Fisher's principle

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Fisher's principle explains why the sex ratio of most species is approximately 1:1. It was famously outlined by R.A. Fisher in his his 1930 book The Genetical Theory of Natural Selection[1] (but incorrectly attributed to Fisher as original[2]). Nevertheless, A.W.F. Edwards has remarked that it is "probably the most celebrated argument in evolutionary biology"[2][3]. Specifically, Fisher couched his argument in terms of parental expenditure, and predicted that parental expenditure on both sexes should be equal. Sex ratios that are 1:1 are hence known as "Fisherian", and those that are not 1:1 are "non-Fisherian" or "extraordinary" and occur because they break the assumptions made in Fisher's model.[4]

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[edit] Basic explanation

W.D. Hamilton gave the following basic explanation in his 1967 paper on "Extraordinary sex ratios"[4], given the condition that males and females cost equal amounts to produce:

  1. Suppose male births are less common than female.
  2. A newborn male then has better mating prospects than a newborn female, and therefore can expect to have more offspring.
  3. Therefore parents genetically disposed to produce males tend to have more than average numbers of grandchildren born to them.
  4. Therefore the genes for male-producing tendencies spread, and male births become commoner.
  5. As the 1:1 sex ratio is approached, the advantage associated with producing males dies away.
  6. The same reasoning holds if females are substituted for males through-out. Therefore 1:1 is the equilibrium ratio.

In modern language, the 1:1 ratio is the evolutionarily stable strategy (ESS)[5]

[edit] Parental expenditure

Specifically, Fisher frames his argument in terms of parental expenditure. In Chapter 6 "Sexual Reproduction and Sexual Selection" under the heading "Natural Selection and the sex-ratio" (p141)[1]:

In organisms of all kinds the young are launched upon their careers endowed with a certain amount of biological capital derived from their parents. This varies enormously in amount in different species, but, in all, there has been, before the offspring is able to lead an independent existence, a certain expenditure of nutriment in addition, almost universally, to some expenditure of time or activity, which the parents are induced by their instincts to make for the advantage of their young. Let us consider the reproductive value of these offspring at the moment when this parental expenditure on their behalf has just ceased. If we consider the aggregate of an entire generation of such offspring it is clear that the total reproductive value of the males in this group is exactly equal to the total value of all the females, because each sex must supply half the ancestry of all future generations of the species. From this it follows that the sex ratio will so adjust itself, under the influence of Natural Selection, that the total parental expenditure incurred in respect of children of each sex, shall be equal; for if this were not so and the total expenditure incurred in producing males, for instance, were less than the total expenditure incurred in producing females, then since the total reproductive value of the males is equal to that of the females, it would follow that those parents, the innate tendencies of which caused them to produce males in excess, would, for the same expenditure, produce a greater amount of reproductive value; and in consequence would be the progenitors of a larger fraction of future generations than would parents having a congenital bias towards the production of females. Selection would thus raise the sex-ratio until the expenditure upon males became equal to that upon females.

[edit] Development of the argument

A.W.F. Edwards has remarked that Fisher's principle is "probably the most celebrated argument in evolutionary biology"[2] (though this seems debatable; if Darwin's original arguments are arbitrarily excepted from consideration, W.D. Hamilton's concept of inclusive fitness at least rivals it), and has significance beyond merely finding an equilibrium value in the sex ratio.

Fisher's principle is an early example of a model showing the power of individual selection over naive group selectionist ideas. In particular it explains why in polygynous species, such as elephant seals, the sex ratio is still 1:1, despite the bachelor males consuming most of the population's food supply.

Fisher's principle was taken and expressed mathematically by population geneticists R.F. Shaw and J. Dawson Mohler [6]. Relating to population genetics, Fisher's model is the first to include three generations rather than just two.

Fisher's principle is also the precursor to evolutionary game theory. R.H. MacArthur (1965) first suggested applying to sex ratios the language of game theory[7], and this was subsequently picked up by W.D. Hamilton (1967) who termed the equilibrium point the "unbeatable strategy"[4]. Hamilton's unbeatable strategy was refined by John Maynard Smith and George R. Price (1973) into their concept of the evolutionarily stable strategy, i.e. one which cannot be invaded by a mutant strategy[5]

Fisher's concept of parental expenditure (now termed parental investment), developed particularly by Robert Trivers is now an important concept in ecology.

[edit] Fisher's sources

Historical research by A.W.F. Edwards[2][8] has shown that the argument is incorrectly attributed to Fisher (the name is in common use and is unlikely to change, treatise of the subject). Charles Darwin had originally formulated a similar but somewhat confused argument in the first edition of The Descent of Man[9] but withdrew it for the second edition[10] -- Fisher only had a copy of the the latter, and quotes Darwin in The Genetical Theory of Natural Selection[1]

Specifically, Carl Düsing of the University of Jena published this in three works between 1883-1884[8], and this is essentially identical to Show and Mohler's later model[6].

[edit] Further reading

As "probably the most celebrated argument in evolutionary biology"[2], Fisher's principle is a staple of popular science books on evolution. For example, see:

For those wishing more advance treatment, see the 2002 book Sex Ratios: Concepts and Research Methods edited by Ian C.W. Hardy, (chapters 1 and 2 by Ido Pen and Franz J. Weissing.)

[edit] References

  1. ^ a b c Fisher, R.A. 1930 The Genetical Theory of Natural Selection, Clarendon Press, Oxford
  2. ^ a b c d e Edwards, A.W.F. 1998 Natural Selection and the Sex Ratio: Fisher's Sources American Naturalist 151: 564-569
  3. ^ Excepting, we presume, Darwin's arguments which are central to evolutionary theory
  4. ^ a b c Hamilton, W.D. 1967 Extraordinary sex ratios Science 156: 477-488
  5. ^ a b Maynard Smith, J & Price, G.R. 1973 The logic of animal conflict Nature 246: 15-18
  6. ^ a b Shaw, R.F., and J.D. Mohler. 1953. The selective significance of the sex ratio. American Naturalist 87:337–342.
  7. ^ MacArthur, R. H. (1965). in: Theoretical and mathematical biology T. Waterman & H. Horowitz, eds. Blaisdell: New York.
  8. ^ a b Edwards, A.W.F. 2000 Carl Düsing (1884) on The Regulation of the Sex-Ratio Theoretical Population Biology 58: 255-257
  9. ^ Darwin, C.R. 1871 The Descent of Man, and Selection in Relation to Sex 1st ed John Murray, London
  10. ^ Darwin, C.R. 1874 The Descent of Man, and Selection in Relation to Sex 2nd ed John Murray, London