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 Produces a Measurable Range

Continuous variation has many intermediate values and often results from several genes, environmental factors, or both.

Variation Example Useful description
Continuous Human skin colour or height Distribution, range, mean, median and mode
Discrete ABO blood group Counts or proportions in distinct categories

In polygenic inheritance, many loci each contribute to the phenotype; environmental conditions can add further variation, often producing a broad distribution.

For student heights, the mean uses every value, the median identifies the middle position and the mode identifies the most frequent value or interval.

Continuous does not mean entirely environmental, and discrete does not mean that only one gene is always involved.

Continuous variation

Assessment in practice

1–3 marks
How 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

[Maximum number: 7]

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.