Sexual selection is a mode of natural selection in which members of one biological sex choose mates of the other sex to mate with (intersexual selection), and compete with members of the same sex for access to members of the opposite sex (intrasexual selection). These two forms of selection mean that some individuals have greater reproductive success than others within a population, for example because they are more attractive or prefer more attractive partners to produce offspring. In general, males benefit from frequent mating and monopolizing access to a group of fertile females. Females can have a limited number of offspring and maximize the return on the energy they invest in reproduction.
The concept was first articulated by Charles Darwin who wrote of a "second agency" of selection, in which competition between mate candidates could lead to speciation. The theory was given a mathematical basis by Ronald Fisher in the early 20th century. Sexual selection can lead males to extreme efforts to demonstrate their fitness to be chosen by females, producing sexual dimorphism in secondary sexual characteristics, such as the ornate plumage of birds such as birds of paradise and peafowl, or the antlers of deer, or the manes of lions, caused by a positive feedback mechanism known as a Fisherian runaway, where the passing-on of the desire for a trait in one sex is as important as having the trait in the other sex in producing the runaway effect. Although the sexy son hypothesis indicates that females would prefer male offspring, Fisher's principle explains why the sex ratio is most often 1:1. Sexual selection is also found in plants and fungi.
Sexual selection was first proposed by Charles Darwin in The Origin of Species (1859) and developed in The Descent of Man and Selection in Relation to Sex (1871), as he felt that natural selection alone was unable to account for certain types of non-survival adaptations. He once wrote to a colleague that "The sight of a feather in a peacock's tail, whenever I gaze at it, makes me sick!" His work divided sexual selection into male-male competition and female choice.
... depends, not on a struggle for existence, but on a struggle between the males for possession of the females; the result is not death to the unsuccessful competitor, but few or no offspring.
... when the males and females of any animal have the same general habits ... but differ in structure, colour, or ornament, such differences have been mainly caused by sexual selection.
These views were to some extent opposed by Alfred Russel Wallace, mostly after Darwin's death. He accepted that sexual selection could occur, but argued that it was a relatively weak form of selection. He argued that male-male competitions were forms of natural selection, but that the "drab" peahen's coloration is itself adaptive as camouflage. In his opinion, ascribing mate choice to females was attributing the ability to judge standards of beauty to animals (such as beetles) far too cognitively undeveloped to be capable of aesthetic feeling.
Ronald Fisher, the English statistician and evolutionary biologist developed a number of ideas about sexual selection in his 1930 book The Genetical Theory of Natural Selection including the sexy son hypothesis and Fisher's principle. The Fisherian runaway describes how sexual selection accelerates the preference for a specific ornament, causing the preferred trait and female preference for it to increase together in a positive feedback runaway cycle. In a remark that was not widely understood for another 50 years he said:
... plumage development in the male, and sexual preference for such developments in the female, must thus advance together, and so long as the process is unchecked by severe counterselection, will advance with ever-increasing speed. In the total absence of such checks, it is easy to see that the speed of development will be proportional to the development already attained, which will therefore increase with time exponentially, or in geometric progression. —Ronald Fisher, 1930
This causes a dramatic increase in both the male's conspicuous feature and in female preference for it, resulting in marked sexual dimorphism, until practical physical constraints halt further exaggeration. A positive feedback loop is created, producing extravagant physical structures in the non-limiting sex. A classic example of female choice and potential runaway selection is the long-tailed widowbird. While males have long tails that are selected for by female choice, female tastes in tail length are still more extreme with females being attracted to tails longer than those that naturally occur. Fisher understood that female preference for long tails may be passed on genetically, in conjunction with genes for the long tail itself. Long-tailed widowbird offspring of both sexes inherit both sets of genes, with females expressing their genetic preference for long tails, and males showing off the coveted long tail itself.
Richard Dawkins presents a non-mathematical explanation of the runaway sexual selection process in his book The Blind Watchmaker. Females that prefer long tailed males tend to have mothers that chose long-tailed fathers. As a result, they carry both sets of genes in their bodies. That is, genes for long tails and for preferring long tails become linked. The taste for long tails and tail length itself may therefore become correlated, tending to increase together. The more tails lengthen, the more long tails are desired. Any slight initial imbalance between taste and tails may set off an explosion in tail lengths. Fisher wrote that:
The exponential element, which is the kernel of the thing, arises from the rate of change in hen taste being proportional to the absolute average degree of taste. —Ronald Fisher, 1932
The female widowbird chooses to mate with the most attractive long-tailed male so that her progeny, if male, will themselves be attractive to females of the next generation—thereby fathering many offspring that carry the female's genes. Since the rate of change in preference is proportional to the average taste amongst females, and as females desire to secure the services of the most sexually attractive males, an additive effect is created that, if unchecked, can yield exponential increases in a given taste and in the corresponding desired sexual attribute.
