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Evolutionary invasion analysis, also known as adaptive dynamics, is a set of techniques for studying long-term phenotypical evolution developed during the 1990s. It incorporates the concept of frequency dependence from game theory but allows for more realistic ecological descriptions, as the traits vary continuously and gives rise to a non-linear invasion fitness (the classical fitness concept is not directly applicable to situations with frequency dependence).
## Introduction and background

## Fundamental ideas

# Monomorphic evolution

## Invasion exponent and selection gradient

## Pairwise-invasibility plots

## Evolutionarily singular strategies

# Polymorphic evolution

## Invasion exponent and selection gradients in polymorphic populations

## Evolutionary branching

## Trait evolution plots

# Other uses

# See also

# External links

The basic principle of evolution, survival of the fittest, was outlined by the naturalist Charles Darwin in his 1859 book On the origin of species. Though controversial at the time, the central ideas remain virtually unchanged to this date, even though much more is now known about the biological basis of inheritance. Darwin expressed his arguments verbally, but many attempts have since then been made to formalise the theory of evolution. The perhaps most well known are population genetics which aim to model the biological basis of inheritance but usually at the expense of ecological detail, quantitative genetics which incorporates quantitative traits influenced by genes at many loci and evolutionary game theory which ignores genetic detail but incorporates a high degree of ecological realism, in particular that the success of any given strategy depends on the frequency at which strategies are played in the population, a concept known as frequency dependence.

Adaptive Dynamics is a set of techniques developed during the 1990s for understanding the long-term consequences of small mutations in the traits expressing the phenotype. They link population dynamics to evolutionary dynamics and incorporate and generalises the fundamental idea of frequency dependent selection from game theory. The number of papers using Adaptive Dynamics techniques is increasing steadily as Adaptive Dynamics is gaining ground as a versatile tool for evolutionary modelling.

Two fundamental ideas of Adaptive Dynamics are that the resident population can be assumed to be in a dynamical equilibrium when new mutants appear, and that the eventual fate of such mutants can be inferred from their initial growth rate when rare in the environment consisting of the resident. This rate is known as the invasion exponent when measured as the initial exponential growth rate of mutants, and as the basic reproductive number when it measures the expected total number of offspring that a mutant individual will produce in a lifetime. It can be thought of, and is indeed sometimes also referred to, as the invasion fitness of mutants. In order to make use of these ideas we require a mathematical model that explicitly incorporates the traits undergoing evolutionary change. The model should describe both the environment and the population dynamics given the environment, but in many cases the variable part of the environment consists only of the demography of the current population. We then determine the invasion exponent, the initial growth rate of a mutant invading the environment consisting of the resident. Depending on the model, this can be trivial or very difficult, but once determined, the Adaptive Dynamics techniques can be applied independent of the model structure.

A population consisting of individuals with the same trait is called monomorphic. If not explicitly stated differently, we will assume that the trait is a real number, and we will write r and m for the trait value of the monomorphic resident population and that of an invading mutant, respectively.

The invasion exponent $S\_r(m)$ is defined as the expected growth rate of an initially rare mutant in the environment set by the resident, which simply means the frequency of each phenotype (trait value) whenever this suffices to infer all other aspects of the equilibrium environment, such as the demographic composition and the availability of resources. For each r the invasion exponent can be thought of as the fitness landscape experienced by an initially rare mutant. The landscape changes with each successful invasion, as is the case in evolutionary game theory, but in contrast with the classical view of evolution as an optimisation process towards ever higher fitness.

We will always assume that the resident is at its demographic attractor, and as a consequence $S\_r(r)\; =\; 0$ for all r, as otherwise the population would grow indefinitely.

The selection gradient is defined as the slope of the invasion exponent at $m=r$, $S\_r\text{'}(r)$. If the sign of the invasion exponent is positive (negative) mutants with slightly higher (lower) trait values may successfully invade. This follows from the linear approximation

- $S\_r(m)\; approx\; S\_r\text{'}(r)\; (m\; -\; r)$

which holds whenever $m\; approx\; r$.

The invasion exponent represents the fitness landscape as experienced by a rare mutant. In a large (infinite) population only mutants with trait values $m$ for which $S\_r(m)$ is positive are able to successfully invade. The generic outcome of an invasion is that the mutant replaces the resident, and the fitness landscape as experienced by a rare mutant changes. To determine the outcome of the resulting series of invasions pairwise-invasibility plots (PIPs) are often used. These show for each resident trait value $r$ all mutant trait values $m$ for which $S\_r(m)$ is positive. Note that $S\_r(m)$ is zero at the diagonal $m=r$. In PIPs the fitness landscapes as experienced by a rare mutant correspond to the vertical lines where the resident trait value $r$ is constant.

