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Kin Selection

Kin selection refers to changes in gene frequency driven by interactions between related individuals. It explains the evolution of altruistic behaviors that lower an individual's fitness but increase the fitness of relatives who share the same genes. Hamilton's rule provides a quantitative framework, stating that genes for altruism increase in frequency when the cost to the actor is less than the benefit to the recipient weighted by their genetic relatedness.

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500 views6 pages

Kin Selection

Kin selection refers to changes in gene frequency driven by interactions between related individuals. It explains the evolution of altruistic behaviors that lower an individual's fitness but increase the fitness of relatives who share the same genes. Hamilton's rule provides a quantitative framework, stating that genes for altruism increase in frequency when the cost to the actor is less than the benefit to the recipient weighted by their genetic relatedness.

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Eduardo Aguirre Dávila
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Kin selection

From Wikipedia, the free encyclopedia

From the time of antiquity field biologists have observed that some organisms tend
to exhibit strategies that favor the reproductive success of their relatives, even at a
cost to their own survival and/or reproduction. The classic example is a eusocial
insect colony, with sterile females acting as workers to assist their mother in the
production of additional offspring. Many evolutionary biologists explain this by the
theory of kin selection.
The concept was formalized by JBS Haldane (1955)[1] and W. D. Hamilton (1963)[2],
while the actual term "kin selection" may first have been coined by John Maynard
Smith (1964)[3] when he wrote "These processes I will call kin selection and group
selection respectively. Kin selection has been discussed by Haldane and by
Hamilton. ... By kin selection I mean the evolution of characteristics which favour
the survival of close relatives of the affected individual, by processes which do not
require any discontinuities in the population breeding structure."
Kin selection refers to changes in gene frequency across generations that are
driven at least in part by interactions between related individuals, and this forms
much of the conceptual basis of the theory of social evolution. Indeed, some cases
of evolution by natural selection can only be understood by considering how
biological relatives influence one another's fitness. Under natural selection, a gene
encoding a trait that enhances the fitness of each individual carrying it should
increase in frequency within the population; and conversely, a gene that lowers the
individual fitness of its carriers should be eliminated. However, a gene that prompts
behaviour which enhances the fitness of relatives but lowers that of the individual
displaying the behavior, may nonetheless increase in frequency, because relatives
often carry the same gene; this is the fundamental principle behind the theory of
kin selection. According to the theory, the enhanced fitness of relatives can at times
more than compensate for the fitness loss incurred by the individuals displaying the
behaviour. As such, this is a special case of a more general model, called
"inclusive fitness" (in that inclusive fitness refers simply to gene copies in other
individuals, without requiring that they be kin).
Contents

1 Hamilton's rule
2 Mechanisms
3 Kin Selection in Evolutionary Psychology
4 Examples
5 See also
6 References

Hamilton's rule
Formally, such genes should increase in frequency when
rB C > 0
where
r = the genetical relatedness of the recipient to the actor, often defined as
the probability that a gene picked randomly from each at the same locus is
identical by descent.
B = the additional reproductive benefit gained by the recipient of the
altruistic act,
C = the reproductive cost to the individual of performing the act.

This inequality is known as Hamilton's rule after W. D. Hamilton who published, in


1964, the first formal quantitative treatment of kin selection to deal with the
evolution of apparently altruistic acts. The phrase Kin selection, however, was
coined by John Maynard Smith.
Originally, the definition for relatedness (r) in Hamilton's rule was explicitly given as
Sewall Wright's coefficient of relationship: the probability that at a random locus,
the alleles there will be identical by descent (Hamilton 1963, American Naturalist,
p. 355). Subsequent authors, including Hamilton, sometimes reformulate this with a
regression, which, unlike probabilities, can be negative, and so it is possible for
individuals to be negatively related, which simply means that two individuals can be
2

less genetically alike than two random ones on average (Hamilton 1970, Nature &
Grafen 1985 Oxford Surveys in Evolutionary Biology). This has been invoked to
explain the evolution of spiteful behaviours.
In the 1930s J.B.S. Haldane had full grasp of the basic quantities and
considerations that play a role in kin selection. He famously said that, "I would lay
down my life for two brothers or eight cousins".[4] Kin altruism is the term for
altruistic behaviour whose evolution is supposed to have been driven by kin
selection.
Haldane's remark alluded to the fact that if an individual loses its life to save two
siblings, four nephews, or eight cousins, it is a "fair deal" in evolutionary terms, as
siblings are on average 50% identical by descent, nephews 25%, and cousins
12.5% (in a diploid population that is randomly mating and previously outbred). But
Haldane also joked that he would truly die only to save more than one identical set
of twins or more than two full siblings.
Mechanisms
Hamilton (1964) outlined two ways in which kin selection altruism could be
favoured.
Firstly, if individuals have the capacity to recognize kin (kin recognition) and to
adjust their behaviour on the basis of kinship (kin discrimination), then the average
relatedness of the recipients of altruism could be high enough for this to be
favoured. Because of the facultative nature of this mechanism, it is generally
regarded that kin recognition and discrimination are unimportant except among
'higher' forms of life (although there is some evidence for this mechanism among
protozoa). A special case of the kin recognition/discrimination mechanism is the
hypothetical 'green beard', where a gene for social behaviour also causes a
distinctive phenotype that can be recognised by other carriers of the gene.
Hamilton's discussion of greenbeard altruism serves as an illustration that
relatedness is a matter of genetic similarity and that this similarity is not necessarily
caused by genealogical closeness (kinship).
Secondly, even indiscriminate altruism may be favoured in so-called viscous
populations, i.e. those characterized by low rates or short ranges of dispersal.
Here, social partners are typically genealogically-close kin, and so altruism may be
able to flourish even in the absence of kin recognition and kin discrimination
3

