Mate choice in humans

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In humans, males and females differ in their strategies to acquire mates and focus on certain qualities. There are two main categories of strategies that both sexes utilize: short-term and long-term. Human mate choice, an aspect of sexual selection in humans, depends on a variety of factors, such as ecology, demography, access to resources, rank/social standing, genes, and parasite stress.

Contents

While there are a few common mating systems seen among humans, the amount of variation in mating strategies is relatively large. This is due to how humans evolved in diverse niches that were geographically and ecologically expansive. This diversity, as well as cultural practices and human consciousness, have all led to a large amount of variation in mating systems. Below are some of the overarching trends of mate choice.

Female mate choice

Although human males and females are both selective in deciding with whom to mate, females exhibit more mate choice selectivity than males, as is seen in nature. Relative to most other animals however, female and male mating strategies are found to be more similar to each other. According to Bateman's principle of Lifespan Reproductive Success (LRS), human females display the least variance of the two sexes in their LRS due to their high obligatory parental investment, that is a nine-month gestational period, as well as lactation following birth in order to feed offspring so that their brain can grow to the required size. [1]

Human female sexual selection can be examined by looking at ways in which males and females are sexually dimorphic, especially in traits that serve little other evolutionary purpose. For example, male traits such as the presence of beards, overall lower voice pitch, and average greater height are thought to be sexually selected traits as they confer benefits to either the women selecting for them, or to their offspring. Experimentally, women have reported a preference for men with beards and lower voices. [2] [3] [4]

Female mate choice hinges on many different coinciding male traits, and the trade-off between many of these traits must be assessed. The ultimate traits most salient to female human mate choice, however, are parental investment, resource provision and the provision of good genes to offspring. Many phenotypic traits are thought to be selected for as they act as an indication of one of these three major traits. The relative importance of these traits when considering mate selection differ depending on the type of mating arrangement females engage in. Human women typically employ long-term mating strategies when choosing a mate, however they also engage in short-term mating arrangements, so their mate choice preferences change depending on the function of the type of arrangement. [5]

Mating strategies

Female short-term

David Buss outlines several hypotheses as to the function of women's short-term mate choices:

Female long-term

The provision of economic resources, or the potential to acquire many economic resources, is the most obvious cue towards the ability of a man to provide resources, and women in the United States have been shown experimentally to rate the importance of their partner's financial status more highly than men. [5] However, many other traits exist that may act as cues towards a man's ability to provide resources that have been sexually selected for in women's evolutionary history. These include older age—older males have had more time to accrue resources—industriousness, dependability and stability—if a woman's long-term partner is not emotionally stable or is not dependable then their provision of resources to her and her offspring are likely to be inconsistent. Additionally, the costs associated with an emotionally unstable partner such as jealousy and manipulation may outweigh the benefits associated with the resources they are able to provide. [5]

Women's mate choices will also be constrained by the context in which they are making them, resulting in conditional mate choices. [1] Some of the conditions that may influence female mate choice include the woman's own perceived attractiveness, the woman's personal resources, mate copying and parasite stress. [5] Romantic love is the mechanism through which long-term mate choice occurs in human females. [6]

Male short-term

When finding a short-term mate, males highly value women with sexual experience and physical attractiveness. [7] Men seeking short-term sexual relationships are likely to avoid women who are interested in commitment or require investment. In short-term sexual relationships, men are less choosy because of low parental investment.

Examples of short-term mating strategies in males:

Male long-term

Humans have the ability to rely on biological signals of reproductive success and non-biological signals, such as the female's willingness to marry. [8] Unlike many animals, humans are not able to consciously display physical changes to their body when they are ready to mate, so they have to rely on other forms of communication before engaging in a consensual relationship. Romantic love is the mechanism through which long-term mate choice occurs in human males. [6] For long-term sexual relationships, men are usually equally choosy because they have a similar parental investment like the women, as they heavily invest in the offspring in form of resource provisioning.

Males may look for:

Parasite stress on mate choice

The parasite-stress theory, otherwise known as pathogen stress, states that parasites or diseases put stress on the life development of an organism, leading to a change in the appearance of their sexually attractive traits. The initial research on the Hamilton–Zuk hypothesis [14] (see indicator traits) showed that, within one species (brightly colored birds), there was greater sexual selection for males that had brighter plumage (feathers). In addition, Hamilton and Zuk showed that, comparing across multiple species, there is greater selection for physical attributes in species under greater parasitic stress. This has influenced research regarding human mate choice.

