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Monogamy
Monogamy
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Monogamy (/məˈnɒɡəmi/ mə-NOG-ə-mee) is a relationship of two individuals in which they form a mutual and exclusive intimate partnership. Having only one partner at any one time, whether for life or serial monogamy, contrasts with various forms of non-monogamy (e.g., polygamy or polyamory).[1]

The term monogamy, derived from Greek for "one marriage," has multiple context-dependent meanings—genetic, sexual, social, and marital—each varying in interpretation across cultures and disciplines, making its definition complex and often debated. The term is typically used to describe the behavioral ecology and sexual selection of animal mating systems, referring to the state of having only one mate at any one given time. In a human cultural context, monogamy typically refers to the custom of two individuals, regardless of orientation, committing to a sexually exclusive relationship.

Monogamy in humans varies widely across cultures and definitions. While only a minority of societies are strictly monogamous, many practice serial monogamy or tolerate extramarital sex. Genetic monogamy is relatively unstudied and often contradicted by evidence of extrapair paternity. Monogamy in humans likely evolved through a combination of biological factors such as the need for paternal care and ecological pressures, alongside cultural developments like agriculture, property inheritance, and religious or societal norms promoting social stability.

Biologists distinguish between social, sexual, and genetic monogamy to reflect how animal pairings may involve cohabitation, sexual exclusivity, and reproductive fidelity in varying combinations, while serial monogamy describes successive exclusive relationships over time.

Terminology

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The word monogamy derives from the Greek μονός, monos ("one"), and γάμος, gamos ("marriage"), referring to the functional social behaviour of pair-bonding.[1] The term can then be subsequently subclassified by context-dependent relational types. Generally, there are four intersecting definitions.

  • genetic monogamy refers to sexually monogamous relationships with genetic evidence of paternity.[2]
  • sexual monogamy refers to two partners remaining sexually exclusive with each other and having no outside sex partners.[2]
  • social monogamy refers to two individuals co-habitating, maintaining a sexual relationship, and sharing basic resources such as shelter, food, and parenting responsibilities.
  • marital monogamy refers to marriages of only two people, within the context of the institution of marriage.

For instance, biologists, biological anthropologists, and behavioral ecologists often use monogamy in the sense of sexual, if not genetic (reproductive), exclusivity.[3] When cultural or social anthropologists and other social scientists use the term monogamy, the meaning is social or marital monogamy.[3][2]

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"[4]
  2. serial monogamy, marriage with only one other person at a time, in contrast to bigamy or polygamy[1]

Defining monogamy across cultures can be difficult because of different cultural assumptions. Some societies believe that monogamy requires limiting sexual activity to a single partner for life.[5] Others accept or endorse pre-marital sex prior to marriage.[6] Some societies consider sex outside of marriage[7] or "spouse swapping"[8] to be socially acceptable. Some consider a relationship monogamous even if partners separate and move to a new monogamous relationship through death, divorce, or simple dissolution of the relationship, regardless of the length of the relationship (serial monogamy).[9] The need to accurately define monogamy was highlighted in a 2012 work, which defined practices as either formal or informal polyandry. The researchers found 53 communities studied between 1912 and 2010 that practiced polyandry (in which women have multiple male partners). This broader definition indicated that polyandry was more common worldwide than previously believed.[10]

Terminology may also affect how data on polygamy is interpreted. While the genetic record indicates that genetic monogamy increased within the last 5,000-10,000 years,[11] the form of prehistoric non-monogamy is less clear. A lack of genetic monogamy could be interpreted as polygamy despite other plausible explanations. Anthropological observations indicate that even when polygyny is accepted in the community, the majority of relationships in the society are monogamous in practice – while couples remain in the relationship, which may not be lifelong.[9] Thus, in prehistoric communities and communities categorized as polygamous, short- or long-term serial monogamy may be the most common practice rather than a lifelong monogamous bond.[9]

Frequency in humans

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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[12]

Distribution of social monogamy

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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.[13] (This does not take into account the relative population of each of the societies studied; the actual practice of polygamy in a tolerant society may actually be low, with the majority of aspirant polygamists practicing de facto monogamous marriage.)[14]

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.[15]

Prevalence of sexual monogamy

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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.[16][17] 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.[18] Studies in Nigeria have found around 47–53% of men and to 18–36% of women engage in extramarital sex.[19][20] 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.[21]

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).[22] Convenience samples may not accurately reflect the population of the United States as a whole, which can cause serious biases in survey results.[23] Sampling bias may, therefore, be why early surveys of extramarital sex in the United States have produced widely differing results:[22] such early studies using convenience samples (1974, 1983, 1993) reported the wide ranges of 12–26% of married women and 15–43% of married men engaged in extramarital sex.[24][25][26] Three studies have used nationally representative samples. These studies in 1994 and 1997 found that about 10–15% of women and 20–25% of men engage in extramarital sex.[27][28][29]

Research by Colleen Hoffon of 566 homosexual male couples from the San Francisco Bay Area (2010) found that 45% had monogamous relationships.[30] However, the Human Rights Campaign has stated, based on a Rockway Institute report, that "LGBT" 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.[31]

Prevalence of genetic monogamy

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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.[32] 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.[33] 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.[34] 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%.[35]

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[36][37] by sociologist Michael Gilding traced these overestimates back to an informal remark at a 1972 conference.[38]

The detection of unsuspected illegitimacy can occur in the context of medical genetic screening,[39] in genetic family name research,[40][41] and in immigration testing.[42] 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.[39]

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 non-paternity rates and pedigree errors. There are numerous software packages and procedures that exist for correcting research data for pedigree errors.[43][44][45]

Evolutionary and historical development in humans

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A pair of kākā parrots at Auckland Zoo

Biological arguments

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Monogamy exists in many societies around the world,[46] resulting in extensive scientific research which tries 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;[2] however, in humans, the main theoretical sources of monogamy are paternal care and extreme ecological stresses.[3] Paternal care should be particularly important in humans due to the extra nutritional requirement of having larger brains and the lengthier developmental period.[47][48][49] Therefore, the evolution of monogamy could be a reflection of this increased need for bi-parental care.[47][48][49] 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.[3] Due to the extreme sociality and increased intelligence of humans, Homo sapiens have solved many problems that generally lead to monogamy, such as those mentioned above.[3] For example, monogamy is certainly correlated with paternal care, as shown by Marlowe,[48] 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.[3] 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.[3] However, some scientists argue that monogamy evolved by reducing within-group conflict, thus giving certain groups a competitive advantage against less monogamous groups.[50]

Paleoanthropology and genetic studies offer two perspectives on when monogamy evolved in the human species: paleoanthropologists offer tentative evidence that monogamy may have started very early in human history[51] whereas genetic studies suggest that monogamy might have increased much more recently, less than 10,000 to 20,000 years ago.[52][11]

