- Chapter 1 Control And Coordination In Living Organisms MCQs
- Chapter 2 Continuity Of Life MCQs
- Chapter 3 Heredity and Common Genetic Diseases MCQs
- Chapter 4 Evolution And Adaptation MCQs
- Chapter 5 Environment Its Resources And Their Conservation MCQs

Question 1. The bacteria that bring about ammonification is
Answer: 1. Bacillus ramosus
Question 2. The bacteria helping in nitrification is
Answer: 2. Nitrosomonas sp
Read and Learn More WBBSE Class 10 Life Science Multiple Choice Questions
Question 3. The absorption of nitrogen in plants occurs in the form of
Answer: 1. N03
Question 4. The bacteria that cause denitrification is
Answer: 3. Nitrobacter sp
Question 5. Which of the plants does not have endophytic cyanobacteria?
Answer: 3. Anthoceros sp

Question 6. Which one of the greenhouse gases causes the acidification of soil?
Answer: 3. N2O
WBBSE Class 10 Life Science Chapter 5 MCQs
Question 7. Which process increases nitrogen concentration in the atmosphere?
Answer: 4. Denitrification
Question 8. Which of the bacteria is a free-living nitrogen fixer?
Answer: 2. Clostridium
Question 9. Which bacteria remains associated with the root valgus?
Answer: 2. Azospirillum
Question 10. The key enzyme for nitrogen fixation is
Answer: 2. Nitrogenase
WBBSE Class 10 Life Science Chapter 5 MCQs
Question 11. The elements required for nitrogenase are
Answer: 2. Fe and mo
Question 12. The chemical process involving the production of NH3 is
Answer: 1. Haber-bosch process
Question 13. The following cyanobacteria fix nitrogen
Answer: 3. Anabaena
Question 14. The following fern is used as a biofertilizer in paddy field
Answer: 2. Azolla
Question 15. The number of ATP molecules required for fixing one molecule of nitrogen is
Answer: 4. 16 Atp
Question 16. The nodule appears red due to the presence of
Answer: 4. Leg-haemoglobin
WBBSE Class 10 Life Science Chapter 5 MCQs
Question 18. Rhizobium to legume root is
Answer: 3. Lectin
Question 19. Leghaemoglobin creates
Answer: 3. Required oxygen concentration for optimum activity of nitrogenase
Question 20. Arrange the following processes of the N2 cycle in proper sequence: Denitrification, Nitrogen fixation, Ammonification, and Nitrification
Answer: 1. (2) — (3)— (4) — (1)
Question 21. One of the following is a way by which atmospheric nitrogen is converted to nitrates-
Answer: 4. Lightning
Question 22. Rhizobium bacteria and root nodules of a pea plant an examples of
Answer: 2. Symbiosis
Question 23. Which of the following phases of the nitrogen cycle Pseudomonas is associated with—
Answer: 3. Denitrification
Life Science Class 10 Chapter 5 Mcqs With Answers
Question 24. Which one of the folio wing microbes takes part in nitrification—
Answer: 1. Nitrosomonas
Question 25. In almost all metropolitan cities, the major atmospheric pollutant(s) is/are
Answer: 3. Suspended particulate matter (SPM)
Question 26. SPM include
Answer: 4. Minute dust particles
Question 27. Which of the following is not a particulate matter?
Answer: 3. Ozone
Question 28. The diameter of the rpm is
Answer: 4. SPM2
Question 29. Which one of the following is a secondary pollutant?
Answer: 3. Both
Question 30. Which one of the following is not a greenhouse gas?
Answer: 4. Co
Life Science Class 10 Chapter 5 Mcqs With Answers
Question 31. The percentage of air pollution that comes from combustion is
Answer: 4. 40-50%
Question 32. Which of the following gases may be used as a coolant?
Answer: 2. Cfc
Question 33. Which layer is damaged due to supersonic jets?
Answer: 1. O3 layer
Question 34. The following gas causes depletion of 02 from hemoglobin
Answer: 2. Co
Question 35. Which are the primary constituents of photochemical smog?
Answer: 3. NO2 & hydrocarbons
Question 36. The greenhouse effect corresponds to
Answer: 3. Global warming
Question 37. Excessive nutrients in the water body are also called
Answer: 4. Eutrophication
Life Science Class 10 Chapter 5 Mcqs With Answers
Question 38. The nitrogen-fixing bacteria only become active
Answer: 3. In the absence of nitrogen
Question 39. The following element is highest in seawater
Answer: 3. P
Question 40. Radiation may induce
Answer: 1. Leukemia
Question 41. The following metal blocks hemoglobin biosynthesis
Answer: 4. Pb
Question 42. Acid rain may include
Answer: 4. All of them
Question 44. Exposure to the following radioactive elements causes bone cancer & leukemia
Answer: 3. Strontium90
Life Science Class 10 Chapter 5 Mcqs With Answers
Question 45. The gradual increase of a pollutant along the food chain is also called
Answer: 4. Bio-magnification
Question 46. A pollutant is any substance, chemical, or other factor, that changes
Answer: 1. The natural balance of our environment
Question 47. Which of the following is associated with biological amplification?