It is important to notice that the conditions of relative stability brought about by these or other means, will be far longer duration than the process in which the ornaments are evolved. In most existing species the runaway process must have been already checked, and we should expect that the more extraordinary developments of sexual plumage are not due like most characters to a long and even course of evolutionary progress, but to sudden spurts of change. —Ronald Fisher, 1930
Since Fisher's initial conceptual model of the 'runaway' process, Russell Lande and Peter O'Donald have provided detailed mathematical proofs that define the circumstances under which runaway sexual selection can take place. Alongside this, biologists have extended Darwin's formulation; Malte Andersson's widely-accepted 1994 definition is that "sexual selection is the differences in reproduction that arise from variation among individuals in traits that affect success in competition over mates and fertilizations". Despite some practical challenges for biologists, the concept of sexual selection is "straightforward".
Sexual preference creates a tendency towards assortative mating or homogamy. The general conditions of sexual discrimination appear to be (1) the acceptance of one mate precludes the effective acceptance of alternative mates, and (2) the rejection of an offer is followed by other offers, either certainly or at such high chance that the risk of non-occurrence is smaller than the chance advantage to be gained by selecting a mate. Bateman's principle states that the sex which invests the most in producing offspring becomes a limiting resource for which the other sex competes, illustrated by the greater nutritional investment of an egg in a zygote, and the limited capacity of females to reproduce; for example, in humans, a woman can only give birth every ten months, whereas a male can become a father numerous times in the same period. More recently, researchers have doubted whether Bateman was correct.
Darwin's ideas on sexual selection were met with scepticism by his contemporaries and not considered of great importance until in the 1930s biologists decided to include sexual selection as a mode of natural selection. Only in the 21st century have they become more important in biology; the theory is now seen as generally applicable and analogous to natural selection.
The handicap principle of Amotz Zahavi, Russell Lande and W. D. Hamilton, holds that the male's survival until and through the age of reproduction with seemingly maladaptive traits is taken by the female as a signal of his overall fitness. Such handicaps might prove he is either free of or resistant to disease, or that he possesses more speed or a greater physical strength that is used to combat the troubles brought on by the exaggerated trait. Zahavi's work spurred a re-examination of the field and several new theories. In 1984, Hamilton and Marlene Zuk introduced the "Bright Male" hypothesis, suggesting that male elaborations might serve as a marker of health, by exaggerating the effects of disease and deficiency.
In 1990, Michael Ryan and A.S. Rand, working with the Túngara frog, proposed the hypothesis of "Sensory Exploitation", where exaggerated male traits may provide a sensory stimulation that females find hard to resist. In the late 1970s, Janzen and Mary Willson, noting that male flowers are often larger than female flowers, expanded the field of sexual selection into plants.
More recently, the field has grown to include other areas of study, not all of which fit Darwin's definition of sexual selection. A "bewildering" range of models variously attempt to relate sexual selection not only to the fundamental questions of anisogamy and parental roles, but also to mechanisms such as sex ratios, parental care, having sexy sons, sexual conflict, and the "most-debated effect", namely mate choice.
Elaborated characteristics that might seem costly for their bearers (e.g., the tail of the swordfish Xiphophorus montezumae) do not always have an energetics, performance or even survival cost; this may be because "compensatory traits" have evolved in concert with the sexually selected traits.
Male mountain gorilla, a tournament species
Toolkit of natural selectionEdit
Sexual selection may explain how characteristics such as feathers had survival value at an early stage in their evolution. Geoffrey Miller proposes that the feathers of proto-birds like Archaeopteryx were originally sexual ornaments. The earliest proto-birds such as Protarchaeopteryx had well-developed feathers but no sign of the top/bottom asymmetry that gives wings lift. One proposal is that the feathers served as insulation, helping females incubate their eggs. But if proto-bird courtship combined displays of forelimb feathers with energetic jumps, then the transition from display to aerodynamic functions could have been relatively smooth.
