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
Exam analysis
Chance of appearing12%of analysed past papers
Latest appearanceMay 2025
Most common paperPaper1
Typical marks1–3
Common command terms
- Identify
- State
- Outline
- Distinguish
- Explain
Recent exam appearances
May 2025Paper1B ["HL"] · TZ14(b)[ 2 ]D3.2.14—Continuous variation
May 2024Paper1 ["HL"] · TZ136[ 1 ]D3.2.14—Continuous variation
May 2022Paper2 ["HL"] · TZ18(c)[ 7 ]D3.2.14—Continuous variation
November 2021Paper2 ["HL"] · TZ06(c)[ 4 ]D3.2.14—Continuous variation
November 2018Paper2 ["HL"] · TZ07(b)[ 5 ]D3.2.14—Continuous variation
Practice this objective
Coverage 2013–2025 · Updated 16 Jul 2026
Continuous Variation Forms a Range
Continuous variation produces many intermediate values because multiple genes and environment influence the trait.
Polygenic effects add small contributions; nutrition and other conditions shift outcomes; populations show a distribution rather than a few classes. Trace the allele combination through the stated biological mechanism before predicting the result.
Look for a measurable range and ask whether many genes and environment contribute.; compare the stated alleles and outcome
Human height forms a broad range, and nutrition can shift an individual’s height. This gives a concrete prediction from the stated parental information.
A smooth distribution can still have a strong genetic component. Interpret the result within the stated inheritance model and its sample or environmental limits.
Continuous variation
Assessment in practice
1–3 marksHow it is assessed
This objective is assessed through structured response, commonly using Identify / State / Outline.
Command terms
Identify / State / Outline / Distinguish / Explain
What earns marks
Build the answer around this relationship: Continuous variation shows a range rather than separate phenotype classes.
Representative question
Question 1
Explain the reasons for variation in human height.
Retrieve the Core Inheritance Route
Core D3.2 is secure when the student can move from allele rules into predictions and evidence: gametes form genotypes, genotypes can produce phenotypes, different dominance patterns need different notation, and pedigrees or plots require evidence-based interpretation.
- haploid gametes carry one allele and fertilization restores a diploid genotype
- dominance, codominance, incomplete dominance, environment, and plasticity affect the observed trait
- PKU, ABO, sex determination, and haemophilia use different inheritance rules and notation
- pedigrees infer inheritance patterns and box plots summarize continuous variation
Solve Core Inheritance Questions
Core inheritance exam questions reward disciplined reasoning. First identify the inheritance rule, then write the correct notation or evidence, then state the phenotype, ratio, or conclusion. This prevents the common mistake of writing definitions without solving the genetic problem.
- Use allele and genotype notation correctly for monohybrid, ABO, PKU, haemophilia, and sex-determination contexts.
- Connect genotype, dominance pattern, environment, or plasticity to phenotype.
- Use pedigree or box-plot evidence to justify an inheritance or variation conclusion.
Concept essentials
- Continuous variation shows a range rather than separate phenotype classes.
- Polygenic inheritance can produce many intermediate phenotypes.
- Environmental factors can contribute to continuous variation.