Answer: 3. Ddt
Question 48. Non-biodegradable organic pollutants include
Answer: 2. Ddt
Question 49. The threshold of pain in human ears is
Answer: 4. 120-140 Db
Class 10 Life Science Multiple Choice Questions
Question 50. The component of living cells affected by the pollutant SO2 is
Answer: 1. All cell membrane system
Question 51. The following organism produces biodegradable plastic
Answer: 3. Bacteria
Question 52. The pollutant responsible for the luxuriant growth of algae which forms water bloom is
Answer: 1. Phosphates
Question 53. The highest ddt deposition shall occur in
Answer: 2. Seagull
Question 54. Drained sewage has a bod
Answer: 1. More than that of clear water
Question 55. Who among the following are nature’s water cleaners?
Answer: 4. Decomposers & scavengers
Question 56. Population is
Answer: 1. Individuals in a species
Question 57. The rate of adding new ones produced in a specific period is termed as
Answer: 4. Natality
Class 10 Life Science Multiple Choice Questions
Question 58. Resources are of two types- renewable resources and non-renewable resources.
Answer: 4. Natural
Question 59. Is the destruction or clearing of forested lands, usually to expand agricultural land or for timber harvesting.
Answer: 2. Deforestation
Question 60. Shrinking fields is one of the biggest challenges for making food available to the world population.
Answer: 1. Agricultural
Question 61. The human carrying capacity of the earth is between
Answer: 4. 9 To 10 billion
Question 62. Pollution has been linked to health problems like asthma and lung disease.
Answer: 1. Air
Question 63. Zero population growth is characterized by
Answer: 1. No growth in population recorded in the last decade
Class 10 Life Science Multiple Choice Questions
Question 64. Problem(s) due to ever-increasing population is/are
Answer: 4. All of these
Question 65. Wetlands act as the biological of the landscape
Answer: 4. Kidneys
Question 66. Lower rates, along with better management of land and water resources, are necessary to avert chronic food shortages.
Answer: 2. Birth
Question 67. Produce an exaggerated response of the immune system in which a specific antibody initiates the inflammatory response.
Answer: 3. Allergens
Question 68. Bronchitis is a disease in which the mucus membrane in the lung’s bronchial passages becomes inflamed.
Answer: 2. Respiratory
Question 69. Is an uncontrolled growth of cells that disrupts body tissues and organs.
Answer: 2. Cancer
Question 70. Experts agree that is the single biggest avoidable cause of cancer in the world.
Answer: 1. Tobacco
Class 10 Life Science Multiple Choice Questions
Question 71. The declining phase of a population is defined by
Answer: 1. Mortality > natality
Question 72. An example of an indoor allergen is
Answer: 2. Dust mites
Question 73. Factor(s) responsible for bronchitis is/are
Answer: 4. All of these
Question 74. An example of a disease caused due to air pollution is
Answer: 3. Asthma
Question 75. A common symptom of asthma is
Answer: 2. Breathing difficulty
Life Science Chapter 5 Class 10 Mcq Solutions
Question 76. If the number of pollen grains, fungal spores, and dust particles increase suddenly in the air, decide which of the following problems may increase-
Answer: 2. Asthma
Question 77. Biodiversity describes the diversity of
Answer: 3. Life
Question 78. Is a unit of the biosphere.
Answer: 1. Ecosystem
Question 79. The worst dangerous threat to wildlife is by
Answer: 2. Habitat destruction
Question 80. The Equatorial region of the earth is rich in
Answer: 2. Biodiversity
Life Science Chapter 5 Class 10 Mcq Solutions
Question 81. Sexual reproduction plays an important role in diversity.
Answer: 3. Genetic
Question 82. A buffer zone of the biosphere reserve is where
Answer: 4. Limited human activity is permitted
Question 83. The gums and adhesives are produced from the tree
Answer: 1. Acacia
Question 84. Resins are a useful product of gymnospermous wood like
Answer: 3. Pinus
Question 85. Apis indica produces
Answer: 4. Both ‘1’ and ‘2’ correct
Question 86. The incorrect match for tiger reserve amongst the following is
Answer: 4. Palamau – tamilnadu
Question 87. Pearls are produced by
Answer: 2. Oysters
Life Science Chapter 5 Class 10 Mcq Solutions
Question 88. Globally, the number of biodiversity hotspots are
Answer: 3. 35
Question 89. In India, rhinoceros is found in the biodiversity hotspot of
Answer: 1. Eastern Himalayas
Question 90. Which is not a reason for the loss of biodiversity?
Answer: 2. Over-eating
Question 91. Which is the first national park established in India?
Answer: 4. Corbett
Question 92. Is considered a a world heritage site by UNESCO.