Sexual selection sometimes generates features that may help cause a species' extinction, as has been suggested for the giant antlers of the Irish elk (Megaloceros giganteus) that became extinct in Pleistocene Europe. Or it may do the opposite, driving species divergence—sometimes through elaborate changes in genitalia—such that new species emerge.
This section needs additional citations for verification. (May 2021)
Sex differences directly related to reproduction and serving no direct purpose in courtship are called primary sexual characteristics. Traits amenable to sexual selection, which give an organism an advantage over its rivals (such as in courtship) without being directly involved in reproduction, are called secondary sex characteristics.
In most sexual species the males and females have different equilibrium strategies, due to a difference in relative investment in producing offspring. As formulated in Bateman's principle, females have a greater initial investment in producing offspring (pregnancy in mammals or the production of the egg in birds and reptiles), and this difference in initial investment creates differences in variance in expected reproductive success and bootstraps the sexual selection processes. (Pipefish and Wilson's phalarope are classic examples of sex role reversal.) Also, unlike a female, a male (except in monogamous species) has some uncertainty about whether or not he is the true parent of a child, and so is less interested in spending his energy helping to raise offspring that may or may not be related to him. As a result of these factors, males can be expected to be more willing to mate than females, while females are expected to be the ones doing the choosing (except in cases of forced copulations, which has been observed in numerous species, including mammals, birds, insects and fish). The effects of sexual selection are thus often more pronounced in males than in females.
Differences in secondary sexual characteristics between males and females of a species are referred to as sexual dimorphisms. These can be as subtle as a size difference (sexual size dimorphism, often abbreviated as SSD) or as extreme as horns and colour patterns. Sexual dimorphisms abound in nature. Examples include the possession of antlers by only male deer, the brighter coloration of many male birds in comparison with females of the same species, or even more distinct differences in basic morphology, such as the drastically increased eye-span of the male stalk-eyed fly. The peacock, with its elaborate and colourful tail feathers, which the peahen lacks, is often referred to as perhaps the most extraordinary example of a dimorphism. Male and female black-throated blue warblers and Guianan cock-of-the-rocks also differ radically in their plumage. Early naturalists even believed the females to be a separate species. The largest sexual size dimorphism in vertebrates is the shell dwelling cichlid fish Neolamprologus callipterus in which males are up to 30 times the size of females. Many other fish such as guppies are sexually dimorphic. Extreme sexual size dimorphism, with females larger than males, is quite common in spiders and birds of prey.
The maintenance of sexual reproduction in a highly competitive world is one of the major puzzles in biology given that asexual reproduction can reproduce much more quickly as 50% of offspring are not males, unable to produce offspring themselves. Many non-exclusive hypotheses have been proposed, including the positive impact of an additional form of selection, sexual selection, on the probability of persistence of a species.
Male intrasexual competitionEdit
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Male-male competition occurs when two males of the same species compete for the opportunity to mate with a female. Sexually dimorphic traits, size, sex ratio, and the social situation may all play a role in the effects male-male competition has on the reproductive success of a male and the mate choice of a female. Larger males tend to win male-male conflicts due to their sheer strength and ability to ward off other males from taking over their females. For instance, in the fly Dryomyza anilis, size shows the strongest correlation to the outcome of male-male conflicts over resources like territory and females.
There are multiple types of male-male competition that may occur in a population at different times depending on the conditions. Competition variation occurs based on the frequency of various mating behaviours present in the population. One factor that can influence the type of competition observed is the population density of males. When there is a high density of males present in the population, competition tends to be less aggressive and therefore sneak tactics and disruptions techniques are more often employed. These techniques often indicate a type of competition referred to as scramble competition. In Japanese medaka, Oryzias latipes, sneaking behaviours refer to when a male interrupts a mating pair during copulation by grasping on to either the male or the female and releasing their own sperm in the hopes of being the one to fertilize the female. Disruption is a technique which involves one male bumping the male that is copulating with the female away just before his sperm is released and the eggs are fertilized.
However, all techniques are not equally successful when in competition for reproductive success. Disruption results in a shorter copulation period and can therefore disrupt the fertilization of the eggs by the sperm, which frequently results in lower rates of fertilization and smaller clutch size.
