Class 10 Science Β· Chapter 8 NotesHeredity

Class 10 Science Heredity notes covering variation, Mendel's laws of inheritance, dominant and recessive traits, chromosomes, genes and sex determination in humans.

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Chapter contents

Chapter summary

Heredity is the branch of biology that explains how traits pass from parents to offspring. In this chapter, you will first see how variations arise during reproduction and why some variations help organisms survive better in a changing environment. You will then study the rules of inheritance worked out by Gregor Johann Mendel using garden peas, including dominant and recessive traits, the F1 and F2 generations, and the independent inheritance of two separate traits. The chapter also explains how genes, which are sections of DNA, control traits through proteins and enzymes, how germ cells carry a single set of chromosomes, and how the sex of a child is determined in human beings. These ideas help you understand why individuals of a species look similar yet are never exactly alike, and how inheritance maintains the basic body design of a species across generations.

What you'll learn

1Explain how variations are created during asexual and sexual reproduction
2Describe why some variations give individuals a better chance of survival
3State Mendel's conclusions about dominant and recessive traits
4Interpret the results of Mendel's experiments on one trait and on two traits
5Explain how genes control traits through proteins and enzymes
6Describe the role of chromosomes and germ cells in inheritance
7Explain how the sex of a child is determined in human beings

Chapter at a glance

01Chapter Overview
02Mendel's Laws of Inheritance
03Chromosomes and Gene Expression
04Human Heredity and Genetic Disorders
05Accumulation of Variation during Reproduction
06Inherited Traits
07Sex Determination

Detailed chapter notes

01

Accumulation of Variation During Reproduction

Reproduction produces new individuals that are similar to their parents but not identical. In asexual reproduction, differences are very small and arise mainly from minor inaccuracies in DNA copying. In sexual reproduction, the combining of genetic material from two parents creates much greater diversity. These variations are inherited by the next generation, and each new generation adds its own newly created differences. Not all variations are equally useful. Depending on their nature, different individuals may have different advantages in a given environment. For example, bacteria that can withstand heat survive better in a heat wave. Environmental factors select variants that are better suited to survive, and this selection forms the basis of evolutionary processes.

  • Asexual reproductionsmall variations, mainly from DNA copying errors
  • Sexual reproductionlarger diversity because two parents contribute genetic material
  • Selection of variants by environmental factors is the basis of evolution
02

Heredity and Inherited Traits

The rules of heredity decide how traits and characteristics are reliably passed on from one generation to the next. A child shows all the basic features of a human being but does not look exactly like either parent, and human populations show a great deal of variation. Traits such as free or attached earlobes are inherited from parents. Since both the father and the mother contribute practically equal amounts of genetic material to the child, each trait can be influenced by both paternal and maternal DNA. This means that for each trait there are two versions in every child, and the trait that is actually seen depends on the rules of inheritance.

  • Hereditythe passing of traits from parents to offspring
  • Both parents contribute almost equal amounts of genetic material
  • Each trait exists in two versions in a sexually reproducing organism
03

Mendel's Experiments and the Rules of Inheritance

Gregor Johann Mendel studied contrasting visible characters of garden peas, such as round or wrinkled seeds, tall or short plants, and white or violet flowers. He crossed a tall plant with a short plant and found that all the first-generation, or F1, progeny were tall; there were no medium-height plants. This showed that only one parental trait was expressed, not a mixture. When the F1 tall plants were self-pollinated, the second-generation, or F2, progeny were not all tall: about one quarter of them were short. This showed that both tallness and shortness were inherited in the F1 plants, but only tallness was expressed. Mendel therefore proposed that two copies of a factor, now called a gene, control each trait in sexually reproducing organisms.

  • F1 generationall tall, no halfway characteristics
  • F2 generationtall and short plants appear, with short plants making up about one quarter
  • Two copies of a factor (gene) control each trait
04

Dominant and Recessive Traits

In Mendel's explanation, both TT and Tt plants are tall, while only tt plants are short. This means a single copy of T is enough to make the plant tall, but both copies must be t for the plant to be short. Traits like T are called dominant traits, and traits that behave like t are called recessive traits. When pea plants showing two different characteristics are bred, the F1 progeny of a tall plant with round seeds and a short plant with wrinkled seeds are all tall with round seeds, so tallness and round seeds are dominant. When these F1 plants are self-pollinated, the F2 progeny include tall plants with round seeds, short plants with wrinkled seeds, and also new combinations such as tall plants with wrinkled seeds and short plants with round seeds. This shows that the tall/short trait and the round/wrinkled seed trait are inherited independently.