Answer: 3. Sundarbans
WBBSE Class 10 Life Science Chapter 5 MCQs
Question 93. The diversity of organisms sharing the same community or habitat is called
Answer: 1. Alpha diversity
Question 94. Ex-situ conservation may be done in
Answer: 3. Zoo gardens
Question 95. The joint forest management system originated in
Answer: 1. West Bengal
Question 96. Tiger conservation initiative in India was started in
Answer: 2. 1973
Question 97. In India, the red panda is found in
Answer: 4. Sikkim
Question 98. In India, lions are conserved in
Answer: 4. Gir forest
Question 99. The first biosphere reserve established in India for conserving the gene pool of flora and fauna and the lifestyle of tribals is
Answer: 1. Nilgiri Biosphere reserve
WBBSE Class 10 Life Science Chapter 5 MCQs
Question 100. The ex-situ conservation of biodiversity is done through
Answer: 3. Cryopreservation of gametes
Question 101. Environmental problems affecting the Sunderban ecosystem is/are due to
Answer: 4. All of these
Question 102. One endangered species of the Eastern Himalayan biodiversity hotspot is
Answer: 3. Red Panda
Question 103. An example of ex-situ conservation is
Answer: 4. Cryopreservation
Question 104. Gorumara, Corbett, Kulik, Nandadevi— choose the correct sequence from the following which is correct for the above forests in sequence
Answer: 3. National Park, National Park, Sanctuary, Biosphere Reserve
Question 1. Animal migration is an example of adaptation.
Answer: 1. Behavioral
Question 2. Most species have reduced or lost true leaves, retaining only spines, which are highly modified leaves.
Answer: 3. Cacti
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Question 3. The spines protect the cactus from
Answer: 4. Predators
WBBSE Class 10 Life Science Chapter 4 MCQs
Question 4. Over time, animals that are better adapted to their environment survive and
Answer: 2. Breed
Question 5. Evolution is the result of
Answer: 2. Adaptation
Question 6. The swim bladder of a fish helps in
Answer: 3. Buoyancy
Question 7. In fish rete mirabile is found in
Answer: 1. Swim bladder
WBBSE Class 10 Life Science Chapter 4 MCQs
Question 8. The number of air sacs in birds is usually
Answer: 4. 9
Question 9. An example of a mangrove plant is
Answer: 2. Garan
Question 10. In their hump camels store
Answer: 2. Fat

Question 11. One of the chimpanzees’ favorite foods is
Answer: 3. Nuts
WBBSE Class 10 Life Science Chapter 4 MCQs
Question 12. Did extensive study of the behavior of chimps.
Answer: 1. Kohler
Question 13. The language of honey bees was decoded by
Answer: 4. Karl von frisch
Question 14. Honeybees indicate the direction of food sources by
Answer: 2. Waggle dance
Question 15. The erythrocytes of camels are
Answer: 4. All of these
Question 16. An example of behavioral adaptation is
Answer: 4. Presence of swim bladder
Question 17. Phyllocladeisfoundin
Answer: 1. Xerophytes
Life Science Class 10 MCQs Chapter 4 Solutions
Question 18. Which of the following adaptations enables the camel to live in deserts?
Answer: 3. Decreased GFR in kidney
Question 19. Which of the following animals shows double respiration?
Answer: 4. Pigeon
Question 20. Physiologically dry soil contains
Answer: 3. A large amount of saline water
Question 21. The approximate age of the Earth is
Answer: 4. 4.6 billion years
Question 22. Life was first formed in
Answer: 1. Sea
Question 23. The most powerful proof of organic evolution is
Answer: 1. Fossil
Life Science Class 10 MCQs Chapter 4 Solutions
Question 24. The biogenetic law was proposed by
Answer: 2. Haeckel
Question 25. The atmosphere of primitive earth consisted of
Answer: 1. Methane, water, ammonia & hydrogen
Question 26. The wing of a bird and the wing of an insect is
Answer: 2. Analogous organ
Question 27. The tendril of gourd and that of pea is
Answer: 2. Analogous organ
Question 28. The second molar in human beings is
Answer: 2. Functional organ
Question 29. The duration of chemical evolution is
Answer: 1. 1 Billion years
Question 30. The following plant is a living fossil
Answer: 2. Ginkgo
Life Science Class 10 MCQs Chapter 4 Solutions
Question 31. The two groups of animals, whose characters are present in Peripetus are
Answer: 3. Arthropoda and Annelida
Question 32. The following reptile has 4 chambered heart
Answer: 3. Crocodile
Question 33. The organ which has been reduced due to evolution is
Answer: 1. Vestigial
Question 34. The organs which are structurally similar and functionally different are called
Answer: 2. Homologous organ
Question 35. The following animal is an example of the missing link.
