WBBSE Chapter 3 Heredity And Common Genetic Diseases Topic A Heredity Introduction To Heredity and Genetics
All living organisms reproduce. Reproduction results in the formation of offspring of the same kind. A pea plant, for example, produces only pea plants each time it reproduces.
Likewise, a rat produces only rats or humans produce only humans. On the other hand, members of a family share many similarities in appearance, such as height, eye color, hair color, etc.
However, the resulting offspring need not and most often do not resemble the parent. Several characteristic differences do occur between individuals belonging to the same species.

It should be noted that the similarities and differences among the members of a species are not coincidental. Both the similarities and differences are received from their parents.
The mechanism of transmission of characters or traits comprising both resemblances as well as differences, from the parental generation to the offspring through reproduction is called heredity.
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WBBSE Chapter 3 Topic A Heredity Introduction To Heredity And Genetics Heredity And Variation
The offspring of all the organisms (plants and animals) resemble their parents in several aspects. This is only due to the phenomenon of heredity.
Heredity is the transmission of characters from one generation to successive generations or from parents to their offspring.
Thus, heredity is the cause of similarities between the offspring, so that the individuals of the same parents resemble each other in many aspects.
Heredity involves the transfer of genetic characteristics from parents to the offspring via the egg and sperm.
On the other hand, though offsprings receive all the characteristics of their parents, still they are not exactly alike.
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Differences are found even between the offspring of the same parents in terms of the shape of faces, hair color, or even skin color.
It is thus difficult to find identical individuals. The progeny differs not only in itself but also with the parents.
These differences are called variations.
Thus, variations may be defined as the differences (morphological, physiological, cytological, and behavioral) between the parents and the offspring or between the offspring of the same parents, family, and race.
Significance Of Variations:
Variations differentiate one individual from another.
Variations enable individuals to adapt themselves according to the changing environment, ie. they make some individuals better fitted or suited to face the struggle for existence.
Discontinuous variations introduce new traits in the species.
Variations are the key to the evolution and development of new species.
WBBSE Chapter 3 Topic A Heredity Types Of Variation
Primarily Variations May Be Classified Into the Following Two Types:
Hereditary Variation:
The variations that arise as a result of any change in the structure and function of the gene and are inherited from one generation to another are called hereditary variations.
Environmental Variations:
Two individuals with the same genotype may become different in phenotype when they come in contact with different conditions of food, temperature, light, humidity, and other external factors.
Such differences among organisms of similar heredity are known as environmental variation. These are not heritable.
Variations may also be classified based on the following parameters:
Based On The Type Of Cells Involved,
Variation Is Classified Into Two Types:
Somatic Variation:
The variation which occurs in somatic cells is called somatic variation. It is generally insignificant because it is not inherited from parents.
It is acquired by the organisms during their lifetime and is lost with death. Hence, it is also called acquired variation.
Somatic variations are caused by three types of factors:
Environmental factors include temperature, light, nutrition, water supply, habitat, topography, enemies, etc.
Use & disuse of organs as may be found in singers whose vocal organs are far more developed than the non-singers.
Conscious efforts include receiving education, developing certain good or bad, or unhealthy habits, etc.
Germinal Variation:
The variation which affects the germinal or reproductive cells is called germinal variation. It is heritable and genetically significant.
It provides raw materials for evolution.
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The factors that cause germinal variations include chance separation of chromosomes, a chance combination of chromosomes, crossing over, chromosomal aberrations, change in chromosome number, genetic mutations, etc.
Based On The Degree Of Differences, Variation Is Classified Into Two Types:
Continuous Variation:
Small and indistinct variations are called continuous variations, eg. the shape of the nose or the color of the skin, etc.
These fluctuate with environmental conditions.
These are non-heritable.
They have no role in evolution.
They are most common and occur in all organisms or races of a species.
Discontinuous Variation:
Large, distinct, and sudden variations are called discontinuous variations, or mutations, eg. the appearance of six fingers in a man, polydactyly, etc.
These are relatively unaffected by environmental conditions.
These are mostly heritable. However, not all the discontinuous variations pass to the next generations because of their appearance in the body cells after the differentiation of germ cells.
They provide raw materials for evolution on which selection is based.
They are not common and appear suddenly.
Based on the affected traits, variations may be of four types:
Morphological variation:
These are the differences that are found in the form and structure of organisms.
Physiological variation:
These are the variations observed in various functions of the body like BMR etc.
Cytological variation:
These variations occur in the number of cells, cell constituents, and their products.
Behaviouristic variation:
These variations are connected with the behavior of the organisms towards different conditions.
Based on impact, variations are of three types:
Beneficial Variation:
These are the variations that help the organisms skillfully adapt to the particular environment.
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Harmful variations:
These variations make organisms unfit for their environment.
Neutral variations:
These variations do not affect the organisms in any way.
WBBSE Chapter 3 Topic A Heredity Sources Of Variation
Variations are more pronounced in sexually reproducing organisms. In sexual reproduction, the production of offspring takes place by the fusion of two types of gametes.
These gametes are formed by the reduction division. Thus, sexual reproduction introduces unlimited genetic variation into the population. The more closely related the sexual partners are, the lesser the variations in their offspring.
Common sources of variations are-
Recombination:
Recombination results in offspring that have a combination of characteristics different from that of their parents. Different types of combinations of characters bring about variation.
Crossing Over:
At the time of gamete formation, crossing over occurs during meiosis division, which causes variations in genetic characteristics.
Mutation:
It is a spontaneous, sudden, heritable, and permanent change in genetic characteristics that causes a detectable effect in the organisms. It occurs in nature or it can be caused artificially in an organism.
WBBSE Chapter 3 Topic A Heredity Mendel The Father Of Genetics
There have been several explanations on the possible mechanism of inheritance of traits from the parent to the offspring, put forth from time to time by different biologists.
All these early theories presume that the characteristics of the two parents somehow mix during inheritance. Hence these ideas came to be known as blending theories of inheritance.
Gregor Johann Mendel (1822-1884) was born in a family of poor peasants in Moravia, Austria. He received his school education with utmost difficulty due to poverty in the family.
Wbbse Class 10 Life Science Heredity Notes
In 1843 he joined a church as a monk where, in 1847, he became the abbot (head) of the monastery at Brunn, Austria (now called Bruno in Czechoslovakia).
In addition to his normal duties of preaching in the church, Mendel evinced a keen interest in the maintenance of the garden in the premises of the church.
In the course of his routine rounds in the garden, Mendel was keenly observing the pattern of inheritance of certain characters in some of the plants.

He became interested in investigating the mechanism by which the characters are transferred from the parent plants to their offspring. He decided to conduct some experiments in this direction.
After careful examination and thinking, Mendel selected the pea plants (Pisum sativum) for his experiments.
Gregor Mendel, through his work on pea plants, discovered the fundamental laws of inheritance.
He deduced that genes come in pairs and are inherited as distinct units, one from each parent. Mendel tracked the segregation of parental genes and their appearance in the offspring as dominant or recessive traits.
He recognized the mathematical patterns of inheritance from one generation to the next.
Thus, Mendel’s concept gave birth to the particulate theory of inheritance. Mendel’s excellent experiments, valid mathematical analysis, and formulation of laws of inheritance are collectively known as Mendelism.
The genetic experiments Mendel did with pea plants took him eight years (1856-1863) and he published his results in 1865. During this time, Mendel grew over 10,000 pea plants, keeping track of progeny number and type.
Wbbse Class 10 Life Science Heredity Notes
Mendel’s work and his Laws of Inheritance were not appreciated in his time. As a result, Mendel died in 1884 without any sort of recognition.
It was not until 1900, after the rediscovery of his Laws, that his experimental results were understood.
Three botanists – Hugo DeVries, Carl Corrensand Erich von Tschermak – independently rediscovered Mendel’s work in the year 1900, a generation after Mendel published his papers.
They helped expand awareness of the Mendelian laws of inheritance in the scientific world. The three Europeans, unknown to each other, were working on different plant hybrids when they each worked out the laws of inheritance.
WBBSE Chapter 3 Topic A Heredity Hereditary Variation
The variations that arise as a result of any change in the structure and function of the gene and that are inherited from one generation to another are called hereditary variations.
The ultimate source of all genetic variation is mutation. It leads to changes in gene function and permanent alteration to the DNA sequence.
It is a rare, random change in the genetic material and it can be inherited. The permanent alteration in the DNA sequence that makes up a gene results in difference which is found in most people.
Mutations range in size; they can affect anywhere from a single DNA building block (base pair) to a large segment of a chromosome that includes multiple genes.
This is the only way new alleles (varieties of a gene) are produced. Mutations are rare events: the average rate of mutation is about one per 100,000 genes.
Wbbse Class 10 Life Science Heredity Notes
Thus it would take on average 100,000 generations for a mutation to occur at any one specific gene. However, each individual has many, many functional genes.
Thus, at the level of the whole individual, mutations occur quite often. It is estimated that each human gamete (egg or sperm cell) has, on average, one mutation.
The heritable change in the composition of a gene that leads to the formation of a mutant gene having changed function and with the consequent appearance of a new phenotype is known as mutation.
Types Of Mutations:
There Are Two Types Of Mutations:
Gene mutations or point mutations, and
Chromosomal mutations.
1. Gene mutations:
A chemical change that occurs in the DNA of a cell is called a gene mutation or point mutation. Such a mutation may alter the sequence of the nucleotides within a part of the DNA molecule.
This alternation changes the information of the DNA chain and results in differences in the proteins being produced.
For Example:
In sickle cell anemia, the mutation of a single gene causes a slight change in the structure of the protein molecule of hemoglobin, and because of that slight change, the blood cell that carries the hemoglobin takes a sickle shape.
According to many scientists, the mutations may be caused naturally by the radiation that constantly enters the earth’s atmosphere from the cosmos.
For example, gene mutations are probably caused when the sex cells (gametes) of an organism are exposed to X-rays, gamma rays, cosmic rays, and ultraviolet rays. In addition to this radiation, certain chemicals called mutagens can change nucleotides within DNA molecules.
Wbbse Class 10 Life Science Heredity Notes
The chance for a particular human gene to mutate in one generation is about 1 in 10,000 to 1 in 1,000,000. Since humans have at least 30,000 genes, each person likely carries at least one mutation.
2. Chromosomal Aberrations (Chromosome mutations):
Another way for the genetic traits of an organism to be altered is through changes involving whole chromosomes or parts of chromosomes.
Structural changes in chromosomes are also caused by radiation, chemicals, and even some virus infections.
Chromosomal mutations may be of two basic types-
- Change of structure, and
- Change of number.
Chromosome structure changes:
Changes occur in the structure of chromosomes, during cell division. When homologous chromosomes pair up, linked genes on the chromosomes may break apart. The genes may join another chromosome, or they may be lost.
Thus, a deletion involves the loss of a piece of chromosome.
If a chromosome breaks and the parts do not reattach, the pieces may be lost. This is the most serious kind of chromosome mutation. Here, bits of genetic information are not available to the offspring.
Duplication occurs when one extra, but identical piece of a chromosome is added to the normal chromosome When an inversion occurs, the pieces of chromosomes break apart and pieces rejoin the same chromosome in a different order. Usually, inversions have no harmful effects on the offspring.
The joining of a fragmented chromosome to a non-homologous chromosome is a translocation. The piece of chromosome detaches from one chromosome and moves to a new position on another chromosome.