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.[53] According to Reno et al., the sexual dimorphism of Australopithecus afarensis, a human ancestor from approximately 3.9–3.0 million years ago,[54] was within the modern human range, based on dental and postcranial morphology.[51] 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".[51] However, Gordon, Green and Richmond claim that in examining postcranial remains, A. afarensis is more sexually dimorphic than modern humans and chimpanzees with levels closer to those of orangutans and gorillas.[52] Furthermore, Homo habilis, living approximately 2.3 mya,[54] is the most sexually dimorphic early hominid.[55] 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.[56]

Currently the oldest ethnic group in Africa, the continent where Homo sapiens species emerged, is the San people of Southern Africa.[57] Most San are monogamous, but if a hunter is able to obtain enough food, he can afford to have a second wife as well. The monogamy practiced by this ethnic group is the serial monogamy.[58]

Cultural arguments

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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.[3] 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).[59] Goody demonstrates a statistical correlation between this cultural complex and the development of intensive plough agriculture in those areas.[60] 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.[61] 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.[11] 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.[62] 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.[63]

Woman farming, using a digging stick in the Nuba Mountains, southern 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.[3][64][65] 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.[64] 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.[65] Thus, the wealth and power of the family would pass to the "celibate" younger brother of the church.[65] 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.[64][65] 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.[3]

Other theorists use cultural factors influencing reproductive success to explain monogamy. During times of major economic/demographic transitions, investing more in fewer offspring (social monogamy not polygyny) increases reproductive success by ensuring the offspring themselves have enough initial wealth to be successful.[3] This is seen in both England and Sweden during the industrial revolution[3] and is currently being seen in the modernization of rural Ethiopia.[66] 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.[3]

Arguments from outside the scientific community

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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.[67] Some writers have suggested that monogamy may solve the problems they view as associated with non-monogamy and hypergamy such as inceldom.[68][69]

Alexandra Kollontai in Make Way for the Winged Eros[70] 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)."

Havelock Ellis advocates for monogamy in sexual relationships and considers it an expression closest to nature with a sufficient amount of mutuality.

Monogamy is the most natural expression of an impulse which cannot, as a rule, be so adequately realized in full fruition under conditions involving a less prolonged period of mutual communion and intimacy.

— Havelock Ellis (1921), Studies in the Psychology of Sex, Volume VI, Sex in Relation to Society, p. 426

This belief is said to be the case because of the fact that "the sexes are always approximately equal" and that living organisms were designed around a sole partner, "while the needs of the emotional life, even apart from the needs of offspring, demand that such unions based on mutual attraction should be so far as possible permanent." The connection between a sexual partner, independent of the purpose of offspring, is prominently and stated to be akin to a necessity for the fulfillment of the "emotional life", and that this fulfillment can be reached in a monogamous relationship. Ellis acknowledges the existence of "variations" and considers it "inevitable oscillations around the norm", but excludes polygamy and discourages the practice of it. Monogamy as a whole being widely accepted in society is not seen as a notable accomplishment, and Ellis states that "the mere acceptance of a monogamic rule carries us but a little way".[71]

Prehistoric societies

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Recent anthropological data suggest that the modern concept of life-long monogamy has been in place for only the last 10,000 years.[72] Genetic evidence has demonstrated that a greater proportion of men began contributing to the genetic pool between 5,000–10,000 years ago (i.e., there was an increase in women reproducing with different men rather than multiple women reproducing with the same man), which suggests that reproductive monogamy became more common at that time.[11] This would correspond to the Neolithic agricultural revolution. During this time, formerly nomadic societies began to claim and settle land for farming, leading to the advent of property ownership and therefore inheritance. Men would therefore seek to ensure that their land would go to direct descendants and had a vested interest in limiting the sexual activities of their reproductive partners. It is possible that the concept of marriage and permanent monogamy evolved at this time.[73] See also Cultural arguments above.

More recent genetic data has clarified that, in most regions throughout history, a smaller proportion of men contributed to human genetic history compared to women.[11][74] This could occur if male mortality outpaced female mortality. This cannot be assumed with the available evidence. If an equal number of men and women are born and survive to reproduce, however, this would indicate that historically, only a subset of men fathered children and did so with multiple women (and may suggest that many men either did not procreate or did not have children that survived to create modern ancestors). This circumstance could occur for several reasons, but there are three common interpretations:

  1. The first interpretation is a harem model, where one man will out-compete other men (presumably through acts of violence or power) for exclusive sexual access to a group of women. Groups of women could be related or unrelated. This does not seem to reflect real-world observations in more modern polygyny societies, where the majority of individuals seldom have more than one partner at a time.[9]
  2. Second, it may suggest that some men had either more sex or more reproductive success with multiple women simultaneously; this could be caused by sexual liaisons outside of a lifelong "monogamous" relationship (which may or may not be acceptable in their society), having multiple committed partners at once (polygyny), or simply sexual reproduction with multiple partners entirely outside of committed relationships (i.e., casual sex without relationships or pair-bonding).
  3. Third, it may suggest that some men were more likely than other men to have a series of monogamous relationships that led to children with different women throughout the man's life (serial monogamy).[9] There are a variety of explanations for this that range from the woman's influence (more woman choosing a specific man based on his perceived attractiveness or ability to produce food) to the man's (social or coercive power or increased mortality/absence in men compared to women).

The serial monogamy interpretation of genetic history would be congruent with other findings, such as the fact that humans form pair bonds (although not necessarily for life) and that human fathers invest in at least the early upbringing of their children.[9] Serial monogamy would also be consistent with the existence of a "honeymoon period", a period of intense interest in a single sexual partner (with less interest in other women) which may help to keep men invested in staying with the mother of their child for this period.[75] When reciprocated, this "honeymoon period" lasts 18 months to three years in most cases.[76][77] This would correspond to the period necessary to bring a child to relative independence in the traditionally small, interdependent, communal societies of pre-Neolithic humans, before they settled into more separate agricultural communities.[11]

While genetic evidence typically displays a bias towards a smaller number of men reproducing with more women, some regions or time periods have shown the opposite. In a 2019 investigation, Musharoff et al. applied modern techniques to the 1000 Genomes Project Phase 3 high-coverage Complete Genomics whole-genome dataset.[78] They found that the Southern Han Chinese had a male bias (45% female, indicating that women were likely to reproduce with multiple men). This region is known for its lack of a concept of paternity and for a sense of female equality or superiority.[79] The Musharoff study also found a male bias in Europeans (20% female) during an out-of-Africa migration event that may have increased the number of men successfully reproducing with women, perhaps by replenishing the genetic pool in Europe. The study did confirm a more typical female bias in Yorubans (63% female), Europeans (84%), Punjabis (82%), and Peruvians (56%).[80]

According to other studies, coupling began or evolved gradually towards monogamy since millions of years ago.[81]