Answer: 2. Archaeopteryx
Question 36. The lungfish is advanced over other fishes apart from having lungs that they have
Answer: 3. 3 Chambered heart
Class 10 Life Science MCQ With Answers
Question 37. The abdominal muscles in humans are
Answer: 2. Vestigial organ
Question 38. Some complex inorganic and organic compounds in the hot sea aggregated in different combinations forming
Answer: 4. Coacervates
Question 39. The theory of use and disuse was denoted by
Answer: 1. Lamarck
Question 40. The following statement which Darwin made but could not explain was
Answer: 4. Origin of new species
Question 41. Mutation theory was denoted by
Answer: 2. Hugo devries
Question 42. The following flower shows staminode
Answer: 3. Mango male flower
Class 10 Life Science MCQ With Answers
Question 43. The following animal fossil shows the presence of characters of both reptiles and bird
Answer: 3. Archaeopteryx
Question 44. The following organ is vestigial in human being
Answer: 3. Appendix
Question 45. The scientific name of the present-day horse is
Answer: 4. Equus
Question 46. The name of the egg-laying mammal is
Answer: 3. Platypus
Question 47. The book called “philosophic zoologique” was written by
Answer: 2. Lamarck
Class 10 Life Science MCQ With Answers
Question 48. Stromatolites, the first found fossils, were of
Answer: 3. Cyanobacteria
Question 49. The process of evolution
Answer: 2. Is a continuous process
Question 50. The number of digits in the hind limb of eohippus is
Answer: 3. Three
Question 51. The following fish is cartilaginous
Answer: 3. Shark
Question 52. The phylum that joins invertebrates and vertebrates is
Answer: 3. Hemichordata
Question 53. The theory of homogeny was proposed by
Answer: 2. Oparin
WBBSE Class 10 Life Science Multiple Choice
Question 54. The phylum showing a diploblastic body wall for the first time is
Answer: 3. Cnidaria
Question 55. Fossils were discovered for the first time by
Answer: 2. Tenophen
Question 56. Biogenetic law states that
Answer: 4. Ontogeny repeats phylogeny
Question 57. The following organ of a plant is vestigial
Answer: 3. Pistillode
WBBSE Class 10 Life Science Multiple Choice
Question 58. The venous heart is found in
Answer: 1. Fishes
Question 59. Germplasm theory was propounded by
Answer: 3. Weisman
Question 60. The tuber of potato and rhizome of turmeric is
Answer: 1. Homologous organ
Question 61. Undifferentiated mass of cell is present in
Answer: 2. Poriferra
Question 62. An incomplete septum in the heart ventricle is found in
Answer: 2. Reptilia
Question 63. To justify that a fossil ‘a’ is older than ‘b’, which one of the following can be selected?
Answer: 3. Fossil a was found in deeper sedimentation
Question 64. Missing links are
Answer: 2. Fossil forms exhibiting two different group characters
WBBSE Class 10 Life Science Multiple Choice
Question 65. Which one of the following is a living fossil?
Answer: 1. Coelacanth
Question 66. Analogous organs have a
Answer: 4. Different embryonic origin but perform similar functions
Question 67. An organism which is an animal and plants
Answer: 3. Euglena
Question 68. The unit of evolution is
Answer: 3. Population
Question 69. Modern evolution theory involves
Answer: 4. All of these.
Question 70. Darwin’s theory does not include
Answer: 2. Evolution through inheritance
Question 71. The Gas that was Absent In The environment during The Origin Of Life Is
Answer: Oxygen
Question 72. The Feature Of Analogous Organs Is
Answer: Different In Origin But Functions Are Same.
Question 73. Which One Of The Following Is The Intraspecific Struggle For The Same Food?
Answer: Struggle Among The Members Of Rohu Fish In Pond
Question 74. Which Of The Following Changes Did Not Occur During The Course Of the Evolution Of the Horse?
Answer: Increase In The Length And Thickness Of All Digits In Limbs.
Question 75. According To The Opinion Of The Scientists, The Prebiotic Environment Of The Earth That Led To The Origin Of Life Was Like
Answer: Hot Dilute Soup In The Sea Water
Question 76. Identify Which Of The Following Indicates Interspecific Struggle?
Answer: Struggle Between Snakes And Owls For Capturing Rats For Eating
WBBSE Class 10 Life Science Multiple Choice
Question 77. Determine The Term Related To The Theory Of Lamarck
Answer: Inheritance Of Acquired Characters
Question 78. Which of the following absorbs the gas of the swim bladder in bony fishes
Answer: 4. Retia mirabilia
Question 79. Identify the animal that communicates information with other members of its own group through specific dancing patterns regarding the sources of food
Answer: 4. Honeybee
Question 1. The mechanism of transmission of characters from the parental generation to the offspring is called as
Answer: 4. Eugenics
Question 2. The idea of mixing parental characters with the offspring is known as
Answer: 3. Blending inheritance
Question 3. Environmental variations are
Answer: 1. Not inherited
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Question 4. Somatic variations are
Answer: 1. Acquired
Question 5. Variations are usually caused by
Answer: 4. Mutation
Question 6. Which one of the following pairs is not contrasting?
Answer: 4. Round & light
Wbbse Class 10 Life Science Mcqs
Question 7. Mendel performed experiments on
Answer: 3. Garden pea (Pisum sativum)
Question 8. Mendel’s concept gave birth to the theory of inheritance.