Chromosome number changes:
A chromosome mutation that causes individuals to have an abnormal number of chromosomes is termed aneuploidy. Aneuploid cells occur as a result of chromosome breakage or non-disjunction errors that happen during meiosis or mitosis.
Non-disjunction is the failure of homologous chromosomes to separate properly during cell division. It produces individuals with either extra or missing chromosomes.
Sex chromosome abnormalities that result from non-disjunction can lead to conditions such as Klinefelter and Turner syndromes. In Klinefelter syndrome, males have one or more extra X chromosomes.
In Turner syndrome, females have only one X chromosome. Down syndrome is an example of a condition that occurs due to non-disjunction in autosomal (non-sex) cells. Individuals with Down syndrome have an extra chromosome on autosomal chromosome 21.
Mendel’S Laws Of Heredity Class 10
A chromosome mutation that results in individuals with more than one haploid set of chromosomes in a cell is termed polyploidy. A haploid cell is a cell that contains one complete set of chromosomes.
Our sex cells are considered haploid and contain 1 complete set of 23 chromosomes. Our autosomal cells are diploid and contain 2 complete sets of 23 chromosomes.
If a mutation causes a cell to have three haploid sets, it is called triploidy. If the cell has four haploid sets, it is called tetraploidy.
Due to the mutagens, two types of mutations are found visible and lethal mutations. Mutations are located on either sex chromosomes or autosomes.
Common Variations In Human Population
Some examples of often un-noticed human traits are the ability or inability to roll the tongue, attached or unattached earlobes, dimples or freckles, naturally curly or straight hair, smooth or cleft chin, color blindness or normal vision, etc.
There are numerous traits in humans, but some traits occur more frequently than others. Between 70-90% of the human population have free-hanging earlobes, can roll their tongue, are right-handed, and can taste a chemical called PTC (Phenyl-thio-carbamide).
But these characters have nothing to do with life efficiencies.
Some common examples are-
Ear Lobe:
Some people have earlobes that curve up between the lowest point of the earlobe and the point where the ear joins the head; these are known as “free” or “unattached” earlobes.
Other people have earlobes that blend in with the side of the head, known as “attached” or “adherent” earlobes [Fig 3.3(b)]. Attached vs.
free earlobes are often used to illustrate basic genetics. The major form of the gene that determines the shape of the earlobe is known as an allele. An allele is a gene that is found at a specific position on a chromosome.

If the genes from the parents get expressed by the dominant allele, then the child will be born with free earlobes.
The structural formation of the attached earlobe is due to the absence of the dominant allele in the chromosomes. The recessive allele is expressed in the chromosomes to form an attached earlobe.
Thus, if a person is homozygous recessive for this trait, the earlobes attach directly to the head and do not hang free. However, it is not necessary that parents with attached earlobes should give birth only to the attached earlobe child.
If, on the other hand, parents with free earlobes give birth to a baby with attached earlobes, it is certain that both of them have a copy of the dominant and recessive alleles.
Tongue Rolling:
Tongue rolling is the ability to roll the lateral edges of the tongue upwards into a tube. A dominant allele enables some people to roll their tongues into a distinct U-shape. If you cannot roll your tongue you carry the recessive trait.
Recent studies have shown that this tongue-rolling could be dependent on multiple genes or alleles & some kind of environmental influences.

WBBSE Chapter 3 Topic A Heredity Key Terms Associated With Heredity
Some basic key terms associated with heredity and genetics are—
Characteristics Or Trait:
A characteristic or phenotypic trait, or simply trait, is a distinct variant of a phenotypic characteristic of an organism that may be inherited, environmentally determined, or maybe a combination of the two.
For example, eye color is a character or abstraction of an attribute, while blue, brown, and hazel are traits.
Individuals and groups differ among themselves biologically, in a practically endless succession of more or less visible elements of their descriptions, which are named as traits, features, marks, nature, characteristics, characters, and others.
Mendel’s Laws Of Heredity Class 10
Each of these components is a description of, say, the observational nature, i.e. selected part of our vision or measuring the actual condition of the individual body or group structure.
Allele:
An allele is an alternative or some form of a gene (one member of a pair) that is located at a specific position (locus) on a specific chromosome.
These DNA codings determine distinct traits that can be passed on from parents to offspring through sexual reproduction. Alleles may occur in pairs, or there may be multiple alleles affecting the expression (phenotype) of a particular trait.
The word “allele” is a short form of allelomorph (“other form”), which was used in the early days of genetics to describe variant forms of a gene detected as different phenotypes.
Organisms generally have two alleles for each trait, for example- yellow or green seed colors of pea plants; in humans, the gene for eye color has an allele for blue eye color and an allele for brown.
For any gene, a person may have the same two alleles or two different ones.
Locus:
In genetics, a locus (plural loci) is the specific location of a gene, DNA sequence, or position on a chromosome.
Each chromosome carries many genes; in humans, the estimated number of ‘haploid’ protein-coding genes is 20,000-25,000, located on 23 different chromosomes. A variant of a similar DNA sequence located at a given locus is called an allele.
A locus is the specific physical location of a gene or other DNA sequence on a chromosome, like a genetic street address.
A locus is a spot or “address” on a chromosome at which a gene for a particular trait is located in all members of a species. It can also refer to the location of a mutation or other genetic marker.
A given locus can be found on any pair of homologous chromosomes. For example, in Drosophila, the locus of red and white eye colors is present on the X chromosome.
Unit of inheritance (Factor/Gene):
A gene is a stretch of DNA that helps to control the development and function of all organs and working systems in the body.
Mendel didn’t know about genes or discover genes, but he did speculate that there were two factors for each basic trait and that 1 factor was inherited from each parent.
We now know that Mendel’s inheritance factors are genes (the term was first used by Johannsen, 1909), or more specifically alleles – different variants of the same gene. It is now known that Mendelian factors, determinants, or genes are present in a linear sequence on the chromosomes.
Therefore, the gene is also defined as a unit of inheritance that consists of linear chromosome segments that can be assigned to the expression of a particular Character.
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Its effect is, however, influenced by its allele, other genes, and the environment.
Genes are passed from parent to offspring; the combination of these genes affects all aspects of the human body, from eye and hair color to how well the liver can process toxins.
Monohybrid and dihybrid cross:
A monohybrid cross is a breeding experiment between P-generation (parental generation) organisms that differ in one trait.
It is a genetic cross between parents that differ in the alleles they possess for one particular gene, one parent having two dominant alleles and the other two recessives.
All the offspring (called monohybrids) have one dominant and one recessive allele for that gene (i.e. they are hybrid at that one locus). Generally, the monohybrid cross is used to determine the dominance relationship between two alleles.
Example:
The allele for green pod color is dominant and the allele for yellow pod color is recessive. The cross-pollination between a P-generation green pod pea plant and a P-generation yellow pod plant results in all green offspring.
Crossing between these offspring yields a characteristic 3:1 (monohybrid) ratio in the following generation of dominant recessive phenotypes.
A dihybrid cross is a cross between two pure lines (varieties, strains) that differ in two observed traits. A dihybrid cross describes a mating experiment between two organisms that are identically hybrid for two traits.
A hybrid organism is heterozygous, which means that it carries two different alleles at a particular genetic position or locus.
Therefore, a dihybrid organism is heterozygous at two different genetic loci. Mendel used these results as the basis for his Law of Independent Assortment.
Example:
Mendel performed a dihybrid cross using pea plants and the characteristics of seed color and texture: the parental plants had either smooth yellow seeds- the dominant characteristics – or wrinkled green seeds- the recessive characteristics.
All the offspring had smooth yellow seeds, being heterozygous for the two alleles. Crossing between these offsprings produced an F2 generation of plants with smooth yellow, smooth green, wrinkled yellow, and wrinkled green seeds in the ratio of 9:3:3:1.
Homozygous and heterozygous organisms:
Organisms can be homozygous or heterozygous for a gene. Homozygous means that the organism has two copies of the same allele for a gene.
An organism can be homozygous dominant if it carries two copies of the same dominant allele, or homozygous recessive if it carries two copies of the same recessive allele.
Heterozygous means that an organism has two different alleles of a gene. For example, pea plants can have red flowers and either be homozygous dominant (red-red), or heterozygous (red-white).
If they have white flowers, then they are homozygous recessive (white-white). Carriers are always heterozygous.
Example:
An organism is referred to as being homozygote or homozygous at a specific locus when it carries two identical copies of the gene affecting a given trait on the two corresponding homologous chromosomes (e.g., the genotype is PP or pp when P and prefers to different possible alleles of the same gene).
Such a cell or such an organism is called a homozygote.
An organism is a heterozygote or is heterozygous at a locus or gene when it has different alleles occupying the gene’s position in each of the homologous chromosomes.

