The human sex ratio is of particular interest to anthropologists and demographers. In human societies, however, sex ratios at birth may be considerably skewed by factors such as the age of mother at birth, and by sex-selective abortion and infanticide. The CIA estimates that the current world wide sex ratio at birth is 107 boys to 100 girls, though during the late 1990s there was concern that the ratio of males to females was declining too rapidly. In 2010, the global adult sex ratio was 986 females per 1,000 males and trended to reduce to 984 in 2011.
- 1 Types of sex ratio
- 2 Sex ratio theory
- 3 Fisher’s principle
- 4 Examples in non-human species
- 5 See also
- 6 Notes
- 7 References
- 8 External links
Types of sex ratio
In most species, sex ratio varies according to the age profile of the population. It is generally divided into four subdivisions:
- primary sex ratio — ratio at fertilization
- secondary sex ratio — ratio at birth
- tertiary sex ratio — ratio in sexually active organisms.
- Also called adult sex ratio and abbreviated to ASR. ASR is defined as the proportion of adults in a population that are male.
- quaternary sex ratio — ratio in post-reproductive organisms
Measuring these is a problem since they lack clear boundaries.
Sex ratio theory
The theory of sex ratio is a field of study concerned with the accurate prediction of sex ratios in all sexual species, based on a consideration of their natural history. The field continues to be heavily influenced by Eric Charnov’s 1982 book, Sex Allocation. He defines five major questions, both for his book and the field in general (slightly abbreviated here):
- For a dioecious species, what is the equilibrium sex ratio maintained by natural selection?
- For a sequential hermaphrodite, what is the equilibrium sex order and time of sex change?
- For a simultaneous hermaphrodite, what is the equilibrium allocation of resources to male versus female function in each breeding season?
- Under what conditions are the various states of hermaphroditism or dioecy evolutionarily stable? When is a mixture of sexual types stable?
- When does selection favour the ability of an individual to alter its allocation to male versus female function, in response to particular environmental or life history situations?
Biological research mostly concerns itself with sex allocation rather than sex ratio, sex allocation denoting the allocation of energy to either sex. Common research themes are the effects of local mate and resource competition (often abbreviated LMC and LRC, respectively).
Fisher’s principle explains why for most species, the sex ratio is approximately 1:1. Bill Hamilton expounded Fisher’s argument in his 1967 paper on “Extraordinary sex ratios” as follows, given the assumption of equal parental expenditure on offspring of both sexes.
- Suppose male births are less common than female.
- A newborn male then has better mating prospects than a newborn female, and therefore can expect to have more offspring.
- Therefore parents genetically disposed to produce males tend to have more than average numbers of grandchildren born to them.
- Therefore the genes for male-producing tendencies spread, and male births become more common.
- As the 1:1 sex ratio is approached, the advantage associated with producing males dies away.
- The same reasoning holds if females are substituted for males throughout. Therefore 1:1 is the equilibrium ratio.
Examples in non-human species
Environmental and individual control
Spending equal amounts of resources to produce offspring of either sex is an evolutionarily stable strategy: if the general population deviates from this equilibrium by favoring one sex, one can obtain higher reproductive success with less effort by producing more of the other. For species where the cost of successfully raising one offspring is roughly the same regardless of its sex, this translates to an approximately equal sex ratio.
Bacteria of the genus Wolbachia cause skewed sex ratios in some arthropod species as they kill males. Sex-ratio of adult populations of pelagic copepods is usually skewed towards dominance of females. However, there are differences in adult sex ratios between families: in families in which females require multiple matings to keep producing eggs, sex ratios are less biased (close to 1); in families in which females can produce eggs continuously after only one mating, sex ratios are strongly skewed towards females.
Several species of reptiles have temperature-dependent sex determination, where incubation temperature of eggs determines the sex of the individual. In the American Alligator, for example, females are hatched from eggs incubated between 27.7 to 30 °C (82 to 86 °F), whereas males are hatched from eggs 32.2 to 33.8 °C (90 to 93 °F). In this method, however, all eggs in a clutch (20–50) will be of the same sex. In fact, the natural sex ratio of this species is five females to one male.