In societies with a high prevalence of parasites or pathogens, members would derive greater evolutionary advantage from selecting for physical attractiveness/good looks in mate choice compared to that derived by members of societies with lower prevalence. Humans could use physical attractiveness to determine resistance to parasites and diseases, which are believed to lower their sufferers' ability to portray attractive traits from then on and limit the number of high-quality pathogen-resistant mates. [15] In cultures where parasitic infection is especially high, members could use cues available to them to determine the physical health status of the potential mate. [16] Regardless of the wealth or ideology, the females in areas that are more at risk or have higher rates of parasites and diseases would weigh masculinity more highly when rating potential mates.

Criticisms

Gangested and Buss (2009) say that research indicates that parasite stress may have only influenced mate choice through females searching for "good genes" which show parasite resistance, in areas which have high prevalence of parasites. [25] John Cartwright also points out that females may be simply avoiding the transmission of parasites to themselves rather than it being them choosing males with good genes and that females look for more than just parasite-resistant genes. [16]

MHC-correlated mate choice

Major histocompatibility complex (MHC) or, in humans, human leukocyte antigen (HLA) produces proteins that are essential for immune system functioning. The genes of the MHC complex have extremely high variability, assumed to be a result of frequency-dependent parasite-driven selection and mate choice. This is believed to be so it promotes heterozygosity improving the chances of survival for the offspring.

Odor preferences

In humans, there is evidence that women will rate men's odor as more pleasant if the odor has MHC-dissimilar antigens, which is proposed as a way of avoiding inbreeding and increasing heterozygosity. [26] [27] However, women on contraceptive pills rate the odor of MHC-similar men as being more pleasant, it is unknown why women on contraceptive pills rate smell in this way. It was found that when processing MHC-similar smells were processed faster. [28] Contrary to these findings, other studies have found that there is no correlation between attraction and odor by testing males' odor preferences on women's odors. The study concludes that there is no correlation in attraction between men and women of dissimilar HLA proteins. [29] Research completed on a Southern Brazilian student population resulted in similar findings that found significant differences in the attraction ratings of giving to male sweat and MHC-difference. [30]

Facial preferences

Human facial preferences have been shown to correlate with both MHC-similarity and MHC-heterozygosity. [31] Research into MHC-similarity with regards to facial attractiveness is limited. One study found that women may prefer mates with MHC-similar faces, despite evidence that they prefer men with dissimilar body odors. [26] While facial asymmetry hasn't been correlated with MHC-heterozygosity, the perceived healthiness of skin appears to be. [32] It appears to be that only MHC-heterozygosity and no other genetic markers are correlated with facial attractiveness in males [33] and it has been shown that so far that there is no correlation that has been found in females. [34] [35] Slightly different from facial attractiveness, facial masculinity is not shown to correlate with MHC heterogeneity (a common measure of immunocompetence). [36]

Criticisms

A review article published in June 2018 concluded that there is no correlation between HLA and mate choice. [37] In addition to assessing previous studies on HLA-Mate choice analysis to identify errors in their research methods (such as small population sizes), the study collects a larger set of data and re-runs the analysis of the previous studies. By using the larger data set to conduct analysis on 30 couples of European descent, they generate findings contrary to previous studies that identified significant divergence in the mate choice with accordance to HLA genotyping. Additional studies have been conducted simultaneously on African and European populations that only show correlation of MHC divergence in European but not African populations. [38]

See also

Related Research Articles

<span class="mw-page-title-main">Sexual attraction</span> Attraction on the basis of sexual desire

Sexual attraction is attraction on the basis of sexual desire or the quality of arousing such interest. Sexual attractiveness or sex appeal is an individual's ability to attract other people sexually, and is a factor in sexual selection or mate choice. The attraction can be to the physical or other qualities or traits of a person, or to such qualities in the context where they appear. The attraction may be to a person's aesthetics, movements, voice, among other things. The attraction may be enhanced by a person's body odor, sex pheromones, adornments, clothing, perfume or hair style. It can be influenced by individual genetic, psychological, or cultural factors, or to other, more amorphous qualities. Sexual attraction is also a response to another person that depends on a combination of the person possessing the traits and on the criteria of the person who is attracted.