In diploid organisms, the two different alleles are inherited from the organism’s two parents. For example, a heterozygous individual would have the allele combination Pp.
Hybridization:
Genetic hybridization is the process of interbreeding individuals from genetically distinct populations to produce a hybrid. A genetic hybrid would therefore carry two different alleles of the same gene.
During the 20th century planned hybridization between carefully selected parents has become dominant in the breeding of self-pollinated species.
The object of hybridization is to combine desirable genes found in two or more different varieties and to produce pure-breeding progeny superior in many respects to the parental types.
The process of hybridization is important biologically because it increases the genetic variety (number of different gene combinations) within a species, which is necessary for evolution to occur.
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Example: Hybridization is the process of crossing two genetically different individuals to create new genotypes.
For example, a cross between parent 1, with the genetic makeup (genotype) BB, and parent 2, with bb, produces progeny with the genetic makeup Bb, which is a hybrid (the first filial generation or FI).

Hybridization was the basis of Gregor Mendel’s historic experiments with garden peas. Inheritance studies require crossing plants with contrasting or complementary traits.
Pure and hybrid:
A diploid organism has paired chromosomes, each with a similar arrangement of genetic loci.
Variations of these genes are called alleles. If an organism has one of the same types of alleles on each of its chromosomes, that organism has a pure trait.
If an organism has two different types of alleles on its chromosomes, that organism has a hybrid trait. Pure breed or true breeding are individuals that are homozygous and that will always produce the same offspring when crossed together.
A hybrid is an organism that has two different alleles for a trait.
In the simplest possible terms, purebreds are the offsprings that result from mating between genetically similar parents while hybrids are the offsprings that are the result of mating between two genetically dissimilar parents.
Thus, purebreds are composed of two (or more) like components while hybrids are created using two or more similar but not like components.
Parental generation:
The parental generation (P) is the first set of parents crossed. It is the generation of individuals of different genotypes that are mated, usually for scientific purposes, to produce hybrids.
These parental strains are purified and obtained by repeated cycles of self-fertilization. In a parental generation, two individuals are mated or crossed to determine or predict the genotypes of their offspring, called the first filial generation.
Immediate parents are designated as Pv grandparents P2; great grandparents are P3 and so on.

Filial generation:
Filial generation is the offspring generation. It is a generation in a breeding experiment that is successive to mating between parents of two distinctively different but usually relatively pure genotypes.
F1 is the first offspring or filial generation; F2 is the second; and so on.
Successive generations of progeny result in a controlled series of crosses, starting with two specific parents (the P generation) and selfing or intercrossing the progeny of each new (F1F2; etc. ) generation.
Filial 1 (F1) generation is the one resulting from the cross of such two selected parent generations; this generation expresses a high degree of uniformity (hybrids).
The progeny/generation derived from the Filial 1 generation is termed the Filial 2 generation (F2); this generation can show a very high degree of variation from progeny to progeny depending upon the parental generation used.
Dominant and recessive characteristics:
The terms dominant and recessive describe the inheritance patterns of certain traits. Sexually reproducing species, including people and other animals, have two copies of each gene.
The two copies, called alleles, can be slightly different from each other. The differences can cause variations in the proteins that are produced.
Proteins affect traits, so variations in protein activity or expression can produce different phenotypes. A dominant allele produces a dominant phenotype in individuals who have one copy of the allele, which can come from just one parent.
For a recessive allele to produce a recessive phenotype, the individual must have two copies, one from each parent.
An individual with one dominant and one recessive allele for a gene (heterozygous) will have the dominant phenotype.
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For example, in humans, the allele for brown eyes is dominant, therefore offspring only need one copy of the ‘brown eye’ allele to have brown eyes (although, with two copies they will still have brown eyes).
Recessive alleles only show their effect if the individual has two copies of the allele (also known as being homozygous).
For example, the allele for blue eyes is recessive, therefore to have blue eyes the offsprings need to have two copies of the ‘blue eye’ allele.

Phenotype And Genotype:
Genotype is the genetic makeup of an individual organism that functions as a set of instructions for the growth and development of the body.
The word ‘genotype’ is usually used when talking about the genetics of a particular trait (like eye color).
Phenotype is the observable physical or biochemical characteristics of an individual organism, determined by both genetic makeup and environmental influences, for example, height, weight, and skin color.
An organism’s genotype is the set of genes that it carries. An organism’s phenotype is all of its observable characteristics—which are influenced both by its genotype and by the environment.
The “internally coded, inheritable information”, or Genotype, carried by all living organisms, holds the critical instructions that are used and interpreted by the cellular machinery of the cells to produce the “outward, physical manifestation”, or Phenotype of the organism.
The entire set of genes or the genotype in a black mouse. It comprises a set of alleles that determines the expression of a particular characteristic or trait (phenotype). Her black hair is the trait or phenotype concerned.
All the key terms described in this article (3A.2), are explained with sample crosses in the following articles.

WBBSE Chapter 3 Topic A Heredity Mendel’s Work On Pea Plants
In 1854, Mendel began a series of breeding experiments with the garden pea Pisum sativum in an attempt to learn something about the mechanisms of heredity.
The bisexual flower of pea normally reproduces by self-fertilization.
That is, the stamen (male reproductive organs) produces pollens, which land on the pistil (female reproductive organs) within the same flower and consequently fertilize the plant. This process is called selfing.
To prevent selfing and to carry out cross-pollination in pea plants, three steps of emasculation, dusting and bagging are to be carried out as elaborated here:
It is relatively a simple procedure to prevent self-fertilization of the pea by removing the stamens from a developing flower bud before they produce any mature pollen.
For this purpose, the stamens are cut off by a scissor from the selected bisexual flowers to remove the masculine part of the flower.
This process is known as emasculation. The pollen taken from the stamens of another flower can then be dusted onto the stigma of the pistil of the emasculated one to cross-pollinate it. After cross-pollination, all the
flowers are covered with paper bags to avoid any contamination by undesired pollen grains.
Cross-fertilization, or more simply a cross, is the term used for the fusion of male gametes (pollen) from one individual and female gametes (eggs) from another.
Once cross-fertilization has occurred, the zygote develops in the seeds (peas), which are then planted.
For his experiment, Mendel obtained 34 strains of pea plants that differed in a number of traits.
He allowed each strain to self-fertilize for many generations to ensure that he only worked with pea strains in which the trait under investigation remained unchanged from parent to offspring for many generations.
Wbbse Class 10 Life Science Heredity Notes
Such strains are called true-breeding or pure-breeding strains.
In Mendel’s work true breeding or pure breeding homozygous strains constitute the parental (P) generation.
Once cross-fertilization is carried out in a parental generation, the progeny that is obtained is known as the First generation offspring or First filial (F1) generation.

WBBSE Chapter 3 Topic A Heredity Mendel’s Experiment And Laws For Monohybrid Cross
Mendel performed several mono-hybridization experiments on pea plants involving crosses between parents that differ in a single gene.
WBBSE Chapter 3 Topic A Heredity The seven pairs of characters as chosen by Mendel
Mating between individuals that differ in only one trait, such as seed color or stem length is known as a monohybrid cross.
In each monohybrid cross, one parent carries one form of the trait, and the other parent carries an alternative form of the same trait. Mendel selected seven such traits to study the monohybrid breeding experiment.
Each trait had two easily distinguishable, alternative appearances (phenotypes).
These are—

WBBSE Chapter 3 Topic A Heredity Experiment And Observation
Mendel carried out a series of monohybrid crosses.
For example, in the spring of 1854, he planted pure-breeding green peas and pure-breeding yellow peas and allowed them to grow into the parental (P) generation.
Later that spring when the plants had flowered, he dusted the female stigma of green-pea plant flowers with pollens from yellow-pea plants. He also performed the reciprocal cross between the female yellow pea plant and the male green pea plant.
In the fall (autumn), when he collected and separately analyzed the progeny peas he found that in both cases, the peas were all yellow.
The yellow peas, the progeny of the P generation, were the beginning of what we now call the first filial (Fx) generation. Mendel planted them and allowed the F1 plants to self-fertilize.
He then harvested and counted the peas of the resulting second filial (F2) generation, the progeny of the Fx generation.