The selection gradient $S\_r\text{'}(r)$ determines the direction of evolutionary change. If it is positive (negative) a mutant with a slightly higher (lower) trait-value will generically invade and replace the resident. But what will happen if $S\_r\text{'}(r)$ vanishes? Seemingly evolution should come to a halt at such a point. While this is a possible outcome, the general situation is more complex. Traits or strategies $r^*$ for which $S\_\{r^*\}\text{'}(r^*)=0$, are known as evolutionarily singular strategies. Near such points the fitness landscape as experienced by a rare mutant is locally `flat'. There are three qualitatively different ways in which this can occur. First, a degenerate case similar to the qubic where finite evolutionary steps would lead past the local 'flatness'. Second, a fitness maximum which is known as an evolutionarily stable strategy (ESS) and which, once established, cannot be invaded by nearby mutants. Third, a fitness minimum where disruptive selection will occur and the population branch into two morphs. This process is known as evolutionary branching. In a pairwise invasibility plot the singular strategies are found where the boundary of the region of positive invasion fitness intersects the diagonal.

Singular strategies can be located and classified once the selection gradient is known. To locate singular strategies, it is sufficient to find the points for which the selection gradient vanishes, i.e. to find $r^*$ such that $S\text{'}\_\{r^*\}(r^*)\; =\; 0$. These can be classified then using the second derivative test from basic calculus. If the second derivative evaluated at $r^*$ is negative (positive) the strategy represents a local fitness maximum (minimum). Hence, for an evolutionarily stable strategy $r^*$ we have

- $S\_\{r^*\}\text{'}\text{'}(r^*)\; <\; 0$

If this does not hold the strategy is evolutionarily unstable and, provided that it also convergence stable, evolutionary branching will eventually occur. For a singular strategy $r^*$ to be convergence stable monomorphic populations with slightly lower or slightly higher trait values must be invadable by mutants with trait values closer to $r^*$. That this can happen the selection gradient $S\_r\text{'}(r)$ in a neighbourhood of $r^*$ must be positive for $r\; <\; r^*$ and negative for $r\; >\; r^*$. This means that the slope of $S\_r\text{'}(r)$ as a function of $r$ at $r^*$ is negative, or equivalently

- $frac\{d\}\{dr\}\; S\_r\text{'}(r)Big|\; \_\{r=r^*\}\; <\; 0.$

The criterion for convergence stability given above can also be expressed using second derivatives of the invasion exponent, and the classification can be refined to span more than the simple cases considered here.

The normal outcome of a successful invasion is that the mutant replaces the resident. However, other outcomes are also possible; in particular both the resident and the mutant may persist, and the population then becomes dimorphic. Assuming that a trait persists in the population if and only if its expected growth-rate when rare is positive, the condition for coexistence among two traits $r\_1$ and $r\_2$ is

- $S\_\{r\_1\}\; (r\_2)\; >\; 0$

and

- $S\_\{r\_2\}\; (r\_1)\; >\; 0,$

where $r\_1$ and $r\_2$ are often referred to as morphs. Such a pair is a protected dimorphism. The set of all protected dimorphisms is known as the region of coexistence. Graphically, the region consists of the overlapping parts when a pair-wise invasibility plot is mirrored over the diagonal

The invasion exponent is generalised to dimorphic populations in a straightforward manner, as the expected growth rate $S\_\{r\_1,\; r\_2\}(m)$ of a rare mutant in the environment set by the two morphs $r\_1$ and $r\_2$. The slope of the local fitness landscape for a mutant close to $r\_1$ or $r\_2$ is now given by the selection gradients

- $S\_\{r\_1,\; r\_2\}\text{'}(r\_1)$

and

- $S\_\{r\_1,\; r\_2\}\text{'}(r\_2)$

In practise, it is often difficult to determine the dimorphic selection gradient and invasion exponent analytically, and one often has to resort to numerical computations.

The emergence of protected dimorphism near singular points during the course of evolution is not unusual, but its significance depends on whether selection is stabilising or disruptive. In the latter case, the traits of the two morphs will diverge in a process often referred to as evolutionary branching. Geritz 1998 presents a compelling argument that disruptive selection only occurs near fitness minima. To understand this heuristically consider a dimorphic population $r\_1$ and $r\_2$ near a singular point. By continuity

- $S\_r(m)\; approx\; S\_\{r\_1,r\_2\}(m)$

and, since

- $S\_\{r\_1,\; r\_2\}(r\_1)\; =\; S\_\{r\_1,\; r\_2\}(r\_2)\; =\; 0,$

the fitness landscape for the dimorphic population must be a perturbation of that for a monomorphic resident near the singular strategy.

Evolution after branching is illustrated using trait evolution plots. These show the region of coexistence, the direction of evolutionary change and whether points where points where the selection gradient vanishes are fitness maxima or minima. Evolution may well lead the dimorphic population outside the region of coexistence, in which case one morph is extinct and the population once again becomes monomorphic.

Adaptive dynamics effectively combines game theory and population dynamics. As such, it can be very useful in investigating how evolution affects the dynamics of populations. One interesting finding to come out of this is that individual-level adaptation can sometimes result in the extinction of the whole population/species, a phenomenon known as evolutionary suicide.

- The Hitchhiker's guide to Adaptive Dynamics on which the first version of this article was based (GFDL).
- Adaptive Dynamics Papers a comprehensive list of papers about Adaptive Dynamics.

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Last updated on Sunday June 01, 2008 at 14:11:53 PDT (GMT -0700)

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This article is licensed under the GNU Free Documentation License.

Last updated on Sunday June 01, 2008 at 14:11:53 PDT (GMT -0700)

View this article at Wikipedia.org - Edit this article at Wikipedia.org - Donate to the Wikimedia Foundation

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