Fitness (biology)




The average contribution to the gene pool of the next generation made by individuals of the specified genotype or phenotype

























Fitness (often denoted w{displaystyle w}w or ω in population genetics models) is the quantitative representation of natural and sexual selection within evolutionary biology. It can be defined either with respect to a genotype or to a phenotype in a given environment. In either case, it describes individual reproductive success and is equal to the average contribution to the gene pool of the next generation that is made by individuals of the specified genotype or phenotype. The fitness of a genotype is manifested through its phenotype, which is also affected by the developmental environment. The fitness of a given phenotype can also be different in different selective environments.


With asexual reproduction, it is sufficient to assign fitnesses to genotypes. With sexual reproduction, genotypes are scrambled every generation. In this case, fitness values can be assigned to alleles by averaging over possible genetic backgrounds. Natural selection tends to make alleles with higher fitness more common over time, resulting in Darwinian evolution.


The term "Darwinian fitness" can be used to make clear the distinction with physical fitness.[1] Fitness does not include a measure of survival or life-span; Herbert Spencer's well-known phrase "survival of the fittest" should be interpreted as: "Survival of the form (phenotypic or genotypic) that will leave the most copies of itself in successive generations."


Inclusive fitness differs from individual fitness by including the ability of an allele in one individual to promote the survival and/or reproduction of other individuals that share that allele, in preference to individuals with a different allele. One mechanism of inclusive fitness is kin selection.




Contents






  • 1 Fitness is a propensity


  • 2 Models of fitness: asexuals


    • 2.1 Absolute fitness


    • 2.2 Relative fitness


    • 2.3 Change in genotype frequencies due to selection




  • 3 History


  • 4 Genetic load


  • 5 See also


  • 6 Notes and references


  • 7 Bibliography


  • 8 External links





Fitness is a propensity


Fitness is often defined as a propensity or probability, rather than the actual number of offspring. For example, according to Maynard Smith, "Fitness is a property, not of an individual, but of a class of individuals — for example homozygous for allele A at a particular locus. Thus the phrase ’expected number of offspring’ means the average number, not the number produced by some one individual. If the first human infant with a gene for levitation were struck by lightning in its pram, this would not prove the new genotype to have low fitness, but only that the particular child was unlucky." [2]


Alternatively, "the fitness of the individual - having an array x of phenotypes — is the probability, s(x), that the individual will be included among the group selected as parents of the next generation."[3]



Models of fitness: asexuals


To avoid the complications of sex and recombination, we initially restrict our attention to an asexual population without genetic recombination. Then fitnesses can be assigned directly to genotypes rather than having to worry about individual alleles. There are two commonly used measures of fitness; absolute fitness and relative fitness.



Absolute fitness


The absolute fitness (W{displaystyle W}W) of a genotype is defined as the proportional change in the abundance of that genotype over one generation attributable to selection. For example, if n(t){displaystyle n(t)}{displaystyle n(t)} is the abundance of a genotype in generation t{displaystyle t}t in an infinitely large population (so that there is no genetic drift), and neglecting the change in genotype abundances due to mutations, then[4]




n(t+1)=Wn(t){displaystyle n(t+1)=Wn(t)}{displaystyle n(t+1)=Wn(t)}.


An absolute fitness larger than 1 indicates growth in that genotype's abundance; an absolute fitness smaller than 1 indicates decline.



Relative fitness


Whereas absolute fitness determines changes in genotype abundance, relative fitness (w{displaystyle w}w) determines changes in genotype frequency. If N(t){displaystyle N(t)}N(t) is the total population size in generation t{displaystyle t}t, and the relevant genotype's frequency is p(t)=n(t)/N(t){displaystyle p(t)=n(t)/N(t)}{displaystyle p(t)=n(t)/N(t)}, then




p(t+1)=ww¯p(t){displaystyle p(t+1)={frac {w}{overline {w}}}p(t)}{displaystyle p(t+1)={frac {w}{overline {w}}}p(t)},


where {displaystyle {overline {w}}}{displaystyle {overline {w}}} is the mean relative fitness in the population (again setting aside changes in frequency due to drift and mutation). Relative fitnesses only indicate the change in prevalence of different genotypes relative to each other, and so only their values relative to each other are important; relative fitnesses can be any nonnegative number, including 0. It is often convenient to choose one genotype as a reference and set its relative fitness to 1. Relative fitness is used in the standard Wright-Fisher and Moran models of population genetics.