Disassortative mating is a mating pattern in which individuals with dissimilar phenotypes mate with one another more frequently than would be expected under random mating. Disassortative mating reduces the mean genetic similarities within the population and produces a greater number of heterozygotes. The pattern is character specific, but does not affect allele frequencies. This nonrandom mating pattern will result in deviation from the Hardy-Weinberg principle.

Sociosexuality, sometimes called sociosexual orientation, is the individual difference in the willingness to engage in sexual activity outside of a committed relationship. Individuals who are more restricted sociosexually are less willing to engage in casual sex; they prefer greater love, commitment and emotional closeness before having sex with romantic partners. Individuals who are more unrestricted sociosexually are more willing to have casual sex and are more comfortable engaging in sex without love, commitment or closeness.

<span class="mw-page-title-main">Physical attractiveness</span> Aesthetic assessment of physical traits

Physical attractiveness is the degree to which a person's physical features are considered aesthetically pleasing or beautiful. The term often implies sexual attractiveness or desirability, but can also be distinct from either. There are many factors which influence one person's attraction to another, with physical aspects being one of them. Physical attraction itself includes universal perceptions common to all human cultures such as facial symmetry, sociocultural dependent attributes, and personal preferences unique to a particular individual.

Assortative mating is a mating pattern and a form of sexual selection in which individuals with similar phenotypes or genotypes mate with one another more frequently than would be expected under a random mating pattern.

<span class="mw-page-title-main">David Buss</span> American evolutionary psychologist (born 1953)

David Michael Buss is an American evolutionary psychologist at the University of Texas at Austin, researching human sex differences in mate selection. He is considered one of the founders of evolutionary psychology.

<span class="mw-page-title-main">Psychological adaptation</span> Psychological theory

A psychological adaptation is a functional, cognitive or behavioral trait that benefits an organism in its environment. Psychological adaptations fall under the scope of evolved psychological mechanisms (EPMs), however, EPMs refer to a less restricted set. Psychological adaptations include only the functional traits that increase the fitness of an organism, while EPMs refer to any psychological mechanism that developed through the processes of evolution. These additional EPMs are the by-product traits of a species’ evolutionary development, as well as the vestigial traits that no longer benefit the species’ fitness. It can be difficult to tell whether a trait is vestigial or not, so some literature is more lenient and refers to vestigial traits as adaptations, even though they may no longer have adaptive functionality. For example, xenophobic attitudes and behaviors, some have claimed, appear to have certain EPM influences relating to disease aversion, however, in many environments these behaviors will have a detrimental effect on a person's fitness. The principles of psychological adaptation rely on Darwin's theory of evolution and are important to the fields of evolutionary psychology, biology, and cognitive science.

<span class="mw-page-title-main">Mate choice</span> Mechanism for evolution

Mate choice is one of the primary mechanisms under which evolution can occur. It is characterized by a "selective response by animals to particular stimuli" which can be observed as behavior. In other words, before an animal engages with a potential mate, they first evaluate various aspects of that mate which are indicative of quality—such as the resources or phenotypes they have—and evaluate whether or not those particular trait(s) are somehow beneficial to them. The evaluation will then incur a response of some sort.

Claus Wedekind is a Swiss biological researcher notable for his 1995 study that determined a major histocompatibility complex (MHC) dependent mate preference in humans.

<span class="mw-page-title-main">Sexual selection in humans</span> Evolutionary effects of sexual selection on humans

Sexual selection in humans concerns the concept of sexual selection, introduced by Charles Darwin as an element of his theory of natural selection, as it affects humans. Sexual selection is a biological way one sex chooses a mate for the best reproductive success. Most compete with others of the same sex for the best mate to contribute their genome for future generations. This has shaped human evolution for many years, but reasons why humans choose their mates are not fully understood. Sexual selection is quite different in non-human animals than humans as they feel more of the evolutionary pressures to reproduce and can easily reject a mate. The role of sexual selection in human evolution has not been firmly established although neoteny has been cited as being caused by human sexual selection. It has been suggested that sexual selection played a part in the evolution of the anatomically modern human brain, i.e. the structures responsible for social intelligence underwent positive selection as a sexual ornamentation to be used in courtship rather than for survival itself, and that it has developed in ways outlined by Ronald Fisher in the Fisherian runaway model. Fisher also stated that the development of sexual selection was "more favourable" in humans.