  • Dominant traitexpressed even when only one copy is present
  • Recessive traitexpressed only when both copies are the same recessive form
  • Two separate traits are inherited independently, producing new combinations in the F2 generation
05

How Traits Are Expressed

Cellular DNA is the information source for making proteins in the cell. A section of DNA that provides information for one protein is called the gene for that protein. Proteins control the characteristics of an organism. For example, plant height depends on the amount of a particular plant hormone, and the amount of hormone made depends on the efficiency of the process that produces it. An enzyme is important in this process. If the enzyme works efficiently, a lot of hormone is made and the plant grows tall. If the gene for that enzyme is altered so that the enzyme becomes less efficient, less hormone is made and the plant remains short. In this way, genes control characteristics or traits.

  • Genea section of DNA that provides information for one protein
  • Proteins control the traits of an organism
  • A change in a gene can change the efficiency of an enzyme and therefore the trait
06

Chromosomes and Germ Cells

If both parents contribute equally to the DNA of the progeny, each parent must contribute one copy of the same gene, so each pea plant must have two sets of all genes. For this to work, each germ cell must carry only one set of genes. This is possible because each gene set is not one long thread of DNA but is present as separate independent pieces called chromosomes. Each body cell has two copies of each chromosome, one from each parent. Every germ cell takes one chromosome from each pair, which may be of maternal or paternal origin. When two germ cells combine, the normal number of chromosomes is restored in the progeny, ensuring the stability of the DNA of the species. This mechanism explains Mendel's results and is used by all sexually reproducing organisms.

  • Chromosomea separate independent piece of DNA carrying many genes
  • Body cells have two copies of each chromosome; germ cells have one
  • Fusion of two germ cells restores the normal chromosome number in the offspring
07

Sex Determination in Human Beings

Different species determine sex in different ways. In some reptiles, the temperature at which fertilised eggs are kept decides whether the young ones are male or female. In snails, individuals can change sex, showing that sex is not genetically determined in them. In human beings, sex is largely genetically determined. Human beings have 22 pairs of chromosomes in which each chromosome has a maternal and a paternal copy. The remaining pair, called the sex chromosomes, is not always a perfect pair. Women have a perfect pair of sex chromosomes, both called X, so they are XX. Men have a mismatched pair with one normal-sized X and one short Y, so they are XY. All children inherit an X chromosome from their mother. A child who inherits an X chromosome from the father is a girl, and one who inherits a Y chromosome from the father is a boy. Thus, the sex of the child is determined by what is inherited from the father.

  • WomenXX; Men: XY
  • Mother always contributes an X chromosome
  • Father's contribution decides the sex of the child: X for a girl, Y for a boy
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Quick revision: key points

  • Variations arising during reproduction can be inherited and may increase the chances of survival.
  • Sexually reproducing individuals have two copies of the gene for each trait.
  • A trait that is expressed when the two copies are different is dominant; the other is recessive.
  • Mendel's F1 plants were all tall, but the F2 generation included short plants, showing that both traits were inherited.
  • Traits can be inherited independently, giving new combinations of traits in the offspring.
  • A gene is a section of DNA that provides information for one protein.
  • Genes control traits by controlling the proteins and enzymes made in the cell.
  • Chromosomes are separate pieces of DNA; body cells have two copies of each, germ cells have one.
  • In humans, women are XX and men are XY; the father's chromosome decides the sex of the child.

Test yourself

Try each question first, then reveal the answer.

Question 01

What is the structural unit of heredity that carries genetic information?

  • AChromosome
  • BGene
  • CRibosome
  • DMitochondria
Show answer
Answer: (B) Gene

A gene is the basic unit of heredity that carries specific genetic information for a trait, while chromosomes are structures containing many genes.

Question 02

Which of the following is an example of a sex-linked trait in humans?

  • AHeight
  • BColor blindness
  • CSkin color
  • DAbility to roll tongue
Show answer
Answer: (B) Color blindness

Color blindness is a sex-linked recessive trait carried on the X chromosome. Males are more frequently affected than females.

Question 03

How many pairs of chromosomes are present in a normal human somatic cell?

  • A20 pairs
  • B23 pairs
  • C46 pairs
  • D92 pairs
Show answer
Answer: (B) 23 pairs

Humans have 23 pairs of chromosomes (46 total) in their somatic cells. This includes 22 pairs of autosomes and 1 pair of sex chromosomes.

