Inbreeding Depression Calculator
Calculate inbreeding coefficient F and expected fitness reduction from inbreeding.
What the Inbreeding Coefficient Measures
F is the probability that both alleles at a locus are identical by descent — inherited from the same ancestral copy. It is not a measure of general similarity but of shared ancestry at that specific locus.
| Relationship | F of offspring |
|---|---|
| Parent–offspring or full sibs | 0.25 |
| Half sibs, uncle–niece | 0.125 |
| First cousins | 0.0625 |
| Second cousins | 0.0156 |
Repeated inbreeding compounds. Three generations of full-sib mating gives F = 1 − 0.75³ = 0.578, not 0.75 — each generation acts on the remaining heterozygosity rather than the original.
Why Inbreeding Reduces Fitness
| Mechanism | Explanation | Purgeable? |
|---|---|---|
| Partial dominance | Recessive deleterious alleles become homozygous | Yes, partly |
| Overdominance | Heterozygote advantage is lost | No |
The distinction matters for conservation. If depression comes mainly from recessive deleterious alleles, slow inbreeding can purge them — selection removes homozygotes and the load declines. If it comes from heterozygote advantage, purging is impossible because the heterozygous state itself is what confers fitness.
Evidence supports partial dominance as the larger contributor in most species, which is why some captive breeding programmes tolerate slow inbreeding while avoiding rapid crashes.
Practical Thresholds
Conservation genetics commonly cites a ceiling of 1% increase in F per generation, corresponding to an effective population size of 50 — enough to limit short-term depression. Long-term retention of adaptive potential is usually put at Ne of 500, the basis of the 50/500 rule.
Note that outbreeding depression is the opposite risk: crossing populations adapted to different environments, or with chromosomal differences, can also reduce fitness. Genetic rescue programmes weigh both.
Worked Examples
Common Mistakes
Inbreeding compounds multiplicatively on remaining heterozygosity. Three generations of full-sib mating gives 0.578, not 0.75.
Only the partial dominance component is purgeable. Depression from heterozygote advantage cannot be removed by selection, since the heterozygous state itself confers the advantage.
It measures probability of identity by descent at a locus, not overall relatedness or genome-wide similarity.
Crossing populations adapted to different environments can also reduce fitness. Genetic rescue requires weighing both risks.