young do need nourishment and protection, but the genetic parents do not actually contribute in the effort to raise their own offspring. For example, in Bombus terrestris, oftentimes sterile female workers will not reproduce on their own, but will raise their mother's brood instead. This is common in social Hymenoptera due to haplodiploidy, whereby males are haploid and females are diploid. This ensures that sisters are more related to each other than they ever would be to their own offspring, incentivizing them to help raise their mother's young over their own. Overall, parents are selected to maximize the difference between the benefits and the costs, and parental care will be likely to evolve when the benefits exceed the costs.

Reproduction is costly. Individuals are limited in the degree to which they can devote time and resources to producing and raising their young, and such expenditure may also be detrimental to their future condition, survival, and further reproductive output. However, such expenditure is typically beneficial to the offspring, since it enhances their condition, survival, and reproductive success. These differences may lead to parent offspring conflict. Parents are naturally selected to maximize the difference between the benefits and the costs, and parental care will tend to exist when the benefits are substantially greater than the costs. Parents are equally related to all offspring, and so in order to optimize their fitness and chance of reproducing their genes, they should distribute their investment equally among current and future offspring. However, any single offspring is more related to themselves (they have 100% of their DNA in common with themselves) than they are to their siblings (siblings usually share 50% of their DNA), so it is best for the offspring's fitness if the parent(s) invest more in them. To optimize fitness, a parent would want to invest in each offspring equally, but each offspring would want a larger share of parental investment. The parent is selected to invest in the offspring up until the point at which investing in the current offspring is costlier than investing in future offspring. In iteroparous species, where individuals may go through several reproductive bouts during their lifetime, a tradeoff may exist between investment in current offspring and future reproduction. Parents need to balance their offspring's demands against their own self maintenance. This potential negative effect of parental care was explicitly formalized by Trivers in 1972, who originally defined the term parental investment to mean any investment by the parent in an individual offspring that increases the offspring's chance of surviving (and hence reproductive success) at the cost of the parent's ability to invest in other offspring. It shows that these penguins initially show a trade off of their own health, in hopes of increasing the survivorship of their egg. But there comes a point where the male penguin's costs become too high in comparison to the gain of a successful breeding season. Olof Olsson investigated the correlation between how many experiences in breeding an individual has and the duration an individual will wait until abandoning his egg. He proposed that the more experienced the individual, the better that individual will be at replenishing his exhausted body reserves, allowing him to remain at the egg for a longer period of time. Likelihood of survival and availability of resources within the village were factors that played into this decision of whether or not to keep the baby. During one illustrated birth, the mother felt the child was too ill and would not survive, so she wrapped the child up, preparing to leave the child in the brush; however, upon seeing the child moving, the mother unwrapped the child and brought it into the village, demonstrating a shift of life and death. or if a medical crisis arose and the baby needed an emergency baptism. This conflict between survival, both emotional and physical, prompted a shift in cultural practices, thus resulting in new forms of investment from the mother towards the child.

Alloparental care also referred to as 'Allomothering,' is when a member of a community, apart from the biological parents of the infant, partake in offspring care provision. A range of behaviors fall under the term alloparental care, some of which are: carrying, feeding, watching over, protecting, and grooming. Through alloparental care stress on parents, especially the mother, can be reduced, therefore reducing the negative effects of the parent offspring conflict on the mother. The apparent altruistic nature of the behavior may seem at odds with Darwin's theory of natural selection, as taking care of offspring which are not one's own would not increase one's direct fitness, while taking time, energy and resources away from raising one's own offspring. However, the behavior can be explained evolutionarily as increasing indirect fitness, as the offspring is likely to be non descendent kin, therefore carrying some of the genetics of the alloparent. Parentally investing individuals are not more vulnerable to being exploited by other adults.

Parental investment as defined by Robert Trivers in 1972 is the investment in offspring by the parent that increases the offspring's chances of surviving and hence reproductive success at the expense of the parent's ability to invest in other offspring. A large parental investment largely decreases the parents' chances of investing in other offspring. Parental investment can be split into two main categories: mating investment and rearing investment. Mating investment consist of the sexual act and the sex cells invested. The rearing investment is the time and energy expended to raise the offspring after conception. In most species, the female's parental investment in both mating and rearing efforts greatly surpasses that of the male. In terms of sex cells (egg and sperms cells), the female's investment is typically a larger portion of both genetic material and overall virility, while typically males produce thousands of sperm cells on a daily basis.