Question 04

Hemophilia is inherited as a recessive trait. If a carrier mother (XHXh) has children with a normal father (XHY), what is the probability of having an affected son?

  • A0%
  • B25%
  • C50%
  • D75%
Show answer
Answer: (C) 50%

From the cross XHXh Γ— XHY, sons can be XHY (normal) or XhY (affected). The probability of an affected son is 50%.

Question 05

Which of the following best describes gene expression?

  • AThe physical appearance of an organism
  • BThe process by which genetic information is used to synthesize functional products
  • CThe mutation of DNA sequences
  • DThe replication of chromosomes
Show answer
Answer: (B) The process by which genetic information is used to synthesize functional products

Gene expression is the process where genetic information in DNA is transcribed into RNA and translated into proteins, resulting in functional products.

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Sample questions and answers

Sample question3 marks

Q1. How does the creation of variations in a species promote survival?

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Model answer

Variations provide different advantages to individuals. Some variations may help individuals survive better in a changing environment, such as bacteria that can withstand heat surviving a heat wave. Environmental factors select variants that are better adapted, leading to increased survival and evolution.

Sample question3 marks

Q2. How do Mendel’s experiments show that traits may be dominant or recessive?

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Model answer

Mendel crossed tall and short pea plants. In the F1 generation, all plants were tall, showing that tallness is dominant and shortness is recessive. When F1 tall plants were self-pollinated, the F2 generation had both tall and short plants in a 3:1 ratio, indicating that the recessive trait reappeared. This shows that a single copy of the dominant trait (T) is enough to express tallness, while both copies must be recessive (tt) for shortness to appear.

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Q3. What are chromosomes and how do they ensure the independent inheritance of traits? Explain with reference to Mendel's experiments.

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Model answer

Chromosomes are separate independent pieces of DNA, each carrying many genes. Each cell has two copies of each chromosome, one from each parent. During germ cell formation, each germ cell takes one chromosome from each pair, so traits located on different chromosomes are inherited independently. This explains Mendel's observation that seed shape and seed colour are inherited independently, giving new combinations in the F2 generation.

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Q4. How is the sex of a child determined in human beings? Explain with the help of the chromosomes inherited from the parents.

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Model answer

In humans, women have a perfect pair of sex chromosomes, XX, while men have a mismatched pair, XY. All children inherit an X chromosome from their mother. If the child inherits an X chromosome from the father, the child is a girl (XX); if the child inherits a Y chromosome from the father, the child is a boy (XY). Thus, the father determines the sex of the child.

Sample question3 marks

Q5. How do Mendel's experiments show that traits may be dominant or recessive?

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Model answer

Mendel crossed tall and short pea plants. In the F1 generation, all plants were tall, showing that tallness is dominant. When F1 plants self-pollinated, the F2 generation had both tall and short plants in a 3:1 ratio, indicating that shortness is recessive and was masked in F1 but reappeared in F2.

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Frequently asked questions

What is heredity?

Heredity is the process by which traits and characteristics are passed from parents to their offspring. The rules of heredity determine how features such as plant height, seed shape or human earlobe type are reliably inherited from one generation to the next.

What is the difference between dominant and recessive traits?

A dominant trait is expressed even when only one copy of its gene is present, as with tallness in pea plants. A recessive trait is expressed only when both copies of the gene are the recessive form, as with shortness in pea plants.

Why did Mendel's F1 plants all look tall even though shortness was also inherited?

The F1 plants received one copy for tallness and one for shortness. Since tallness is dominant, a single copy of T was enough for the plants to appear tall. The shortness trait was present but not expressed, and it reappeared in the F2 generation.

How is the sex of a child determined in human beings?

A child always inherits an X chromosome from the mother. If the father contributes an X chromosome, the child is a girl (XX). If the father contributes a Y chromosome, the child is a boy (XY). So the father's chromosome decides the sex of the child.

How do genes control traits?

A gene is a section of DNA that provides information for making one protein. Proteins, including enzymes, control the characteristics of an organism. For example, the efficiency of an enzyme affects how much plant hormone is made, which in turn affects the height of the plant.

Why are germ cells important for inheritance?

Body cells have two copies of each chromosome, but germ cells carry only one chromosome from each pair. When two germ cells combine during sexual reproduction, the normal number of chromosomes is restored in the offspring, keeping the DNA of the species stable.

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