Among the progeny of one series of F1 self-fertilization, there were 6022 yellow and 2001 green peas, an almost perfect ratio of 3 yellow to 1 green.
The results of reciprocal crosses produced a similar ratio. Monohybrid crosses involving other traits (such as long and short stem length) also showed similar results.
WBBSE Chapter 3 Topic A Heredity Mendel’s explanation
To explain these results, Mendel proposed the existence of what he called particulate unit factors for each trait. He suggested that these factors served as the basic unit of heredity and passed unchanged from generation to generation, determining various traits expressed by each individual plant.
WBBSE Chapter 3 Topic A Heredity Mendel’s First Three Postulates
Using the constant pattern of result in the monohybrid crosses, Mendel derived the following three postulates or principles of inheritance
Unit Factors in Pairs:
Genetic characters are controlled by unit factors existing in pairs in individual organisms.
In the monohybrid cross involving yellow (Y) and green (y) seeds, a specific unit factor exists for each trait. Each diploid individual receives one factor from each parent.
Because the factors occur in pairs, three combinations are possible:
YY, Yy, and Yy. The seeds having unit factor combinations of either YY or yy have two copies of the same allele for a gene. Hence these are homozygous.
The seeds having a unit factor combination of Yy have two different alleles of a gene. Hence these are heterozygous.
Dominance/Recessiveness:
When two unlike unit factors, responsible for a single character, are present in a single individual, one unit factor is dominant to the other, which is said to be recessive.
In each monohybrid cross, the trait expressed in the F1 generation results from the presence of the dominant unit factor.
The trait that is not expressed in the F1 but which reappears in the F2 is under the genetic influence of the recessive unit factor.
In the above-mentioned case, the trait yellow seed color (Y) is said to be dominant to the recessive trait, green seed (y). Hence, the progeny of P, i.e. the F1 generation had all yellow pea plants.
Among the progeny of ie. in the F2 generation, green pea plants reappeared along with yellow pea plants.
Segregation:
During the formation of gametes, the paired unit factors responsible for contrasting traits do not blend with each other but separate or segregate randomly, so that each garnet receives one or the other with equal likelihood.
This is known as the 1st law of Mendel or the law of Segregation.
WBBSE Chapter 3 Topic A Heredity Analysis Of Monohybrid Cross And Checker Board

WBBSE Chapter 3 Topic A Heredity Punnett Squares
The genotypes and phenotypes resulting from the recombination of gametes during fertilization can be easily visualized by constructing a Punnett square, named after R. C.
Punnett who first devised this approach. In this construction, each of the possible gametes is assigned an individual column or a row, with the vertical column representing those of the female parent and the horizontal row those of the male parent.
After the gametes are entered in rows and columns, the new generation can be predicted by combining the male and female gametic information for each combination and entering the resulting genotype in the boxes. This process represents all possible random fertilization events.
WBBSE Chapter 3 Topic A Heredity Mendel’s Experiment And Laws For Dihybrid Cross
As a natural extension of the monohybrid cross, Mendel also designed experiments in which he examined two characters simultaneously. Such a cross, involving two pairs of contrasting traits, is called a dihybrid cross.
WBBSE Chapter 3 Topic A Heredity Experiment and Observation
Mendel-crossed pea plants that are heterozygous for two genes at the same time.
To construct such a dihybrid, he mated true-breeding plants grown from yellow round peas (YYRR) with true-breeding plants grown from green wrinkled peas (year).
From this cross, he obtained a dihybrid F1 generation (YyRr) showing only the two dominant phenotypes, yellow and round. He then allowed these F1 dihybrids to self-fertilize to produce the F2 generation.
When Mendel counted the F2 generation of one experiment, he found 315 yellow round, 101 yellow wrinkled, 108 round green, and 32 wrinkled green peas. There were, in fact, yellow wrinkled and green round recombinant phenotypes, providing evidence that some shuffling of alleles had taken place.
Explanation
From the observed ratios, Mendel inferred the biological mechanism of shuffling the independent assortment of gene pairs during gamete formation.
Because the genes for peas’ color and for shape assort independently, Y can be with R or r in any gamete with equal probability.
Thus, the presence of a particular allele of one gene, say, the dominant Y for pea color, provides no information whatsoever about the alleles of the second gene.
That is, the allele for pea shape in Y carrying game could with equal likelihood be either R or r.
Each dihybrid of the F1 generation can, therefore, make four kinds of gametes:
YR, Yr, yR, and yr. In a large number of gametes, the four kinds will appear in an almost perfect ratio of 1:1:1:1.
At fertilization then, in a mating of dihybrids, 4 different kinds of eggs can combine with any one of 4 different kinds of pollen, producing a total of 16 possible zygotes in the F2 generation.
Wbbse Class 10 Life Science Heredity Notes
Once again, a Punnett square is a convenient way to visualize the process.
In fact, there are only nine different F2 genotypes — YYRR, YYRr, YyRr, YyRR, yyRR, yyRr, YYrr, Yyrr, and yyrr — because the source of the alleles (egg or pollen) does not make any difference.
If we look at the combination of the traits determined by nine genotypes, we will see only four phenotypes— yellow round, yellow wrinkled, green round, and green wrinkled — observed in a ratio of 9 : 3 : 3: 1.
If, however, we look at just pea color or just pea shape, we can see that each trait is inherited in the 3: 1 ratio as predicted by Mendel’s law of segregation.
Punnet Square or Checker Board of Dihybrid cross


WBBSE Chapter 3 Topic A Heredity Mendel’s Fourth Postulate
The above analysis became the basis of Mendel’s second general principle or the fourth postulate, the law of independent assortment.
Independent Assortment:
During gamete formation, segregating pairs of unit factors assort independently of each other and undergo random recombination in all possible combinations governed by chance alone.
This postulate stipulates that any pair of unit factors segregate independently of all other unit factors. Thus, according to the postulate of independent assortment, all possible combinations of gametes will be formed in equal frequency.
WBBSE Chapter 3 Topic A Heredity Reasons for Mendel’s Success
Mendel’s success was dependent upon the following factors:
First, he chose the garden pea (Pisum sativum) as his experimental organism.
These plants can easily be cultivated, crossed, and for each successive generation, Mendel could thus obtain large members of individuals within a relatively short growing season.
By comparison, if he had worked with sheep, each mating would have generated only a few offspring and the time between generations would have been several years.
Second, Mendel examined the inheritance of clearcut contrasting forms of particular traits — round versus wrinkled seed, yellow versus green pod color, etc.
Using such ‘either-or’ traits, he could distinguish and trace unambiguously the transmission of one or the other observed characteristics, because there were neither any intermediate forms nor any of these characters located on separate chromosomes.
Third, Mendel isolated and perpetuated lines of peas that breed true. Mating with such pure breeding lines produce offsprings carrying specific parental traits that remain constant from generation to generation.
Fourth, Mendel carefully controlled his matings, going to great lengths to ensure that the progeny he observed really resulted from the specific fertilization he intended.
Thus he painstakingly prevented the intrusion of any foreign pollen and assured self or cross-pollination as the experiment demanded.
He also performed reciprocal crosses, in which by reversing the traits of male and female parents, he efficiently controlled the path of transmission of a particular trait either via the egg cell within the ovule or via the pollen as per experimental demand.
Fifthly, Mendel worked with a large number of plants, counted and subjected his findings to statistical analysis, and then compared his results with predictions based on mathematical models.
Wbbse Class 10 Life Science Heredity Notes
Finally, Mendel was a brilliant practical experimentalist. He could call and observe an optimum number of individuals from the limited space of the monastery garden.
In short, Mendel purposely set up a simplified ‘black and white’ experimental system and then successfully out how it worked.
Genetic Crosses With Guineapig
Mendel worked on pea plants but the application of his laws on animals was carried out by his successors.
WBBSE Chapter 3 Topic A Heredity Monohybrid Cross
When a pure (homozygous) black-haired guineapig (BB) is crossed with a pure white-haired guineapig (bb), all the F1 offsprings (Bb) are found to be black-haired despite the presence of two contrasting genes for black hair and white hair.
It means black color is dominant to white color in guineapig and F1 black offsprings (Bb) are heterozygous. Here the gene for the black color is represented by B and for the recessive white color by b.
When the F1 heterozygous guineapigs are bred among themselves, individuals of the F2 generation are produced. The F2 phenotypic ratio is 3 (black): 1 (white) whereas the F2 genotypic ratio is (pure black, BB) 1: (heterozygous black, Bb) 2: (pure white, bb) 1.
This shows that the inheritance of hair color in guinea pigs follows Mendel’s first law of Segregation.
The monohybrid cross in guinea pig is shown here with a checkerboard.

