Class 10Science · BiologyFull chapter

Heredity

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Heredity and Variation

Quick answer Heredity is the transmission of characters from parents to offspring, while variation is the differences that arise among individuals of a species. Sexual reproduction produces more variation than asexual reproduction.

Heredity is the passing on of features or characters from one generation to the next. The rules of heredity decide how a plant or animal inherits its traits from its parents. Variation means the differences seen among individuals of the same species.

When organisms reproduce, offspring resemble their parents because they inherit a set of instructions in the form of genes. However, offspring are never exactly identical to their parents or to one another. For example, in a group of human children of the same parents, we see differences in height, complexion, ear-lobe shape and blood group. These differences are variations.

Variations arise mainly during sexual reproduction, because the offspring gets one set of genes from the mother and one from the father, and these combine in new ways. Small errors while copying DNA also create variation. In asexual reproduction (like in bacteria), offspring are nearly identical, so only tiny variations from copying errors occur.

Variation is useful for a species. If the environment changes suddenly — say the temperature of water rises for bacteria — individuals with a variation that lets them survive the heat will live and reproduce, while others die. So variation gives a species a better chance of survival over time. Variations that are inherited by offspring accumulate generation after generation.

Heredity Inheritance of characters from parents to offspring via genes Genes are units of inheritance located on chromosomes
Source of variation Sexual reproduction (recombination of parental genes) + DNA copying errors Asexual reproduction gives least variation
Remember
  • Heredity is the transmission of characters (traits) from parents to offspring through genes.
  • Variation is the difference among individuals of a species; it is greater in sexual than in asexual reproduction.
  • Sexual reproduction mixes genes from two parents, creating new combinations and more variation.
  • Only inherited variations pass to the next generation and can accumulate over generations.
  • Variation increases a species' chances of survival when the environment changes.

Mendel's Monohybrid Cross and the 3:1 Ratio

Quick answer A cross involving one pair of contrasting traits (e.g. tall vs dwarf) gives an F2 phenotypic ratio of 3:1 and a genotypic ratio of 1:2:1, showing that traits are controlled by pairs of factors, one being dominant.

Gregor Mendel used the garden pea plant (Pisum sativum) for his experiments because it has clear contrasting traits, such as tall/dwarf plants and round/wrinkled seeds. A cross that follows the inheritance of a single pair of contrasting characters is called a monohybrid cross.

Mendel crossed a pure tall plant (TT) with a pure dwarf plant (tt). All the plants in the first generation (F1) were tall (Tt). The dwarf character seemed to disappear. This showed that the tall factor (T) is dominant and the dwarf factor (t) is recessive. Both parents contribute one factor each, so the F1 plant carries both T and t but looks tall.

Mendel then self-pollinated the F1 tall plants (Tt × Tt). In the second generation (F2), the dwarf trait reappeared. He obtained tall and dwarf plants in the ratio 3 tall : 1 dwarf. Working out the cross: the gametes T and t combine to give TT, Tt, Tt and tt.

  • 1 TT (tall)
  • 2 Tt (tall)
  • 1 tt (dwarf)

So the phenotypic ratio is 3 : 1 (tall : dwarf) and the genotypic ratio is 1 : 2 : 1 (TT : Tt : tt). This proves that a trait is controlled by a pair of factors (alleles) that separate during gamete formation, and that a recessive trait is not lost — it is only hidden in the presence of a dominant factor.

Monohybrid F2 phenotypic ratio 3 : 1 (dominant : recessive) e.g. 3 tall : 1 dwarf
Monohybrid F2 genotypic ratio 1 : 2 : 1 (TT : Tt : tt) Pure dominant : hybrid : pure recessive
Monohybrid cross TT x tt -> F1 all Tt (tall); Tt x Tt -> F2 1 TT + 2 Tt + 1 tt Parental gametes: T and t
Remember
  • A monohybrid cross studies the inheritance of one pair of contrasting traits.
  • TT (tall) × tt (dwarf) gives all tall Tt plants in F1; dwarf is masked because T is dominant.
  • F1 selfing (Tt × Tt) gives F2 phenotypic ratio 3 tall : 1 dwarf.
  • The F2 genotypic ratio is 1 TT : 2 Tt : 1 tt.
  • Recessive traits reappear in F2, proving factors occur in pairs and separate during gamete formation.