Another factor that can influence male-male competition is the value of the resource to competitors. Male-male competition can pose many risks to a male's fitness, such as high energy expenditure, physical injury, lower sperm quality and lost paternity. The risk of competition must therefore be worth the value of the resource. A male is more likely to engage in competition for a resource that improves their reproductive success if the resource value is higher. While male-male competition can occur in the presence or absence of a female, competition occurs more frequently in the presence of a female. The presence of a female directly increases the resource value of a territory or shelter and so the males are more likely to accept the risk of competition when a female is present. The smaller males of a species are also more likely to engage in competition with larger males in the presence of a female. Due to the higher level of risk for subordinate males, they tend to engage in competition less frequently than larger, more dominant males and therefore breed less frequently than dominant males. This is seen in many species, such as the Omei treefrog, Rhacophorus omeimontis, where larger males obtain more mating opportunities and mate with larger females.
A third factor that can impact the success of a male in competition is winner-loser effects. Burrowing crickets, Velarifictorus aspersus, compete for burrows to attract females using their large mandibles for fighting. Female burrowing crickets are more likely to choose winner of a competition in the 2 hours after the fight. The presence of a winning male suppresses mating behaviours of the losing males because the winning male tends to produce more frequent and enhanced mating calls in this period of time.
Effect on female fitnessEdit
Male-male competition can both positively and negatively affect female fitness. When there is a high density of males in a population and a large number of males attempting to mate with the female, she is more likely to resist mating attempts, resulting in lower fertilization rates. High levels of male-male competition can also result in a reduction in female investment in mating. Many forms of competition can also cause significant distress for the female negatively impacting her ability to reproduce. An increase in male-male competition can affect a female's ability to select the best mates, and therefore decrease the likelihood of successful reproduction.
However, group mating in Japanese medaka has been shown to positively affect the fitness of females due to an increase in genetic variation, a higher likelihood of paternal care and a higher likelihood of successful fertilization. Exposure to environmental estrogens, such as some herbicides, can confuse female choice of males.
In different taxaEdit
- In detail, see Sexual selection in birds, mammals, humans, scaled reptiles, amphibians, insects, spiders
Sexual selection has been observed to occur in plants, animals and fungi. In certain hermaphroditic snail and slug species of molluscs the throwing of love darts is a form of sexual selection. Certain male insects of the order Lepidoptera cement the vaginal pores of their females.
Today, biologists say that certain evolutionary traits can be explained by intraspecific competition—competition between members of the same species—distinguishing between competition before or after sexual intercourse.
Before copulation, intrasexual selection—usually between males—may take the form of male-to-male combat. Also, intersexual selection, or mate choice, occurs when females choose between male mates. Traits selected by male combat are called secondary sexual characteristics (including horns, antlers, etc.), which Darwin described as "weapons", while traits selected by mate (usually female) choice are called "ornaments". Due to their sometimes greatly exaggerated nature, secondary sexual characteristics can prove to be a hindrance to an animal, thereby lowering its chances of survival. For example, the large antlers of a moose are bulky and heavy and slow the creature's flight from predators; they also can become entangled in low-hanging tree branches and shrubs, and undoubtedly have led to the demise of many individuals. Bright colourations and showy ornamenations, such as those seen in many male birds, in addition to capturing the eyes of females, also attract the attention of predators. Some of these traits also represent energetically costly investments for the animals that bear them. However, one must also consider that intersexual selection can occur with an emphasis on resources that one sex possesses rather than morphological and physiological differences. For example, males of Euglossa imperialis, a non-social bee species, form aggregations of territories considered to be leks, to defend fragrant-rich primary territories. The purpose of these aggregations is only facultative, since the more suitable fragrant-rich sites there are, the more habitable territories there are to inhabit, giving females of this species a large selection of males with whom to potentially mate.
After copulation, male–male competition distinct from conventional aggression may take the form of sperm competition, as described by Parker in 1970. More recently, interest has arisen in cryptic female choice, a phenomenon of internally fertilised animals such as mammals and birds, where a female can get rid of a male's sperm without his knowledge.
Finally, sexual conflict is said to occur between breeding partners, sometimes leading to an evolutionary arms race between males and females. Sexual selection can also occur as a product of pheromone release, such as with the stingless bee, Trigona corvina.
Female mating preferences are widely recognized as being responsible for the rapid and divergent evolution of male secondary sexual traits. Females of many animal species prefer to mate with males with external ornaments—exaggerated features of morphology such as elaborate sex organs. These preferences may arise when an arbitrary female preference for some aspect of male morphology—initially, perhaps, a result of genetic drift—creates, in due course, selection for males with the appropriate ornament. One interpretation of this is known as the sexy son hypothesis. Alternatively, genes that enable males to develop impressive ornaments or fighting ability may simply show off greater disease resistance or a more efficient metabolism, features that also benefit females. This idea is known as the good genes hypothesis.