Absolute fitnesses can be used to calculate relative fitness, since p(t+1)=n(t+1)/N(t+1)=(W/W¯)p(t){displaystyle p(t+1)=n(t+1)/N(t+1)=(W/{overline {W}})p(t)}{displaystyle p(t+1)=n(t+1)/N(t+1)=(W/{overline {W}})p(t)} (we have used the fact that N(t+1)=W¯N(t){displaystyle N(t+1)={overline {W}}N(t)}{displaystyle N(t+1)={overline {W}}N(t)}, where {displaystyle {overline {W}}}{displaystyle {overline {W}}} is the mean absolute fitness in the population). This implies that w/w¯=W/W¯{displaystyle w/{overline {w}}=W/{overline {W}}}{displaystyle w/{overline {w}}=W/{overline {W}}}, or in other words, relative fitness is proportional to W/W¯{displaystyle W/{overline {W}}}{displaystyle W/{overline {W}}}. It is not possible to calculate absolute fitnesses from relative fitnesses alone, since relative fitnesses contain no information about changes in overall population abundance N(t){displaystyle N(t)}N(t).



Change in genotype frequencies due to selection




Increase in frequency over time of genotype A{displaystyle A}A, which has a 1% greater relative fitness than the other genotype present, B{displaystyle B}B.


The change in genotype frequencies due to selection follows immediately from the definition of relative fitness,




Δp=p(t+1)−p(t)=w−p(t){displaystyle Delta p=p(t+1)-p(t)={frac {w-{overline {w}}}{overline {w}}}p(t)}{displaystyle Delta p=p(t+1)-p(t)={frac {w-{overline {w}}}{overline {w}}}p(t)}.


Thus, a genotype's frequency will decline or increase depending on whether its fitness is lower or greater than the mean fitness, respectively.


In the particular case that there are only two genotypes of interest (e.g. representing the invasion of a new mutant allele), the change in genotype frequencies is often written in a different form. Suppose that two genotypes A{displaystyle A}A and B{displaystyle B}B have fitnesses wA{displaystyle w_{A}}{displaystyle w_{A}} and wB{displaystyle w_{B}}{displaystyle w_{B}}, and frequencies p{displaystyle p}p and 1−p{displaystyle 1-p}1-p, respectively. Then =wAp+wB(1−p){displaystyle {overline {w}}=w_{A}p+w_{B}(1-p)}{displaystyle {overline {w}}=w_{A}p+w_{B}(1-p)}, and so




Δp=w−p=wA−wBw¯p(1−p){displaystyle Delta p={frac {w-{overline {w}}}{overline {w}}}p={frac {w_{A}-w_{B}}{overline {w}}}p(1-p)}{displaystyle Delta p={frac {w-{overline {w}}}{overline {w}}}p={frac {w_{A}-w_{B}}{overline {w}}}p(1-p)}.


Thus, the change in genotype A{displaystyle A}A's frequency depends crucially on the difference between its fitness and the fitness of genotype B{displaystyle B}B. Supposing that A{displaystyle A}A is more fit than B{displaystyle B}B, and defining the selection coefficient s{displaystyle s}s by wA=(1+s)wB{displaystyle w_{A}=(1+s)w_{B}}{displaystyle w_{A}=(1+s)w_{B}}, we obtain




Δp=w−p=s1+spp(1−p)≈sp(1−p){displaystyle Delta p={frac {w-{overline {w}}}{overline {w}}}p={frac {s}{1+sp}}p(1-p)approx sp(1-p)}{displaystyle Delta p={frac {w-{overline {w}}}{overline {w}}}p={frac {s}{1+sp}}p(1-p)approx sp(1-p)},


where the last approximation hold for s≪1{displaystyle sll 1}{displaystyle sll 1}. In other words, the fitter genotype's frequency grows approximately logistically.



History





Herbert Spencer.