Anthropologists characterize human beings as "mildly polygynous" or "monogamous with polygynous tendencies."[82][83][84][85] This slight inclination towards polygamy is reinforced by the low rate of polygamy even in polygamist societies; less than five percent of men marry more than one woman in approximately half of polygynous societies.[86] This slight inclination towards men reproducing with a small number of women is also seen in genetic evidence. Depending on the period of history, the average man with modern descendents appears to have had children with between 1.5 women (70,000 years ago) to 3.3 women (45,000 years ago), except in East Asia. This rate varied dramatically by era, possibly due to male mortality, environmental conditions, food availability, and other influences on mortality, and migration patterns.[87][88] These rates may be consistent with a society that practices serial monogamy. However, there was a temporary but sharp decrease in the ratio during the start of the Neolithic resolution, where the average man with modern descendants had children with 17 women (circa 8,000 years ago).[89][90] Given the dramatic cultural shifts towards sedentary agriculture at the time, this is speculated to represent a dramatic change from a community-based society towards the hoarding of power and resources more consistent with a harem model; however, the rapid movement back towards 4.5 women per man after this dip, accompanied by evidence for the move towards monogamy as the agricultural revolution progressed, may suggest a dramatic, unknown factor such as catastrophic male mortality.[91] Some researchers have postulated alternative explanations for the reduction in male effective population size, such as the extinction of male lineages through warfare. In patrilineal clan-based societies, entire male bloodlines could be eradicated by a conquering tribe, while women were often absorbed into the victorious group. Women also traditionally joined their husband's family upon marriage, and this gene flow would have increased the likelihood of their lineages surviving.[92] Another study proposed a more peaceful explanation involving variance in reproductive success among patrilineal groups combined with the gradual splitting of groups over time.[93] These mechanisms could have led to a drastic reduction in male genetic diversity over time without requiring equivalently drastic reproductive ratios between the sexes.

Ancient societies

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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.[94]

Tribal societies

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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 Christian monogamous paradigm.[95]

Ancient Mesopotamia and Assyria

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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.[96] 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.[97]

Ancient Egypt

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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.[98] 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 the right to ask for a divorce if their husband took a second wife. Many tomb reliefs testify to the 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 she is not capable of pregnancy.[99]

Ancient Israel

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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.[100][101] 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.[100] Study shows that ancient Middle East societies, though not strictly monogamous, were practically (at least on commoners' level) monogamous.[97][98] 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.[100] 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."[102]

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, record only one instance of commoner polygamy - that of Samuel's father. The wisdom 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".[101][103]

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[original research?] - especially after 212 AD, when all the Jews became Roman citizens.[100] However, some Jews continued to practice bigamy (e.g. up to medieval times in Egypt and Europe).[citation needed] Fourth-century Roman law forbade Jews to contract plural marriages.[104]

A synod convened by Gershom ben Judah around 1000 CE banned polygamy among Ashkenazi and Sephardic Jews.[105]

Ancient Greece and ancient Rome

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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.[105][106]

Early Christianity

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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.[107]

[dubiousdiscuss]

Contemporary societies

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International

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Western European societies established monogamy as their marital norm.[108] Monogamous marriage is normative and is legally enforced in most developed countries.[109] Laws prohibiting polygyny were adopted in Japan (1880), China (1953), India (1955) and Nepal (1963).[109] Polyandry is illegal in most countries.

The women's rights movements seek to make monogamy the only legal form of marriage.[citation needed] 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)[110] to monitor the progress of nations implementing the convention.

People's Republic of China

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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.[111]

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."[112]

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."[113][114] The protocol entered into force on 25 November 2005.

Varieties in biology

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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.[115][116] 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.[117] 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, [118](p. 4)

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".[119]

Serial monogamy

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Serial monogamy is a mating practice in which individuals may engage in sequential monogamous pairings,[120] or in terms of humans, when men or women can marry another partner but only after ceasing to be married to the previous partner.[121]

Serial monogamy may effectively resemble polygyny in its reproductive consequences because both men and women are able to utilize both sexes reproductive lifespan through repeated marriages.[122]

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.[123][124]

Reproductive success

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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.[122] Men with more serial marriages are likely to have more children than men with only one spouse, whereas the same is not true of women with consecutive spouses.[122] 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.[125][126]

Breakup

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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.[127] As divorce has continued to become more accessible, more individuals have availed themselves of it, and many go on to remarry.[128] Barry Schwartz, author of The Paradox of Choice: Why More is Less, 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.[129][130][131]

Similarity with polygamy

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According to Danish scholar Miriam K. Zeitzen, anthropologists treat serial monogamy, in which divorce and remarriage occur, as a form of polygamy as it also can establish a series of households that may continue to be tied by shared paternity and shared income.[132] As such, they are similar to the household formations created through divorce and serial monogamy.[133] [134][135]

Mating system

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Monogamy is one of several mating systems observed in animals. However, a pair of animals may be socially monogamous without necessarily being sexually or genetically monogamous. Social monogamy, sexual monogamy, and genetic monogamy can occur in different combinations.[118]

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.[118] 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.[136][137] Social monogamy has also been observed in reptiles, fish, and insects.[citation needed]

Sexual monogamy is defined as an exclusive sexual relationship between a female and a male based on observations of sexual interactions.[118] 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.[118]

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% or more of the baby birds in any nest [are] sired by someone other than the resident male."[138] Patricia Adair Gowaty has estimated that, out of 180 different species of socially monogamous songbirds, only 10% are sexually monogamous.[139] Offspring are far more successful when both the male and the female members of the social pair contribute food resources.

The highest known frequency of reproductively successful extra-pair copulations are found among fairywrens Malurus splendens and Malurus cyaneus where more than 65% of chicks are fathered by males outside the supposed breeding pair.[137] 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.[140] Fish of this genus frequently mate with a new partner after they are widowed.

Evolution in animals

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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.[citation needed] There is even a parasitic worm, Schistosoma mansoni, that in its female-male pairings in the human body is monogamous.[141] 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.[citation needed]

The low occurrence of social monogamy in placental mammals has been claimed[by whom?] to be related to the presence or absence of estrus—or oestrus—the duration of sexual receptivity of a female.[citation needed] This, however, does not 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.

