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Friday, December 6, 2019

Monogamy

From Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Monogamy
 
Monogamy (/məˈnɒɡəmi/ mə-NOG-ə-mee) is a form of dyadic relationship in which an individual has only one partner during their lifetime—alternately, only one partner at any one time (serial monogamy)—as compared to non-monogamy (e.g., polygamy or polyamory). The term is also applied to the social behavior of some animals, referring to the state of having only one mate at any one time.

Terminology

The word monogamy derives from the Greek μονός, monos ("alone"), and γάμος, gamos ("marriage").

The term "monogamy" may be referring to one of various relational types, depending upon context. Generally, there are four overlapping definitions.
  • marital monogamy refers to marriages of only two people.
  • social monogamy refers to two partners living together, having sex with each other, and cooperating in acquiring basic resources such as shelter, food and money.
  • sexual monogamy refers to two partners remaining sexually exclusive with each other and having no outside sex partners.
  • genetic monogamy refers to sexually monogamous relationships with genetic evidence of paternity.
For instance, biologists, biological anthropologists, and behavioral ecologists often use monogamy in the sense of sexual, if not genetic (reproductive), exclusivity. When cultural or social anthropologists and other social scientists use the term monogamy, the meaning is social or marital monogamy.

Marital monogamy may be further distinguished between:
  1. classical monogamy, "a single relationship between people who marry as virgins, remain sexually exclusive their entire lives, and become celibate upon the death of the partner"
  2. serial monogamy, marriage with only one other person at a time, in contrast to bigamy or polygamy.

Frequency in humans

Bronze sculpture of an elderly Kashubian married couple located in Kaszubski square, Gdynia, Poland, which commemorates their monogamous fidelity, through the time of their separation, while he temporarily worked in the United States.
 

Distribution of social monogamy

According to the Ethnographic Atlas by George P. Murdock, of 1,231 societies from around the world noted, 186 were monogamous; 453 had occasional polygyny; 588 had more frequent polygyny; and 4 had polyandry. However, this does not take into account the relative population of each of the societies studied, and the actual practice of polygamy in a tolerant society may actually be low, with the majority of aspirant polygamists practicing monogamous marriage.

Divorce and remarriage can thus result in "serial monogamy", i.e. multiple marriages but only one legal spouse at a time. This can be interpreted as a form of plural mating, as are those societies dominated by female-headed families in the Caribbean, Mauritius and Brazil where there is frequent rotation of unmarried partners. In all, these account for 16 to 24% of the "monogamous" category.

Prevalence of sexual monogamy

The prevalence of sexual monogamy can be roughly estimated as the percentage of married people who do not engage in extramarital sex. The Standard Cross-Cultural Sample describes the amount of extramarital sex by men and women in over 50 pre-industrial cultures. The amount of extramarital sex by men is described as "universal" in 6 cultures, "moderate" in 29 cultures, "occasional" in 6 cultures, and "uncommon" in 10 cultures. The amount of extramarital sex by women is described as "universal" in 6 cultures, "moderate" in 23 cultures, "occasional" in 9 cultures, and "uncommon" in 15 cultures.

Surveys conducted in non-Western nations (2001) also found cultural and gender differences in extramarital sex. A study of sexual behavior in Thailand, Tanzania and Côte d'Ivoire suggests about 16–34% of men engage in extramarital sex while a much smaller (unreported) percentage of women engage in extramarital sex. Studies in Nigeria have found around 47–53% of men and to 18–36% of women engage in extramarital sex. A 1999 survey of married and cohabiting couples in Zimbabwe reports that 38% of men and 13% of women engaged in extra-couple sexual relationships within the last 12 months.

Many surveys asking about extramarital sex in the United States have relied on convenience samples: surveys given to whoever happens to be easily available (e.g., volunteer college students or volunteer magazine readers). Convenience samples do not accurately reflect the population of the United States as a whole, which can cause serious biases in survey results. It should not be surprising, therefore, that surveys of extramarital sex in the United States have produced widely differing results. These studies (1974, 1983, 1993) reported that 12–26% of married women and 15–43% of married men engaged in extramarital sex. The only way to get scientifically reliable estimates of extramarital sex is to use nationally representative samples. Three studies have used nationally representative samples. These studies (1994, 1997) found that about 10–15% of women and 20–25% of men engage in extramarital sex.

Research by Colleen Hoffon of 566 homosexual male couples from the San Francisco Bay Area (2010) found that 45% had monogamous relationships. However, the Human Rights Campaign has stated, based on a Rockway Institute report, that "GLBT young people… want to spend their adult life in a long-term relationship raising children." Specifically, over 80% of the homosexuals surveyed expected to be in a monogamous relationship after age 30.

Prevalence of genetic monogamy

The incidence of genetic monogamy may be estimated from rates of extrapair paternity. Extrapair paternity is when offspring raised by a monogamous pair come from the female mating with another male. Rates of extrapair paternity have not been extensively studied in people. Many reports of extrapair paternity are little more than quotes based on hearsay, anecdotes, and unpublished findings. Simmons, Firman, Rhodes, and Peters reviewed 11 published studies of extra-pair paternity from various locations in the United States, France, Switzerland, the United Kingdom, Mexico, and among the native Yanomami Indians of Amazon forest in South America. The rates of extrapair paternity ranged from 0.03% to 11.8% although most of the locations had low percentages of extrapair paternity. The median rate of extrapair paternity was 1.8%. A separate review of 17 studies by Bellis, Hughes, Hughes, and Ashton found slightly higher rates of extrapair paternity. The rates varied from 0.8% to 30% in these studies, with a median rate of 3.7% extrapair paternity. A range of 1.8% to 3.7% extrapair paternity implies a range of 96% to 98% genetic monogamy. Although the incidence of genetic monogamy may vary from 70% to 99% in different cultures or social environments, a large percentage of couples remain genetically monogamous during their relationships. A review paper, surveying 67 other studies, reported rates of extrapair paternity, in different societies, ranging from 0.4% to over 50%.