The British sociologist Herbert Spencer coined the phrase "survival of the fittest" in his 1864 work Principles of Biology to characterise what Charles Darwin had called natural selection.[5]


The British biologist J.B.S. Haldane was the first to quantify fitness, in terms of the modern evolutionary synthesis of Darwinism and Mendelian genetics starting with his 1924 paper A Mathematical Theory of Natural and Artificial Selection. The next further advance was the introduction of the concept of inclusive fitness by the British biologist W.D. Hamilton in 1964 in his paper on The Genetical Evolution of Social Behaviour.



Genetic load



Genetic load measures the average fitness of a population of individuals, relative either to a theoretical genotype of optimal fitness, or relative to the most fit genotype actually present in the population.[6] Consider n genotypes A1…An{displaystyle mathbf {A} _{1}dots mathbf {A} _{n}} mathbf{A} _1 dots mathbf{A} _n, which have the fitnesses w1…wn{displaystyle w_{1}dots w_{n}}w_1 dots w_n and the genotype frequencies p1…pn{displaystyle p_{1}dots p_{n}}p_1 dots p_n respectively. Ignoring frequency-dependent selection, then genetic load (L{displaystyle L}L) may be calculated as:


L=wmax−wmax{displaystyle L={{w_{max }-{bar {w}}} over w_{max }}}{displaystyle L={{w_{max }-{bar {w}}} over w_{max }}}

Genetic load may increase when deleterious mutations, migration, inbreeding, or outcrossing lower mean fitness. Genetic load may also increase when beneficial mutations increase the maximum fitness against which other mutations are compared; this is known as the substitutional load or cost of selection.



See also



  • Gene-centered view of evolution

  • Inclusive fitness

  • Lineage selection

  • Natural selection

  • Reproductive success

  • Selection coefficient

  • Universal Darwinism



Notes and references





  1. ^ Wassersug, J. D., and R. J. Wassersug, 1986. Fitness fallacies. Natural History 3:34-37.


  2. ^ Maynard-Smith, J. (1989) Evolutionary Genetics .mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
    ISBN 0-19-854215-1



  3. ^ Hartl, D. L. (1981) A Primer of Population Genetics
    ISBN 0-87893-271-2



  4. ^ Kimura, James F. Crow, Motoo (1970). An introduction to population genetics theory ([Reprint] ed.). New Jersey: Blackburn Press. p. 5. ISBN 978-1-932846-126.


  5. ^ "Letter 5140 – Wallace, A. R. to Darwin, C. R., 2 July 1866". Darwin Correspondence Project. Retrieved 12 January 2010.

    "Letter 5145 – Darwin, C. R. to Wallace, A. R., 5 July (1866)". Darwin Correspondence Project. Retrieved 12 January 2010.


    ^ "Herbert Spencer in his Principles of Biology of 1864, vol. 1, p. 444, wrote: 'This survival of the fittest, which I have here sought to express in mechanical terms, is that which Mr. Darwin has called "natural selection", or the preservation of favoured races in the struggle for life.'" Maurice E. Stucke, Better Competition Advocacy, retrieved 29 August 2007, citing HERBERT SPENCER, THE PRINCIPLES OF BIOLOGY 444 (Univ. Press of the Pac. 2002.)



  6. ^ Ewens, Warren J. (2003). Mathematical population genetics (2nd ed.). New York: Springer. pp. 78–86. ISBN 978-0387201917.




Bibliography




  • Sober, E. (2001). The Two Faces of Fitness. In R. Singh, D. Paul, C. Krimbas, and J. Beatty (Eds.), Thinking about Evolution: Historical, Philosophical, and Political Perspectives. Cambridge University Press, pp. 309–321. Full text


  • Orr HA (August 2009). "Fitness and its role in evolutionary genetics". Nat. Rev. Genet. 10 (8): 531–9. doi:10.1038/nrg2603. PMC 2753274. PMID 19546856.



External links



  • Video: Using fitness landscapes to visualize evolution in action

  • BEACON Blog--Evolution 101: Fitness Landscapes

  • Pleiotrophy Blog--an interesting discussion of Sergey Gavrilets's contributions

  • Evolution A-Z: Fitness

  • Stanford Encyclopedia of Philosophy entry









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