Answer: 1. Particulate
Question 9. An organism with two copies of the same allele is
Answer: 3. Homozygous for that trait

Question 10. Mendelian laws of heredity are connected with
Answer: 1. Segregation, dominance & independent assortment
Wbbse Class 10 Life Science Mcqs
Question 11. Gene mutations are also known as
Answer: 2. Point mutation
Question 12. A diploid individual’s chromosome is
Answer: 4. 2N+l
Question 13. In humans, tongue-rolling characteristics are found in
Answer: 4. Most
Question 14. The attached ear lobe character in humans is
Answer: 3. Recessive
Question 15. An alternative form of a gene, located at a specific position on a specific chromosome is called
Answer: 4. Variety
Question 16. The specific location of a gene on a chromosome is called its
Answer: 1. Locus
Wbbse Class 10 Life Science Chapter 3 Solutions
Question 17. Mendelian factors are now called
Answer: 2. Genes
Question 18. A genetic cross dealing with two character differences is called
Answer: 2. Dihybrid cross
Question 19. The genotype ‘as’ is
Answer: 2. Heterozygous
Question 20. The character that is expressed in the heterozygous condition is
Answer: 3. Dominant
Question 21. The outer expression of a character is its
Answer: 1. Phenotype
Question 22. Pea plants normally perform
Answer: 4. Self-fertilization
Wbbse Class 10 Life Science Chapter 3 Solutions
Question 23. In case of incomplete dominance in the F2 generation
Answer: 3. The genotypic ratio = phenotypic ratio
Question 24. The F2 phenotypic ratio of the Mendelian dihybrid cross is
Answer: 3. 3:1
Question 25. The case of incomplete dominance is observed in
Answer: 3. Mirabilis jalapa
Question 26. Human males are
Answer: 2. Heterogametic
Question 27. Sry is present in human
Answer: 1. Y chromosome
Class 10 Life Science Mcq With Answers
Question 28. In men, sperm contain autosomes and
Answer: 2. Either x or y chromosome
Question 29. If a homozygous dominant red-flowered plant is crossed with a homozygous recessive white-flowered plant, the offspring will be
Answer: 3. All red flowered
Question 28. Independent assortment can be proved by
Answer: 2. Test cross
Question 29. A cross between black and white birds results in all blue in the F1 generation. Then the cross between bluebirds in the F2 generation would result in
Answer: 3. 9 Blue : 3 black : 3 white
Question 30. The four daughter cells derived from single meiosis differ from each other due to
Answer: 4. Crossing over and independent assortment of chromosomes
Question 31. The number of distinct traits selected by Mendel in garden peas for his breeding experiments are
Answer: 4. 8
Class 10 Life Science Mcq With Answers
Question 32. When two hybrids undergo crossing in a monohybrid cross, then the percentage of recessive is
Answer: 4. 75
Question 33. If a couple has 5 daughters, the percentage probability of the other child being a girl is
Answer: 1. 25
Question 1. Which of the following traits in the pea plant is recessive?
Answer: wrinkled seed.
Question 2. How many types of gametes are formed from pea plants having the genotype yy rr?
Answer: 4.
Question 3. Which one of the following is the genotypic ratio at the F2 generation of Mendel’s monohybrid cross?
Answer: 1:2:1
Question 4. What would be the phenotypic ratio in the F2 generation of a monohybrid cross in case of incomplete dominance?
Answer: 1:2:1
Question 5. Identify which of the following is a dominant trait
Answer: the color of the cotyledon – yellow
Life Science Class 10 Wbbse Multiple Choice
Question 6. Assess how many types of gametes are produced from the pea plant having the genotype rryy —
Answer: one type
Question 7. Select which of the following two genotypes are responsible for the expression of the phenotype wrinkled yellow in Pea plant
Answer: rrYY and rrYy
Life Science Class 10 Wbbse Multiple Choice
Question 1. Genetic Disorders Are
Answer: 2. Inherited
Question 2. Haemophilia Is Related To
Answer: 1. Blood
Question 3. Color Blindness Is
Answer: 3. Sex-Linked Recessive
Question 4. Thalassemia Is
Answer: 4. Genetic
Wbbse Class 10 Life Science Mcqs
Question 5. Haemophilia B Is Also Known As
Answer: 3. Christmas Disease
Question 6. The Most Common Type Of Colour Blindness Is
Answer: 1. Red-Green
Question 7. The Chromosome Carrying Sex-Linked Gene Is
Answer: 3. X Chromosome
Question 8. Holandric Genes Are Ones Situated On
Answer: 2. Y Chromosome
Question 9. A Man Known To Be A Victim Of Haemophilia Mar-Ries A Normal Woman Whose Father Was Known To Be Bleeder; Then It May Be Expected That
Answer: 2. Half Of Their Sons Would Be Bleeders
Wbbse Class 10 Life Science Chapter 3 Solutions
Question 10. Red Green Colour Blindness Is Also Known As
Answer: 4. Both 1&2
Question 11. A Colourblind Man, Both Of Whose Parents Had Normal Vision And Whose Paternal And Maternal Grandparents Had Normal Vision, Probably Inher-Ited The Gene For Colourblindness From His
Answer: 3. Mother
Question 12. Daltonism Can Occur In Females Due To
Answer: 1. Homozygous Condition In Which Both X chromosomes Are Mutated At The Same Locus
Question 13. The Daughters Born To a Haemophilic Father And Normal Mother Could Be
Answer: 2. Carrier
Question 14. Color Blindness Is Related to a Defect In
Answer: 2. Cones
Question 15. Haemophilia Is A Genetic Disorder In Which
Answer: 2. There Is Delayed Coagulation Of Blood
Question 16. A Cross Between A Normal Homozygous Woman And A Haemophilic Man Will Result In How Many Sons Having The Above Disease?