Genetic and neuroendocrine bases

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The prairie vole is an animal example for its monogamous social behaviour, since the male is usually socially faithful to the female, and shares in the raising of pups. The woodland vole is also usually monogamous. Another species from the same genus, the meadow vole, has promiscuously mating males, and scientists have changed adult male meadow voles' behaviour to resemble that of prairie voles in experiments in which a single gene was introduced into the brain by a virus.[142]

The behaviour is influenced by the number of repetitions of a particular string of microsatellite DNA. Male prairie voles with the longest DNA strings spend more time with their mates and pups than male prairie voles with shorter strings.[143] However, other scientists have disputed the gene's relationship to monogamy, and cast doubt on whether the human version plays an analogous role.[144] Physiologically, pair-bonding behavior has been shown to be connected to vasopressin, dopamine, and oxytocin levels, with the genetic influence apparently arising via the number of receptors for these substances in the brain; the pair-bonding behavior has also been shown in experiments to be strongly modifiable by administering some of these substances directly.[145]

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 Microtus 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.[146] This difference in neuropeptide effect is attributed to the location, density, and distribution of OT and AVP receptors.[147] 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.[146] 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.[147]

See also

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References

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Bibliography

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Further reading

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Monogamy is a mating system in which individuals form a pair bond with one partner, typically involving cohabitation, biparental care, and varying degrees of sexual and genetic exclusivity during the bond's duration. In biological terms, it distinguishes between social monogamy (pair-living and cooperation in offspring rearing) and genetic monogamy (exclusive reproduction with the partner), though empirical studies reveal frequent discrepancies, with extra-pair paternity common even in socially monogamous species. Among mammals, monogamy is empirically rare, occurring in only 3-5% of approximately 5,000 species, with most examples limited to rodents, primates, and canids rather than strict genetic fidelity across taxa. In humans, the system manifests primarily as social monogamy, with normative pair-bonding in over 80% of societies despite pockets of polygyny, low genetic non-paternity rates (around 2%), and prevalent serial monogamy marked by divorce and remarriage. Evolutionary models attribute its emergence to factors like high paternal investment in offspring, avoidance of infanticide by guarding mates, and resource scarcity favoring pair stability over promiscuity, though these drivers do not preclude infidelity or dissolution. Key characteristics include reduced intrasexual competition and violence in monogamous populations, alongside improved child survival from biparental provisioning, but costs arise from enforced exclusivity, such as opportunity losses for high-fitness individuals and elevated divorce rates in modern contexts where cultural enforcement wanes. Controversies center on its "naturalness," with data showing humans deviate from lifelong bonds via infidelity (affecting 20-25% of pairs in some studies) and sequential partnering, challenging idealizations of perpetual fidelity while affirming its adaptive role in stabilizing kin networks and curbing inequality.

Definitions and Terminology

Core Concepts and Distinctions

Monogamy constitutes a mating system wherein an individual forms a pair bond with a single partner, typically involving in or resource sharing. This framework contrasts with polygamy, where multiple partners are involved simultaneously, and is observed across species, though its prevalence and strictness vary. Biologists delineate three primary forms of monogamy—social, sexual, and genetic—to account for divergences in behavioral, reproductive, and genetic outcomes. Social monogamy entails the sustained association of one male and one female, characterized by cohabitation, territorial defense, and cooperative offspring provisioning, without necessitating exclusivity in mating. Sexual monogamy requires fidelity in copulation, limiting sexual activity to the paired partner over a defined period, such as a breeding season. Genetic monogamy, the strictest variant, occurs when all progeny within the pair bond result exclusively from the mated individuals, excluding extra-pair fertilizations. These categories often dissociate in nature; for instance, social pairs may exhibit sexual infidelity, yielding cuckoldry and undermining genetic monogamy, as documented in avian studies where up to 30% of offspring in socially monogamous species derive from extra-pair copulations. In human contexts, social monogamy aligns with institutionalized marriage or cohabitation, yet surveys indicate sexual non-exclusivity in 20-25% of committed relationships, per self-reported data from longitudinal studies. Serial monogamy further qualifies the paradigm, involving successive exclusive pairings rather than lifelong commitment, predominant in modern Western societies where average marriage duration approximates 8 years before dissolution or repartnering. Distinctions extend to emotional monogamy, denoting exclusive affective attachment, though empirical measurement remains challenging due to reliance on subjective reports; neuroendocrine markers like oxytocin levels correlate with pair-bond maintenance but do not preclude behavioral infidelity. These concepts underscore that monogamy functions as a spectrum rather than a binary, shaped by ecological pressures and verifiable through genetic assays, observational ethology, and demographic records.

Biological Foundations

Monogamy in Non-Human Animals

Social monogamy, characterized by long-term pair bonding and biparental care of , predominates in avian species, with approximately 90% of bird species exhibiting this to ensure chick in resource-scarce environments where dual provisioning is essential. In contrast, genetic monogamy—exclusive mating within the pair—is rarer, as extra-pair copulations occur in many socially monogamous birds, reducing paternity certainty despite stable partnerships. Among mammals, monogamy of any form is far less common, affecting only 3-5% of the roughly 5,000 mammalian species, largely due to females' capacity for solitary lactation and male tendencies toward polygyny for reproductive maximization. Social monogamy appears in select lineages like rodents (e.g., prairie voles, where vasopressin receptor distribution promotes pair bonding) and primates (e.g., owl monkeys and some callitrichids), often linked to male infanticide avoidance or female dispersion in habitats favoring territorial defense over harem formation. However, genetic monogamy remains exceptional in these groups, with DNA analyses revealing frequent cuckoldry even in pair-living species; for instance, in pair-living primates, extra-pair paternity rates can exceed 20-30% in some populations. True lifelong monogamy, combining social and genetic exclusivity, is documented in few taxa, such as certain voles and seabirds like albatrosses, but empirical studies emphasize that most "monogamous" animals divorce or cheat opportunistically, challenging romanticized views of fidelity. In primates, where pair-living evolved multiple times independently, social bonds facilitate cooperative foraging and infant carrying, yet mate guarding does not preclude genetic polygamy, as constrained choice in small groups limits alternatives but not infidelity.

Evolutionary Drivers

Social monogamy has evolved independently in only about 5% of mammalian , primarily as an adaptive response to ecological and demographic pressures that limit male access to multiple mates. In mammals with dispersed or solitary females, males face challenges in monopolizing multiple partners due to spatial constraints and high search costs, favoring pair- as a to secure reproductive opportunities. This is evident in phylogenetic analyses showing that social monogamy often derives from ancestral states of female solitariness rather than group-living polygyny. A primary driver in primates, where monogamy has arisen multiple times across major clades, is the risk of male-inflicted infanticide. Incoming males frequently kill unrelated infants to shorten female interbirth intervals and accelerate their own reproductive access, imposing high fitness costs on cuckolded or absent sires; pair-living allows resident males to guard mates and offspring, reducing such losses. Quantitative trait analyses across 230 primate species confirm that infanticide risk, rather than direct benefits of paternal care alone, best predicts the transition to monogamy, with solitary female ranging preceding pair formation. In human evolution, analogous pressures in ancestral groups—where lethal male competition and resource scarcity amplified infanticide threats—likely reinforced social monogamy to enhance offspring survival amid prolonged dependency periods. Biparental care emerges as a complementary selective force, particularly for species with altricial young requiring extended provisioning. Monogamy facilitates male investment in offspring, which boosts viability in environments where single-parent rearing yields low success; however, this often co-evolves with paternity assurance mechanisms like mate guarding, as genetic monogamy remains imperfect even in socially paired systems. Empirical correlates in socially monogamous mammals show that pair-living predicts higher genetic fidelity when combined with factors like territoriality, though extra-pair mating persists due to residual polygynous incentives. In humans, the evolution of large brains and slow maturation intensified biparental demands, with pair-bonding providing a stable framework for cooperative child-rearing, though serial monogamy likely predominated given high adult mortality and divorce rates in ethnographic data. These drivers underscore monogamy's origin in pragmatic fitness maximization, not romantic attachment, with reversals to polygyny occurring under conditions of male-biased sex ratios or resource abundance.