In sexual relationships between men and women, concepts of age disparity, including what defines an age disparity, have developed over time and vary among societies. Differences in age preferences for mates can stem from partner availability, gender roles, and evolutionary mating strategies, and age preferences in sexual partners may vary cross-culturally. There are also social theories for age differences in relationships as well as suggested reasons for 'alternative' age-hypogamous relationships. Age-disparate relationships have been documented for most of recorded history and have been regarded with a wide range of attitudes dependent on sociocultural norms and legal systems.

Genetic matchmaking is the idea of matching couples for romantic relationships based on their biological compatibility. The initial idea was conceptualized by Claus Wedekind through his "sweaty t-shirt" experiment. Males were asked to wear T-shirts for two consecutive nights, and then females were asked to smell the T-shirts and rate the body odors for attractiveness. Human body odor has been associated with the human leukocyte antigens (HLA) genomic region. They discovered that females were attracted to men who had dissimilar HLA alleles from them. Furthermore, these females reported that the body odors of HLA-dissimilar males reminded them of their current partners or ex-partners providing further evidence of biological compatibility.

Odour is sensory stimulation of the olfactory membrane of the nose by a group of molecules. Certain body odours are connected to human sexual attraction. Humans can make use of body odour subconsciously to identify whether a potential mate will pass on favourable traits to their offspring. Body odour may provide significant cues about the genetic quality, health and reproductive success of a potential mate.

<span class="mw-page-title-main">Major histocompatibility complex and sexual selection</span> Adaptive immune gene selection

Major histocompatibility complex (MHC) genes code for cell surface proteins that facilitate an organism's immune response to pathogens as well as its ability to avoid attacking its own cells. These genes have maintained an unusually high level of allelic diversity throughout time and throughout different populations. This means that for each MHC gene, many alleles consistently exist within the population, and many individuals are heterozygous at MHC loci.

Mate preferences in humans refers to why one human chooses or chooses not to mate with another human and their reasoning why. Men and women have been observed having different criteria as what makes a good or ideal mate. A potential mate's socioeconomic status has also been seen important, especially in developing areas where social status is more emphasized.

<span class="mw-page-title-main">Human mating strategies</span> Courtship behavior of humans

In evolutionary psychology and behavioral ecology, human mating strategies are a set of behaviors used by individuals to select, attract, and retain mates. Mating strategies overlap with reproductive strategies, which encompass a broader set of behaviors involving the timing of reproduction and the trade-off between quantity and quality of offspring.

Strategic pluralism is a theory in evolutionary psychology regarding human mating strategies that suggests women have evolved to evaluate men in two categories: whether they are reliable long term providers, and whether they contain high quality genes. The theory of strategic pluralism was proposed by Steven Gangestad and Jeffry Simpson, two professors of psychology at the University of New Mexico and Texas A&M University, respectively.

Mate value is derived from Charles Darwin's theory of evolution and sexual selection, as well as the social exchange theory of relationships. Mate value is defined as the sum of traits that are perceived as desirable, representing genetic quality and/or fitness, an indication of a potential mate's reproductive success. Based on mate desirability and mate preference, mate value underpins mate selection and the formation of romantic relationships.

<span class="mw-page-title-main">Parasite-stress theory</span> Theory of human evolution

Parasite-stress theory, or pathogen-stress theory, is a theory of human evolution proposing that parasites and diseases encountered by a species shape the development of species' values and qualities, proposed by researchers Corey Fincher and Randy Thornhill.

The ovulatory shift hypothesis holds that women experience evolutionarily adaptive changes in subconscious thoughts and behaviors related to mating during different parts of the ovulatory cycle. It suggests that what women want, in terms of men, changes throughout the menstrual cycle. Two meta-analyses published in 2014 reached opposing conclusions on whether the existing evidence was robust enough to support the prediction that women's mate preferences change across the cycle. A newer 2018 review does not show women changing the type of men they desire at different times in their fertility cycle.