Human women have a fixed supply of around 400 ova, while sperm cells in men are supplied at a rate of twelve million per hour. Also, fertilization and gestation occur in women, investments which outweigh the man's investment of a single effective sperm cell. Furthermore, for women, one act of sexual intercourse could result in a nine month commitment such as human gestation and subsequent commitments related to rearing such as breastfeeding. From Trivers' theory of parental investment, several implications follow. The first implication is that women are often but not always the more investing sex. The fact that they are often the more investing sex leads to the second implication that evolution favors females who are more selective of their mates to ensure that intercourse would not result in unnecessary or wasteful costs. The third implication is that because women invest more and are essential for the reproductive success of their offspring, they are a valuable resource for men; as a result, males often compete for sexual access to females.

For many species the only type of male investment received is that of sex cells. In those terms, the female investment greatly exceeds that of male investment as previously mentioned. However, there are other ways in which males invest in their offspring. For example, the male can find food as in the example of balloon flies. He may find a safe environment for the female to feed or lay her eggs as exemplified in many birds. He may also protect the young and provide them with opportunities to learn as young, as is the case with many wolves. Overall, the main role that males overtake is that of protection of the female and their young. That often can decrease the discrepancy of investment caused by the initial investment of sex cells. There are some species such as the Mormon cricket, pipefish seahorse and Panamanian poison arrow frog males invest more. Among the species where the male invests more, the male is also the pickier sex, placing higher demands on their selected female. For example, the female that they often choose usually contain 60% more eggs than rejected females. This links Parental Investment Theory (PIT) with sexual selection: where parental investment is bigger for a male than a female, it is usually the female who competes for a mate, as shown by Phalaropidae and polyandrous bird species. In these species females are usually more aggressive, brightly colored, and larger than males, suggesting the more investing sex has more choice while selecting a mate compared to the sex engaged in intra sexual selection.

The second prediction that follows from Trivers' theory is that the fact that females invest more heavily in offspring makes them a valuable resource for males as it ensures the survival of their offspring which is the driving force of natural selection. Therefore, the sex that invests less in offspring will compete among themselves to breed with the more heavily investing sex. In other words, males will compete for females. It has been argued that jealousy has developed to avert the risk of potential loss of parental investment in offspring. shows that males are tuned into physical attractiveness as it signals youth and fertility and ensures male reproductive success, which is increased by copulating with as many fertile females as possible. Women on the other hand are tuned into resources provided by potential mates, as their reproductive success is increased by ensuring their offspring will survive, and one way they do so is by getting resources for them. Alternatively, another study shows that men are more promiscuous than women, giving further support to this theory. Clark and Hatfield found that 75% of men were willing to have sex with a female stranger when propositioned, compared to 0% of women. On the other hand, 50% of women agreed to a date with a male stranger. This suggests males seek short term relationships, while women show a strong preference for long term relationships. However, these preferences (male promiscuity and female choosiness) can be explained in other ways. In Western cultures, male promiscuity is encouraged through the availability of pornographic magazines and videos targeted to the male audience. Alternatively, both Western and Eastern cultures discourage female promiscuity through social checks such as slut shaming. PIT (Parental Investment Theory) also explains patterns of sexual jealousy. as it seems to rationalise rape and sexual coercion of females. Thornhill and Palmer claimed rape is an evolved technique for obtaining mates in an environment where women choose mates. As PIT claims males seek to copulate with as many fertile females as possible, the choice women have could result in a negative effect on the male's reproductive success. If women did not choose their mates, Thornhill and Palmer claim there would be no rape. This ignores a variety of sociocultural factors, such as the fact that not only fertile females are raped – 34% of underage rape victims are under 12, which means they are not of fertile age, thus there is no evolutionary advantage in raping them. 14% of rapes in England are committed on males, who cannot increase a man's reproductive success as there will be no conception. Thus, what Thornhill and Palmer called an 'evolved machinery' might not be very advantageous.

Trivers' theory overlooks that women do have short term relationships such as one night stands, while not all men behave promiscuously. An alternative explanation to PIT (Parental Investment Theory) and mate preferences would be Buss and Schmitt's sexual strategies theory. SST argues that both sexes pursue short term and long term relationships, but seek different qualities in their short and long term partners. For a short term relationship women will prefer an attractive partner, but in a long term relationship they might be willing to trade off that attractiveness for resources and commitment. On the other hand, men might be accepting of a sexually willing partner in a short term relationships, but to ensure their paternal certainty they will seek a faithful partner instead.

