Edexcel A-Level Biology B 9BI0
Biological Molecules
Cells, Viruses and Reproduction of Living Things
Classification and Biodiversity
Exchange and Transport
Energy for Biological Processes
Microbiology and Pathogens
Modern Genetics
Origins of Genetic Variation
Control Systems
Ecosystems
Origins of Genetic Variation
- 8 subtopics
- 24 things to know
- Papers 2 and 3
What Origins of Genetic Variation covers
Where genetic variation comes from, how it is passed on through monohybrid, dihybrid and sex-linked crosses, how a chi-squared test judges whether results fit a prediction, and how allele frequencies change in a population.
Where it is assessed
Papers 2 and 3
Advanced Physiology, Evolution and Ecology, then the general and practical principles paper.
Check the Pearson Edexcel specification ↗The 8 subtopics
Each one has its own page.
- Mutation, meiosis and random fertilisationRecall questions on mutation, crossing over, independent assortment and random fertilisation as sources of variation.Open →
- Genotype, phenotype and monohybrid inheritanceRecall questions on the key terms, dominance and codominance, and constructing a monohybrid cross.Open →
- Dihybrid crosses and pedigree diagramsRecall questions on the symbols and lines of a pedigree diagram, what a dihybrid cross is, the 9:3:3:1 ratio, and why unlinked genes assort independently.Open →
- Autosomal linkage and sex linkageRecall questions on autosomal linkage and why linked genes do not assort independently, crossing over and recombinant phenotypes, body colour and wing length in Drosophila, and sex linkage, hemizygous males and the X-linked inheritance of haemophilia.Open →
- The chi-squared test in geneticsRecall questions on the null hypothesis, calculating the statistic, degrees of freedom, and interpreting the result against the critical value.Open →
- Selection pressures and allele frequencyRecall questions on selection pressures, stabilising selection and birth mass, disruptive selection, bimodal distributions and speciation, and why selection changes allele frequencies without creating new alleles.Open →
- Genetic drift and the founder effectRecall questions on chance change in small populations, genetic bottlenecks, and the founder effect.Open →
- The Hardy-Weinberg equationRecall questions on the conditions the principle assumes, using the two equations, and what a departure from equilibrium indicates.Open →
What you need to know
Answer each one before you reveal it.
State the formula for the chi-squared statistic and the purpose of the chi-squared test in genetics.
In the chi-squared formula, what does E represent?
How are degrees of freedom calculated for a chi-squared test?
In the Hardy-Weinberg equation, what do p², 2pq and q² each represent?
State the formula for the number of possible gamete combinations produced by independent assortment, and define the variable.
What is calculated from a completed Punnett square?
What is the genotype of a female carrier of haemophilia?
State the Hardy-Weinberg equation that describes genotype frequencies.
What is meant by the term genotype?
After identifying parental genotypes in a genetic cross, what must be determined next?
What do horizontal lines represent in a pedigree diagram?
How are gametes used in a Punnett square to show offspring genotypes?
Under what environmental conditions does stabilising selection usually operate?
What happens to allele frequencies and to the range of variation in a population undergoing stabilising selection?
Why might allele frequencies change following a population bottleneck?
How does the founder effect begin?
What is the ultimate source of new genetic variation in a population?
Define phenotype.
What do vertical lines represent in a pedigree diagram?
Define autosomal linkage.
Explain how disruptive selection can lead to speciation.
What is the consequence of the founder effect for allele frequencies in the new population?
In the Hardy-Weinberg equations, what do p and q represent?
Take Origins of Genetic Variation further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Gene mutation vs Chromosome mutation
Gene mutation: change in the base sequence of DNA. Chromosome mutation: change in chromosome structure or number.
Horizontal gene transfer vs Vertical gene transfer
Horizontal gene transfer: movement of genetic material between organisms without reproduction. Vertical gene transfer: inheritance of genetic material from parent to offspring.
Genetic drift vs Natural selection
Genetic drift: random change in allele frequencies. Natural selection: non-random change caused by differential reproductive success.
Questions from this topic
Each one with the model answer underneath.
- 1
What is the ultimate source of new genetic variation in a population?
Model answer
Mutations are the ultimate source of new genetic variation, creating new alleles that did not previously exist in a population.
- 2
Why are mutations considered the only way to generate truly novel alleles?
Model answer
Mutations alter the DNA sequence itself, producing alleles that have never existed before, rather than simply rearranging pre-existing alleles.
- 3
During random assortment, where do homologous chromosome pairs align?
Model answer
Homologous pairs align independently at the metaphase plate during metaphase I.
- 4
Explain how the orientation of each homologous pair at metaphase I is determined.
Model answer
Each homologous pair can orient with either parental chromosome facing either pole; this orientation is random and independent of other pairs.
- 5
State the formula for the number of possible gamete combinations produced by independent assortment, and define the variable.
Model answer
The formula is 2ⁿ, where n is the haploid chromosome number.
- 6
At which stage of meiosis does crossing over occur?
Model answer
Crossing over occurs during prophase I when homologous chromosomes pair up.
What is inside Levo
Six ways to work the same material.
Origins of Genetic Variation revision questions
- What does Origins of Genetic Variation cover in Edexcel A-Level Biology B?
- 8 subtopics: mutation, meiosis and random fertilisation, genotype, phenotype and monohybrid inheritance, dihybrid crosses and pedigree diagrams, autosomal linkage and sex linkage, the chi-squared test in genetics, selection pressures and allele frequency, genetic drift and the founder effect and the hardy-weinberg equation. Each one has its own page with questions and model answers.
- How is Origins of Genetic Variation organised?
- By the Edexcel 9BI0 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Origins of Genetic Variation, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
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