References

  1. 1 2 Barrett, Louise; Dunbar, Robin; Lycett, John (2002). Human Evolutionary Psychology. Hampshire: Palgrave. ISBN   978-0-333-72558-0.[ page needed ]
  2. Collins, Sarah A. (2000). "Men's voices and women's choices". Animal Behaviour. 60 (6): 773–780. doi:10.1006/anbe.2000.1523. PMID   11124875. S2CID   15165482.
  3. Barber, Nigel (1995). "The evolutionary psychology of physical attractiveness: Sexual selection and human morphology". Ethology and Sociobiology. 16 (5): 395–424. doi:10.1016/0162-3095(95)00068-2.
  4. Buss, David M.; Shackelford, Todd K. (2008). "Attractive Women Want it All: Good Genes, Economic Investment, Parenting Proclivities, and Emotional Commitment". Evolutionary Psychology . 6 (1). doi: 10.1177/147470490800600116 .
  5. 1 2 3 4 5 6 7 8 Buss, David (2016). Evolutionary Psychology, The New Science of Mind. New York: Routledge. pp. 103–104. ISBN   978-0-205-99212-6.
  6. 1 2 Bode, Adam; Kushnick, Geoff (2021). "Proximate and Ultimate Perspectives on Romantic Love". Frontiers in Psychology. 12: 573123. doi: 10.3389/fpsyg.2021.573123 . ISSN   1664-1078. PMC   8074860 . PMID   33912094.
  7. 1 2 3 4 5 Buss, David (2016). Evolutionary Psychology, The New Science of Mind. New York: Routledge. pp. 163–176. ISBN   978-0-205-99212-6.
  8. 1 2 3 4 5 6 7 Buss, David (2016). Evolutionary Psychology, The New Science of Mind. New York: Routledge. pp. 133–162. ISBN   978-0-205-99212-6.
  9. Rowland, Hannah; Burriss, Robert (2017). "Human color in mate choice and competition". Philosophical Transactions of the Royal Society B: Biological Sciences. 372 (1724): 20160350. doi:10.1098/rstb.2016.0350. PMC   5444069 . PMID   28533465. The luminance of the eyebrows, eyes and mouth is lower than that of the surrounding skin in younger women [55], and decreasing the luminance of the features and increasing that of overall facial skin makes female faces more attractive and male faces less attractive [56]. Female faces exhibit greater facial contrast at the eyes and mouth than do male faces, to the extent that varying the contrast of an androgynous face while keeping the shape of the face constant can induce the viewer to perceive the face as male or female [57].
  10. Russell, Richard (1 January 2009). "A Sex Difference in Facial Contrast and its Exaggeration by Cosmetics". Perception. 38 (8). SAGE Publications: 1211–1219. doi:10.1068/p6331. ISSN   0301-0066. PMID   19817153. S2CID   136762. P.1213: "Female faces had greater facial contrast than male faces in both the East Asian and the Caucasian samples, and the East Asian faces (with dark eyes) had greater facial contrast than the Caucasian faces (with lighter eyes). A 2 (sex) 62 (race) analysis of variance (ANOVA) of facial contrast found significant main effects of sex and race.
  11. 1 2 Dixson, Barnaby J.; Grimshaw, Gina M.; Linklater, Wayne L.; Dixson, Alan F. (19 February 2010). "Eye Tracking of Men's Preferences for Female Breast Size and Areola Pigmentation". Archives of Sexual Behavior. 40 (1). Springer Science and Business Media LLC: 51–58. doi:10.1007/s10508-010-9601-8. ISSN   0004-0002. PMID   20169468.
  12. Antfolk, Jan (2017). "Age Limits: Men's and Women's Youngest and Oldest Considered and Actual Sex Partners". Evolutionary Psychology. 15 (1): 147470491769040. doi: 10.1177/1474704917690401 . PMC   10367477 . PMID   28127998.