Covert illegitimacy is a situation which arises when someone who is presumed to be a child's father (or mother) is in fact not the biological father (or mother). Frequencies as high as 30% are sometimes assumed in the media, but research by sociologist Michael Gilding traced these overestimates back to an informal remark at a 1972 conference.

The detection of unsuspected illegitimacy can occur in the context of medical genetic screening, in genetic family name research, and in immigration testing. Such studies show that covert illegitimacy is in fact less than 10% among the sampled African populations, less than 5% among the sampled Native American and Polynesian populations, less than 2% of the sampled Middle Eastern population, and generally 1%-2% among European samples.

Pedigree errors are a well-known source of error in medical studies. When attempts are made to try to study medical afflictions and their genetic components, it becomes very important to understand nonpaternity rates and pedigree errors. There are numerous software packages and procedures that exist for correcting research data for pedigree errors.

Evolutionary and historical development in humans

A pair of New Zealand kaka parrots at Auckland Zoo
 

Biological arguments

Monogamy exists in many societies around the world, and it is important to understand how these marriage systems might have evolved. In any species, there are three main aspects that combine to promote a monogamous mating system: paternal care, resource access, and mate-choice; however, in humans, the main theoretical sources of monogamy are paternal care and extreme ecological stresses. Paternal care should be particularly important in humans due to the extra nutritional requirement of having larger brains and the lengthier developmental period. Therefore, the evolution of monogamy could be a reflection of this increased need for bi-parental care. Similarly, monogamy should evolve in areas of ecological stress because male reproductive success should be higher if their resources are focused on ensuring offspring survival rather than searching for other mates. However, the evidence does not support these claims. Due to the extreme sociality and increased intelligence of humans, H. sapiens have solved many problems that generally lead to monogamy, such as those mentioned above. For example, monogamy is certainly correlated with paternal care, as shown by Marlowe, but not caused by it because humans diminish the need for bi-parental care through the aid of siblings and other family members in rearing the offspring. Furthermore, human intelligence and material culture allows for better adaptation to different and rougher ecological areas, thus reducing the causation and even correlation of monogamous marriage and extreme climates. However, some scientists argue that monogamy evolved by reducing within-group conflict, thus giving certain groups a competitive advantage against less monogamous groups.

Paleoanthropology and genetic studies offer two perspectives on when monogamy evolved in the human species: paleoanthropologists offer tentative evidence that monogamy may have evolved very early in human history whereas genetic studies show that monogamy evolved much more recently, less than 10,000 to 20,000 years ago.

Orangutan males are not monogamous and compete for access to females.
 
Paleoanthropological estimates of the time frame for the evolution of monogamy are primarily based on the level of sexual dimorphism seen in the fossil record because, in general, the reduced male-male competition seen in monogamous mating results in reduced sexual dimorphism. According to Reno et al., the sexual dimorphism of Australopithecus afarensis, a human ancestor from approximately 3.9–3.0 million years ago, was within the modern human range, based on dental and postcranial morphology. Although careful not to say that this indicates monogamous mating in early hominids, the authors do say that reduced levels of sexual dimorphism in A. afarensis "do not imply that monogamy is any less probable than polygyny". However, Gordon, Green and Richmond claim that in examining postcranial remains, A. afarensis is more sexually dimorphic than modern humans and chimps with levels closer to those of orangutans and gorillas. Furthermore, Homo habilis, living approximately 2.3 mya, is the most sexually dimorphic early hominid. Plavcan and van Schaik conclude their examination of this controversy by stating that, overall, sexual dimorphism in australopithecines is not indicative of any behavioral implications or mating systems.

Cultural arguments

Plough agriculture. The castle in the background is Lusignan. Detail from the calendar Les très riches heures from the 15th century. This is a detail from the painting for March.
 
Despite the human ability to avoid sexual and genetic monogamy, social monogamy still forms under many different conditions, but most of those conditions are consequences of cultural processes. These cultural processes may have nothing to do with relative reproductive success. For example, anthropologist Jack Goody's comparative study utilizing the Ethnographic Atlas demonstrated that monogamy is part of a cultural complex found in the broad swath of Eurasian societies from Japan to Ireland that practice social monogamy, sexual monogamy and dowry (i.e. "diverging devolution", that allow property to be inherited by children of both sexes). Goody demonstrates a statistical correlation between this cultural complex and the development of intensive plough agriculture in those areas. Drawing on the work of Ester Boserup, Goody notes that the sexual division of labour varies in intensive plough agriculture and extensive shifting horticulture. In plough agriculture farming is largely men's work and is associated with private property; marriage tends to be monogamous to keep the property within the nuclear family. Close family (endogamy) are the preferred marriage partners to keep property within the group. A molecular genetic study of global human genetic diversity argued that sexual polygyny was typical of human reproductive patterns until the shift to sedentary farming communities approximately 10,000 to 5,000 years ago in Europe and Asia, and more recently in Africa and the Americas. A further study drawing on the Ethnographic Atlas showed a statistical correlation between increasing size of the society, the belief in "high gods" to support human morality, and monogamy. A survey of other cross-cultural samples has confirmed that the absence of the plough was the only predictor of polygamy, although other factors such as high male mortality in warfare (in non-state societies) and pathogen stress (in state societies) had some impact.

Woman farming, using a digging stick in the Nuba Mountains, South Sudan.
 