Bright colors that develop in animals during mating season function to attract partners. It has been suggested that there is a causal link between strength of display of ornaments involved in sexual selection and free radical biology. To test this idea, experiments were performed on male painted dragon lizards. Male lizards are brightly conspicuous in their breeding coloration, but their color declines with aging. Experiments involving administration of antioxidants to these males led to the conclusion that breeding coloration is a reflection of innate anti-oxidation capacity that protects against oxidative damage, including oxidative DNA damage. Thus color could act as a "health certificate" that allows females to visualize the underlying oxidative stress induced damage in potential mates.
Darwin conjectured that heritable traits such as beards and hairlessness in different human populations are results of sexual selection in humans. Geoffrey Miller has hypothesized that many human behaviours not clearly tied to survival benefits, such as humour, music, visual art, verbal creativity, and some forms of altruism, are courtship adaptations that have been favoured through sexual selection. In that view, many human artefacts could be considered subject to sexual selection as part of the extended phenotype, for instance clothing that enhances sexually selected traits. Some argue that the evolution of human intelligence is a sexually selected trait, as it would not confer enough fitness in itself relative to its high maintenance costs.
- Cecie Starr (2013). Biology: The Unity & Diversity of Life (Ralph Taggart, Christine Evers, Lisa Starr ed.). Cengage Learning. p. 281.
- Vogt, Yngve (January 29, 2014). "Large testicles are linked to infidelity". Phys.org. Archived from the original on January 31, 2014. Retrieved January 31, 2014.
- Darwin, Charles (1858). "On the Tendency of Species to form Varieties; and on the Perpetuation of Varieties and Species by Natural Means of Selection" (PDF). Journal of the Proceedings of the Linnean Society of London. Zoology. 3 (9): 46–50. doi:10.1111/j.1096-3642.1858.tb02500.x. Archived (PDF) from the original on 2012-10-22.
- Moore, Jamie C.; Pannell, John R. (2011). "Sexual selection in plants". Current Biology. 21 (5): R176–R182. doi:10.1016/j.cub.2010.12.035. PMID 21377091. S2CID 18044399.
- Nieuwenhuis, B. P. S.; Aanen, D.K. (2012). "Sexual selection in fungi". Journal of Evolutionary Biology. 25 (12): 2397–2411. doi:10.1111/jeb.12017. PMID 23163326. S2CID 5657743.
- Leonard, Janet L. (2006-08-01). "Sexual selection: lessons from hermaphrodite mating systems". Integrative and Comparative Biology. 46 (4): 349–367. doi:10.1093/icb/icj041. ISSN 1540-7063. PMID 21672747.
- Darwin, Charles (1859). On the Origin of Species (1st edition). Chapter 4, p. 88. "And this leads me to say a few words on what I call Sexual Selection. This depends ..." "Archived copy". Archived from the original on 2011-11-05. Retrieved 2011-05-22.CS1 maint: archived copy as title (link)
- Darwin, Charles (1859). On the Origin of Species (1st edition). Chapter 4, p. 89. "Archived copy". Archived from the original on 2011-11-05. Retrieved 2011-05-22.CS1 maint: archived copy as title (link)
- Wallace, Alfred Russel (1892). "Note on Sexual Selection (S459: 1892)". Charles Smith. Archived from the original on 17 February 2017. Retrieved 13 January 2017.
- Dawkins, Richard (1996). The Blind Watchmaker: Why the Evidence of Evolution Reveals a Universe Without Design. Norton. pp. Chapter 8, Explosions and Spirals. ISBN 978-0-393-31570-7.
- Andersson, M. (1994). Sexual Selection. Princeton University Press.[page needed]
- Ronald Fisher in a letter to Charles Galton Darwin, 22 November 1932, cited in Fisher, R. A., Bennett, J. H. 1999. The genetical theory of natural selection: A complete variorum edition, Oxford University Press, Oxford, p. 308
- Lande, Russell (1981). "Models of speciation by sexual selection on polygenic traits". PNAS. 78 (6): 3721–3725. Bibcode:1981PNAS...78.3721L. doi:10.1073/pnas.78.6.3721. PMC 319643. PMID 16593036.