  13. Antfolk, Jan; Salo, Benny; Alanko, Katarina; Bergen, Emilia; Corander, Jukka; Sandnabba, N. Kenneth; Santtila, Pekka (2015). "Women's and men's sexual preferences and activities with respect to the partner's age: Evidence for female choice". Evolution and Human Behavior. 36 (1): 73–79. Bibcode:2015EHumB..36...73A. doi:10.1016/j.evolhumbehav.2014.09.003.
  14. Hamilton, William; Zuk, Marlene (1982). "Heritable True Fitness and Bright Birds: A Role for Parasites?". Science. 218 (4570): 384–387. Bibcode:1982Sci...218..384H. doi:10.1126/science.7123238. JSTOR   1688879. PMID   7123238.
  15. Fincher, Corey; Thornhill, Randy; Murray, Damian; Schaller, Mark (7 June 2018). "Pathogen prevalence predicts human cross-cultural variability in individualism/collectivism". Proceedings of the Royal Society B: Biological Sciences. 275 (1640): 1279–1285. doi:10.1098/rspb.2008.0094. PMC   2602680 . PMID   18302996.
  16. 1 2 Cartwright, John (2000). Evolution and human behavior: Darwinian perspectives on human nature. Basingstoke: Macmillan. pp. 146–147. ISBN   978-0-333-71457-7.
  17. Ludvico, L.R.; Kurland, J.A. (1995). "Symbolic or not-so symbolic wounds: The behavioral ecology of human scarification". Ethology and Sociobiology. 16 (2): 155–172. doi:10.1016/0162-3095(94)00075-i.
  18. Singh, Devendra; Mathew, Bronstad (1997). "Sex differences in the anatomical locations of human body scarification and tattooing as a function of pathogen prevalence". Evolution and Human Behavior. 18 (6): 403–416. Bibcode:1997EHumB..18..403S. doi: 10.1016/S1090-5138(97)00089-5 .
  19. DeBruine, Lisa M.; Jones, Benedict C.; Crawford, John R.; Welling, Lisa L. M.; Little, Anthony C. (2010). "The health of a nation predicts their mate preferences: cross-cultural variation in women's preferences for masculinized male faces". Proceedings of the Royal Society B: Biological Sciences. 277 (1692): 2405–2410. doi:10.1098/rspb.2009.2184. PMC   2894896 . PMID   20236978.
  20. Jones, Benedict C.; Feinberg, David R.; Watkins, Christopher D.; Fincher, Corey L.; Little, Anthony C.; DeBruine, Lisa M. (2012). "Pathogen disgust predicts women's preferences for masculinity in men's voices, faces, and bodies". Behavioral Ecology. 24 (2): 373–379. doi: 10.1093/beheco/ars173 .
  21. Thornhill, R; Gangestad, S. W.; Scheib, J. E. (1999). "Facial attractiveness, symmetry and cues of good genes". Proceedings of the Royal Society B: Biological Sciences. 266 (1431): 1913–1917. doi:10.1098/rspb.1999.0866. PMC   1690211 . PMID   10535106.
  22. DeBruine, Lisa M.; Little, Anthony C.; Jones, Benedict C. (2012). "Extending parasite-stress theory to variation in human mate preferences". Behavioral and Brain Sciences. 35 (2): 86–87. doi:10.1017/s0140525x11000987. hdl: 1893/17923 . PMID   22289354. S2CID   7420555.
  23. White, D. R.; Burton, M. L. (1988). "Causes of polygyny: Ecology, economy, kinship, and warfare". American Anthropologist. 90 (4): 871–887. doi:10.1525/aa.1988.90.4.02a00060. S2CID   5158340.
  24. Low, Bobbi S. (1990). "Marriage Systems and Pathogen Stress in Human Societies". American Zoologist. 30 (2): 325–339. doi: 10.1093/icb/30.2.325 .
  25. Gangestad, Steven W.; Buss, David M. (1993). "Pathogen prevalence and human mate preferences". Ethology and Sociobiology. 14 (2): 89–96. CiteSeerX   10.1.1.496.1320 . doi:10.1016/0162-3095(93)90009-7.