Betzig postulated that culture/society can also be a source of social monogamy by enforcing it through rules and laws set by third-party actors, usually in order to protect the wealth or power of the elite. For example, Augustus Caesar encouraged marriage and reproduction to force the aristocracy to divide their wealth and power among multiple heirs, but the aristocrats kept their socially monogamous, legitimate children to a minimum to ensure their legacy while having many extra-pair copulations. Similarly—according to Betzig—the Christian Church enforced monogamy because wealth passed to the closest living, legitimate male relative, often resulting in the wealthy oldest brother being without a male heir. Thus, the wealth and power of the family would pass to the “celibate” younger brother of the church. In both of these instances, the rule-making elite used cultural processes to ensure greater reproductive fitness for themselves and their offspring, leading to a larger genetic influence in future generations. Furthermore, the laws of the Christian Church, in particular, were important in the evolution of social monogamy in humans. They allowed, even encouraged, poor men to marry and produce offspring which reduced the gap in reproductive success between the rich and poor, thus resulting in the quick spread of monogamous marriage systems in the western world. According to B. S. Low, culture would appear to have a much larger impact on monogamy in humans than the biological forces that are important for non-human animals.

Other theorists use cultural factors influencing reproductive success to explain monogamy. During times of major economic / demographic transitions, investing more in a fewer offspring (social monogamy not polygyny) increases reproductive success by ensuring the offspring themselves have enough initial wealth to be successful. This is seen in both England and Sweden during the industrial revolution and is currently being seen in the modernization of rural Ethiopia. Similarly, in modern industrialized societies, fewer yet better-invested offspring, i.e. social monogamy, can provide a reproductive advantage over social polygyny, but this still allows for serial monogamy and extra-pair copulations.

Arguments from outside the scientific community

Karol Wojtyła (later, Pope John Paul II) in his book Love and Responsibility postulated that monogamy, as an institutional union of two people being in love with one another, was an embodiment of an ethical personalistic norm, and thus the only means of making true human love possible. Some writers have suggested that monogamy may solve the problems they view as associated with non-monogamy and hypergamy such as inceldom.

Alexandra Kollontai in Make Way for the Winged Eros argues that monogamy is an artifact of capitalist concepts of property and inheritance and wrote, "The social aims of the working class are not affected one bit by whether love takes the form of a long and official union or is expressed in a temporary relationship. The ideology of the working class does not place any formal limits on love." Later, "Modern love always sins, because it absorbs the thoughts and feelings of 'loving hearts' and isolates the loving pair from the collective. In the future society, such a separation will not only become superfluous but also psychologically inconceivable." One of the tenets of the new proletarian morality is "mutual recognition of the rights of the other, of the fact that one does not own the heart and soul of the other (the sense of property, encouraged by bourgeois culture)."

Ancient societies

The historical record offers contradictory evidence on the development and extent of monogamy as a social practice. Laura Betzig argues that in the six large, highly stratified early states, commoners were generally monogamous but that elites practiced de facto polygyny. Those states included Mesopotamia, Egypt, Aztec Mexico, Inca Peru, India and China.

Tribal societies

Monogamy has appeared in some traditional tribal societies such as the Andamanese, Karen in Burma, Sami and Ket in northern Eurasia, and the Pueblo Indians of the United States, apparently unrelated to the development of the Judeo-Christian monogamous paradigm.

Ancient Mesopotamia and Assyria

Both the Babylonian and Assyrian families were monogamous in principle but not entirely so in practice since polygyny was frequently practiced by the rulers.

In the patriarchal society of Mesopotamia the nuclear family was called a "house". In order "to build a house" a man was supposed to marry one woman and if she did not provide him with offspring, he could take a second wife. The Code of Hammurabi states that he loses his right to do so if the wife herself gives him a slave as concubine. According to Old Assyrian texts, he could be obliged to wait for two or three years before he was allowed to take another wife. The position of the second wife was that of a "slave girl" in respect to the first wife, as many marriage contracts explicitly state.

Ancient Egypt

Although an Egyptian man was free to marry several women at a time, and some wealthy men from Old and Middle Kingdoms did have more than one wife, monogamy was the norm. There may have been some exceptions, e.g. a Nineteenth Dynasty official stated as proof of his love to his deceased wife that he had stayed married to her since their youth, even after he had become very successful (P. Leiden I 371). This may suggest that some men abandoned first wives of a low social status and married women of higher status in order to further their careers although even then they lived with only one wife. Egyptian women had right to ask for a divorce if her husband took a second wife. Many tomb reliefs testify to monogamous character of Egyptian marriages, officials are usually accompanied by a supportive wife. "His wife X, his beloved" is the standard phrase identifying wives in tomb inscriptions. The instruction texts belonging to wisdom literature, e.g. Instruction of Ptahhotep or Instruction of Any, support fidelity to monogamous marriage life, calling the wife a Lady of the house. The Instruction of Ankhsheshonq suggests that it is wrong to abandon a wife because of her barrenness.

Ancient Israel

As against Betzig's contention that monogamy evolved as a result of Christian socio-economic influence in the West, monogamy appeared widespread in the ancient Middle East much earlier. In Israel's pre-Christian era, an essentially monogamous ethos underlay the Jewish creation story (Gn 2) and the last chapter of Proverbs. During the Second Temple period (530 BCE to 70 CE), apart from an economic situation which supported monogamy even more than in earlier period, the concept of "mutual fidelity" between husband and wife was a quite common reason for strictly monogamous marriages.[citation needed] Some marriage documents explicitly expressed a desire for the marriage to remain monogamous. Examples of these documents were found in Elephantine. They resemble those found in neighbouring Assyria and Babylonia. Study shows that ancient Middle East societies, though not strictly monogamous, were practically (at least on commoners' level) monogamous.[65][66] Halakha of the Dead Sea Sect saw prohibition of polygamy as coming from the Pentateuch (Damascus Document 4:20–5:5, one of the Dead Sea Scrolls). Christianity adopted a similar attitude (cf. 1 Tm 3:2,12; Tt 1:6), which conformed with Jesus' approach. Michael Coogan, in contrast, states that "Polygyny continued to be practised well into the biblical period, and it is attested among Jews as late as the second century CE."