Mendel's Dihybrid Cross and the 9:3:3:1 Ratio

Quick answer A cross involving two pairs of contrasting traits gives an F2 phenotypic ratio of 9:3:3:1, and shows that the two pairs of traits are inherited independently of each other.

A dihybrid cross follows the inheritance of two pairs of contrasting characters at the same time. Mendel crossed pea plants having round, yellow seeds (RRYY) with plants having wrinkled, green seeds (rryy). Here round (R) is dominant over wrinkled (r), and yellow (Y) is dominant over green (y).

All F1 plants had round, yellow seeds (RrYy), showing round and yellow are the dominant traits. Mendel then self-pollinated the F1 plants (RrYy × RrYy). In the F2 generation he obtained four types of seeds in the ratio 9 : 3 : 3 : 1:

  • 9 round, yellow
  • 3 round, green
  • 3 wrinkled, yellow
  • 1 wrinkled, green

The important point is that new combinations appeared in F2 — round-green and wrinkled-yellow — which were not present in the original parents. This proves that the two pairs of traits (seed shape and seed colour) are inherited independently of each other. The gene for seed shape assorts separately from the gene for seed colour during gamete formation.

This is why a child can, for example, inherit the mother's hair type together with the father's eye colour — different traits are shuffled independently.

Dihybrid F2 phenotypic ratio 9 : 3 : 3 : 1 9 round-yellow : 3 round-green : 3 wrinkled-yellow : 1 wrinkled-green
Dihybrid cross RRYY x rryy -> F1 all RrYy; RrYy x RrYy -> F2 in 9:3:3:1 F1 gametes: RY, Ry, rY, ry
Law of Independent Assortment Two pairs of traits are inherited independently of each other New (recombinant) trait combinations appear in F2
Remember
  • A dihybrid cross studies two pairs of contrasting traits together.
  • RRYY (round, yellow) × rryy (wrinkled, green) gives all round-yellow (RrYy) in F1.
  • F1 selfing gives an F2 phenotypic ratio of 9 : 3 : 3 : 1.
  • New combinations (round-green and wrinkled-yellow) appear in F2.
  • This proves the two pairs of traits are inherited independently of each other.

Rules of Inheritance and How Traits Are Expressed

Quick answer Traits are controlled by genes that make proteins; each organism carries two copies of a gene, one from each parent. A dominant allele is expressed even when a single copy is present, while a recessive allele shows only when both copies are recessive.

Each trait of an organism is controlled by a pair of genes (alleles), one inherited from the mother and one from the father, located on chromosomes. A gene works by giving instructions to make a specific protein, often an enzyme, and this protein controls how the trait appears.

Consider plant height. Let us say a gene codes for an enzyme that helps make a plant hormone which makes the plant grow tall. The dominant allele T makes an efficient enzyme, so enough hormone is produced and the plant is tall. The recessive allele t makes a less efficient enzyme, so less hormone is made. A plant with even one T allele (Tt) makes enough hormone and is tall — this is why T is dominant. Only a plant with both recessive alleles (tt) is dwarf.

This explains the rules of inheritance:

  1. Traits are controlled by pairs of alleles.
  2. During gamete (sex-cell) formation, the two alleles separate, so each gamete carries only one allele of a pair.
  3. At fertilisation, the offspring again gets one allele from each parent, restoring the pair.
  4. A dominant allele is expressed even in a single dose (Tt); a recessive allele is expressed only when present in a double dose (tt).

Because each parent contributes one allele of every gene, both parents make an equal genetic contribution to the offspring, even though the offspring's appearance may resemble one parent more for a given trait.