  26. 1 2 Roberts, S. C.; Little, A. C.; Gosling, L. M.; Jones, B. C.; Perrett, D. I.; Carter, V.; Petrie, M (2005). "MHC-assortative facial preferences in humans". Biology Letters. 1 (4): 400–403. doi:10.1098/rsbl.2005.0343. PMC   1626373 . PMID   17148217.
  27. Wedekind, C.; Fu¨ri, S. (1997). "Body odour preferences in men and women: do they aim for specific MHC combinations or simply heterozygosity?". Proceedings of the Royal Society B: Biological Sciences. 264 (1387): 1471–1479. doi:10.1098/rspb.1997.0204. PMC   1688704 . PMID   9364787.
  28. Pause, B. M.; Krauel, K.; Schraders, C.; Sojka, B.; Westphal, E.; Muller-Ruchholtz, W.; Ferstl, R. (2005). "The human brain is a detector of chemosensorily transmitted HLA-class I-similarity in same- and opposite-sex relations". Proceedings of the Royal Society B: Biological Sciences. 273 (1585): 471–478. doi:10.1098/rspb.2005.3342. PMC   1560206 . PMID   16615215.
  29. Probst, F., Fischbacher, U., Lobmaier, J. S., Wirthmüller, U., & Knoch, D. (2017). Men's preferences for women's body odours are not associated with human leucocyte antigen. Proceedings. Biological sciences, 284(1864), 20171830.
  30. Santos, Pablo; Schinemann, Juliano; Gabardo, Juarez; Bicalho, Maria (2005). "New evidence that the MHC influences odor perception in humans: a study with 58 Southern Brazilian students". Hormones and Behavior. 47 (4): 384–388. doi:10.1016/j.yhbeh.2004.11.005. PMID   15777804. S2CID   8568275.
  31. Havlicek, Jan; Roberts, S. Craig (2009). "MHC-correlated mate choice in humans: A review". Psychoneuroendocrinology. 34 (4): 497–512. doi:10.1016/j.psyneuen.2008.10.007. PMID   19054623. S2CID   40332494.
  32. Roberts, S. C.; Little, A. C.; Gosling, L. M.; Perrett, D. I.; Carter, V.; Jones, B. C.; Penton-Voak, I. S.; Petrie, M. (2005). "MHC-heterozygosity and human facial attractiveness". Evolution and Human Behavior. 26 (3): 213–226. Bibcode:2005EHumB..26..213R. doi:10.1016/j.evolhumbehav.2004.09.002.
  33. Lie, H.; Simmons, L.; Rhodes, G. (2008). "Genetic diversity revealed in human faces". Evolution. 62 (10): 2473–2486. doi:10.1111/j.1558-5646.2008.00478.x. PMID   18691260. S2CID   20020857.
  34. Thornhill, R.; Gangestad, S. W.; Miller, R.; Scheyd, G.; McCollough, J. K.; Franklin, M. (2003). "Major histocompatibility complex genes, symmetry, and body scent attractiveness in men and women". Behavioral Ecology. 14 (5): 668–678. doi: 10.1093/beheco/arg043 .
  35. Coetzee, V.; Barrett, L.; Greeff, J. M.; Henzi, S. P.; Perrett, D. I.; Wadee, A. A. (2007). "Common HLA alleles associated with health, but not with facial attractiveness". PLOS ONE. 2 (7): e640. Bibcode:2007PLoSO...2..640C. doi: 10.1371/journal.pone.0000640 . PMC   1919430 . PMID   17653267.
  36. Zaidi, Arslan; White, Julie; Mattern, Brooke; Liebowitz, Corey; Puts, David; Claes, Peter; Shriver, Mark (2018). "Facial masculinity does not appear to be a condition-dependent male ornament in humans and does not reflect MHC heterozygosity" (PDF). doi: 10.1101/322255 .{{cite journal}}: Cite journal requires |journal= (help)
  37. Stancu, Mircea; Kloosterman, Wigard; Pulit, Sara (2018). "No evidence that mate choice in humans is dependent on the MHC" (PDF). doi: 10.1101/339028 .{{cite journal}}: Cite journal requires |journal= (help)
  38. Chaix, Raphaelle; Cao, Chen; Donnelley, Peter (2008). "Is Mate Choice in Humans MHC-Dependent?". PLOS Genetics. 4 (9): e1000184. doi: 10.1371/journal.pgen.1000184 . PMC   2519788 . PMID   18787687.