D3.2.14—Continuous variation
Continuous variation produces a range of phenotypes, often influenced by many genes and environmental factors in inheritance problems in inheritance problems.
- Syllabus
- First assessment 2025
- Objective
- D3.2.14
- Level
- HL
Continuous variation produces a range of phenotypes, often influenced by many genes and environmental factors in inheritance problems in inheritance problems.

Coverage 2013–2025 · Updated 16 Jul 2026
| Feature | Continuous variation | Discrete variation |
|---|---|---|
| possible values | many intermediate measurements | separate categories |
| common cause | polygenic effects plus environment | often one or few major loci |
| examples | height, body mass, skin pigmentation | ABO group, biological sex chromosome category |
| useful display | histogram or box plot | bar chart or counts table |
Ask whether the variable is measured on a scale or counted in named categories. Height remains continuous even if a researcher later groups measurements into artificial height bands.
Continuous does not mean every imaginable value must occur in one sample, and discrete does not mean the categories are controlled by only one allele.
In polygenic inheritance, several loci contribute to one characteristic. Different combinations of small allele effects generate many genotypic values rather than a few Mendelian phenotype classes.
many contributing genotypes + nutrition, health, temperature or other environmental effects + genotype-specific responses to those conditions → overlapping phenotypes across a continuous range
| Trait | Genetic contribution | Environmental contribution |
|---|---|---|
| height | many growth-related loci | nutrition, disease and developmental conditions |
| body mass | metabolism and appetite loci | diet, activity and health |
| skin pigmentation | several melanin-related loci | ultraviolet exposure changes melanin production |
Do not confuse multiple genes contributing to one trait with multiple alleles at one gene locus. These are different levels of genetic variation.
X and Y contributions establish the usual chromosomal starting point → unequal X-linked gene dosage changes inheritance risk → pedigrees reveal transmission across families → polygenes and environment create continuous population variation → box plots summarize centre and spread
| Evidence source | Reliable question |
|---|---|
| X-linked cross | which parent supplies the allele to sons or daughters? |
| pedigree | which inheritance hypotheses are contradicted by family relationships? |
| continuous measurements | where is the median and how wide is the middle 50%? |
| apparent outlier | biological extreme, data error or different process? |
Match the claim to the evidence scale. One Punnett grid predicts a fertilization probability, a pedigree constrains family genotypes, and a box plot describes a sample distribution; none alone proves a universal biological rule.
[ 7 ]
Explain the reasons for variation in human height.