Geometric and Exponential Growth
Applied Population Dynamics
WILD 5700/7700
The equations for geometric and exponential growth.
The relationship between geometric growth and the BIDE model.
The difference between continuous and discrete time models of population growth.
The definition of density independent population growth.
The study of spatial and temporal variation in population size and structure.
How does abundance go from \(N_t\) to \(N_{t+1}\)?
Answer: The BIDE Model
\[N_{t+1} = N_t + B_t + I_t - D_t - E_t\]
B=Births, I=Immigrations, D=Deaths, E=Emigrations
Geometric growth is a simplification of BIDE.
Exponential growth is a continuous time version of geometric growth.
Charles Darwin Origin of Species
“There is no exception to the rule that every organic being increases at so high a rate, that if not destroyed, the earth would soon be covered by the progeny of a single pair.”
“Hence, as more individuals are produced than can possibly survive, there must in every case be a struggle for existence…”
“Every wild species has certain fixed habits which govern the reproductive process, and determine its maximum rate. Thus one pair of quail, if entirely unmolested in an ‘ideal’ environment, would increase at this rate:”
| At End of | Young | Adults | Total |
|---|---|---|---|
| 1st year | 14 | 2 | 16 |
| At End of | Young | Adults | Total |
|---|---|---|---|
| 1st year | 14 | 2 | 16 |
| 2nd year | (16/2)14=112 | 16 | 128 |
| At End of | Young | Adults | Total |
|---|---|---|---|
| 1st year | 14 | 2 | 16 |
| 2nd year | (16/2)14=112 | 16 | 128 |
| 3rd year | (128/2)14=896 | 128 | 1024 |
“The maximum rate of increase is of course never attained in nature. Part of it never takes place, part of it is absorbed by natural enemies, and part of it absorbed by hunters.”


For an arbitrary time step (\(t\)):
\[N_t = N_0(1+r)^t\]
Or, for one time step:
\[N_{t+1} = N_t + N_tr\]
\(r\) = discrete-time version of intrinsic rate of increase
\[N_{t+1} = N_t + N_t r\]











| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | |
| 2 | |
| 3 | |
| 4 | |
| 5 | |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | |
| 3 | |
| 4 | |
| 5 | |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | |
| 4 | |
| 5 | |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | |
| 5 | |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | 640 |
| 7 | |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | 640 |
| 7 | 1280 |
| 8 | |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | 640 |
| 7 | 1280 |
| 8 | 2560 |
| 9 | |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | 640 |
| 7 | 1280 |
| 8 | 2560 |
| 9 | 5120 |
| 10 |
| Time | Population size (\(N\)) |
|---|---|
| 0 | 10 |
| 1 | 20 |
| 2 | 40 |
| 3 | 80 |
| 4 | 160 |
| 5 | 320 |
| 6 | 640 |
| 7 | 1280 |
| 8 | 2560 |
| 9 | 5120 |
| 10 | 10240 |
\[N_{t+1} = N_t + N_t r\]
\(-1 \leq r < 0\)
population goes extinct

\(r = 0\)
population is at equilibrium

\(r > 0\)
population grows to \(\infty\)

\[N_{t+1} = N_t + B_t + I_t - D_t - E_t\]
| \(N_t\) | = | Abundance at year \(t\) |
| \(B\) | = | Births |
| \(I\) | = | Immigrations |
| \(D\) | = | Deaths |
| \(E\) | = | Emigrations |
Step 1: Ignore immigration and emigration
\[ N_{t+1} = N_t + B_t - D_t \]
Step 2: Divide both sides by \(N_{t}\).
\[ \frac{N_{t+1}}{N_t} = \frac{N_t + B_t - D_t}{N_t}\]
Step 3: Write in terms of birth and death rates, with \(r=b-d\).
\[ \begin{aligned} \frac{N_{t+1}}{N_{t}} \quad &= \quad 1 + b - d \\ \quad &= \quad 1 + r %\\ % \quad &= \quad \lambda \end{aligned} \]
Step 4: Multiply through by \(N_t\) to get the solution:
\[N_{t+1} = N_t + N_tr\]
Note
The finite rate of increase is defined as: \(\lambda = N_{t+1}/N_t\), which for geometric growth is equivalent to \(\lambda = 1+r\).
Geometric and exponential growth are examples of density independent growth.
Definition: Population growth rate (\(r\) or \(\lambda\)) is not affected by population size (\(N\)).
Implications: Resources are unlimited and there is no carrying capacity!
All models are wrong, but some are useful. (George Box)
Is exponential growth a useful model?
Possibly for describing some populations during short time periods.
And as foundation for more realistic models.

Is the human population exhibiting exponential growth?
Read pages 15–19 in Conroy and Carroll.
Be prepared for a quiz.