Genetic and Neuroendocrine Mechanisms

In socially monogamous prairie voles (Microtus ochrogaster), genetic variation in the vasopressin receptor 1a gene (Avpr1a) promoter region, characterized by a microsatellite expansion, leads to higher receptor expression in brain areas such as the ventral pallidum, facilitating pair bond formation and partner preference. This contrasts with non-monogamous montane voles (Microtus montanus), which lack this expansion and exhibit lower Avpr1a expression in the same regions, correlating with reduced affiliative behaviors toward mates. Experimental introduction of the human AVPR1A variant into prairie voles alters brain Avpr1a distribution, impairing social bonding and underscoring the gene's causal role in monogamous traits. Neuroendocrinologically, arginine vasopressin (AVP) in males and oxytocin (OT) in females mediate pair bonding via receptors in the nucleus accumbens and ventral pallidum, where they interact with dopamine to reinforce partner-specific reward circuits during mating. Central infusion of AVP or OT promotes selective partner preference in voles, while receptor antagonists disrupt bond formation, indicating these neuropeptides' necessity for the transition from promiscuity to monogamy. Dopamine release in the nucleus accumbens during cohabitation with a mate synergizes with AVP/OT signaling to sustain bonds, as blocking D2 receptors prevents affiliation. In humans, polymorphisms in AVPR1A, such as the RS3 repeat, associate with pair-bonding behaviors, including lower marital satisfaction and higher divorce risk in carriers of certain alleles, mirroring vole findings but with weaker effect sizes due to environmental confounders. Transcriptomic analyses across vertebrates reveal conserved gene expression profiles in monogamous species, including upregulated AVP/OT pathways, suggesting shared neuroendocrine mechanisms evolved for paternal investment and mate guarding, though genetic monogamy remains rare even in socially monogamous lineages. These mechanisms explain variation in fidelity but do not preclude extra-pair mating, as evidenced by field studies showing incomplete genetic monogamy in voles despite social pairing.

Empirical Evidence in Humans

Genetic Monogamy and Paternity Certainty

Genetic monogamy in humans is assessed through the rate at which offspring conceived within socially monogamous pairs are biologically sired by the social father, with low non-paternity rates indicating high genetic fidelity. Empirical DNA-based studies, using methods such as Y-chromosomal STR analysis and autosomal SNPs, have consistently found these rates to be low in most populations, typically ranging from 0.8% to 2%. For instance, a large-scale genetic analysis of over 2,000 individuals from rural West Africa spanning 400 years revealed a non-paternity rate of 0.9% (95% CI: 0.4-1.5%), demonstrating stability over time in a pre-modern context. Paternity certainty, the male's confidence in his biological fatherhood, aligns closely with these actual rates, particularly among men reporting high confidence, such as long-term married couples, where non-paternity drops to under 1%. Earlier anecdotal or clinic-based estimates suggesting 10% or higher non-paternity were biased toward disputed cases, such as child support litigations or immigrant paternity tests, inflating figures beyond population-representative samples. Population-wide genetic surveys, unbiased by suspicion, confirm that extra-pair paternity (EPP) remains rare, supporting the evolutionary utility of social monogamy in securing male parental investment through assured relatedness. Exceptions exist in specific small-scale or high-fertility groups; for example, a study of 1,846 children in a Bolivian community reported an EPP rate of 48%, attributed to local socioecological factors like partner scarcity and seasonal labor migration, though this outlier contrasts with broader human patterns and may reflect non-representative dynamics. Cross-cultural data remain limited, but available evidence from Europe, North America, and parts of Africa indicates that non-paternity does not exceed 3% in stable monogamous unions, with no systemic evidence for higher rates undermining pair-bonding. These findings underscore that human genetic monogamy, while not absolute, achieves sufficient paternity certainty to facilitate biparental care, distinguishing humans from many promiscuous primates.

Sexual and Social Fidelity Rates

Empirical studies indicate that sexual fidelity, defined as adherence to exclusive sexual partnering within a monogamous relationship, is imperfect among humans despite widespread social norms favoring it. Self-reported lifetime rates of extramarital sexual infidelity in the United States, drawn from the General Social Survey (GSS), show approximately 20% of married men and 13% of married women admitting to sex with someone other than their spouse. These figures likely understate true prevalence due to social desirability bias in self-reporting, with some analyses suggesting actual rates could be higher, particularly among men. Annual rates of sexual fidelity are substantially higher, exceeding 90% for both sexes among married individuals across age groups, per the same GSS data, reflecting episodic rather than chronic infidelity in most cases. Genetic evidence provides an indirect measure of female sexual fidelity through extra-pair paternity (EPP) rates, which average 1-2% in modern Western populations, indicating high overall adherence to sexual exclusivity by women despite self-reported infidelity. This low EPP rate contrasts with higher self-reported male infidelity, as male extrapair copulations do not typically affect paternity certainty in monogamous pairings. Factors influencing sexual infidelity include relative income disparities, with higher-earning spouses more prone to affairs under social exchange models tested in longitudinal data. Social fidelity, involving public commitment to a single partner without dissolution of the pair bond, generally exceeds sexual fidelity rates, as many relationships persist despite sexual breaches. Approximately 60-75% of couples remain together following discovery of an affair, according to multiple clinical and survey-based studies of infidelity outcomes. Social monogamy can thus tolerate sexual infidelity without immediate relational collapse, aligning with observations that humans often maintain pair bonds for child-rearing and resource stability even amid lapses in sexual exclusivity. Peer-reviewed reviews emphasize that while sexual monogamy is not universal within socially monogamous unions, the latter's prevalence underscores adaptive pressures favoring long-term partnering over strict genetic fidelity. Self-report limitations persist here as well, with underreporting common due to stigma, though behavioral persistence in marriage serves as a proxy for social adherence.

Cross-Cultural Prevalence

In George P. Murdock's Ethnographic Atlas, which catalogs marriage practices across 1,231 societies, 186 (approximately 15%) are classified as monogamous, 453 permit occasional polygyny (typically limited to elites), and 588 allow more frequent polygyny; however, even in the latter cases, the actual proportion of polygynous unions remains low, with married men averaging 1.1 to 1.5 wives due to economic and resource constraints that restrict multiple marriages to a minority of high-status individuals. This pattern underscores that monogamy dominates in practice across cultures, even where polygyny is culturally sanctioned. Polygyny, the most common non-monogamous form, is permitted in roughly 80-85% of ethnographic societies but manifests primarily in sub-Saharan Africa and parts of the Middle East and South Asia, where it correlates with pastoralism, unequal resource distribution, and male-biased sex ratios from warfare or infanticide. In these regions, polygynous households comprise 20-50% of marriages in high-prevalence areas like Mali or Niger as of 2020, yet globally, only about 2% of the population lives in such arrangements. In contrast, monogamy is normative and legally enforced in Europe, the Americas, East Asia, and most industrialized societies, often evolving from historical norms tied to agriculture, state formation, and equitable land inheritance that favor pair-bonding. Hunter-gatherer societies, approximating pre-agricultural human baselines, exhibit higher monogamy rates (over 70% in sampled groups), associated with bilateral food sharing and male subsistence contributions exceeding 30-40% of calories, which reduce incentives for polygyny by promoting cooperative pair-bonding. Polyandry, involving one woman with multiple husbands, occurs in fewer than 1% of societies, confined to extreme environments like Tibetan plateaus where fraternal polyandry preserves land holdings amid population pressure and male labor shortages. Group marriages or other variants are negligible in the ethnographic record.