- O'Donald, Peter (1980). Genetic Models of Sexual Selection. Cambridge University Press. ISBN 9780521225335.
- Kokko, H.; Jennions, M. D. (18 July 2014). "The Relationship between Sexual Selection and Sexual Conflict". Cold Spring Harbor Perspectives in Biology. Cold Spring Harbor Laboratory. 6 (9): a017517. doi:10.1101/cshperspect.a017517. ISSN 1943-0264. PMC 4142970. PMID 25038050.
- Orr, H. A. (August 2009). "Fitness and its role in evolutionary genetics". Nature Reviews Genetics. 10 (8): 531–9. doi:10.1038/nrg2603. PMC 2753274. PMID 19546856.
- Bateman, Angus J. (1948). "Intra-sexual selection in Drosophila". Heredity. 2 (Pt. 3): 349–368. doi:10.1038/hdy.1948.21. PMID 18103134.
- Newcomer, Scott D.; Zeh, Jeanne A.; Zeh, David W. (31 August 1999). "Genetic benefits enhance the reproductive success of polyandrous females". Proceedings of the National Academy of Sciences. 96 (18): 10236–10241. Bibcode:1999PNAS...9610236N. doi:10.1073/pnas.96.18.10236. ISSN 0027-8424. PMC 17872. PMID 10468592.
- Miller, Geoffey, The Mating Mind, p. 24
- Sexual Selection and the Mind Archived 2015-06-10 at the Wayback Machine
- Hosken, David J.; House, Clarissa M. (January 2011). "Sexual Selection". Current Biology. 21 (2): R62–R65. doi:10.1016/j.cub.2010.11.053. PMID 21256434. S2CID 18470445.
- Population benefits of sexual selection explain the existence of males phys.org May 18, 2015 Report on a study by the University of East Anglia Archived August 21, 2015, at the Wayback Machine
- Zahavi, Amotz (1975). "Mate selection—A selection for a handicap". Journal of Theoretical Biology. Elsevier BV. 53 (1): 205–214. Bibcode:1975JThBi..53..205Z. doi:10.1016/0022-5193(75)90111-3. ISSN 0022-5193. PMID 1195756.
- Zahavi, Amotz (1977). "The cost of honesty". Journal of Theoretical Biology. Elsevier BV. 67 (3): 603–605. doi:10.1016/0022-5193(77)90061-3. ISSN 0022-5193. PMID 904334.
- Zahavi, Amotz; Zahavi, Avishag (1997). The handicap principle: a missing piece of Darwin's puzzle (PDF). New York: Oxford University Press. ISBN 978-0-19-510035-8. OCLC 35360821.
- Hamilton, W. D.; Zuk, M. (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. ISSN 0036-8075. PMID 7123238.
- Ryan, Michael J.; Fox, James H.; Wilczynski, Walter; Rand, A. Stanley (1990). "Sexual selection for sensory exploitation in the frog Physalaemus pustulosus". Nature. 343 (6253): 66–67. Bibcode:1990Natur.343...66R. doi:10.1038/343066a0. ISSN 0028-0836. PMID 2296291. S2CID 4358189.
- Wilson, Mary F. (June 1979). "Sexual Selection In Plants". The American Naturalist. 113 (6): 777–790. doi:10.1086/283437. S2CID 84970789.
- Kokko, Hanna; Jennions, Michael D.; Brooks, Robert (2006). "Unifying and Testing Models of Sexual Selection" (PDF). Annual Review of Ecology, Evolution, and Systematics. 37 (1): 43–66. doi:10.1146/annurev.ecolsys.37.091305.110259. hdl:1885/22652. ISSN 1543-592X.
- Oufiero, Christopher E. (May 2015). "Sexual Selection, Costs, and Compensation". University of California Riverside. Archived from the original on 6 June 2014.
- Miller, Geoffrey (2000). The Mating Mind. Anchor Books.[page needed]
- Gould, Stephen Jay (1974). "Origin and Function of 'Bizarre' Structures – Antler Size and Skull Size in 'Irish Elk', Megaloceros giganteus". Evolution. 28 (2): 191–220. doi:10.2307/2407322. JSTOR 2407322. PMID 28563271.
- Eberhard, William G. (2009-03-24). "Evolution of genitalia: theories, evidence, and new directions" (PDF). Genetica. 138 (1): 5–18. doi:10.1007/s10709-009-9358-y. ISSN 0016-6707. PMID 19308664. S2CID 1409845.