In several different groups of fish, such as wrasses, parrotfish and clownfish, dichogamy — or sequential hermaphoditism — is normal. This can cause a discrepancy in the sex ratios as well. In the Bluestreak cleaner wrasse, there is only one male for every group of 6-8 females. If the male fish dies, the strongest female changes its sex to become the male for the group. All of these wrasse are born female, and only become male in this situation. Other species, like clownfish, do this in reverse, where all start out as non-reproductive males, and the largest male becomes a female, with the second-largest male maturing to become reproductive.
Traditionally, farmers have discovered that the most economically efficient community of animals will have a large number of females and a very small number of males. A herd of cows with a few prize bulls or a flock of hens with one rooster are the most economical sex ratios for domesticated livestock.
Dioecious plants secondary sex ratio and amount of pollen
It was found that the amount of fertilizing pollen can influence secondary sex ratio in dioecious plants. Increase in pollen amount leads to decrease in number of male plants in the progeny. This relationship was confirmed on four plant species from three families – Rumex acetosa (Polygonaceae), Melandrium album (Cariophyllaceae), Cannabis sativa and Humulus japonicus (Cannabinaceae).
Polyandrous and cooperatively breeding homiotherms
In charadriiform birds, recent research has shown clearly that polyandry and sex-role reversal (where males care and females compete for mates) as found in phalaropes, jacanas, painted snipe and a few plover species is clearly related to a strongly male-biased adult sex ratio. Those species with male care and polyandry invariably have adult sex ratios with a large surplus of males, which in some cases can reach as high as six males per female.
Male-biased adult sex ratios have also been shown to correlate with cooperative breeding in mammals such as alpine marmots and wild canids. This correlation may also apply to cooperatively breeding birds, though the evidence is less clear. It is known, however, that both male-biased adult sex ratios and cooperative breeding tend to evolve where caring for offspring is extremely difficult due to low secondary productivity, as in Australia and Southern Africa. It is also known that in cooperative breeders where both sexes are philopatric like the Varied Sittella, adult sex ratios are equally or more male-biased than in those cooperative species, such as fairy-wrens, treecreepers and the Noisy Miner where females always disperse.
- Bride kidnapping
- Demographic transition
- Evolution of sex
- Human sex ratio
- List of countries by sex ratio
- Operational sex ratio
- Sex allocation
- Sex selection
- Sex-selective abortion and infanticide
- Trivers–Willard hypothesis
- XY sex-determination system
- Youth bulge
- "Trend Analysis of the sex Ratio at Birth in the United States". U.S. Department of Health and Human Services, National Center for Health Statistics.
- "CIA Fact Book". The Central Intelligence Agency of the United States.
- Davis, Devra Lee; Gottlieb, Michelle and Stampnitzky, Julie; “Reduced Ratio of Male to Female Births in Several Industrial Countries” in Journal of the American Medical Association; April 1, 1998, volume 279(13); pp. 1018-1023
- "Decline in sex ratio is a global trend". The Times Of India. August 17, 2011.
- Coney, N.S. Mackey, W.C. (May 1998). “The woman as final arbiter: a case for the facultative character of the human sex ratio”; in Journal of Sex Research 35 (2): 169–175. doi:10.1080/00224499809551930.
- Wilson, K. & Hardy, I.C.W. (2002) “Statistical analysis of sex ratios: an introduction”; in Hardy, Ian C.W. (editor), Sex Ratios: Concepts and Research Methods, pp. 48–92. ISBN 0521665787
- Eric L. Charnov. (1982) Sex allocation. Princeton University Press, Princeton, New Jersey. ISBN 0-691-08312-6
- Hamilton W.D. (April 1967). "Extraordinary sex ratios. A sex-ratio theory for sex linkage and inbreeding has new implications in cytogenetics and entomology". Science 156 (3774): 477–88. Bibcode:1967Sci...156..477H. doi:10.1126/science.156.3774.477. PMID 6021675. "references"
- Maynard Smith, J., Price, G.R. (1973). "The logic of animal conflict". Nature 246 (5427): 15–8. Bibcode:1973Natur.246...15S. doi:10.1038/246015a0.
- Kiørboe, T. (2006). "Sex, sex-ratios, and the dynamics of pelagic copepod populations". Oecologia 148 (1): 40–50. doi:10.1007/s00442-005-0346-3. PMID 16425044.
- Ferguson, M.W.J., Joanen, T. (April 1982). "Temperature of egg incubation determines sex in Alligator mississippiensis". Nature 296 (5860): 850–3. Bibcode:1982Natur.296..850F. doi:10.1038/296850a0. PMID 7070524.
