In humans, the sex of a child is determined by the sex chromosomes contributed by the parents. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY). During reproduction, the mother always contributes an X chromosome, while the father can contribute either an X or a Y chromosome. If the child inherits an X chromosome from the father, the child will be female (XX); if a Y chromosome is inherited, the child will be male (XY).


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Introduction to Sex Determination in Humans

Sex determination in humans is a genetic process where the sex of a child is established based on the chromosomes inherited from the parents. This process is crucial for the development of sexual characteristics and is determined at the moment of conception.

The Role of Chromosomes in Sex Determination

Humans have 23 pairs of chromosomes, with one pair being the sex chromosomes. These are crucial in determining the genetic sex of an individual. Females typically have two X chromosomes (XX), while males have one X and one Y chromosome (XY).

Contribution of the Mother

The mother contributes one of her X chromosomes to the child. Since females have two X chromosomes, the mother’s contribution is always an X chromosome. This is a constant factor in the sex determination process.

Contribution of the Father

The father, having one X and one Y chromosome, can contribute either chromosome to the child. The sex chromosome that the father contributes determines the sex of the child. If the father contributes an X chromosome, the child will be female (XX), and if he contributes a Y chromosome, the child will be male (XY).

The Genetic Mechanism

At conception, when the sperm (carrying either an X or a Y chromosome) fertilizes the egg (carrying an X chromosome), the combination of these chromosomes determines the sex of the embryo. This combination is a matter of chance, with approximately a 50% probability for each sex.

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The Determination of Sex

In conclusion, the sex of a child in humans is determined by the specific combination of sex chromosomes inherited from the parents. The mother’s contribution is always an X chromosome, while the father’s contribution, either an X or a Y chromosome, is what ultimately decides whether the child will be male or female. This genetic mechanism is a fundamental aspect of human reproduction and development.

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Questions of 10th Science Chapter 8 in Detail

If a trait A exists in 10% of a population of an asexually reproducing species and a trait B exists in 60% of the same population, which trait is likely to have arisen earlier?
How does the creation of variations in a species promote survival?
How do Mendel’s experiments show that traits may be dominant or recessive?
How do Mendel’s experiments show that traits are inherited independently?
A man with blood group A marries a woman with blood group O and their daughter has blood group O. Is this information enough to tell you which of the traits – blood group A or O – is dominant? Why or why not?
How is the sex of the child determined in human beings?
A study found that children with light-coloured eyes are likely to have parents with light-coloured eyes. On this basis, can we say anything about whether the light eye colour trait is dominant or recessive? Why or why not?
Outline a project which aims to find the dominant coat colour in dogs.
How is the equal genetic contribution of male and female parents ensured in the progeny?