Parental investment theory is not only used to explain evolutionary phenomena and human behavior but describes recurrences in international politics as well. Specifically, parental investment is referred to when describing competitive behaviors between states and determining aggressive nature of foreign policies. The parental investment hypothesis states that the size of coalitions and the physical strengths of its male members determines whether its activities with its foreign neighbors are aggressive or amiable. According to Trivers, men have had relatively low parental investments, and were therefore forced into fiercer competitive situations over limited reproductive resources. Sexual selection naturally took place and men have evolved to address its unique reproductive problems. Among other adaptations, men's psychology has also developed to directly aid men in such intra sexual competition.). In species where both sexes invest highly in parental care, mutual choosiness is expected to arise. An example of this is seen in crested auklets, where parents share equal responsibility in incubating their single egg and raising the chick. In crested auklets, both sexes are ornamented.

Humans have evolved increasing levels of parental investment, both biologically and behaviorally. The fetus requires high investment from the mother, and the altricial newborn requires high investment from a community. Species whose newborn young are unable to move on their own and require parental care have a high degree of altriciality. Human children are born unable to care for themselves and require additional parental investment post birth in order to survive.

As altriciality increased, investment from individuals other than the mother became more necessary. High sociality meant that female relatives were present to help the mother, but paternal investment increased as well. Paternal investment increases as it becomes more difficult to have additional children, and as the effects of investment on offspring fitness increase. Men are more likely than women to give no parental investment to their children, and the children of low investing fathers are more likely to give less parental investment to their own children. Father absence is a risk factor for both early sexual activity and teenage pregnancy. Father absence raises children's stress levels, which are linked to earlier onset of sexual activity and increased short term mating orientation. Daughters of absent fathers are more likely to seek short term partners, and one theory explains this as a preference for outside (non partner) social support because of the perceived uncertain future and uncertain availability of committing partners in a high stress environment.

Women can only get pregnant while ovulating. Human ovulation is concealed, or not signaled externally. Concealed ovulation decreases paternity certainty because men are unsure when women ovulate. The evolution of concealed ovulation has been theorized to be a result of altriciality and increased need for paternal investment—if men are unsure of the time of ovulation, the best way to successfully reproduce would be to repeatedly mate with a woman throughout her cycle, which requires pair bonding, which in turn increases paternal investment.

Sociosexuality was first described by Alfred Kinsey as a willingness to engage in casual and uncommitted sexual relationships. Sociosexual orientation describes sociosexuality on a scale from unrestricted to restricted. Individuals with an unrestricted sociosexual orientation have higher openness to sex in less committed relationships, and individuals with a restricted sociosexual orientation have lower openness to casual sexual relationships. However, today it is acknowledged that sociosexuality does not in reality exist on a one dimensional scale. Individuals who are less open to casual relationships are not always seeking committed relationships, and individuals who are less interested in committed relationships are not always interested in casual relationships. Short and long term mating orientations are the modern descriptors of openness to uncommitted and committed relationships, respectively. Parental investment theory, as proposed by Trivers, argues that the sex with higher obligatory investment will be more selective in choosing sex partners, and the sex with lower obligatory investment will be less selective and more interested in "casual" mating opportunities. The more investing sex cannot reproduce as frequently, causing the less investing sex to compete for mating opportunities. In humans, women have higher obligatory investment (pregnancy and childbirth), than men (sperm production). When marriage is not involved, women put greater emphasis on physical attractiveness. Generally, women prefer men who are likely to perform high parental investment and have good genes. Women prefer men with good financial status, who are more committed, who are more athletic, and who are healthier. Some inaccurate theories have been inspired by parental investment theory. The "structural powerlessness hypothesis" proposes that women strive to find mates with access to high levels of resources because as women, they are excluded from these resources directly. However, this hypothesis has been disproved by studies which found that financially successful women place an even greater importance on financial status, social status, and possession of professional degrees.

Sexual dimorphism is the difference in body size between male and female members of a species as a result of both intersexual and intrasexual selection, which is sexual selection that acts both within and between the sexes. High levels of sexual dimorphism and larger body size in males is driven by a combination of male male competition and female selective pressure. Primate species in which groups are formed of many females and one male have higher sexual dimorphism than species that have both multiple females and males, or one female and one male. Polygynous primates have the highest sexual dimorphism, and polygamous and monogamous primates have less. Decreased polygyny is associated with increased paternal investment.

The demographic transition describes the modern decrease in both birth and death rates. From a Darwinian perspective, it does not make sense that families with more resources are having fewer children. One explanation for the demographic transition is the increased parental investment required to raise children who will be able to maintain the same level of resources as their parents.