Historical Development

Prehistoric and Societies

Evidence from paleoanthropological and genetic studies indicates that prehistoric humans, including early Homo sapiens, likely practiced social monogamy through pair-bonding, inferred from low levels of and indicators of reduced male intrasexual . The body dimorphism of approximately 1.15 in aligns more with pair-bonding like gibbons than the higher dimorphism (1.2–1.5) seen in polygynous great apes, suggesting mating systems where males competed less intensely for multiple females. Testis relative to body in humans also points to adaptations for at levels consistent with social rather than strict genetic monogamy, but with predominant pair-bonding to ensure paternal investment. Genetic analyses of modern and ancient DNA reveal low extra-pair paternity rates, with medians of 1.7–3.3% across populations, supporting high in prehistoric contexts where biparental care was crucial for offspring survival amid high juvenile mortality. archaeological of systems remains scarce to the absence of written records or unambiguous grave associations indicating polygynous harems, but isotopic studies of skeletal remains from sites like Sunghir (, ~34,000 years ago) show resource sharing patterns consistent with units rather than elite of females. Ethnographic data from extant societies, serving as analogs for foragers, confirm monogamy as the dominant pattern, often serial in nature due to frequent , , and adult mortality rates exceeding 30–40% before age 45. occurs but at low frequencies, typically involving fewer than 10–20% of married men, constrained by egalitarian , minimal inequality, and the inability to support multiple wives without surplus production. For instance, in the of forager societies, polygyny rates are markedly lower than in agricultural groups, with fishing-based foragers exhibiting near-exclusive monogamy due to high male provisioning reliability. Among specific groups like the Hadza or !Kung, monogamous pair bonds facilitate cooperative hunting and gathering, with men contributing 40–60% of calories via big game, incentivizing female mate choice for reliable partners over polygynous males. Gathering-dominant societies, such as some Ache or Hiwi subgroups, show slightly elevated polygyny (up to 20–30% in rare cases), linked to lower male subsistence input and higher intergroup raiding, but even here, serial monogamy prevails, with divorce rates over 50% within years of marriage. These patterns underscore causal drivers like offspring dependency—human infants requiring years of dual parental investment—and ecological pressures favoring stable bonds over resource-limited polygyny. Overall, such evidence counters narratives of inherent human promiscuity, highlighting adaptive monogamy in resource-scarce, mobile forager lifeways.

Ancient Civilizations

In ancient Mesopotamia, marriage was predominantly monogamous among the general population, structured as a contractual alliance between families for economic and social stability, with the Code of Hammurabi (c. 1750 BCE) regulating dowries, inheritance, and spousal rights under this framework. Polygyny was permitted and practiced by elites and kings, who maintained harems of secondary wives or concubines, as evidenced by royal records and legal allowances for multiple sexual partners outside the primary union. This distinction arose from resource availability, where affluent men could support additional dependents, while commoners faced practical constraints limiting them to one wife. Ancient Egyptian society enforced monogamy for non-royal couples, viewing marriage as cohabitation without formal ceremonies, aimed at producing heirs and maintaining household unity, as depicted in tomb art and Herodotus's accounts from the 5th century BCE. Pharaohs deviated with polygamous or sibling unions for dynastic purity, but these were exceptional and not emulated by the populace, where divorce and remarriage were common yet fidelity idealized in mutual obligations. Economic factors, including limited arable land along the Nile, reinforced serial monogamy over concurrent polygyny for most families. Greco-Roman civilizations institutionalized legal monogamy, prohibiting men from holding multiple wives simultaneously, a norm established by the Archaic period in Greece (c. 800–480 BCE) and codified in Roman law, distinguishing them from contemporaneous polygynous empires like Persia. Greek sources, such as Euripides, condemned polygyny as barbaric, emphasizing one legal spouse for legitimate inheritance, though extramarital relations with concubines or slaves were tolerated for men. In Rome, the Lex Julia (18 BCE) further entrenched this by penalizing adultery while upholding marital exclusivity for citizen unions, driven by concerns over paternity certainty and civic order. This system prioritized social monogamy to curb elite competition for women, reducing violence as inferred from comparative historical data. In ancient China, Confucian ideals from the Zhou dynasty (1046–256 BCE) promoted one principal wife per man, with concubines subordinate and not equivalent in status, reflecting a hierarchy where monogamy applied to the nuclear family core amid elite polygyny. Legal texts like the Rites of Zhou emphasized mutual fidelity for social harmony, but emperors and nobles amassed concubines for lineage expansion, limited only by imperial bureaucracy. Similarly, in Vedic India (c. 1500–500 BCE), texts such as the Rigveda describe monogamy as normative for commoners, with kings engaging polygyny for alliances, though polyandry appeared in resource-scarce regions like the Himalayas. Across these societies, monogamy's prevalence correlated with agricultural intensification and property inheritance needs, favoring pair-bonding over elite harems for population stability.

Religious and Medieval Influences

Christian doctrine, drawing from New Testament teachings such as Matthew 19:4-6 where Jesus affirms marriage as the union of one man and one woman based on Genesis, established monogamy as the normative marital form from the early centuries AD. Early Church Fathers, including Tertullian (c. 155-220 AD), explicitly condemned polygamy, arguing it contradicted the singular marital bond modeled in creation. This stance contrasted with historical Jewish allowances for polygyny under Mosaic law, though rabbinic traditions increasingly favored monogamy by the medieval period, and diverged from Islamic permissions for up to four wives as outlined in Quran 4:3. In Europe, Christianity's adoption and reinforcement of Roman monogamous legal traditions transformed it into a sacramental institution emphasizing fidelity and indissolubility. During the medieval era, the Catholic Church exerted profound influence over marriage practices, prohibiting consanguineous unions—extending bans to seventh cousins by the 11th century—and spiritual kinships, which disrupted extended clan structures that had previously facilitated polygynous mating among elites. These reforms, formalized through councils like the Fourth Lateran Council in 1215 which restricted prohibitions to fourth-degree relatives, promoted nuclear family units and reduced incentives for polygyny by prioritizing individual consent and monogamous pairings over kin-based alliances. The Church's assertion of jurisdiction over marriage as a sacrament, evident by the 9th century when it controlled annulments and dispensations, generated institutional power and wealth while embedding monogamy in canon law, supplanting Germanic customs of serial monogamy or concubinage. Despite formal monogamous marriages, powerful medieval men often maintained concubines or extramarital relations, indicating that while the Church curtailed legal polygyny—absent among European nobility after the early Middle Ages—de facto polygynous behaviors persisted among the elite until reinforced by secular laws. This ecclesiastical framework, however, fostered broader societal adherence to monogamy, as evidenced by the decline of polygynous practices in Christianized regions by 1000 AD, contributing to the psychological and social orientations toward individualism and pair-bonding that characterize Western kinship systems. In Judaism, medieval Ashkenazi communities largely abandoned polygyny following Gershom ben Judah's 11th-century ban, aligning with Christian Europe's monogamous norms amid shared legal and cultural pressures.