Answer: 1. 0%
Question 17. If You Are Missing One Of The Four Alpha Chain Genes, Then You Are Suffering From Which Type Of Alpha Thalassemia?
Answer: 1. Silent Carrier
Wbbse Class 10 Life Science Chapter 3 Solutions
Question 18. Which Type Of Thalassemia Is Also Called Cooley’s Anaemia?
Answer: 2. Beta Thalassemia Major
Question 19. What Are The Factors That Increase The Risk Of Thalassemia Disease?
Answer: 3. Both 1 & 2
Question 20. A Good Genetic Counsellor Should Have Skills Of
Answer: 4. All Of These
Answer: 3. Virchow
Question 2. Which statement about the cell cycle is incorrect?
Answer: 2. Chromosomes
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Question 4. The main function of a gene is to
Answer: 4. All the above
WBBSE Class 10 Life Science Chapter 2 MCQs
Question 5. Which is not a nitrogenous base of DNA?
Answer: 4. Uracil(u)

Question 6. Are long thread-like structures made of a DNA molecule and protein.
Answer: 2. Chromosomes
Question 7. Each of our body cells contains pairs of chromosomes.
Answer: 1. 23
Question 8. The sex chromosomes of human males are
Answer: 2. XY
Question 9. Pictures of chromosomes arranged in pairs are known as
Answer: 4. Karyogram
WBBSE Class 10 Life Science Chapter 2 MCQs
Question 10. Cells with a haploid number of chromosomes are produced by
Answer: 3. Meiosis
Question 11. The twenty-third pair of chromosomes in man is known as
Answer: 1. Heterosome
Question 12. At mitotic metaphase, each chromosome consists of two symmetrical structures called
Answer: 4. Chromatids
Question 13. Are v-shaped chromosomes in which the centromere lies in the middle of the chromosome so that the two arms are almost equal.
Answer: 3. Metacentric
Question 14. Secondary constrictions are also called
Answer: 2. NOR
WBBSE Class 10 Life Science Chapter 2 MCQs
Question 15. Different types of chromosomes can be recognized by the position of the following separating the two arms
Answer: 4. Centromeres
Question 16. Chromatin is composed of DNA, RNA and
Answer: 3. Protein
Question 17. Deoxyribose sugar is
Answer: 1. Pentose
Question 18. Chromosomes contain proteins.
Answer: 1. Histone
Question 19. Regions of the chromosomes containing genes are
Answer: 1. Euchromatin
Continuity Of Life MCQs For Class 10 Board Exams
Question 20. Cytokinesis refers to
Answer: 2. Division of cytoplasm
Question 21. In sexual reproduction
Answer: 3. Gametes are usually haploid
Question 22. Microtubules are thick, strong spirals of thousands of subunits known as\
Answer: 4. Tubulin
Question 23. Mitochondrial production is also vital for cell division.
Answer: 2. ATP
Question 24. Is also known as reductional cell division.
Answer: 2. Meiosis
Question 25. Is the time when a cell will leave the cycle and quit dividing.
Answer: 1. G0
Class 10 Life Science Chapter 2 Multiple Choice
Question 26. The chromosome set is
Answer: 4. Constant for a given species
Question 27. Mitotic nuclear division is called
Answer: 3. Karyokinesis
Question 28. Karyokinesis does not include
Answer: 4. Cytokinesis
Question 29. Chromosomes are arranged in the equator of the cell during
Answer: 2. Metaphase
Question 30. Crossing over occurs during
Answer: 1. Meiosis I
MCQs For Continuity Of Life WBBSE
Question 31. Which of the following statements is true?
Answer: 4. The daughter cell receives both maternal and paternal chromosomes of the homologous pair in meiosis
Question 32. During mitosis, each chromosome at the beginning of the prophase is
Answer: 2. Paired structure
Question 33. In mitotic cell division the
Answer: 4. Both (1) & (2)
Question 34. Which of the following is true for mitosis?
Answer: 4. All of these
West Bengal Board Class 10 Life Science MCQs
Question 35. Identify the pair of nucleotides that are joined by hydrogen bonds in double-stranded DNA.
Answer: 3. AT & CG
Question 36. Chromosomes do not have a well-defined structure in
Answer: 1. Interphase
Question 37. Crossing over is the
Answer: 1. Exchange of genetic material
Question 38. If the number of chromosomes in most body cells of a mammal is 40, the cells in the seminiferous tubule will have
Answer: 3. 20 Chromosomes
Question 39. Chromosomes which have a definite role in sex determination are
Answer: 2. Allosomes
Question 40. Crossing over occurs between
Answer: 1. Non-sister chromatids of homologous chromosomes
Question 41. Which of the following is true?