Gene to trait Gene -> Protein (enzyme) -> Trait An efficient enzyme allele is usually dominant
Dominant expression TT or Tt -> dominant trait shown (tall) One dominant allele is enough
Recessive expression tt -> recessive trait shown (dwarf) Needs both alleles recessive
Remember
  • Genes are units of inheritance on chromosomes; each organism has two alleles per trait, one from each parent.
  • A gene expresses a trait by directing the making of a specific protein/enzyme.
  • A dominant allele shows its effect even in a single copy (Tt is tall).
  • A recessive trait is expressed only when both alleles are recessive (tt is dwarf).
  • Alleles separate during gamete formation and pair up again at fertilisation, so both parents contribute equally.

Sex Determination in Human Beings

Quick answer Humans have 23 pairs of chromosomes, of which one pair is the sex chromosomes. Females are XX and males are XY; the sex of a child is determined by whether the sperm carries an X or a Y chromosome from the father.

In human beings the sex of an individual is decided genetically by a special pair of sex chromosomes. A human cell has 23 pairs (46) of chromosomes. Of these, 22 pairs are autosomes and one pair is the sex chromosomes.

A female has two X chromosomes, written as XX. A male has one X and one Y chromosome, written as XY. During gamete formation the pair separates:

  • All eggs (ova) produced by the mother carry one X chromosome.
  • Half of the sperms produced by the father carry an X chromosome and the other half carry a Y chromosome.

When a sperm carrying an X chromosome fertilises the egg (X), the child is XX — a girl. When a sperm carrying a Y chromosome fertilises the egg (X), the child is XY — a boy.

Since the egg always contributes an X chromosome, the sex of the child depends entirely on whether the fertilising sperm carries an X or a Y chromosome. Therefore, the sex of the child is determined by the father, not the mother. Because X- and Y-bearing sperms are produced in roughly equal numbers, the chance of having a boy or a girl is about 50 : 50.

Human chromosome number 23 pairs = 46 chromosomes (22 autosome pairs + 1 sex-chromosome pair) Present in each body cell
Sex chromosomes Female = XX ; Male = XY Egg always X; sperm X or Y
Sex determination X-sperm + X-egg -> XX (girl) ; Y-sperm + X-egg -> XY (boy) Father determines sex of child; ~50:50 ratio
Remember
  • Human cells have 23 pairs of chromosomes: 22 pairs of autosomes + 1 pair of sex chromosomes.
  • Females are XX and males are XY.
  • All eggs carry an X chromosome; sperms are of two kinds — half carry X, half carry Y.
  • X-sperm + egg → XX girl; Y-sperm + egg → XY boy.
  • The sex of the child is determined by the father, with about a 50:50 chance of a boy or girl.

Key facts & terms

Every formula in this chapter, in one place — screenshot it before your exam.

Inheritance of characters from parents to offspring via genes
Heredity
Sexual reproduction (recombination of parental genes) + DNA copying errors
Source of variation
3 : 1 (dominant : recessive)
Monohybrid F2 phenotypic ratio
1 : 2 : 1 (TT : Tt : tt)
Monohybrid F2 genotypic ratio
TT x tt -> F1 all Tt (tall); Tt x Tt -> F2 1 TT + 2 Tt + 1 tt
Monohybrid cross
9 : 3 : 3 : 1
Dihybrid F2 phenotypic ratio
RRYY x rryy -> F1 all RrYy; RrYy x RrYy -> F2 in 9:3:3:1
Dihybrid cross
Two pairs of traits are inherited independently of each other
Law of Independent Assortment
Gene -> Protein (enzyme) -> Trait
Gene to trait
TT or Tt -> dominant trait shown (tall)
Dominant expression
tt -> recessive trait shown (dwarf)
Recessive expression
23 pairs = 46 chromosomes (22 autosome pairs + 1 sex-chromosome pair)
Human chromosome number
Female = XX ; Male = XY
Sex chromosomes
X-sperm + X-egg -> XX (girl) ; Y-sperm + X-egg -> XY (boy)
Sex determination

Test yourself

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0 correct · 0/12 answered
Q1 Mendel's experiments easy

Which plant did Mendel use for his experiments on inheritance?

