Poisson Distributions

Comparison to Binomial Distribution

A Poisson distribution is an extreme case of the binomial distribution when n is very large and p is very small. Thus, the product np is "normal". We call this product λ=np

P(k)=λkk!e−λ

We could prove this formula from the Binomial Formula P(k)=(nk)pk(1−p)n−k. For our purposes it suffices to that the two formulas are basically the same.

Example: Mutations over time

Like in Population Genetics

Probability of getting one specific gene in one generation:

Mutation rate in one allele in one generation:
p=10−6
Looking at Drosophila, which has n=104 genes

λ=np=0.01

Probability of no mutations (k=0):

P(k)=λkk!e−λ

Not sure why she wrote this:
P(0)=(1−10−6)104

Using Poisson dist:
P(0)=(0.010)0!e−0.01=11e−0.01=0.990055

Probability of female having surviving offspring

Population Dynamics
If fecundity λ=2
(a female on average needs to produce two offpsring to maintain population. p is probability of survival of offspring and n is offspring population so in a stable population np=2)

P(0)=200!e−2=e−2=...
P(1)=211!e−2=2e−2
P(2)=222!e−2=2e−2
P(3)=233!e−2=43e−2
Then it decreases from here.

What is the lowest possible n for Poisson to be valid

Skellam model for plant population size

We have m possible sites for plants. n sites occupied and m−n are empty

Each plant produces α seeds, so we have αn seeds produced each year.

If we have many sites, m→∞

Probability of a site being occupied p
p=1m→∞→0
Seeds produced:
αn→∞

λ=αnp=αnm

Let's call the fraction of sites occupied n/m: =x
And ξ is the number of seeds in our "focal" site.

P(k)=λkk!e−λ

Fraction of sites occupied in the next time step

In the next year, every site will be occupied (m=n,x=1), minus the ones that had zero seeds. P(0) from a Poisson distribution will give us the probability of zero seeds reaching a site:

P(0)=λ00!e−λ=e−λ

So, combining our theory with this equation gives us:

xt+1=1−P(0)=1−e−αxt

At equilibrium

When there is no change, xt+1=xt. We call this value x^.

x^=1−e−αx^

If we plot xt+1 (y axis) and xt (α=2 for this example):

bottom=-0.5
top=2
left=-0.5
right=4
---
a= 2
y=1-e^{a(-x)}

We cannot solve this for x. But we can solve it for alpha, so let's try that, and use that solution to figure out how the equilibrium varies with alpha:

ln⁡(e−αx^)=ln⁡(1−x^)α=−ln⁡(1−x^)x^

Here is a new function. What does this look like? Plotting alpha as a function of x^:

left=-0.1
right=1.5
---
y=-(\ln(1-x))/x

If we swap axes (x as a function of alpha):

bottom=-0.1
top=1.5
---
x=-(\ln(1-y))/y

So, as alpha (seeds produced per occupied site) increases to 5, the equilibrium value of x approaches 1.

Each plant needs to produce at least one seed for the model to work. When alpha is one (produces one seed), the equilibrium population size (ratio) is zero.

When alpha gets close to five, nearly every site is occupied - every site gets many seeds and there is lots of competition.

Introducing a second species (Competition)

Let's say there is a second species that is more fecund but less competitive. If seeds from both species land in the same site, species A will always outcompete, but species B produces more seeds overall. This is a competition-colonization Trade-off.

Eva leaves this as an exercise to us to try and figure out how these relate.