faculties. This suggests a rather general explanation for altruism. Directional


selection will always favor those with higher rates of fecundity within a certain
population. Social individuals can often ensure the survival their own kin by
participating in, and following the rules of a group.

Kin Selection in Evolutionary Psychology


Evolutionary psychologists have attempted to explain prosocial behavior through
kin selection by stating that behaviors that help a genetic relative are favored by
natural selection. Human beings have developed a tendency over time to frame
and interpret their actions as an avenue to the survival of their genetic material,
making kin selection not a completely altruistic form of prosocial behavior and is
perhaps better described as a component of social exchange theory. This theory
does not necessarily imply that people compute genetic benefit when helping
others, but there is an indication that those who behave in such a way are more
likely to pass on their genes to future generations. [5]
Examples
Social insects are an excellent example of organisms that display presumed kin
selected traits. The workers of some species are sterile, a trait that would not occur
if individual selection was the only process at work. The relatedness coefficient r is
abnormally high between the worker sisters in a colony of Hymenoptera due to
haplodiploidy, and Hamilton's rule is presumed to be satisfied because the benefits
in fitness for the workers are believed to exceed the costs in terms of lost
reproductive opportunity, though this has never been demonstrated empirically.
There are competing hypotheses, as well, which may also explain the evolution of
social behavior in such organisms (see Eusociality).
Alarm calls in ground squirrels are another example. While they may alert others of
the same species to danger, they draw attention to the caller and expose it to
increased risk of predation. Paul Sherman, of Cornell University, studied the alarm
calls of ground squirrels. He observed that they occurred most frequently when the
caller had relatives nearby.[6]
Alan Krakauer of University of California, Berkeley has studied kin selection in the
courtship behavior of wild turkeys. Like a teenager helping her older sister prepare

for prom night, a subordinate turkey may help his dominant brother put on an
impressive team display that is only of direct benefit to the dominant member.[7]
Recent studies provide evidence that even certain plants can recognize and
respond to kinship ties. Using sea rocket for her experiments, Susan Dudley at
McMaster University in Canada compared the growth patterns of unrelated plants
sharing a pot to plants from the same clone. She found that unrelated plants
competed for soil nutrients by aggressive root growth. This did not occur with
sibling plants.[8]

See also

Altruism
Group selection
Inclusive fitness
Selfish gene

References
1.

^ Haldane, JBS. 1955. Population Genetics. New Biology 18:34-51

2.

^ Hamilton, WD. 1963. The evolution of altruistic behavior. American


Naturalist 97:354-356

3.

^ Maynard Smith, J. 1964. Group Selection and Kin Selection, Nature


201:1145-1147.

4.

^ (1999) "Altruism", in Kevin Connolly and Margaret Martlew:


Psychologically Speaking: A Book of Quotations. BPS Books, 10. ISBN 185433-302-X. (see also: Haldane's Wikiquote entry)

5.

^ Aronson, W. A. (2007). Social Psychology 6th Edition. New Jersey:


Pearson Education, Inc.

6.

^ The science of eeeeek: what a squeak can tell researchers about life,
society, and all that Science News, Sept 12, 1998 by Susan Milius
5

7.

^ http://www.berkeley.edu/news/media/releases/2005/03/02_turkeys.shtml
In the mating game, male wild turkeys benefit even when they do not get the
girl

8.

^ http://www.nature.com/news/2007/070611/full/070611-4.html Plants can


tell who's who.

Hamilton, W.D. (1964). The genetical evolution of social behaviour I and II.
Journal of Theoretical Biology 7: 1-16 and 17-52. pubmed I pubmed II
Lucas, J.R., Creel, S.R. & Waser, P.M. (1996) How to measure inclusive fitness,
revisited, Animal Behaviour, 51, 225-228.
Madsen, E.A., Tunney, R., Fieldman, G., Plotkin, H.C., Dunbar, R.I.M., Richards,
J.M., & McFarland, D. (2007) Kinship and altruism: A cross-cultural
experimental study. British Journal of Psychology, 98, 2 [1]
Queller, D.C. & Strassman, J.E. (2002) Quick Guide: Kin Selection. Current
Biology,12,R832. [2]
West, S.A., Gardner, A. & Griffin, A.S. (2006) Quick Guide: Altruism. Current
Biology,16,R482-R483. [3]

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