Q2 Monohybrid cross easy

In a monohybrid cross between a pure tall (TT) and a pure dwarf (tt) pea plant, the F1 generation is:

Q3 3:1 ratio easy

The phenotypic ratio obtained in the F2 generation of a monohybrid cross is:

Q4 Monohybrid genotype medium

The genotypic ratio of the F2 generation in a monohybrid cross (Tt × Tt) is:

Q5 Dihybrid cross medium

In a dihybrid cross, the F2 phenotypic ratio obtained by Mendel was:

Q6 Independent assortment medium

The appearance of round-green and wrinkled-yellow seeds in the F2 of a dihybrid cross shows that:

Q7 Dominant and recessive easy

A trait that is expressed only when present in a double recessive condition is called:

Q8 Sex determination easy

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

Q9 Sex determination easy

The sex chromosome constitution of a human male and female respectively is:

Q10 Sex determination medium

In humans, the sex of a child is determined by:

Q11 Sex determination medium

If a father contributes a Y-bearing sperm and it fertilises an egg, the child will be:

Q12 How traits are expressed hard

A gene expresses a trait mainly by directing the making of a:

NCERT solutions & previous-year questions

Step-by-step model answers — tap a question to reveal the full solution.

NCERT questions 6

1 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?

In an asexually reproducing species, new traits arise only by small variations (DNA copying errors) and are then passed on to all descendants. A trait that appeared earlier has had more time to be inherited and spread through many generations, so it will be present in a larger fraction of the population.

Here, trait B is present in 60% of the population while trait A is present in only 10%. Since B is more widespread, it must have appeared earlier and had more time to spread. Trait A, being present in fewer individuals, arose more recently.

Answer: Trait B arose earlier than trait A.

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

Mendel crossed a pure tall pea plant (TT) with a pure dwarf pea plant (tt).

  • In the F1 generation, all plants were tall (Tt). The dwarf character did not appear, even though a dwarf parent was used.
  • When these F1 tall plants were self-pollinated (Tt × Tt), the F2 generation showed both tall and dwarf plants in the ratio 3 tall : 1 dwarf.

The dwarf trait disappeared in F1 but reappeared in F2. This shows that the tall factor (T) suppressed the dwarf factor (t) in the F1 hybrid. The trait that appears in F1 and masks the other is the dominant trait (tall), and the trait that is hidden in F1 but reappears in F2 is the recessive trait (dwarf).

3 How do Mendel's experiments show that traits are inherited independently?

Mendel performed a dihybrid cross using two pairs of traits together. He crossed plants with round, yellow seeds (RRYY) with plants having wrinkled, green seeds (rryy).

  • The F1 plants all had round, yellow seeds (RrYy).
  • On self-pollination, the F2 generation showed four types of seeds in the ratio 9 round-yellow : 3 round-green : 3 wrinkled-yellow : 1 wrinkled-green.

Two of these — round-green and wrinkled-yellow — are new combinations that were not present in either parent. Their appearance shows that the gene for seed shape and the gene for seed colour are passed on independently of each other during gamete formation. This is the basis of independent inheritance of traits.

4 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?

We can work out the genotypes. Blood group O has the genotype ii (a double recessive condition). The daughter has blood group O (ii), so she must have received one i allele from each parent. Since the man is of blood group A, his genotype must therefore be IAi (heterozygous), because he had to pass an i allele to the daughter.

No, this information alone is NOT enough to decide which trait — blood group A or blood group O — is dominant.

To establish which trait is dominant, we need to see which trait appears in the offspring of a cross between two pure-breeding (homozygous) parents. From a single family like this, the observed pattern (father A, mother O, daughter O) is equally consistent with either possibility — A being dominant over O, or O being dominant over A. Knowing only the parents' and one child's phenotypes lets us deduce the genotypes but does not, by itself, prove which allele is dominant. Hence the given information is insufficient to determine dominance.

5 How is the sex of a newborn individual determined in human beings?

In humans, each body cell has 23 pairs of chromosomes. Of these, 22 pairs are autosomes and one pair is the sex chromosomes.

  • A female has two X chromosomes (XX). All her eggs carry one X chromosome.
  • A male has one X and one Y chromosome (XY). Half his sperms carry an X chromosome and half carry a Y chromosome.