- Hosken, David J.; Stockley, Paula. "Sexual selection and genital evolution Archived 2017-10-12 at the Wayback Machine." Trends in Ecology & Evolution 19.2 (2004): 87–93.
- Arnqvist, Göran. "Comparative evidence for the evolution of genitalia by sexual selection Archived 2012-01-27 at the Wayback Machine." Nature 393.6687 (1998): 784.
- Eberhard, William G. (1985). Sexual Selection and Animal Genitalia. Harvard University Press, Cambridge, Mass.[page needed]
- Sagebakken, Gry; Kvarnemo, Charlotta; Ahnesjö, Ingrid (22 March 2017). "Nutritional state – a survival kit for brooding pipefish fathers". Biological Journal of the Linnean Society. 121 (2): 312–318. doi:10.1093/biolinnean/blx002. ISSN 0024-4066.
- Garner, S. R., Bortoluzzi, R. N., Heath, D. D. & Neff, B. D. Sexual conflict inhibits female mate choice for major histocompatibility complex dissimilarity in Chinook salmon. Proceedings: Biological Sciences 277, 885–94 (2010).
- Ota, Kazutaka; Kohda, Masanori; Sato, Tetsu (1 May 2010). "Unusual allometry for sexual size dimorphism in a cichlid where males are extremely larger than females". Journal of Biosciences. 35 (2): 257–265. doi:10.1007/s12038-010-0030-6. ISSN 0250-5991. PMID 20689182. S2CID 12396902.
- Hartfield, Matthew; P. D. Keightley (2012). "Current hypotheses for the evolution of sex and recombinationn" (PDF). Integrative Zoology. 7 (2): 192–209. doi:10.1111/j.1749-4877.2012.00284.x. PMID 22691203. Archived (PDF) from the original on 2016-08-26.
- Weir, Laura K. (2012-11-22). "Male–male competition and alternative male mating tactics influence female behavior and fertility in Japanese medaka (Oryzias latipes)". Behavioral Ecology and Sociobiology. 67 (2): 193–203. doi:10.1007/s00265-012-1438-9. ISSN 0340-5443. S2CID 15410498.
- Proctor, D. S.; Moore, A. J.; Miller, C. W. (2012-03-09). "The form of sexual selection arising from male-male competition depends on the presence of females in the social environment". Journal of Evolutionary Biology. 25 (5): 803–812. doi:10.1111/j.1420-9101.2012.02485.x. ISSN 1010-061X. PMID 22404372. S2CID 594384.
- Otronen, Merja (1984-08-01). "Male contesis for territories and females in the fly Dryomyza Anilis". Animal Behaviour. 32 (3): 891–898. doi:10.1016/S0003-3472(84)80167-0. ISSN 0003-3472. S2CID 53188298.
- Nelson-Flower, Martha J.; Ridley, Amanda R. (2015-09-24). "Male-male competition is not costly to dominant males in a cooperatively breeding bird". Behavioral Ecology and Sociobiology. 69 (12): 1997–2004. doi:10.1007/s00265-015-2011-0. ISSN 0340-5443. S2CID 15032582.
- Luo, Zhenhua; Li, Chenliang; Wang, Hui; Shen, Hang; Zhao, Mian; Gu, Qi; Liao, Chunlin; Gu, Zhirong; Wu, Hua (2016-02-23). "Male-male competition drives sexual selection and group spawning in the Omei treefrog, Rhacophorus omeimontis". Behavioral Ecology and Sociobiology. 70 (4): 593–605. doi:10.1007/s00265-016-2078-2. ISSN 0340-5443. S2CID 13912038.
- Zeng, Yang; Zhou, Feng-Hao; Zhu, Dao-Hong (2018-06-26). "Fight outcome briefly affects the reproductive fitness of male crickets". Scientific Reports. 8 (1): 9695. Bibcode:2018NatSR...8.9695Z. doi:10.1038/s41598-018-27866-4. ISSN 2045-2322. PMC 6018733. PMID 29946077.
- Cayuela, Hugo; Lengagne, Thierry; Kaufmann, Bernard; Joly, Pierre; Léna, Jean-Paul (2016-06-24). "Larval competition risk shapes male–male competition and mating behavior in an anuran". Behavioral Ecology. 27 (6): arw100. doi:10.1093/beheco/arw100. ISSN 1045-2249.