Under Judges and the monarchy, old restrictions went into disuse, especially among royalty, though the Books of Samuel and Kings, which cover entire period of monarchy, do not record a single case of bigamy among commoners — except for Samuel's father. The wisdom books e.g. Book of Wisdom, which provides a picture of the society, Sirach, Proverbs, Qohelet portray a woman in a strictly monogamous family (cf. Pr 5:15-19; Qo 9:9; Si 26:1-4 and eulogy of perfect wife, Proverbs 31:10-31). The Book of Tobias speaks solely of monogamous marriages. Also prophets have in front of their eyes monogamous marriage as an image of the relationship of God and Israel. (Cf. Ho 2:4f; Jer 2:2; Is 50:1; 54:6-7; 62:4-5; Ez 16). Roland de Vaux states that "it is clear that the most common form of marriage in Israel was monogamy".

The Mishnah and the baraitot clearly reflect a monogamist viewpoint within Judaism (Yevamot 2:10 etc.). Some sages condemned marriage to two wives even for the purpose of procreation (Ketubot 62b). R. Ammi, an amora states:
Whoever takes a second wife in addition to his first one shall divorce the first and pay her kettubah (Yevamot 65a)
Roman customs, which prohibited polygamy, may have enhanced such an attitude - especially after 212 AD, when all the Jews became Roman citizens. However, some Jews continued to practice bigamy (e.g. up to medieval times in Egypt and Europe). Fourth-century Roman law forbade Jews to contract plural marriages.

A synod convened by Gershom ben Judah around 1000 CE banned polygamy among Ashkenazi and Sephardic Jews.

Ancient Greece and ancient Rome

The ancient Greeks and Romans were monogamous in the sense that men were not allowed to have more than one wife or to cohabit with concubines during marriage.

Early Christianity

According to Jesus Christ monogamy was a primordial will of the Creator described in Genesis, darkened by the hardness of hearts of the Israelites. As John Paul II interpreted the dialogue between Jesus and the Pharisees (Gospel of Matthew 19:3–8), Christ emphasized the primordial beauty of monogamic spousal love described in the Book of Genesis 1:26–31, 2:4–25, whereby a man and woman by their nature are each ready to be a beautifying, total and personal gift to one another:
Jesus avoids entangling himself in juridical or casuistic controversies; instead, he appeals twice to the "beginning". By doing so, he clearly refers to the relevant words of Genesis, which his interlocutors also know by heart. (...) it clearly leads the interlocutors to reflect about the way in which, in the mystery of creation, man was formed precisely as "male and female," in order to understand correctly the normative meaning of the words of Genesis.

Contemporary societies

International

Western European societies established monogamy as their marital norm. Monogamous marriage is normative and is legally enforced in most developed countries. Laws prohibiting polygyny were adopted in Japan (1880), China (1953), India (1955) and Nepal (1963). Polyandry is illegal in most countries. 

The women's rights movements seek to make monogamy the only legal form of marriage. The United Nations General Assembly in 1979 adopted the Convention on the Elimination of All Forms of Discrimination Against Women, Article 16 of which requires nations to give women and men equal rights in marriage. Polygamy is viewed as inconsistent with the Article as it gives men the right of multiple wives, but not to women. The United Nations has established the Committee on the Elimination of Discrimination against Women (CEDAW) to monitor the progress of nations implementing the Convention. 

People's Republic of China

The founders of Communism determined that monogamous marriage inherently oppressed women and therefore had no place in communist society. Friedrich Engels stated that compulsory monogamy could only lead to increased prostitution and general immorality, with the benefits of restricting capital and solidifying the class structure. As he spelled out in The Origin of the Family, Private Property and the State (1884),
The first class antagonism which appears in history coincides with the development of the antagonism between man and woman in monogamian marriage, and the first class oppression with that of the female sex by the male. …[T]he wellbeing and development of the one group are attained by the misery and repression of the other.
The monogamous family is distinguished from the pairing family by the far greater durability of wedlock, which can no longer be dissolved at the pleasure of either party. As a rule, it is only the man who can still dissolve it and cast off his wife.
However, the communist revolutionaries in China chose to take the Western viewpoint of monogamy as giving women and men equal rights in marriage. The newly formed Communist government established monogamy as the only legal form of marriage.
"The 1950 Marriage Law called for sweeping changes in many areas of family life. It forbade any 'arbitrary and compulsory' form of marriage that would be based on the superiority of men and would ignore women’s interests. The new democratic marriage system was based on the free choice of couples, monogamy, equal rights for both sexes, and the protection of the lawful interests of women. It abolished the begetting of male offspring as the principal purpose of marriage and weakened kinship ties which reduced the pressure on women to bear many children, especially sons. With arranged marriages prohibited, young women could choose their own marriage partners, share the financial cost of setting up a new household, and have equal status in household and family decision-making. The Government then initiated an extensive campaign of marriage-law education, working jointly with the Communist Party, women’s federations, trade unions, the armed forces, schools and other organizations."

Africa

The African Union has adopted the Protocol on the Rights of Women in Africa (the Maputo Protocol). While the protocol does not suggest making polygamous marriage illegal, Article 6 does state that "monogamy is encouraged as the preferred form of marriage and that the rights of women in marriage and family, including in polygamous marital relationships are promoted and protected." The protocol entered into force on 25 November 2005. 

Varieties in biology

Recent discoveries have led biologists to talk about the three varieties of monogamy: social monogamy, sexual monogamy, and genetic monogamy. The distinction between these three are important to the modern understanding of monogamy.

Monogamous pairs of animals are not always sexually exclusive. Many animals that form pairs to mate and raise offspring regularly engage in sexual activities with partners other than their primary mate. This is called extra-pair copulation. Sometimes these extra-pair sexual activities lead to offspring. Genetic tests frequently show that some of the offspring raised by a monogamous pair come from the female mating with an extra-pair male partner. These discoveries have led biologists to adopt new ways of talking about monogamy: 
Social monogamy refers to a male and female's social living arrangement (e.g., shared use of a territory, behaviour indicative of a social pair, and/or proximity between a male and female) without inferring any sexual interactions or reproductive patterns. In humans, social monogamy equals monogamous marriage. Sexual monogamy is defined as an exclusive sexual relationship between a female and a male based on observations of sexual interactions. Finally, the term genetic monogamy is used when DNA analyses can confirm that a female-male pair reproduce exclusively with each other. A combination of terms indicates examples where levels of relationships coincide, e.g., sociosexual and sociogenetic monogamy describe corresponding social and sexual, and social and genetic monogamous relationships, respectively.
Reichard, 2003
Whatever makes a pair of animals socially monogamous does not necessarily make them sexually or genetically monogamous. Social monogamy, sexual monogamy, and genetic monogamy can occur in different combinations. 

