Haploid gametes, diploid zygotes and genetic crosses in plants

Organisms (Continuity and change) · Inheritance · note 1 of 10

Haploid gametes, diploid zygotes and genetic crosses in plantsSpec D3.2.1, D3.2.2

In short

Inheritance in all eukaryotes with a sexual life cycle works by parents producing haploid gametes that fuse to form a diploid zygote, which has two copies of each autosomal gene. Genetic crosses in flowering plants transfer pollen, which contains the male gametes, to the stigma of another plant, and follow the P, F1 and F2 generations using Punnett grids.

Each parent produces haploid gametes by meiosis, carrying one copy of each gene. At fertilization two gametes fuse to give a diploid zygote with two copies of each autosomal gene, one from each parent. This pattern of inheritance is common to all eukaryotes with a sexual life cycle.

Carrying out a cross in flowering plants

Pollen contains the male gametes and the female gametes are in the ovules inside the ovary, so pollination is needed to carry out a cross. Plants such as peas produce male and female gametes in the same flower, so they normally self-pollinate and self-fertilize.

  1. Choose two pure-breeding (homozygous) parents with contrasting traits: the P generation.
  2. Remove the immature anthers from flowers of one parent so it cannot self-pollinate.
  3. Transfer pollen from the other parent to its stigmas with a small brush, then cover the flowers with a bag to stop other pollen arriving.
  4. Collect the seeds and grow them: these plants are the F1 generation. Record their phenotypes.
  5. Allow the F1 plants to self-pollinate (or cross them with each other). The offspring are the F2 generation. Count each phenotype.
  6. Use a Punnett grid to predict the expected ratios and compare them with the counts.

Genetic crosses like these are widely used to breed new varieties of crop and ornamental plants, combining useful traits such as yield, disease resistance or flower colour.

Exam tip:

Always show a full genetic diagram: parental phenotypes and genotypes, gametes, a Punnett grid, then offspring genotypes, phenotypes and ratio.

Written and checked against the IB Biology HL specification · Updated October 2026

Frequently asked questions

What is the difference between genotype and phenotype?

Genotype is the combination of alleles an organism inherits, for example Aa. Phenotype is the observable traits of the organism, which result from its genotype and environmental factors. Some traits depend on genotype only, such as ABO blood group; others, such as height, depend on genes interacting with the environment.

What is the difference between codominance and incomplete dominance?

In codominance the heterozygote has a dual phenotype, with both alleles fully expressed, as in blood group AB with A and B antigens. In incomplete dominance the heterozygote has an intermediate phenotype, as in pink four o'clock flowers from red and white parents. Both give a 1:2:1 phenotype ratio in the F2.

Why are sex-linked disorders more common in males?

Sex-linked disorders such as haemophilia are caused by recessive alleles on the X chromosome. Males have only one X chromosome, so a single recessive allele is expressed. Females have two X chromosomes and are affected only if both carry the recessive allele, so they are usually unaffected carriers.

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