At fertilisation:

  • If an X-bearing sperm fertilises the egg, the child is XX — a girl.
  • If a Y-bearing sperm fertilises the egg, the child is XY — a boy.

Since the egg always contributes an X chromosome, the sex of the child depends only on the type of sperm. Hence the sex of the child is determined by the father.

6 Why do all the gametes formed in human females have an X chromosome?

A human female has the sex-chromosome constitution XX, that is, both her sex chromosomes are of the same type (X). During gamete (egg) formation, the chromosome pair separates and each egg receives one chromosome from the pair.

Because both chromosomes in the female are X, every egg — no matter which one of the pair it receives — will contain an X chromosome. There is no Y chromosome in the female to be passed on. Therefore, all eggs produced by a human female carry an X chromosome, and the female is said to be the homogametic sex.

Previous-year board questions 4

Q1 A cross was made between pure-breeding pea plants, one with round green seeds and another with wrinkled yellow seeds. (a) Write the phenotype of the F1 generation. Give reason. (b) Write the different types of F2 progeny obtained along with their ratio when F1 progeny is selfed. CBSE 2023 5 marks

Let round be R (dominant) and wrinkled be r; yellow be Y (dominant) and green be y. Parents: round-green = RRyy and wrinkled-yellow = rrYY.

(a) F1 generation: All F1 plants have round, yellow seeds (RrYy).

Reason: Round (R) is dominant over wrinkled (r), and yellow (Y) is dominant over green (y). So in the hybrid RrYy, the dominant traits round and yellow are expressed while wrinkled and green remain hidden.

(b) F2 generation (obtained by selfing RrYy × RrYy, whose gametes are RY, Ry, rY and ry) gives four types of seeds in the ratio 9 : 3 : 3 : 1:

  • 9 round, yellow
  • 3 round, green
  • 3 wrinkled, yellow
  • 1 wrinkled, green

The appearance of new combinations (round-green and wrinkled-yellow) shows that the two traits are inherited independently.

Q2 "The sex of a newborn child is a matter of chance and none of the parents may be considered responsible for it." Justify this statement giving a suitable explanation. CBSE 2020 3 marks

In humans, there are 22 pairs of autosomes and one pair of sex chromosomes. A female is XX and a male is XY.

  • All eggs produced by the mother carry an X chromosome (she can give only X).
  • The father produces two kinds of sperm — half carrying X and half carrying Y.

At fertilisation, whether an X-sperm or a Y-sperm fuses with the egg is purely a matter of chance:

  • X-sperm + X-egg → XX (girl)
  • Y-sperm + X-egg → XY (boy)

Since both types of sperm are produced in equal numbers and fertilisation is random, the chance of a boy or girl is about 50:50. Neither parent can control which sperm fertilises the egg, so no parent can be held responsible for the sex of the child.

Q3 Define heredity. State the law of dominance using a suitable example of a monohybrid cross. CBSE 2019 3 marks

Heredity is the transmission of characters (traits) from parents to their offspring from one generation to the next through genes.

Law of Dominance: When two organisms with a pair of contrasting characters are crossed, only one character (the dominant one) is expressed in the F1 generation, while the other (recessive) character remains hidden.

Example (monohybrid cross): When a pure tall pea plant (TT) is crossed with a pure dwarf plant (tt), all F1 plants are tall (Tt). Here the tall trait (T) is dominant and is expressed, while the dwarf trait (t) is recessive and remains masked. This illustrates the law of dominance.

Q4 A Mendelian experiment consisted of breeding tall pea plants bearing violet flowers with short pea plants bearing white flowers. The progeny all bore violet flowers, but almost half of them were short. What can be concluded about the traits tall/violet in the parent plants? CBSE 2018 2 marks

All the progeny bore violet flowers, so the violet flower colour is a dominant trait and white is recessive.

About half the progeny were short. This means the tall parent was not pure-breeding but was a heterozygous (hybrid) tall plant (Tt). When crossed with a short plant (tt), it gives tall (Tt) and short (tt) offspring in nearly equal numbers (1:1). Hence the tall trait is dominant, but the tall parent carried a hidden recessive allele for shortness.

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