WBBSE Chapter 3 Topic A Heredity Dihybrid Cross
In guinea pigs, the black coat (BB) is dominant to the white coat (bb), and short hair (SS) is dominant over long hair (ss).
When a homozygous black short-haired male guinea pig (BBSS) is crossed with a white long-haired female (bass), all the F1 offspring obtained are with black short hair (BbSs).
This shows the dominance of black coats over white coats and the dominance of short hair over long hair.
When the hybrid individuals are allowed to interbreed, F2 generation consisting of four types of individuals is produced in the following phenotypic ratio = 9 (black short) : 3 (black long) : 3 (white short): 1 (white long).
The F1 hybrids (BbSs) produced gametes when Bb and Ss alleles were segregated and assorted independently to produce four types of gametes: BS, Bs, bS, and bs.
Thus four types of male gametes and similar four types of female gametes are produced.
These gametes undergo fertilization at random to produce 16 different types of zygotes in the F2 generation having the above-mentioned four types of phenotypes. This clearly explains Mendel’s law of independent assortment.

WBBSE Chapter 3 Topic A Heredity Deviation Of Menders Laws Of Heredity
Although Mendel formulated the postulates that provide the basis of our understanding of genetic principles, there are many types or modes of inheritance that Mendel simply didn’t encounter.
These modes of inheritance were encountered when investigators began using Mendel’s postulates to study inheritance in other organisms.
Some of these modes of inheritance appear, at first glance, to obey different rules than those that Mendel proposed. So, was Mendel wrong then? Not really.
Wbbse Class 10 Life Science Heredity Notes
His postulates fit the data that he collected, but as stated above, there are situations that he didn’t observe in his study of the pea.
This is a common occurrence in science: when a theory is proposed, it is used as long as it is useful in explaining some aspect of nature.
When data are encountered that don’t fit the theory, the theory may have to be modified (if possible) or discarded. Mendel’s ideas as originally presented may not fit every possible mode of inheritance, but they still provide the basis for explaining those other types of inheritance.
WBBSE Chapter 3 Topic A Heredity Genetic Interaction
According to Mendel each trait or character is controlled by a pair of factors or genes. But later discoveries proved that in many cases the expression of a single character is controlled by the interaction of more than one pair of genes.
The coordinated effect of two or more genes in producing a given phenotypic trait is known as genetic interaction. It was proposed by Bateson and Punnet in the form of a factor hypothesis.
This hypothesis states that certain characters are controlled by the interaction of two or more genes.
The interaction of genes may be classified into two types:
- Non-allelic and
- Allelic gene interaction.
The genetic interactions that occur between genes located in the same chromosome or different chromosomes are known as nonallelic gene interactions.
For instance, in some animals, a gene at one locus on a chromosome totally suppresses the expression of a gene at another locus. Such genes are called inhibiting genes and the phenomenon is known as epistasis, eg. ABO blood group in man.
There may be supplementary genes that interact in such a way that one dominant gene produces its effect whether another dominant gene is present or not, but when the second dominant gene is added to the first, a new character is expressed; eg. coat color in mice.
There may also be collaborator genes that influence the same trait but interact to produce totally new traits that neither of the genes could produce, eg. comb shape in fowls.
The other type of genetic interaction that occurs between the two alleles of a single type of gene is known as allelic gene interaction.
For instance, if genes are within a certain distance on the same chromosomes, they do not follow the Law of independent assortment; instead, they are linked when transmitted to the next generation.
This is called linkage. Genes that are located in the cytoplasm do not follow either of Mendel’s Laws, they exhibit maternal inheritance traits.
If the dominance is incomplete, a dominant trait wouldn’t be observed immediately. Sometimes genes become co-dominant, meaning both alleles will show a phenotype.
There may be multiple genes in which case two or more independent pairs of factors affect the same characters but in an additive manner, eg. human skin color.
WBBSE Chapter 3 Topic A Heredity Incomplete Dominance
A common example of deviation from Mendelism is the phenomenon called incomplete dominance.
A cross between parents with contrasting traits may sometimes generate offspring with an intermediate phenotype.
In a heterozygote organism carrying both a dominant and a recessive allele of the same gene, when the dominant gene cannot express its dominant phenotype completely, a mixed or intermediate, or blended phenotype between the dominant and the recessive is expressed.
Such a situation is known as incomplete dominance. In many plant species, flower color serves as a striking example of incomplete dominance.
With the flowers of Four O’Clocks or floret clusters of Snapdragons Mirabilis jalapeno, a cross between pure breeding red flowered parents and pure breeding white yields hybrids with pink blossoms.
During gametogenesis, the pure red flowered parent plant (AA) produces (A) gametes and the pure white flowered parent plant (aa) produces (a) gametes.

After cross-pollination of parental plants, (A) and (a) unite together to form (Aa) zygote that develops into plants with pink flowers.
Here both the allelomorphic genes have a partial or incomplete dominant relationship and hence, F1 hybrids show a mixture of characters of both parents. This is a case of incomplete dominance.
If allowed to self-pollinate, the F1 pink blooming plants produce F2 progeny bearing red, pink, and white flowers in a ratio of 1: 2 :1. This is the familiar genotypic ratio of an ordinary single gene F1 self-cross.
What is new is that because the heterozygotes look unlike either homozygote, the phenotypic ratios are an exact reflection of the genotypic ratios.
F2 Phenotypic ratio = 1 (Red): 2 (Pink): 1 (White) F2 Genotypic ratio = 1 (AA): 2 (Aa): 1 (aa) In this example of Mirabilis jalapa, the red gene is incompletely dominant over the white gene and so both of them give rise to an intermediate pink colored flower in heterozygous or hybrid condition.
Explanation:
The biochemical explanation for this type of incomplete dominance is that each allele of the gene under analysis specifies an alternative form of a protein molecule with an enzymatic role in pigment production.
If the ‘white’ allele does not give rise to the functional enzyme, no pigment appears.
Thus, in Snapdragons and four o’clock, two ‘red’ alleles per cell produce a double dose of a red-producing enzyme, which generates enough pigment to make the flowers look fully red.
Wbbse Class 10 Life Science Heredity Notes
In the heterozygote, one copy of the ‘red’ allele per cell results in only enough pigment to make the flowers look pink. In the homozygote for the ‘white’ allele, where there is no functional enzyme and thus no red pigment, the flowers appear white.
WBBSE Chapter 3 Topic A Heredity Sex Determination In Human
The term sex refers to sexual phenotype. Most organisms have only two sexual phenotypes—male and female.
We, normally, define the sex of an individual organism about its phenotype. The mechanism by which sex is established is termed sex determination.
Sometimes an individual organism has chromosomes that are normally associated with one sex. For example, the cells of female humans normally have two X chromosomes, and the cells of males have one X chromosome and one Y chromosome.
Sex Determination In Humans:
In humans, Drosophila, and many other species, the cells of males and females have the same number of chromosomes, but the cells of males have a single X chromosome and a smaller sex chromosome, the Y chromosome.
The Y chromosome is not Y-shaped as is commonly assumed but is acrocentric. In this type of sex determination system, the male (44A + XY) is heterogametic because half of the male gametes have an X chromosome and the other half have a Y chromosome.
The female (44A + XX) is homogametic because all the eggs contain a single X chromosome. Fertilization of an egg (always X-bearing) with an X-bearing sperm produces female offspring (XX), but a Y-bearing sperm produces male offspring (XY).

The Total Chromosomes In Humans, In Each Body Cell, Can Be Represented As-
Female chromosomes – 44+XX where 44 are the autosomes and XX chromosomes are the sex chromosomes.
Male chromosomes – 44+XY where 44 are the autosomes and XY chromosomes are the sex chromosomes.
Although the X and Y chromosomes are not homologous, they pair and segregate into different cells in meiosis.
This is because of the fact that these chromosomes are homologous in small regions, called the pseudoautosomal region, in which they carry the same genes. In both types, the human X and Y chromosomes contain pseudoautosomal regions.
In humans and other placental mammals, maleness is due to a dominant effect of the Y chromosome. This is evidenced by the study of individuals with an abnormal number of sex chromosomes or aneuploidy.
XO persons (Turner syndrome) develop as females and XXY persons (Klinefelter syndrome) develop as males.
The dominant effect of the Y chromosome is exhibited early in development when it directs the primordial gonads to develop into testes.
Mendel’S Laws Of Heredity Class 10
Once the testes are formed, they secrete the hormone testosterone, which stimulates the development of male secondary sexual characteristics.
It is now known that the testis-determining factor (TDF) is the product of a gene called SRY (Sex-determining region Y), which is located outside the pseudoautosomal region in the short arm of the Y chromosome.
When fertilization occurs, the zygote (the initial cell from which a fetus grows) always inherits one of the mother’s X chromosomes, and either an X or a Y from the father, depending on which chromosome the fertilizing sperm cell happened to inherit.
One could say, then, that the father or, at least, his sperm determines the sex of the child.
The generally accepted theory is that males determine the sex because males can donate either an X chromosome or Y chromosome, while females can only donate an X chromosome to their offspring, making their contribution constant and the male’s contribution.
The variable, which under normal circumstances, determines the offspring’s genetic sex (at least, in humans Moreover, genetically there is a 50% chance of having a boy and a 50% chance of having a girl, as is found out from.
But there are actually slightly more boys born every year than girls.
It’s unclear why this is the case, but some research points out that more female fetuses die during pregnancy than male.
The Y chromosome contains all the directions that make the human zygote develop into a male. It is a relatively small chromosome with about 30 genes.
In comparison, the X chromosome has between 800 and 900 genes.
With its limited number, the Y chromosome focuses primarily on male traits. It contains the all-important SRY gene, which instructs the embryo to develop male traits such as testicles.
Another gene unique to the Y chromosome is USP9Y, which contributes to sperm production.