- Pike, T.W., Petrie, M. (October 2005). "Maternal body condition and plasma hormones affect offspring sex ration in peafowl". Animal Behaviour 70 (4): 745–51. doi:10.1016/j.anbehav.2004.12.020. [Egg Shell Game Lay summary].
- Соrrеns С. (1922). "Geschlechtsbestimmung und Zahlenverhaltnis der Geschlechter beim Sauerampfer (Rumex acetosa)". Biol. Zbl. 42: 465–80.
- Rychlewski J., Kazlmierez Z. (1975). "Sex ratio in seeds of Rumex acetosa L. as a result of sparse or abundant pollination". Acta Biol Crac Ser Bot 18: 101–14.
- Correns C. (1928). "Bestimmung, Vererbung und Verteilung des Geschlechter bei den hoheren Pflanzen". Handb. Vererbungswiss. 2: 1–138.
- Mulcahy D.L. (1967). "Optimal sex ratio in Silene alba". Heredity 22 (3): 41.
- Riede W. (1925) Beitrage zum Geschlechts- und Anpassungs-problem. “Flora” 18/19
- Kihara H., Hirayoshi J. (1932) Die Geschlechtschromosomen von Humulus japonicus. Sieb. et. Zuce. In: 8th Congr. Jap. Ass. Adv. Sci., p. 363—367 (cit.: Plant Breeding Abstr., 1934, 5, № 3, p. 248, ref. № 768).
- Liker, András; Freckleton, Robert P. and Székely, Tamás; “The evolution of sex roles in birds is related to adult sex ratio”; in Nature Communications 4, No. 1587. Published 12 March 2013
- Kosztolányi, András; Barta, Zoltán; Küpper, Clemens and Székely, Tamás; “Persistence of an extreme male-biased adult sex ratio in a natural population of a polyandrous bird”; in Journal of Evolutionary Biology, volume 24 (August 2011), issue 8, pp. 1842–1846
- Allainé, Dominique; Brondex, Francine; Graziani, Laurent; Coulon, Jacques and Till-Bottraud, Irène; “Male-biased sex ratio in litters of Alpine marmots supports the helper repayment hypothesis”
- Doerr, Erik D. and Doerr, Veronica A.J. “Comparative demography of treecreepers: evaluating hypotheses for the evolution and maintenance of cooperative breeding”; in Animal Behaviour , volume 72, issue 1 (July 2006); pp 147–159
- Kokko, Hanna and Jennions, Michael D.; “Parental investment, sexual selection and sex ratios”; in Journal of Evolutionary Biology volume 21, issue 4 (July 2008), pp 919–948
- Orians Gordon H. and Milewski, Antoni V.; “Ecology of Australia: the effects of nutrient-poor soils and intense fires” in Biological Reviews; volume 82, issue 3 (August 2007); pp. 393–423.
- Noske, R.A.; “Intersexual niche segregation among three bark-foraging birds of eucalypt forests”; in Australian Journal of Ecology volume 11 (1986), pp. 255-267
- “Sex-biased hatching sequences in the cooperatively breeding Noisy Miner”; in Journal of Avian Biology; 32 (September 2001); pp. 219-223
- Coale A.J. (1996). "Five Decades of Missing Females in China". Proceedings of the American Philosophical Society 140 (4): 421–50.
- Hamilton W.D. (April 1967). "Extraordinary sex ratios. A sex-ratio theory for sex linkage and inbreeding has new implications in cytogenetics and entomology". Science 156 (3774): 477–88. Bibcode:1967Sci...156..477H. doi:10.1126/science.156.3774.477. PMID 6021675.
- Nishimura, K., Jahn, G.C. (1996). "Sex allocation of three solitary ectoparasitic wasp species on bean weevil larvae: sex ratio change with host quality and local mate competition". Journal of Ethology 14 (1): 27–34. doi:10.1007/BF02350089.
- Trivers R.L., Willard D.E. (1973). "Natural selection of parental ability to vary the sex ratio of offspring". Science 179 (4068): 90–2. Bibcode:1973Sci...179...90T. doi:10.1126/science.179.4068.90. PMID 4682135.
- Rath, R.M., and Mishra A.K. (2005). Techniques for Sex Ratio Analysis. Association of Professional Geographers.