The Malthusian model is the simplest population growth model: the rate of change of the population is proportional to the population itself.
where is the population at time and is a constant proportionality factor. If , the population grows; if , it decays.
Named for Thomas Malthus (1798), who used it to argue that populations grow geometrically while food supplies grow only arithmetically — predicting (incorrectly, as it turned out) inevitable famine.
Solution
The ODE is separable:
Integrate:
Exponentiate:
where is the initial population.
The solution is exponential growth (when ) or exponential decay (). The doubling time (when growing) is ; the half-life (when decaying) is the same value.
Derivation from rates
Start from the conceptual decomposition: . If both are proportional to :
with . Per-capita growth rate is constant, independent of population size — that’s the Malthusian assumption.
Why it’s wrong (limitations)
The model breaks down at large populations. Real populations face:
- Resource limits: more individuals → less food per individual → lower per-capita growth rate.
- Crowding effects: disease spreads faster, predators concentrate, competition intensifies.
- Carrying capacity: the environment can sustain only so many.
These effects mean the per-capita growth rate decreases with population size, not stays constant. The Malthusian model overpredicts long-term growth.
Where it’s still useful
For early growth (when the population is small relative to environmental limits), the Malthusian model is an excellent approximation. Used for:
- Bacterial cultures in their exponential phase before nutrients run out.
- Cancer cells in early proliferation.
- Compound interest: a bank balance grows Malthusian-style with continuous compounding.
- Radioactive decay: , exactly Malthusian with .
For more realistic population modeling, see Logistic model — adds a competition term to limit growth.
Generalization
A generalized Malthusian allows time-dependent rates: . Solution by Integrating factor or directly:
This handles seasonal birth rates, time-varying decay rates, etc.
For a model with two interacting species (predator-prey style), see Lotka-Volterra equations (not yet in this vault).