Industrial and Modern Shifts

The Industrial Revolution, beginning in the late 18th century in Britain and spreading to Europe and North America by the mid-19th century, facilitated a transition from extended family structures to nuclear families centered on monogamous couples. This shift was driven by urbanization and the separation of home and workplace, as men increasingly engaged in wage labor outside the household, reducing reliance on multi-generational kin networks for economic production. Industrialization also enhanced women's access to labor income, increasing their autonomy within marriages and correlating with a reinforcement of monogamous norms, as economic productivity favored paternal investment in fewer offspring over polygynous competition. By the 19th century, these dynamics solidified monogamous pair-bonding as a social and economic haven amid the disruptions of factory work and city life, though marriage ages and fertility rates remained relatively stable compared to pre-industrial eras. In the 20th century, legal and cultural changes enabled serial monogamy through rising divorce rates, which climbed from 4.1 per 1,000 married women in 1900 to a peak of 22.6 in 1980 in the United States, reflecting easier no-fault divorce laws introduced in the 1970s and shifting gender roles. The sexual revolution of the 1960s and 1970s, propelled by widespread contraception access and delayed marriages, normalized premarital sex and cohabitation, eroding strict lifelong monogamy in favor of more fluid partnerships. However, empirical data indicate monogamy's persistence as the dominant practice; only about 5% of U.S. adults report current involvement in consensual non-monogamy, while global polygamy affects under 2% of households, with monogamous marriage prevailing even in societies historically tolerant of polygyny. Recent trends show stabilizing divorce rates at around 14.6 per 1,000 in 2022, alongside declining marriage rates but continued preference for exclusive pair-bonding among most couples.

Societal and Familial Impacts

Benefits for Child-Rearing and Family Stability

Monogamy promotes paternity certainty, which encourages greater paternal investment in offspring. In species and societies with high paternity uncertainty, males reduce investment to avoid cuckoldry, whereas assured paternity correlates with increased provisioning, protection, and emotional involvement from fathers. This dynamic is evident in human pair-bonding, where monogamous norms minimize extra-pair copulations, fostering direct biological ties and long-term commitment. Children raised in stable monogamous families exhibit superior developmental outcomes compared to those in polygamous or unstable structures. Longitudinal research indicates that offspring of married biological parents demonstrate enhanced cognitive skills, behavioral regulation, and emotional health, attributable to dual parental resources and consistent caregiving. In contrast, polygynous households often show diluted paternal attention and resources, leading to higher child mortality rates and slower recovery from health setbacks. Family stability under monogamy mitigates social disruptions like divorce or serial partnering, which correlate with elevated risks of mental health issues in children. Stable two-parent marriages provide economic security, modeled conflict resolution, and intergenerational continuity, outperforming single-parent or cohabiting arrangements in fostering resilience and academic achievement. Systematic reviews of polygamous impacts reveal increased psychosocial problems and lower educational attainment among children, underscoring monogamy's role in concentrated investment and reduced intra-family competition.

Reduction of Social Pathologies

Normative monogamy mitigates social pathologies by suppressing intrasexual competition among males and reducing the proportion of unmarried men, who exhibit elevated risk-taking behaviors and criminality. In suppressing this competition, monogamous institutions lower overall crime rates, encompassing offenses such as rape, murder, assault, robbery, and fraud, alongside reductions in personal abuses like domestic violence. These effects stem from decreased male-male rivalry over mates, which in polygynous systems exacerbates violence and instability, as evidenced by higher homicide and violent crime rates in societies permitting multiple wives. Monogamy further diminishes intra-household conflict by elevating genetic relatedness within families, promoting greater parental investment—particularly paternal—and yielding improvements in child welfare outcomes. This includes reduced rates of child neglect, abuse, accidental death, and homicide compared to polygamist cultures, where resource competition and fragmented family structures intensify such risks. Father presence, facilitated by stable monogamous pair-bonds, correlates with lower child delinquency and long-term criminal involvement; for instance, children from father-absent homes face incarceration risks 3 to 20 times higher than those from intact families. Empirical data from U.S. jurisdictions underscore these patterns: states with lower percentages of single-parent families report correspondingly reduced juvenile crime rates, independent of other socioeconomic variables. Father absence also heightens poverty exposure, with children in such households four times more likely to live below the poverty line, perpetuating cycles of economic disadvantage and social disruption. In contrast, polygynous societies exhibit amplified gender inequality, poverty, and violence due to surplus unpaired males and unequal resource distribution, reinforcing monogamy's role in fostering societal stability.

Economic and Demographic Effects

Normative monogamy redirects male competitive efforts away from acquiring multiple mates toward increased paternal investment, savings, and economic productivity, as evidenced by comparative analyses of historical and contemporary societies. In polygynous systems, by contrast, resource competition among males for fewer available females reduces capital accumulation and output per worker, with empirical models showing that eliminating polygyny could raise steady-state output by up to 59% in affected regions. Cross-national data from sub-Saharan Africa indicate that polygynous countries exhibit per capita GDP approximately 38% lower than monogamous ones, attributable in part to diminished savings rates and higher fertility that strain productive capacity. These patterns hold after controlling for factors like economic development, suggesting monogamy fosters conditions for sustained growth through stabilized household investments and reduced intrasexual rivalry. Demographically, monogamy correlates with lower total fertility rates compared to polygyny, where women in polygynous unions averaged 6.8 children per woman in 1980 versus 4.6 in monogamous countries, driven by earlier marriage (over five years sooner on average) and less paternal dilution per offspring. This fertility differential contributes to slower population growth in monogamous societies, potentially aiding transitions to lower birth and death rates, though initial shifts from polygyny may sustain high fertility before family sizes contract. Monogamy also mitigates sex ratio distortions and surplus unpaired males prevalent in polygynous systems, which can exacerbate social instability and hinder demographic equilibrium, as institutional monogamy equalizes mating access and promotes pair-bonding stability. In modern contexts, these effects intersect with broader demographic declines, but causal evidence links monogamous norms to more predictable population dynamics and reduced variance in reproductive success.