WBBSE Chapter 3 Topic A Heredity Fill In The Blanks
Question 1. _______________ is the cause of similarities between the offspring.
Answer: Heredity
Question 2. _______________ is considered as the father of genetics.
Answer: Mendel
Question 3. Mendel selected the _______________ plants for his experiments.
Answer: Garden Pea
Question 4. The process of removing stamens from flowers during hybridization is known as _______________.
Answer: Emasculation
Question 5. The mutation is a change in a gene or_______________.
Answer: Chromosome
Question 6. If a person is_______________ recessive for this trait, the earlobes attach directly to the head and do not hang free.
Answer: Homozygous
Heredity Class 10 MCQS
Question 7. If you cannot roll your tongue you carry the_______________ trait.
Answer: Recessive
Question 8. An _______________is an alternative form of a gene that is located at a specific position on a specific chromosome.
Answer: Allele
Question 9. In genetics, a _______________is the specific location of a gene on a chromosome.
Answer: Locus
Question 10. A_______________ cross describes a mating experiment between two organisms that are identically hybrid for two traits.
Answer: Dihybrid
Question 11. _______________ means that the organism has two copies of the same allele for a gene.
Answer: Ghomozygous
Question 12. Heterozygous means that an organism has two different_______________ of a gene.
Answer: Alleles
Question 13. _______________is the process of crossing two genetically different individuals to create new genotypes.
Answer: Hybridization
Question 14. Mating between parents of two distinctly different but usually relatively pure genotypes results in_______________ generation.
Answer: First filial (F1)
Heredity Class 10 MCQS
Question 15. An individual with one dominant and one recessive allele for a gene will have the_______________ phenotype.
Answer: Dominant
Question 16. _______________ is the observable physical or biochemical characteristics of an individual organism.
Answer: Phenotype
Question 17. Two crosses between the same pair of genotypes or phenotypes in which the sources of the gametes are reversed in one cross are known as_______________
Answer: Reciprocal Cross
Question 18. The law of_______________ is known as the first law of Mendel.
Answer: Segregation
Question 19. 9:3:3:1 F2 ratio is found in a _______________cross.
Answer: Dihybrid
Question 20._______________ genes do not show independent assortment.
Answer: Linked
Question 21. _______________dominance was observed in Snapdragons.
Answer: Incomplete
Question 22. In humans, maleness is due to a dominant effect of the_______________ chromosome.
Answer: Y
Question 23. A ratio of 1:2:1 as both the phenotypic and genotypic ratios is found in_______________.
Answer: Incomplete Dominance
Question 24. The genotypes and phenotypes resulting from the recombination of gametes during fertilization can be easily visualized by constructing a_______________
Answer: Punnett Square
Heredity Class 10 MCQS
Question 25. The coordinated effect that occurs between the two alleles of a single type of gene is known as_______________ gene interaction.
Answer: Athletic
WBBSE Chapter 3 Topic A Heredity Write True Or False
Question 1. It is difficult to find out identical individuals due to variations.
Answer: True
Question 2. Genetic variations are caused by environmental changes.
Answer: False
Question 3. Blending theories of inheritance were proposed by Mendel
Answer: False
Question 4. Mendel selected 7 pairs of contrasting traits of the pea plants for his experiments.
Answer: True
Question 5. Small and indistinct variations are referred to as discontinuous variations.
Answer: False
Question 6. Mendel’s concept gave birth to the particulate theory of inheritance.
Answer: True
Question 7. Masculation, dusting, and bagging are the methods to be followed to ensure cross-pollination in bisexual flowers.
Answer: True
Heredity Class 10 MCQS
Question 8. While Mendel is known as the ‘Father of Genetics, Bateson is called the ‘Father of modern genetics’.
Answer: True
Question 9. The mutation is a change in an environment.
Answer: False
Question 10. A dominant allele enables some people to roll their tongues into a distinct U-shape.
Answer: True
Question 11. An allele is a place where a gene is located.
Answer: False
Question 12. In human reproduction, the mother plays a vital role to determine the sex of the child.
Answer: False
Question 13. Mendelian monohybrid cross F2 ratio is 3:1.
Answer: True
Question 14. Homozygous means that an organism has two different alleles of a gene.
Answer: False
Question 15. Hybridization is the process of crossing two genetically different individuals to create new genotypes.
Answer: True
Question 16. A diploid organism has paired chromosomes.
Answer: True
Question 17. The progeny/generation derived from filial 2 generations is termed as filial 1 generation.
Answer: False
Question 18. In humans, the allele for brown eyes is dominant.
Answer: True
Question 19. An organism’s phenotype is the set of genes that it carries.
Answer: False
Question 20. The law of independent assortment is considered the first law of Mendel.
Answer: False
Question 21. Linked genes do not assort independently.
Answer: True
Question 22. The intermediate genotype is caused due to incomplete dominance.
Answer: True
Heredity Class 10 MCQS
Question 23. In humans, persons bearing XX chromosomes are females.
Answer: True
Question 24. Even if the dominance is incomplete, the dominant trait would prevail over the recessive one in the F1 generation.
Answer: False
Question 25. ‘Gametes are never hybrid’—this is a statement of the law of segregation.
Answer: True
WBBSE Chapter 3 Topic A Heredity Match The Column