Social monogamy does not always involve marriage in humans. A married couple is almost always a socially monogamous couple. But couples who choose to cohabit without getting married can also be socially monogamous. The popular science author Matt Ridley in his book The Red Queen: Sex and the Evolution of Human Nature, described the human mating system as "monogamy plagued by adultery". 

Serial monogamy

Serial monogamy is a mating practice in which individuals may engage in sequential monogamous pairings, or in terms of humans, when men or women can marry another partner but only after ceasing to be married to the previous partner.

One theory is that this pattern pacifies the elite men and equalizes reproductive success. This is called the Male Compromise Theory. Such serial monogamy may effectively resemble polygyny in its reproductive consequences because some men are able to utilize more than one woman’s reproductive lifespan through repeated marriages.

Serial monogamy may also refer to sequential sexual relationships, irrespective of marital status. A pair of humans may remain sexually exclusive, or monogamous, until the relationship has ended and then each may go on to form a new exclusive pairing with a different partner. This pattern of serial monogamy is common among people in Western cultures.

Reproductive success

Evolutionary theory predicts that males would be apt to seek more mating partners than females because they obtain higher reproductive benefits from such a strategy. Men with more serial marriages are likely to have more children than men with only one spouse, where the same is not true of women with consecutive spouses. A study done in 1994 found that remarried men often had a larger age difference from their spouses than men who were married for the first time, suggesting that serial monogamy helps some men extract a longer reproductive window from their spouses.

Breakup

Serial monogamy has always been closely linked to divorce practices. Whenever procedures for obtaining divorce have been simple and easy, serial monogamy has been found. As divorce has continued to become more accessible, more individuals have availed themselves of it, and many go on to remarry. Barry Schwartz, author of The Paradox of Choice: Why less is more, further suggests that Western culture's inundation of choice has devalued relationships based on lifetime commitments and singularity of choice. It has been suggested, however, that high mortality rates in centuries past accomplished much the same result as divorce, enabling remarriage (of one spouse) and thus serial monogamy.

Mating system

Monogamy is one of several mating systems observed in animals. However, a pair of animals may be socially monogamous but that does not necessarily make them sexually or genetically monogamous. Social monogamy, sexual monogamy, and genetic monogamy can occur in different combinations.

Social monogamy refers to the overtly observed living arrangement whereby a male and female share territory and engage in behaviour indicative of a social pair, but does not imply any particular sexual fidelity or reproductive pattern. The extent to which social monogamy is observed in animals varies across taxa, with over 90 percent of avian species being socially monogamous, compared to only 3 percent of mammalian species and up to 15 percent of primate species. Social monogamy has also been observed in reptiles, fish, and insects.

Sexual monogamy is defined as an exclusive sexual relationship between a female and a male based on observations of sexual interactions. However, scientific analyses can test for paternity, for example by DNA paternity testing or by fluorescent pigment powder tracing of females to track physical contact. This type of analysis can uncover reproductively successful sexual pairings or physical contact. Genetic monogamy refers to DNA analyses confirming that a female-male pair reproduce exclusively with each other.

The incidence of sexual monogamy appears quite rare in other parts of the animal kingdom. It is becoming clear that even animals that are overtly socially monogamous engage in extra-pair copulations. For example, while over 90% of birds are socially monogamous, "on average, 30 percent or more of the baby birds in any nest [are] sired by someone other than the resident male." Patricia Adair Gowaty has estimated that, out of 180 different species of socially monogamous songbirds, only 10% are sexually monogamous. Offspring are far more successful when both the male and the female members of the social pair contribute food resources. 

An example of this was seen when scientists studied red winged blackbirds. These birds are known for remaining in monogamous relationships during the course of mating season. During the course of the study, the researchers gave a few select males vasectomies just before mating season. The male birds behaved like they do every season, establishing territory, finding a mate, and attempting to make baby birds. Despite apparent social monogamy, the female birds whose partners were surgically altered still became pregnant, indicating that overt social monogamy did not predict for sexual fidelity. These babies were cared for by their sterile adoptive fathers.

The highest known frequency of reproductively successful extra-pair copulations are found among fairywrens Malurus splendens and Malurus cyaneus where more than 65 percent of chicks are fathered by males outside the supposed breeding pair. This discordantly low level of genetic monogamy has been a surprise to biologists and zoologists, as social monogamy can no longer be assumed to determine how genes are distributed in a species. 

Elacatinus, also widely known as neon gobies, also exhibit social monogamy. Hetereosexual pairs of fish belonging to the genus Elacatinus remain closely associated during both reproductive and non-reproductive periods, and often reside in same cleaning station to serve client fish. Fish of this genus frequently mate with a new partner after they are widowed. 

Evolution in animals

Socially monogamous species are scattered throughout the animal kingdom: A few insects, a few fish, about nine-tenths of birds, and a few mammals are socially monogamous. There is even a parasitic worm, Schistosoma mansoni, that in its female-male pairings in the human body is monogamous. The diversity of species with social monogamy suggests that it is not inherited from a common ancestor but instead evolved independently in many different species.

The low occurrence of social monogamy in placental mammals has been claimed to be related to the presence or absence of estrus—or oestrus—the duration of sexual receptivity of a female. This, however, doesn't explain why estrus females generally mate with any proximate male nor any correlation between sexual and social monogamy. Birds, which are notable for a high incidence of social monogamy, do not have estrus.

Researchers have observed a mixed mating system of monogamy and polygyny in the European pied flycatcher.