- McCallum, M.L., M. Matlock, J. Treas, B. Safi, W. Sanson, J.L. McCallum. (2013). Endocrine disruption of sexual selection by an estrogenic herbicide in Tenebrio molitor. Ecotoxicology 22:1461-1466.
- Tales of two snails: sexual selection and sexual conflict in Lymnaea stagnalis and Helix aspersa Oxford Journals Archived 2015-09-04 at the Wayback Machine
- von Byern, Janek; Grunwald, Ingo (2011). Biological Adhesive Systems: From Nature to Technical and Medical Application. Springer Science & Business Media. p. 124. ISBN 9783709102862.
- Campbell, N. A.; J. B. Reece (2005). Biology. Benjamin Cummings. p. 1230. ISBN 978-0-8053-7146-8.
- Kimsey, Lynn Siri (1980). "The behaviour of male orchid bees (Apidae, Hymenoptera, Insecta) and the question of leks". Animal Behaviour. 28 (4): 996–1004. doi:10.1016/s0003-3472(80)80088-1. S2CID 53161684.
- Parker, Geoffrey A. (1970). "Sperm competition and its evolutionary consequences in the insects". Biological Reviews. 45 (4): 525–567. doi:10.1111/j.1469-185x.1970.tb01176.x. S2CID 85156929.
- Eberhard, W.G. (1996) Female control: Sexual selection by cryptic female choice. Princeton, Princeton University Press.
- Rowe, Locke; Arnqvist, Göran. (2013) Sexual conflict, Princeton University Press.[page needed]
- Jarau, Stefan; Dambacher, Jochen; Twele, Robert; Aguilar, Ingrid; Francke, Wittko; Ayasse, Manfred (2010). "The Trail Pheromone of a Stingless Bee, Trigona corvina (Hymenoptera, Apidae, Meliponini), Varies between Populations". Chemical Senses. 35 (7): 593–601. doi:10.1093/chemse/bjq057. ISSN 0379-864X. PMID 20534775.
- Andersson M. (1994). Sexual Selection. Princeton Univ Press, Princeton, NJ.[page needed]
- von Schantz T, Bensch S, Grahn M, Hasselquist D, Wittzell H (January 1999). "Good genes, oxidative stress and condition-dependent sexual signals". Proc. Biol. Sci. 266 (1414): 1–12. doi:10.1098/rspb.1999.0597. PMC 1689644. PMID 10081154.
- Olsson M, Tobler M, Healey M, Perrin C, Wilson M (August 2012). "A significant component of ageing (DNA damage) is reflected in fading breeding colors: an experimental test using innate antioxidant mimetics in painted dragon lizards". Evolution. 66 (8): 2475–2483. doi:10.1111/j.1558-5646.2012.01617.x. PMID 22834746. S2CID 205783815.
- PLoS ONE: Sexual Selection and the Evolution of Brain Size in Primates Archived 2007-09-30 at the Wayback Machine
|Wikimedia Commons has media related to Sexual selection.|
- Andersson, M. (1994) Sexual selection. Princeton University Press. ISBN 0-691-00057-3
- Arnqvist, G. & Rowe, L. (2013) Sexual conflict. Princeton University Press
- Cronin, H. (1991) The ant and the peacock: altruism and sexual selection from Darwin to today. Cambridge University Press.
- Darwin, C. (1871) The Descent of Man and Selection in Relation to Sex. John Murray, London.
- Eberhard, W. G. (1996) Female control: Sexual selection by cryptic female choice. Princeton, Princeton University Press.
- Fisher, R. A. (1930) The Genetical Theory of Natural Selection. Oxford University Press, ISBN 0-19-850440-3, Chapter 6 Memeoid.net
- Lodé, T. (2006) La guerre des sexes chez les animaux. Eds Odile Jacob. ISBN 2-7381-1901-8
- Miller, G. F. (1998) How mate choice shaped human nature: A review of sexual selection and human evolution. In: C. Crawford & D. Krebs (Eds.) Handbook of evolutionary psychology: Ideas, issues, and applications. Lawrence Erlbaum, pp. 87–129
- Miller, G. F. (2000) The Mating Mind: How sexual choice shaped the evolution of human nature. Heinemann, London. ISBN 0-434-00741-2
- Rosenberg, J. & Tunney, R. J. (2008). Human vocabulary use as display. Evolutionary Psychology, 6, 538–549