Answer: 1-E,2-D,3-A,4-B

Answer: 1-C,2-E,3-B,4-A

Answer: 1-C,2-D,3-A,4-B
WBBSE Chapter 3 Topic A Heredity Very Short Answer Type Questions
Question 1. Name two sources of variation.
Answer: Mutation, deletion.
Question 2. Write the scientific name of the plant which Mendel chose for the hybridization experiment.
Answer: Garden pea plant – Pisum sativum.
Question 3. In which year, Mendel’s propositions were rediscovered?
Answer: In 1900.
Question 4. Give an example of a harmful variation.
Answer: Sickle cell anemia.
Question 5. What is mutation?
Answer: Mutation is the spontaneous, sudden, heritable, and permanent change in a gene or chromosome that causes a detectable effect in the organism.
Question 6. What is the average rate of mutation?
Answer: The average rate of mutation is about one per 100,000 genes.
Question 7. Are the environmental variations heritable?
Answer: No, they are not heritable.
Question 8. Give an example of discontinuous variation in man.
Answer: Appearance of six fingers in man.
Question 9. What are germinal variations?
Answer: The heritable variation which affects the germinal or reproductive cells is called germinal variation.
Mendel’s Laws Of Heredity Class 10
Question 10. Give an example of neutral variation.
Answer: Presence of left-handed and right-handed persons.
Question 11. Choose the odd one and write it:
Answer: Wrinkled seed shape, short stem length, round pod shape, terminal flower position.
Round Pod Shape:
It is a dominant trait in pea plants while the other examples are recessive traits.
Question 12. What is a gene mutation or point mutation?
Answer: A chemical change that occurs in the DNA of a cell is called a gene mutation or point mutation.
Question 13. How the structural changes of chromosomes may be caused?
Answer: Structural changes in chromosomes are caused by exposure to radiation, chemicals, and even by some virus infections.
Question 14. What is an inversion?
Answer: When an inversion occurs, the pieces of chromosome break apart and pieces rejoin the same chromosome in a different order.
Question 15. Name a visible dominant character of a human.
Answer: Free, unattached ear lobe.
Question 16. What is the diploid chromosome number of garden peas?
Answer: Diploid (2n) chromosome number = 14.
Question 17. Among the following four terms, one includes the other three. Find out the term and write it: blood type, trait, skin color, height.
Answer: Trait.
Question 18. Who is considered the father of experimental genetics?
Answer: Morgan.
Mendel’s Laws Of Heredity Class 10
Question 19. What is sex determination?
Answer: The mechanism by which sex is determined is known as sex determination.
Question 20. What is the vital role of the Y chromosome in humans?
Answer: It is responsible for male sex determination.
Question 21. A tall (dominant trait) and a dwarf (recessive trait) pea plant are crossed. How would you represent the test cross?
Answer: Ttxtt.
Question 22. Is the organism having a genotype of BbSS homozygous or heterozygous?
Answer: Heterozygous
Question 23. How many different types of gametes would be produced by an individual with genotype SsTt Uu?
Answer: Since the contrasting pairs of characters recombine randomly in all possible combinations, there would be 8 different types of gametes as shown: STU, STU, StU, Stu, sTU, stU, sTu, stu.
Question 24. A pair of related terms is given below. Based on the relationship in the first pair, write the suitable word in the gap of the second pair:
Answer:
1. Complete dominance : (3:1):: Incomplete dominance:1:2:1
2. Tall pea: dwarf pea::guineapig: smooth hair Rough hair guineapig.
3.Female parent: 44+XX:: Male parent:44 +XY.
Mendel’S Laws Of Heredity Class 10
Question 25. A monohybrid cross between two plants, one having 24cm long internodes and the other having 12cm long internodes, produced F1, hybrids all having 18cm long internodes. What type of phenomenon is this one?
Answer: Incomplete dominance.
Question 26. What type of gamete (for a given trait) is produced by a dominant homozygous individual? What is the genotypical proportion of these gametes? What about a recessive homozygous individual?
Answer: If an individual is dominant homozygous (AA say, for a given trait), it will produce only gametes with the allele A. The proportion is therefore 100%.
If an individual is recessive homozygous (aa say, for a given trait), it will produce only gametes with the allele a; also a 100% proportion.
Question 27. What type of gamete is produced by a heterozygous individual? What is the genotypic proportion of these gametes?
Answer: Heterozygous individuals (for example, Aa say, for a given pair of contrasting traits) produce two different types of gametes: one containing the allele A and another type containing the allele a. The proportion is 1:1.
Question 28. According to Mendel’s first law, how many genotypic and phenotypic forms are there in the F2 generation of hybridization for a given trait conditioned by a pair of alleles?
Answer: In the mentioned hybridization, F2 generation shows three different genotypic forms and two different phenotypic forms.
Question 29. What is the condition for Mendel’s second law to be valid?
Answer: Mendel’s second law is valid only for genes located in different chromosomes. For genes located in the same chromosome, such as linked genes, the law is not valid since the assortment of these genes is not independent.
If two white sheep produce a black offspring, what conclusion can you draw regarding the parent’s genotypes for color?
The parents must be heterozygous since black is the recessive trait.
Chapter 3 Topic A Heredity Short Answer Type Questions With Answers
Question 1. Explain the term heredity.
Answer:
Heredity
Hereditary means “tendency of like begets like” i.e. all living organisms tend to produce offspring like themselves.
Hereditary may be defined as the transmission of characters from one generation to successive generations or from parents to their offspring via the egg and the sperm.
Thus, heredity is the cause of similarities between the offspring, so that the individuals of the same parents resemble each other in many aspects.
Question 2. What is the blending theory of inheritance?
Answer:
Blending theory of inheritance
There have been several explanations on the possible mechanism of inheritance of traits from the parent to the offspring, put forth from time to time in the Pre-Mendelian era by different biologists like Swammerdam, Bonnet, Wolff, etc.
All these early theories presume that the characteristics of the two parents somehow mix during inheritance. Hence these ideas came to be known as blending theories of inheritance.
Question 3. Mention the advantages of selecting a pea plant for the experiment by Mendel.
Answer:
The advantages were-
Peas are cheap, easily available, and have many visible contrasting characteristics such as tall/dwarf plants, round/wrinkled seeds, green/yellow pods, purple/white flowers, etc.
Peas have bisexual flowers and therefore undergo self-pollination easily. Thus, pea plants produce offspring with same traits generation after generation, i.e. the plants breed true.
In pea plants, cross-pollination can be easily achieved by emasculation in which the stamen of the flower is removed without affecting the pistil.
Pea plants have a short life span and produce many seeds in one generation. Since the plants are annuals, repeated hybridization experiments could be conducted to study more number of generations.
Question 4. What is gene mutation?
Answer:
Gene mutation
Mutation is a change in a gene or chromosome. It is a rare, random change in the genetic material and it can be inherited.
A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people.
Mutations range in size; they can affect anywhere from a single DNA building block (base pair) to a large segment of a chromosome that includes multiple genes. This is the only way new alleles (varieties of a gene) are produced.
Question 5. Write briefly about the genetics of the ear lobe.
Answer:
The genetics of the ear lobe
Some people have earlobes that curve up between the lowest point of the earlobe and the point where the ear joins the head; these are known as “free” or “unattached” earlobes.
Other people have earlobes that blend in with the side of the head, known as “attached” or “adherent” earlobes. Attached vs.
free earlobes are often used to illustrate basic genetics. If a person is homozygous recessive for this trait, the earlobes attach directly to the head and do not hang free.
The structural formation of the attached earlobe is due to the absence of the dominant allele in the chromosomes. The recessive allele is expressed in the chromosomes to form an attached earlobe.

On the other hand, if the genes from the parents get expressed by the dominant allele, then the child will be born with free earlobes.
However, parents with attached earlobes don’t need to give birth only to the attached earlobe child. If, on the other hand, parents with free earlobes give 10. birth to a baby with attached earlobes, it is certain that both of them had a copy of the dominant and the recessive allele.
Question 6. What is the environmental variation?
Answer:
The environmental variation
Two individuals with the same genotype may become different in phenotype when they come in contact with different conditions of food, temperature, light, humidity, and other external factors.
Such differences among organisms of similar heredity are known as environmental variation. These are not heritable.
Question 7. Write the characteristics of discontinuous variations.
Answer:
Characteristics of discontinuous variations
Large, distinct, and sudden variations are called discontinuous variations.
- These are relatively unaffected by environmental conditions.
- These are heritable.
- They provide raw materials for evolution on which selection is based.
- They are not common and appear suddenly.
Mendel’S Laws Of Heredity Class 10
Question 8. What are inversions and translocations?
Answer:
Inversions and translocations
Inversion and translocation are chromosomal aberrations in the structure of chromosomes. When an inversion occurs, the pieces of chromosome break apart and pieces rejoin the same chromosome in a different order.
Usually, inversions have no harmful effects on the offspring.
The joining of a fragmented chromosome to a non-homologous chromosome is a translocation.
The piece of chromosome detaches from one chromosome and moves to a new position on another chromosome.

Question 9. What is aneuploidy?
Answer:
Aneuploidy
Aneuploidy is the presence of an abnormal number of chromosomes in a cell (too many or too few copies), for example having 45 or 47 chromosomes when 46 is expected in a human cell. Klinefelter syndrome in humans is due to the trisomy condition of aneuploidy (2n + l).
Persons suffering from this clinical syndrome have 47 chromosomes (XXY).
Question 10. What is euploidy?
Answer:
Euploidy
It is a genomic condition of having a chromosome number that is an exact multiple of the haploid number. The individuals may be Triploid (3n), Tetraploid (4n), etc.
Though this condition is frequently found in plants, it is very rare in animals. Euploids above the diploid level may be referred to as polyploids.
Question 11. What is a monohybrid cross?
Answer:
Monohybrid cross
A monohybrid cross is a breeding experiment between P-generation (parental generation) organisms that differ in one trait.
It is a genetic cross between parents that differ in the alleles they possess for one particular gene, with one parent having two dominant alleles and the other two recessives.
All the offspring (called monohybrids) have one dominant and one recessive allele for that gene (i.e. they are hybrid at that one locus).
Generally, the monohybrid cross is used to determine the dominance relationship between two alleles.
Question 12. What is a dihybrid cross?
Answer:
Dihybrid cross
A dihybrid cross is a cross between two pure lines (varieties, strains) that differ in two observed traits. A dihybrid cross describes a mating experiment between two organisms that are identically hybrid for two traits.
A hybrid organism is heterozygous, which means that it carries two different alleles at a particular genetic position or locus.
Therefore, a dihybrid organism is heterozygous at two different genetic loci. Mendel used these results as the basis for his Law of Independent Assortment.
Question 13. What is incomplete dominance?
Answer:
Incomplete dominance
Incomplete dominance is a form of intermediate or blended inheritance in which one allele for a specific trait is not completely expressed over its paired allele.
This results in a third phenotype in which the expressed physical trait is a combination of the phenotypes of both alleles.
Unlike incomplete dominance inheritance, here one allele does not dominate or mask the other allele.
incomplete dominance is seen in cross-pollination experiments between red and white flower-colored snapdragon (Mirabilis jalapa) plants and as a result, pink flower is produced in the F1 generation.
The F2 generation consists of red, pink, and white flowers in a ratio of 1:2:1.
Question 14. What is the law of independent assortment?
Answer:
The law of independent assortment
It is the principle, originated by Gregor Mendel, stating that when two or more characteristics are inherited, individual hereditary factors assort independently during gamete production and undergo random recombination in all possible combinations, giving different traits an equal opportunity of occurring together.
Question 15. What is Mendel’s first law of inheritance?
Answer:
Mendel’s first law of inheritance
The principle of segregation is considered the first Law of Mendel.
It states that the two members of a gene pair (alleles) do not blend but instead segregate (separate) from each other randomly during the formation of gametes.
Therefore, half the gametes carry one allele, and the other half carry the other allele (ie. segregation with equal likelihood).
Question 16. What is Punnett Square?
Answer:
Punnett Square
The Punnett square is a diagram that is used to predict the outcome of a particular cross or breeding experiment. It is named after Reginald C.
Punnett, who devised the approach. The diagram is used by biologists to determine the probability of an offspring having a particular genotype. The Punnett square is a tabular summary of possible combinations of maternal alleles with paternal alleles.
Question 17. State the role of the Y chromosome in the sex determination of humans.
Answer:
The role of the Y chromosome in the sex determination of humans
Every Y chromosome has a gene known as the SRY gene that carries instructions for the development of a male fetus. The presence of the SRY gene and thus the Y chromosome mechanizes the development of testes in the human embryo.
In the absence of a Y chromosome, genes found in the X chromosome take over and develop the ovaries of a female fetus. Thus, in humans, maleness is due to the dominant effect of the Y chromosome.
Mendel’S Laws Of Heredity Class 10
Question 18. Why Mendel did not face the problem of linkage?
Answer:
Pea has seven homologous pairs of chromosomes. Mendel was lucky that he studied those seven traits whose allelic pairs were present on different homologous chromosomes.
So they were not linked. After Mendel, further research work on the pea plant revealed that out of 7 pairs of chromosomes
Genes for the length of the plant, the position of the flower, and the shape of the seed are present in chromosome 4, the shape of the seed in chromosome 7, and the color of the seed and the color of the flower in chromosome 1 and color of a pod in chromosome 5.
Question 19. Two red-eyed fruit flies are mated. They have the following offspring: 140 red-eyed flies and 48 flies with bright orange eyes. Which allele is dominant for the eye color gene: red or orange?
Answer:
This is a monohybrid cross between two heterozygous parents since very nearly the offspring are red-eyed and they are orange-eyed. Hence the red-eyed flies have the dominant phenotype.
A tall plant crossed with a dwarf one produces offspring of which about half are tall and half are dwarf.
Question 20. What are the genotypes of the two parents?
Answer:
The genotypes of the two parents
The genotype of the dwarf plant must be tt. If the tall parent plant were TT, all the offspring would have been tall (Tt) since tall is the dominant trait. Hence the tall parent must be Tt.
Giving and offspring as per the Punnet Square shown here:

Question 21. Define Back cross and test cross.
Answer:
Back cross and test cross
The cross of a progeny individual with its parents is known as a back cross.
The cross of an individual (generally of dominant phenotype) with one having the recessive phenotype is known as a test cross. It is generally used to determine whether an individual of the dominant phenotype is homozygous or heterozygous.
Question 22. What do you mean by pure line or pure breeding line?
List the gametes that an individual with genotype AABbCc can produce.
Answer:
Pure line or pure breeding line
A strain of individuals homozygous for all genes being considered is known as a pure breeding line.
There will be four types of gametes that the individual can produce: ABC, ABc, AbC, and Abe.
Question 23. Variations are more pronounced in sexually reproducing organisms rather than in asexually reproducing organisms- explain why.
Answer:
Replication of DNA is so nearly perfect that there is little scope for variations occurring in the genotypes of asexually reproducing organisms.
Any apparent variation between these organisms is, therefore, almost certainly, newborn. Transmission of a gene from the male parent the result of environmental influences only.
In the case of sexually reproducing organisms, there is ample opportunity for genetic variation to arise.
Meiosis and the fusion of gametes during fertilization provide the means of introducing unlimited genetic variations into the population. Common sources of variations in sexually reproducing organisms include recombination, crossing over, and mutation.
Fill In The Blanks
Question 1. The different_________________of Pea plants may show the same phenotype.
Answer: genotypes
Question 2. The sexual reproduction that occurs among two genotypically different organisms belonging to the same species is called__________________.
Answer: Hybridization
Write True Or False
Question 1. In his monohybrid cross experiment, Mendel obtained 75% pure tall pea plants in the first filial generation.
Answer: False
Question 2. A pair of sex-determining sex chromosomes are present in the ovum of humans.
Answer: False
Long Answer Type Questions
Question 1. With the help of a checkerboard show the types of offspring that might be produced in a cross between a hybrid black guineapig and a pure white guineapig. State the law of segregation as proposed by Mendel.
Answer:
Monohybrid Cross
When a pure (homozygous) black-haired guineapig (BB) is crossed with a pure white-haired guineapig (bb), all the F1 offsprings (Bb) are found to be black-haired despite the presence of two contrasting genes for black hair and white hair.
It means black color is dominant to white color in guineapig and F1 black offsprings (Bb) are heterozygous. Here the gene for the black color is represented by B and for the recessive white color by b.
When the F1 heterozygous guineapigs are bred among themselves, individuals of the F2 generation are produced. The F2 phenotypic ratio is 3 (black): 1 (white) whereas the F2 genotypic ratio is (pure black, BB) 1: (heterozygous black, Bb) 2: (pure white, bb) 1.
This shows that the inheritance of hair color in guinea pigs follows Mendel’s first law of Segregation.
The monohybrid cross in guinea pig is shown here with a checkerboard.
Mendel’s First Three Postulates
Using the constant pattern of result in the monohybrid crosses, Mendel derived the following three postulates or principles of inheritance
Unit Factors in Pairs:
Genetic characters are controlled by unit factors existing in pairs in individual organisms.
In the monohybrid cross involving yellow (Y) and green (y) seeds, a specific unit factor exists for each trait. Each diploid individual receives one factor from each parent.
Because the factors occur in pairs, three combinations are possible:
YY, Yy, and Yy. The seeds having unit factor combinations of either YY or yy have two copies of the same allele for a gene. Hence these are homozygous.
The seeds having a unit factor combination of Yy have two different alleles of a gene. Hence these are heterozygous.
Dominance/Recessiveness:
When two unlike unit factors, responsible for a single character, are present in a single individual, one unit factor is dominant to the other, which is said to be recessive.
In each monohybrid cross, the trait expressed in the F1 generation results from the presence of the dominant unit factor.
The trait that is not expressed in the F1 but which reappears in the F2 is under the genetic influence of the recessive unit factor.
In the above-mentioned case, the trait yellow seed color (Y) is said to be dominant to the recessive trait, green seed (y). Hence, the progeny of P, i.e. the F1 generation had all yellow pea plants.
Among the progeny of ie. in the F2 generation, green pea plants reappeared along with yellow pea plants.
Segregation:
During the formation of gametes, the paired unit factors responsible for contrasting traits do not blend but separate or segregate randomly, so that each garnet receives one or the other with equal likelihood.
This is known as the 1st law of Mendel or the law of Segregation.
Question 2. Color of the seed and shape of the seed of a pea Taking these two characters Mendel performed a Dihybrid cross. Write the genotypes of pea plants having yellow and round seeds produced in the F2 generation of this experiment. State the law of independent assortment of Mendel.
Answer: Let,
R= Dominant allele for round seed shape
r= Recessive allele for wrinkled seed shape
Y= Dominant allele for yellow seed color
y = Recessive allele for green seed color.
Four types of genotypes obtained in the F2 generation of pea plants having yellow and round seeds are the following:
RRYY, RrYY, RrYy and RRYy
Independent Assortment:
During gamete formation, segregating pairs of unit factors assort independently of each other and undergo random recombination in all possible combinations governed by chance alone.
This postulate stipulates that any pair of unit factors segregate independently of all other unit factors. Thus, according to the postulate of independent assortment, all possible combinations of gametes will be formed in equal frequency.
Question 3. State the opposite traits for each of the characters of flowers of the pea plant chosen by Mendel for his experiment.
“For developing the scientific ideas on heredity the experiments performed by Mendel on pea plants are epoch-making”— mention three reasons behind his success in performing these experiments.
Answer:

Flowers of pea plant chosen by Mendel:
Second, Mendel examined the inheritance of clearcut contrasting forms of particular traits — round versus wrinkled seed, yellow versus green pod color, etc.
Using such ‘either-or’ traits, he could distinguish and trace unambiguously the transmission of one or the other observed characteristics, because there were neither any intermediate forms nor any of these characters located on separate chromosomes.
Third, Mendel isolated and perpetuated lines of peas that breed true. Mating with such pure breeding lines produces offspring carrying specific parental traits that remain constant from generation to generation.
Fourth, Mendel carefully controlled his matings, going to great lengths to ensure that the progeny he observed resulted from the specific fertilization he intended.
Heredity And Variation Class 10 Questions
Thus he painstakingly prevented the intrusion of any foreign pollen and assured self or cross-pollination as the experiment demanded.
He also performed reciprocal crosses, in which by reversing the traits of male and female parents, he efficiently controlled the path of transmission of a particular trait either via the egg cell within the ovule or via the pollen as per experimental demand.
Fifthly, Mendel worked with a large number of plants, counted and subjected his findings to statistical analysis, and then compared his results with predictions based on mathematical models.
Finally, Mendel was a brilliant practical experimentalist. He could call and observe an optimum number of individuals from the limited space of the monastery garden.
In short, Mendel purposely set up a simplified ‘black and white’ experimental system and then successfully out how it worked.
Question 4. Show the result of hybridization till F2 generation between a pure black (BB) coarse-haired (RR) guinea pig and a pure white (bb)
smooth-haired (rr) guinea pig by a checkerboard. State the conclusion one can reach from this hybridization experiment.
Answer:

Conclusion:
There exists a biological mechanism of shuffling resulting in an independent assortment of gene pairs during gamete formation.
The genes for hair color (Black or White) and hair texture (coarse or smooth) assort independently in any gamete with equal probability.
Thus the presence of a particular allele for one gene provides no information whatsoever about the allele of the second gene.