Answer: 4. All of these
Question 42. The characteristic structure called phragmoplast formed during plant cell division is the precursor of
Answer: 3. Cell wall
Question 43. There can not be mitotic division in one of the following cells. Identify the cell
Answer: 2. Sperm
Question 44. The complete process of meiosis involves
Answer: 2. Two cytoplasmic divisions with one reduction of chromosomes
Question 45. Amitosis is
Answer: 4. Cleavage of the nucleus without recognizable chromosome distribution
West Bengal Board Class 10 Life Science MCQs
Question 46. Bulbil is a modification of
Answer: 4. Bud
Question 47. The animal that reproduces by multiple fission is
Answer: 4. All of them
Question 48. The organism that shows fragmentation is
Answer: 3. Oscillatoria
Question 49. The most developed artificial propagation method is
Answer: 1. Grafting
Question 50. The following animal may develop by parthenogenesis:
Answer: 2. Worker bee
Question 51. The unit of asexual reproduction is
Answer: 3. Spore
Class 10 Life Science Chapter 2 Important MCQs
Question 52. Which one is related to sexual reproduction?
Answer: 4. Meiosis
Question 53. Production of fruit without fertilization is known as
Answer: 3. Parthenocarpy
Question 54. Which type of reproduction paves the pathway of evolution?
Answer: 3. Sexual reproduction
Question 55. Which one is not formed due to sexual reproduction?
Answer: 1. Zoospore
Question 56. Yeast reproduces by
Answer: 3. Both
Question 57. The first diploid cell resulting from sexual reproduction is
Answer: 2. Zygote
Question 58. Which one is not an underground stem?
Answer: 4. Runner
Question 59. Gametes are
Answer: 1. Haploid
Question 60. The propagating organ for ginger is
Answer: 3. Rhizome
Class 10 Life Science Chapter 2 Important MCQs
Question 61. The propagating organ for onion is
Answer: 3. Bullb
Question 62. The gametes that look identical are called
Answer: 1. Isogamete
Question 63. The following organism may exhibit spore
Answer: 2. Rhizopus
Question 64. The animal that does not show regeneration is
Answer: 3. Ascaris
Question 65. Which one of the following methods is not a method of artificial vegetative propagation?
Answer: 3. Hybridization
Question 66. The vegetative method of reproduction adopted for plants with longer seed dormancy is
Answer: 4. Grafting
Question 67. The part of the plant which remains close to the ground is
Answer: 1. Stock
Question 68. Which one of the following reproduces with the help of a leaf?
Answer: 3. Bryophyllum
Question 69. Which method results in the mixing of features of two separate plants?
Answer: 2. Grafting
Question 70. Which one of the following is true for vegetative reproduction?
Answer: 4. It is both natural and artificial, producing genetically different plants.
Question 71. The following plant reproduces by vegetative means
Answer: 4. All of them
Question 72. The following hormone induces rooting after cutting
Answer: 2. IAA
Class 10 Life Science Chapter 2 Important MCQs
Question 73. The following plant reproduces by root bud
Answer: 3. Both
Question 74. Which one of the following processes is related to root induction
Answer: 1. Cutting
Question 75. In grafting, the plant part that joins with the stock is called
Answer: 1. Scion
Question 76. The following plant reproduces with a fleshy root
Answer: 4. All of them
Question 77. Potato tuber reproduces with
Answer: 3. Both
Question 78. The plant that reproduces by rhizome is
Answer: 4. All of them
Question 79. The plant that reproduces with Gootee is
Answer: 4. All of them
Question 80. The animal that reproduces by conjugation is
Answer: 1. Paramoecium
Question 36. The largest plant production method of vegetative reproduction is
Answer: 3. Micropropagation
Life Science Chapter 2 MCQs with Answers Class 10
Question 37. A totipotent cell means
Answer: 1. An undifferentiated cell capable of developing into a system or entire plant
Question 38. Which of the following plant cells show totipotency?
Answer: 3. Meristem
Question 39. Asexually produced organisms inheriting all the characteristics of the parent are
Answer: 2. Clone
Question 40. Which is connected to asexual reproduction?
Answer: 1. Gemmules
Question 41. Any cell, tissue, or organ removed from a plant for culturing is called
Answer: 2. Scion
Question 42. When two different individuals participate in vegetative reproduction, it is called
Answer: 2. Grafting
Question 43. Parthenogenesis is
Answer: 3. Development of fruit without hormone
Question 44. In which of the following modes of asexual reproduction, a mother cell produces innumerable unicellular uninucleate offspring?
Answer: 2. Multiple fission
Question 45. In oogamy, fertilization involves
Answer: 1. A large nonmotile female gamete and a small nonmotile male gamete
Question 46. Why is asexual reproduction sometimes disadvantageous?
Answer: 2. It allows sedentary animals to produce offspring without mates
Life Science Chapter 2 MCQs with Answers Class 10
Question 47. When an animal is cut into pieces, each piece is found to grow into a complex organism. Name the process.
Answer: 4. Regeneration
Question 48. In grafting contact is made between
Answer: 3. Cambium
Question 49. Which of the following statements supports the view that elaborates sexual reproductive processes appeared much later in the organic evolution?
