Questions: Population Genetics and Hardy-Weinberg Equilibrium
3 questions to test your understanding
Score: 0 / 3
Question 1 Multiple Choice
A population is in Hardy-Weinberg equilibrium for a gene with alleles A (frequency p = 0.6) and a (frequency q = 0.4). What is the expected frequency of heterozygotes (Aa)?
A0.24
B0.48
C0.16
D0.36
The frequency of heterozygotes is 2pq = 2(0.6)(0.4) = 0.48. A common error is computing pq = 0.24 and forgetting the factor of 2, which accounts for the two ways to be heterozygous (receiving A from mother and a from father, or vice versa).
Question 2 True / False
The equation p + q = 1 describes the frequencies of genotypes in a Hardy-Weinberg population.
TTrue
FFalse
Answer: False
p + q = 1 describes *allele* frequencies — p is the frequency of one allele, q of the other, and together they must sum to 1. *Genotype* frequencies are described by p² + 2pq + q² = 1, which is the expanded form of (p + q)². Confusing these two equations is one of the most common errors in population genetics problems.
Question 3 Short Answer
A population is found to have significantly more homozygous individuals than Hardy-Weinberg predicts. Name one evolutionary mechanism that could cause this deviation and explain why it would produce an excess of homozygotes.
Think about your answer, then reveal below.
Model answer: Non-random mating (inbreeding) causes individuals to preferentially mate with relatives, increasing the probability that both copies of a gene descend from the same ancestor and are therefore identical. This increases homozygosity beyond H-W expectations without changing allele frequencies. Alternatively, strong disruptive selection against heterozygotes would reduce 2pq below predicted levels.
This tests whether students understand H-W as a null model: deviations reveal which assumptions are violated. An excess of homozygotes specifically points to mechanisms that reduce heterozygosity — inbreeding, assortative mating, or selection against heterozygotes — rather than mechanisms like drift or mutation that shift allele frequencies.