Have a single set of chromosomes.
Have two sets of paired chromosomes.
The number of chromosomes found in the sex cells (sperms and ova), which is half the number found in the majority of body cells. In humans the haploid number is 23.
A diagram to represent the alleles and gametes present for a particular characteristic in parents and the possible allele combinations in their children.
The number of chromosomes in most ordinary body cells. In humans this number is 46.
The plural of ovum.
The type of cell division, which occurs in the ovaries and testes, to produce cells with a haploid number of chromosomes.
The transfer of characteristics from parents to children through their genes.
The science of genes, heredity and variation.
The sex cells (ova and sperm) that join together to form a new unique diploid cell in sexual reproduction.
Meiosis is the process by which new cells with half the usual number of chromosomes are produced. In humans the full complement of 46 chromosomes is called the diploid number. Meiosis produces cells with 23 chromosomes, known as the haploid number, and these are the gametes, i.e. sperms for males and ova
In meiosis there are two lots of cell division so that a single diploid cell gives rise to four haploid cells. During fertilisation two haploid nuclei join to give a zygote with the diploid number of chromosomes. The zygote then grows and develops by mitosis.
Genetics is the study of inheritance, that is, how characteristics are passed from one generation to the next. Gametes are haploid with only one of each chromosome and therefore one of each gene. When two gametes fuse at fertilisation the zygote now has two of each gene (that is a pair of alleles for each gene) one from the mother and one from the father. Where the alleles are different, one may be recessive and the other dominant and the dominant allele will determine the characteristic.
We can use genetic diagrams to show how a characteristic is passed on. Letters are used to represent the genes and a capital letter means an allele is dominant, and a small letter means a recessive allele. The diagram right shows the possible gametes and offspring for parents who both have homozygous alleles for eye colour, one for blue eyes and one for brown eyes. Note that, any child with Bb alleles will have brown eyes but carries the allele for blue eyes which could be passed on to a later generation.
For parents with heterozygous alleles for eye colour, the outcome is different as shown in the diagram below.
The ability to roll the tongue is something an individual can or cannot do and is passed on genetically. It cannot be learned. In the diagram below, the parents are heterozygous for tongue rolling.
The inheritance of blood group can be represented by the simplified diagram below. It shows the possible blood groups of offspring when the parents are heterozygous A and heterozygous B.
Many characteristics are controlled by a gene (or sometimes a few genes). The gender of the next generation, however, is determined by a whole chromosome. Human chromosome pair number 23 differs between male and female. It can be XX , which is female, or XY, which is male. In the following genetic diagram the letters represent chromosomes.
It shows that the ratio of boys to girls is 1:1, that is, there is always an equal chance of getting a boy or a girl.