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Kin Selection
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According to Hamilton’s kin selection theory (also known as “inclusive fitness” theory), kin selection is the process by which social evolution occurs in nature. The theory extends the genetical theory of natural selection to social behaviors and finds that their evolution is affected by the likelihood that individuals share genes (relatedness). In biology, a social behavior occurs when one individual (the actor) behaves so as to affect the direct fitness (number of offspring) of itself and another individual (the recipient). For example, altruism occurs when the actor’s behavior decreases the actor’s direct fitness and increases the recipient’s direct fitness. Conversely, selfishness occurs when the actor’s behavior increases the actor’s direct fitness and decreases the recipient’s. Social behaviors are widespread in nature. A classic example is the altruism shown by the sterile workers of social insects such as ants, which sacrifice their own reproduction in order to rear the queen’s offspring. At first sight, altruism poses a problem for the genetical theory of natural selection, which seems to preclude the spread of a gene for reduced reproduction. Kin selection was devised by William Hamilton in the early 1960s to address this “problem of altruism.” The basic principle behind kin selection had been hinted at by Darwin, Fisher, and Haldane, but it was Hamilton who provided the first general model. Hamilton called his idea “inclusive fitness” theory, and it was later dubbed “kin selection” by Maynard Smith in 1964. For most purposes, the two can be considered identical, although inclusive fitness theory technically includes kin selection theory because the relatedness it invokes need not involve kin (genealogical relatives). Kin selection theory solved the problem of altruism by showing that a gene for altruism can spread if altruism is directed at individuals likely to bear the same gene. By definition, kin are likely to share genes. So, a gene for altruism can spread if altruism is directed at kin and the loss of gene copies through the actor’s decreased reproduction is more than offset by the gain in gene copies through the increased reproduction of the recipient. The algebraic version of this condition is termed “Hamilton’s rule.” Although kin selection theory was devised to explain altruism, it also applies to the other forms of social behavior such as selfishness. The theory is therefore now widely used to investigate and explain many kinds of social behavior in living organisms as diverse as bacteria and human beings.
Title: Kin Selection
Description:
According to Hamilton’s kin selection theory (also known as “inclusive fitness” theory), kin selection is the process by which social evolution occurs in nature.
The theory extends the genetical theory of natural selection to social behaviors and finds that their evolution is affected by the likelihood that individuals share genes (relatedness).
In biology, a social behavior occurs when one individual (the actor) behaves so as to affect the direct fitness (number of offspring) of itself and another individual (the recipient).
For example, altruism occurs when the actor’s behavior decreases the actor’s direct fitness and increases the recipient’s direct fitness.
Conversely, selfishness occurs when the actor’s behavior increases the actor’s direct fitness and decreases the recipient’s.
Social behaviors are widespread in nature.
A classic example is the altruism shown by the sterile workers of social insects such as ants, which sacrifice their own reproduction in order to rear the queen’s offspring.
At first sight, altruism poses a problem for the genetical theory of natural selection, which seems to preclude the spread of a gene for reduced reproduction.
Kin selection was devised by William Hamilton in the early 1960s to address this “problem of altruism.
” The basic principle behind kin selection had been hinted at by Darwin, Fisher, and Haldane, but it was Hamilton who provided the first general model.
Hamilton called his idea “inclusive fitness” theory, and it was later dubbed “kin selection” by Maynard Smith in 1964.
For most purposes, the two can be considered identical, although inclusive fitness theory technically includes kin selection theory because the relatedness it invokes need not involve kin (genealogical relatives).
Kin selection theory solved the problem of altruism by showing that a gene for altruism can spread if altruism is directed at individuals likely to bear the same gene.
By definition, kin are likely to share genes.
So, a gene for altruism can spread if altruism is directed at kin and the loss of gene copies through the actor’s decreased reproduction is more than offset by the gain in gene copies through the increased reproduction of the recipient.
The algebraic version of this condition is termed “Hamilton’s rule.
” Although kin selection theory was devised to explain altruism, it also applies to the other forms of social behavior such as selfishness.
The theory is therefore now widely used to investigate and explain many kinds of social behavior in living organisms as diverse as bacteria and human beings.
Related Results
Cryptic Kin Selection: Kin Structure in Vertebrate Populations and Opportunities for Kin‐Directed Cooperation
Cryptic Kin Selection: Kin Structure in Vertebrate Populations and Opportunities for Kin‐Directed Cooperation
AbstractAnimal societies of varying complexity have been the favoured testing ground for inclusive fitness theory, and there is now abundant evidence that kin selection has played ...
Kin and Non-Kin Connected Plants Benefit More Than Disconnected Kin and Non-Kin Plants under Nutrient-Competitive Environments
Kin and Non-Kin Connected Plants Benefit More Than Disconnected Kin and Non-Kin Plants under Nutrient-Competitive Environments
In the natural environment, plants grow and interact with both conspecific and heterospecific neighbours under different environmental conditions. In this study, we tested whether ...
Kin-Mediated Male Choice and Alternative Reproductive Tactics in Spider Mites
Kin-Mediated Male Choice and Alternative Reproductive Tactics in Spider Mites
Optimal outbreeding and kin selection theories state that the degree of kinship is a fundamental determinant in any mating system. However, the role of kinship in male choice and a...
Kin terms and fitness interdependence
Kin terms and fitness interdependence
Although genetic relatedness has been shown to be an important determinant of helping and other forms of cooperation among kin, it does not correspond well to the different types o...
Selection Gradients
Selection Gradients
Natural selection and sexual selection are important evolutionary processes that can shape the phenotypic distributions of natural populations and, consequently, a primary goal of ...
Predictive structure emerges during generalisation of kin terms to new referents
Predictive structure emerges during generalisation of kin terms to new referents
Despite crosslinguistic diversity in how kin relations map to terminology, there are constraints on which kin may be categorised together. But what are the constraints on kin term ...
Human kin detection
Human kin detection
Natural selection has favored the evolution of behaviors that benefit not only one's genes, but also their copies in genetically related individuals. These behaviors include optima...