Psychology

Psychological studies of social monogamy have relied heavily on observations of married couples. These studies focus on relationship satisfaction, duration and attachment

Neuroendocrine bases

The North American microtine rodent's (vole) complex social structure and social behavior has provided unique opportunities to study the underlying neural bases for monogamy and social attachment. Data from studies using the Microtis ochrogaster or prairie vole indicate that the neuroendocrine hormones, oxytocin (in female prairie voles) and vasopressin (in male prairie voles) play a central role in the development of affiliative connections during mating. The effects of intracerebroventricular administration of oxytocin and vasopressin have been shown to promote affiliative behavior in the prairie vole but not in similar, but non-monogamous montane voles. This difference in neuropeptide effect is attributed to the location, density, and distribution of OT and AVP receptors. Only in the prairie voles are OT and AVP receptors located along the mesolimbic dopamine reward pathway, presumably conditioning the voles to their mates odor while consolidating the social memory of the mating episode. This finding highlights the role of genetic evolution in altering the neuroanatomical distribution of receptors, resulting in certain neural circuits becoming sensitive to changes in neuropeptides.

Thursday, December 5, 2019

Pair bond

From Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Pair_bond
 
 
In biology, a pair bond is the strong affinity that develops in some species between a mating pair, often leading to the production and rearing of offspring and potentially a lifelong bond. Pair-bonding is a term coined in the 1940s that is frequently used in sociobiology and evolutionary biology circles. The term often implies either a lifelong socially monogamous relationship or a stage of mating interaction in socially monogamous species. It is sometimes used in reference to human relationships.
Monogamous voles (such as prairie voles) have significantly greater density and distribution of vasopressin receptors in their brain when compared to polygamous voles. These differences are located in the ventral forebrain and the dopamine-mediated reward pathway.

Peptide arginine vasopressin (AVP), dopamine, and oxytocin act in this region to coordinate rewarding activities such as mating, and regulate selective affiliation. These species-specific differences have shown to correlate with social behaviors, and in monogamous prairie voles are important for facilitation of pair bonding. When compared to montane voles, which are polygamous, monogamous prairie voles appear to have more of these AVP and oxytocin neurotransmitter receptors. It is important that these receptors are in the reward centers of the brain because that could lead to a conditioned partner in the prairie vole compared to the montane vole which would explain why the prairie vole forms pair bonds and the montane vole does not.
 

Varieties

Black-backed jackals are one of very few monogamous mammals. This pair works together in teamwork to hunt down prey and scavenge. They will stay together until one of the two dies.
 
According to evolutionary psychologists David P. Barash and Judith Lipton, from their 2001 book The Myth of Monogamy, there are several varieties of pair bonds:
  • Short-term pair-bond: a transient mating or associations
  • Long-term pair-bond: bonded for a significant portion of the life cycle of that pair
  • Lifelong pair-bond: mated for life
  • Social pair-bond: attachments for territorial or social reasons, as in cuckold situations
  • Clandestine pair-bond: quick extra-pair copulations
  • Dynamic pair-bond: e.g. gibbon mating systems being analogous to "swingers"

Humans and pair bonding

Pair-bonded human male and female
 
Humans can experience some or all of the above-mentioned varieties of pair bonds in their lifetime. These bonds can be temporary or last a lifetime, same age or with different age groups. In a biological sense there are two main types of pair bonds exhibited in humans: social pair bonding and sexual pair bonding. The social pair bond is a strong behavioral and psychological relationship between two individuals that is measurably different in physiological and emotional terms from general friendships or other acquaintance relationships. On the other hand, the sexual pair bond is a behavioral and physiological bond between two individuals with a strong sexual attraction component. In this bond the participants in the sexual pair bond prefer to have sex with each other over other options. Social pair bonds are usually more wide-ranging than their sexual counterparts due to the sexual nature involved in the latter. In humans and other mammals, these pair bonds are created by a combination of social interaction and biological factors including neurotransmitters like oxytocin, vasopressin, and dopamine. 

Pair bonds (social and/or sexual) are a biological phenomenon and are not equivalent to the human social institution of marriage. Marriage can be associated with a sexual or social pair bond; however, married couples do not necessarily have to experience both or either of these bonds. Marriage can be a consequence of pair bonding and vice versa; however, neither always creates or leads to the other. Pair bonding in humans helps explain extreme "bonds" that we may share with others but are unable to articulate in terms of contemporary "love".
 

Examples

Birds

Close to ninety percent of known avian species are monogamous, compared to five percent of known mammalian species. The majority of monogamous avians form long-term pair bonds which typically result in seasonal mating: these species breed with a single partner, raise their young, and then pair up with a new mate to repeat the cycle during the next season. Some avians such as swans, bald eagles, California condors, and the Atlantic Puffin are not only monogamous, but also form lifelong pair bonds.

When discussing the social life of the bank swallow, Lipton and Barash state:
For about four days immediately prior to egg-laying, when copulations lead to fertilizations, the male bank swallow is very busy, attentively guarding his female. Before this time, as well as after—that is, when her eggs are not ripe, and again after his genes are safely tucked away inside the shells—he goes seeking extra-pair copulations with the mates of other males…who, of course, are busy with defensive mate-guarding of their own.
Male (left) and female (right) mallard ducks form seasonal monogamous pairs.
 
In various species, males provide parental care and females mate with multiple males. For example, recent studies show that extra-pair copulation frequently occurs in monogamous birds in which a "social" father provides intensive care for its "social" offspring.
 

Fishes

A University of Florida scientist reports that male sand gobies work harder at building nests and taking care of eggs when females are present – the first time such “courtship parental care” has been documented in any species.