Criticisms, Alternatives, and Debates

Arguments Against Strict Monogamy

Strict monogamy, defined as lifelong exclusive sexual and romantic pairing, faces challenges from , as human mating strategies exhibit flexibility rather than rigid exclusivity. Genetic and anthropological evidence indicates that humans have adapted both long-term pair-bonding and short-term mating opportunities, with serial monogamy—sequential exclusive partnerships—being more normative than lifelong adherence. Paternity certainty studies reveal non-paternity rates around 2% in socially monogamous human populations, lower than in many pair-bonding birds but suggestive of occasional extra-pair copulations that align with opportunistic rather than strict . This evolutionary legacy, particularly men's predisposition toward sexual variety to maximize genetic dissemination, implies that enforcing strict monogamy may conflict with innate tendencies toward mate variety, potentially fostering psychological strain or covert . In modern hypersexualized societies, these challenges are amplified for some men by unlimited access to pornography and dating apps, which exploit the Coolidge effect—renewed sexual arousal from novel stimuli—and provide abundant casual options, correlating with reduced relationship satisfaction and elevated infidelity risks. Empirical data on relationship outcomes underscore the difficulty of sustaining strict monogamy. Lifetime infidelity rates in heterosexual marriages range from 20% to 25% for women and 20% to 40% for men, with higher prevalence among younger cohorts and those in their peak reproductive years. Sexual dissatisfaction contributes to marital dissolution, as evidenced by studies linking low sexual frequency and dysfunction to elevated divorce risks; for instance, couples reporting infrequent intercourse (less than once weekly) show significantly higher separation rates. In divorce-seeking populations, sexual incompatibility and dissatisfaction are cited as precipitating factors in up to 15-20% of cases, often intertwined with broader relational erosion but rooted in unmet desires for novelty or variety. Comparisons with consensual non-monogamy (CNM) highlight potential drawbacks of strict exclusivity. Recent analyses of over 3,000 participants found no significant differences in relationship or sexual satisfaction between monogamous and CNM individuals, challenging assumptions of monogamous superiority and suggesting CNM as a viable alternative for those prone to dissatisfaction. CNM practitioners often report benefits such as expanded social networks, personal growth through compersion (joy in a partner's other relationships), and fulfillment of diverse needs without the secrecy of affairs, with psychological health metrics comparable or superior to monogamous counterparts in some cohorts. However, these findings derive largely from self-selected samples, warranting caution against overgeneralization, as methodological limitations like reliance on volunteer participants may skew toward more adaptive CNM practitioners. Critics argue that strict monogamy can exacerbate gender asymmetries, particularly for women, by channeling jealousy into controlling behaviors; experimental data link monogamous norms to heightened possessive responses that, in dysfunctional contexts, justify coercion or violence. In polygynous societies historically prevalent among humans, resource inequality enabled multiple partnerships without the universal instability predicted by monogamy proponents, though modern applications remain contested due to equity concerns. Overall, while strict monogamy yields stability for some, its enforcement against prevalent infidelity patterns and evolutionary predispositions risks widespread non-compliance, underscoring the need for flexible models attuned to human behavioral realities.

Evidence on Consensual Non-Monogamy

Research on consensual non-monogamy (CNM) primarily relies on cross-sectional, self-report surveys from convenience samples recruited via social networks or CNM communities, introducing potential self-selection bias where only satisfied participants remain engaged or respond. A 2025 of 35 studies encompassing 24,489 participants found no significant differences in relationship satisfaction (Hedges' g = -0.05, 95% CI [-0.20, 0.10]) or sexual satisfaction (g = 0.06, 95% CI [-0.07, 0.18]) between monogamous and CNM individuals, though high heterogeneity (I² > 80%) suggests variability across subgroups like polyamorous (g = 0.16) and (g = 0.43) reporting slightly higher satisfaction. These null effects challenge assumptions of monogamous superiority but are limited by the absence of longitudinal data, reliance on self-reports prone to —particularly in stigmatized CNM groups motivated to affirm their choices—and underrepresentation of diverse demographics. Longitudinal studies on CNM stability are scarce, with scoping reviews of over 200 publications from 2023 noting few that track outcomes over time, precluding firm conclusions on dissolution rates compared to monogamy. Cross-sectional evidence indicates CNM participants often report effective jealousy management through communication, with lower self-reported jealousy levels than monogamous counterparts in some surveys, though jealousy remains a common challenge and predictor of relational strain. Critics highlight that self-reports may understate emotional costs, as dissatisfaction could prompt reversion to monogamy, inflating observed satisfaction among persisting CNM adherents. CNM is associated with elevated sexually transmitted infection (STI) risks due to higher lifetime partner counts and potential inconsistencies in condom use or disclosure. A 2015 study found CNM individuals reported more STIs and sex partners than monogamous ones, despite similar recent condom practices, underscoring transmission risks even with precautions. Non-monogamy independently predicts STI acquisition and spread, as partners' external involvements amplify exposure chains. While CNM protocols emphasize testing and barriers, empirical data show incomplete adherence, contributing to public health concerns. Overall, CNM outcomes appear comparable in self-assessed quality to monogamy among adherents, but methodological constraints and health risks warrant caution in generalizing viability.

Methodological Critiques of Non-Monogamy Research

Research on consensual non-monogamy (CNM) frequently employs convenience sampling from online communities and advocacy groups, introducing self-selection bias as participants who volunteer are often those with more positive experiences or ideological alignment with CNM, skewing results toward favorable self-reports of relationship satisfaction and well-being. This recruitment method overrepresents demographically similar individuals—typically White, middle-class, urban, and sexually liberal—limiting generalizability to broader populations and confounding comparisons with monogamous groups that differ in traits like openness to experience. Most studies are cross-sectional, capturing snapshots of current subjective experiences via self-reports rather than tracking outcomes over time, which prevents assessment of long-term stability, dissolution rates, or causal effects such as whether CNM causes dissatisfaction or vice versa. Longitudinal research remains scarce; for instance, few investigations extend beyond six months, and those that do often lack robust controls for baseline differences or external stressors. Small sample sizes exacerbate these issues, with many analyses drawing from nonprobability samples of under 200 participants, reducing statistical power and increasing vulnerability to outliers or unmeasured confounders like socioeconomic status. Measurement challenges further undermine reliability, as studies often use unvalidated or single-item scales for key variables like jealousy, commitment, or sexual health risks, while conflating CNM with nonconsensual non-monogamy in broader surveys, which obscures distinct patterns in infidelity versus agreed-upon multiplicity. Self-report data is prone to social desirability effects, particularly in stigmatized practices, where CNM participants may underreport conflicts or overemphasize autonomy to align with prevailing narratives in the literature. Researcher affiliations with pro-CNM organizations can introduce additional bias, as seen in studies where authors serve on boards of sexual freedom coalitions, potentially influencing participant selection or interpretation of equivocal findings on psychological adjustment. These methodological shortcomings collectively weaken claims of CNM's equivalence or superiority to monogamy, highlighting the need for probability-based, diverse, and prospectively designed studies to isolate true relational dynamics.

References

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