In the cichlid species Tropheus moorii, a male and female will form a temporary monogamous pair bond and spawn; after which, the female leaves to mouthbrood the eggs on her own. T. moorii broods exhibit genetic monogamy (all eggs in a brood are fertilized by a single male). Another mouth brooding cichlid - the Lake Tanganyika cichlid (Xenotilapia rotundiventralis) has been shown that mating pairs maintain pair bonds at least until the shift of young from female to male. More recently the Australian Murray cod has been seen maintaining pair bonds over 3 years 
 

Mammals

As noted above, different species of voles vary in their sexual behavior, and these differences correlate with expression levels of vasopressin receptors in reward areas of the brain. Scientists were able to change adult male montane voles' behavior to resemble that of monogamous prairie voles in experiments in which vasopressin receptors were introduced into the brain of male montane voles.

Concealed ovulation

From Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Concealed_ovulation
 
Concealed ovulation or hidden estrus in a species is the lack of any perceptible change in an adult female (for instance, a change in appearance or scent) when she is fertile and near ovulation. Some examples of perceptible changes are swelling and redness of the genitalia in baboons and bonobos, and pheromone release in the feline family. In contrast, the females of humans and a few other species that undergo hidden estrus have few external signs of fecundity, making it difficult for a mate to consciously deduce, by means of external signs only, whether or not a female is near ovulation.

Human females

In humans, an adult woman's fertility peaks for a few days during each roughly monthly cycle. The frequency and length of fertility (the time when a woman can become pregnant) is highly variable between women, and can slightly change for each woman over the course of her lifespan. Humans are considered to have concealed ovulation because there is no outward physiological sign, either to a woman herself or to others, that ovulation, or biological fertility, is occurring. Knowledge of the fertility cycle, learned through experience or from educational sources, can allow a woman to estimate her own level of fertility at a given time (fertility awareness). Whether other humans, potential reproductive partners in particular, can detect fertility in women through behavioral or invisible biological cues is highly debated. Scientists and laypersons are interested in this question because it has implications for human social behavior, and could theoretically offer biological explanations for some human sexual behavior. However, the science here is weak, due to a relatively small number of studies. 

Several small studies have found that fertile women appear more attractive to men than women during infertile portions of her menstrual cycle, or women using hormonal contraception. It has also been suggested that a woman's voice may become more attractive to men during this time. Two small studies of monogamous human couples found that women initiated sex significantly more frequently when fertile, but male-initiated sex occurred at a constant rate, without regard to the woman's phase of menstrual cycle. It may be that a woman's awareness of men's courtship signals increases during her highly fertile phase due to an enhanced olfactory awareness of chemicals specifically found in men's body odor.

Analyses of data provided by the post-1998 U.S. Demographic and Health Surveys found no variation in the occurrence of coitus in the menstrual phases (except during menstruation itself). This is contrary to other studies, which have found female sexual desire and extra-pair copulations (EPCs) to increase during the midfollicular to ovulatory phases (that is, the highly fertile phase). These findings of differences in woman-initiated versus man-initiated sex are likely caused by the woman's subconscious awareness of her ovulation cycle (because of hormonal changes causing her to feel increased sexual desire), contrasting with the man's inability to detect ovulation because of its being "hidden".

In 2008, researchers announced the discovery in human semen of hormones usually found in ovulating women. They theorized that follicle stimulating hormone, luteinising hormone, and estradiol may encourage ovulation in women exposed to semen. These hormones are not found in the semen of chimpanzees, suggesting this phenomenon may be a human male counter-strategy to concealed ovulation in human females. Other researchers are skeptical that the low levels of hormones found in semen could have any effect on ovulation. One group of authors has theorized that concealed ovulation and menstruation were key factors in the development of symbolic culture in early human society.
 

Evolutionary hypotheses

Evolutionary psychologists have advanced a number of different possible explanations for concealed ovulation. Some posit that the lack of signaling in some species is a trait retained from evolutionary ancestors, not something that existed previously and later disappeared. If signaling is supposed to have existed and was lost, then it could have been merely due to reduced adaptive importance and lessened selection, or due to direct adaptive advantages for the concealment of ovulation. Yet another possibility (regarding humans specifically) is that while highly specific signaling of ovulation is absent, human female anatomy evolved to mimic permanent signaling of fertility.
 

Paternal investment hypothesis

The paternal investment hypothesis is strongly supported by many evolutionary biologists. Several hypotheses regarding human evolution integrate the idea that women increasingly required supplemental paternal investment in their offspring. The shared reliance on this idea across several hypotheses concerning human evolution increases its significance in terms of this specific phenomenon. 

This hypothesis suggests that women concealed ovulation to obtain men's aid in rearing offspring. Schoroder[14] summarizes this hypothesis outlined in Alexander and Noonan's 1979 paper: if women no longer signaled the time of ovulation, men would be unable to detect the exact period in which they were fecund. This led to a change in men's mating strategy: rather than mating with multiple women in the hope that some of them, at least, were fecund during that period, men instead chose to mate with a particular woman repeatedly throughout her menstrual cycle. A mating would be successful in resulting in conception when it occurred during ovulation, and thus, frequent matings, necessitated by the effects of concealed ovulation, would be most evolutionarily successful. A similar hypothesis was proposed by Lovejoy in 1981 that argued that concealed ovulation, reduced canines and bipedalism evolved from a reproductive strategy where males provisioned food resources to his paired female and dependent offspring.

Continuous female sexual receptivity suggests human sexuality is not solely defined by reproduction; a large part of it revolves around conjugal love and communication between partners. Copulations between partners while the woman is pregnant or in the infertile period of her menstrual cycle do not achieve conception, but do strengthen the bond between these partners. Therefore, the increased frequency of copulations due to concealed ovulation are thought to have played a role in fostering pair bonds in humans.

The pair bond would be very advantageous to the reproductive fitness of both partners throughout the period of pregnancy, lactation, and rearing of offspring. Pregnancy, lactation and caring for post-lactation offspring require vast amounts of energy and time on the part of the woman. She must at first consume more food, then provide food to her offspring, while her ability to forage is reduced throughout. Supplemental male investment in the mother and her offspring is advantageous to all parties. While the man supplements the woman's limited gathered food, the woman is enabled to devote the necessary time and energy to the care of their offspring. The offspring benefits from the supplemental investment, in the form of food and defense from the father, and receives the full attention and resources of the mother. Through this shared parental investment, both man and woman would increase their offspring's chances for survival, thereby increasing their reproductive fitness. In this way natural selection would favor the establishment of pair bonds in humans. To the extent that concealed ovulation strengthened pair bonding, selective pressure would favor concealed ovulation as well. 

Another, more recent, hypothesis is that concealed ovulation is an adaptation in response to a promiscuous mating system, similar to that of our closest evolutionary relatives, bonobos and chimpanzees. The theory is that concealed ovulation evolved in women to lessen paternity certainty, which would both lessen the chances of infanticide (as a father is less likely to kill offspring that might be his), and potentially increase the number of men motivated to assist her in caring for her offspring (partible paternity). This is supported by the fact that all other mammals with concealed ovulation, such as dolphins and gray langurs, are promiscuous, and that the only other ape species that have multi-male communities, as humans do, are promiscuous. It is argued that evidence such as the Coolidge effect, showing that a man does not seem to be naturally geared towards sexual mate-guarding behavior (that is, preventing other males from having access to his sexual partner), supports the conclusion that sexual monogamy (though perhaps not social monogamy and/or pair bonding) was rare in early modern humans.
 

Reduced infanticide hypothesis

This hypothesis suggests the adaptive advantage for women who had hidden estrus would be a reduction in the possibility of infanticide by men, as they would be unable to reliably identify, and kill, their rivals' offspring. This hypothesis is supported by recent studies of wild Hanuman langurs, documenting concealed ovulation, and frequent matings with males outside their fertile ovulatory period. Heistermann et al. hypothesize that concealed ovulation is used by women to confuse paternity and thus reduce infanticide in primates. He explains that as ovulation is always concealed in women, men can only determine paternity (and thus decide on whether to kill the woman's child) probabilistically, based on his previous mating frequency with her, and so he would be unable to escape the possibility that the child might be his own, even if he were aware of promiscuous matings on the woman's part.

Sex and reward hypothesis

Schoroder reviews a hypothesis by Symons and Hill, that after hunting, men exchanged meat for sex with women. Women who continuously mimicked estrus may have benefited from more meat than those that did not. If this occurred with enough frequency, then a definite period of estrus would have been lost, and with it sexual signaling specific to ovulation would have disappeared. 

Social-bonding hypothesis

Schoroder presents the idea of a "gradual diminution of mid-cycle estrus and concomitant continuous sexual receptivity in human women" because it facilitated orderly social relationships throughout the menstrual cycle by eliminating the periodic intensification of male–male aggressiveness in competition for mates. The extended estrous period of the bonobo (reproductive-age females are in heat for 75% of their menstrual cycle) has been said to have a similar effect to the lack of a "heat" in women. While concealed human ovulation may have evolved in this fashion, extending estrus until it was no longer a distinct period, as paralleled in the bonobo, this theory of why concealed ovulation evolved has frequently been rejected. Schroder outlines the two objections to this hypothesis: (1) natural selection would need to work at a level above the individual, which is difficult to prove; and (2) selection, because it acts on the individuals with the most reproductive success, would thus favor greater reproductive success over social integration at the expense of reproductive success.

However, since 1993 when that was written, group selection models have seen a resurgence.

Cuckoldry hypothesis

Schroder in his review writes that Benshoof and Thornhill hypothesized that estrus became hidden after monogamous relationships became the norm in Homo erectus. Concealed ovulation allowed the woman to mate secretly at times with a genetically superior man, and thus gain the benefit of his genes for her offspring, while still retaining the benefits of the pair bond with her usual sexual partner. Her usual sexual partner would have little reason to doubt her fidelity, because of the concealed ovulation, and would have high, albeit unfounded, paternity confidence in her offspring. His confidence would encourage him to invest his time and energy in assisting her to care for the child, even though it was not his own. Again, the idea of a man's investment being vital to the child's survival is a central fixture of a hypothesis regarding concealed ovulation, even as the evolutionary benefits accrue to the child, the woman, and her clandestine partner, and not to her regular sexual partner. 

As a side effect of bipedalism

Pawlowski presents the importance of bipedalism to the mechanics and necessity of ovulation signaling. The more open savannah environment inhabited by early humans brought greater danger from predators. This would have caused humans to live in denser groups, and, in such a scenario, the long-distance sexual signaling provided by female genital swellings would have lost its function. Concealed ovulation is thus argued to be a loss of function evolutionary change rather than an adaptation. Thermoregulatory systems were also modified in humans with the move to the savannah to conserve water. It is thought that female genital swellings would have incurred added cost because of ineffective evaporation of water from the area. Pawlowski continues by saying the change to bipedalism in early hominins changed both the position of female genitals and the line of vision of males. Since males could no longer constantly see the female genitals, swelling of them during estrus as a mode of signaling would have become useless. Also, anogenital swelling at each ovulatory period may have interfered with the mechanics of bipedal locomotion, and selection may have favored females who were less hindered by this occurrence. This hypothesis ultimately concludes that bipedalism, which was strongly selected for, caused the physiological changes and a loss of function of sexual signaling through female genital swelling, leading to the concealed ovulation we now observe. 

Pawlowski's paper offers views that differ from the other hypotheses regarding concealed ovulation in that it pinpoints physiological changes in early humans as the cause of concealed ovulation rather than social or behavioral ones. One of the strengths of this is derived from the other hypotheses' weaknesses – it is difficult to track the evolution of a behavior as it leaves no verifiable evidence in the form of bone or DNA. However, the fact that the Hanuman langurs also display some concealed ovulation and that it is not directly caused by a physiological change to bipedalism may suggest bipedalism was not, at least, the sole cause of concealed ovulation in humans. As stated earlier, it is possible for many elements of different hypotheses to be true regarding the selective pressures for concealed ovulation in humans.

Operator (computer programming)

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Operator_(computer_programmin...