Choose the correct answer from the given options:
Answer: 3. 2&4
Question 50. There are various types of reproduction. The type of reproduction adopted by an organism depends on
Answer: 4. The habitat, physiology, and genetic makeup of the organism
Question 76. Growth is a permanent increase in
Answer: 3. Dry mass
Question 77. The growth which occurs due to the multiplication of cells by repeated mitosis and in which the size of the cells does not increase is called
Answer: 2. Multiplicative growth
Question 78. Growth requires
Answer: 4. All above are correct
Question 79. Human childhood age is
Answer: 2. 2-10 Years
Question 80. Intelligence is not associated with
Answer: 1. Old age
Class 10 Life Science Chapter 2 Multiple Choice
Question 81. In human beings which part shows the maximum increase in weight from birth to adulthood?
Answer: 3. Muscles
Question 82. The process in which reserve food material is utilized and which shows negative growth is called
Answer: 4. Degrowth
Question 83. Growth curve indicates
Answer: 3. Growth parameter at various interval
Question 84. The shape of the curve that represents the growth pattern of all organisms, plants or animals, unicellular or multicellular forms is
Answer: 1. S
Question 85. Death is
Answer: 4. All Of These
Question 86. Which of the following pairs is correct?
Question 89. Which phase of human development is associated with the maturity of reproductive organs and reproductive glands?
Answer: 2. Adolescence
Question 1. The ability of a plant to react to external stimuli is
Answer: 4. Irritability
Question 2. The instrument with which sir. c. Bose proved the phenomenon of reacting to stimulus is
Answer: 2. Crescograph
Read and Learn More WBBSE Class 10 Life Science Multiple Choice Questions
Question 3. The movement of variation is controlled by
Answer: 2. Osmosis
Question 4. The following plant is capable of locomotion
Answer: 4. Volvox
WBBSE Class 10 Life Science Chapter 1 MCQs
Question 5. The movement offers antherozoid to archegonium is called
Answer: 2. Chemonasty
Question 6. The plant movement that is controlled by auxin is
Answer: 2. Nastic
Question 7. The movement of Chlamydomonas towards light is called
Answer: 3. Photonastism
Question 8. The tactic movement controlled by an electric current is
Answer: 4. Galvanotactic
Question 9. The movement of plant roots against gravity is known as
Answer: 2. Aerotropic
WBBSE Class 10 Life Science Chapter 1 MCQs
Question 10. When a plant stem grows opposite to water, it is called
Answer: 2. Negatively phototropic

Question 11. The movement of drosera lea felt towards insects is called
Answer: 2. Chemonasty
Question 12. The plant movement depending on the intensity of the stimulus is
Answer: 2. Tropic
Question 13. The nastic movement that is controlled by both light and temperature is
Answer: 3. Nyctinasty
Question 14. The movement of plants involving actual displacement is
Answer: 2. Taxism
Question 15. The movement of curvature whose direction is controlled by the direction of the stimulus is
Answer: 2. Tropic
WBBSE Class 10 Life Science Chapter 1 MCQs
Question 16. In comparison to geotropism, which one is a greater force?
Answer: 2. Hydrotropism
Question 17. The following organism shows amoeboid movement
Answer: 2. Fungi
Question 18. The movement that both Chlamys Doonas and Volvox exhibit is
Answer: 3. Phototaxis
Question 19. The movement involved in the opening of the tulip flower is
Answer: 4. Thermonasty
Class 10 Life Science Chapter 1 Multiple Choice
Question 20. The following plant movement is due to the growth
Answer: 4. All of them
Question 21. The closing of leaflets in Cisalpine is
Answer: 4. Seismonasty
Question 22. The primary root is:
Positively geotropic, Positively hydrotropic, Negatively geotropic, Negatively hydrotropic
Answer: 3. 1, 2 Correct
Question 23. The opening and closing of a sunflower are also called
Answer: 1. Photonasty
Question 24. The movement of tendrils of the pea is
Answer: 2. Circumnutation
Question 25. The movement that occurs in plants due to touch is
Answer: 3. Both
Class 10 Life Science Chapter 1 Multiple Choice
Question 26. The response toward a stimulus is said to be
Answer: 3. Positive
Question 27. Who for the first time mentioned plant hormones?
Answer: 2. Charles Darwin
Question 28. Which one is the natural auxin?
Answer: 1. IAA
Question 29. The hormone that helps in the ripening of fruit is
Answer: 3. Ethylene
Class 10 Life Science Chapter 1 Important MCQs
Question 30. Which hormone is produced in the leaf but helps in flowering?
Answer: 3. Gibberellin
Question 31. Which hormone is produced in the coleoptile?
Answer: 1. Auxin
Question 32. Which hormone is used as a weedicide?
Answer: 2. 2,4-D
Question 33. Name the hypothetical hormone that induces flowering.
Answer: 4. Florigen
Question 34. Name the hormone that helps in the growth of the axillary bud.
Answer: 2. Gibberellin
Class 10 Life Science Chapter 1 Important MCQs
Question 35. The hormone that is produced in a maximum amount in the matured seed is
Answer: 2. Gibberellin
Question 36. The hormone that is present in coconut milk is
Answer: 1. Kinetin
Question 37. The hormone that helps in the production of seedless fruit is
Answer: 3. Kinetin
Question 38. The following hormone does not contain nitrogen
Answer: 3. Ga3
Class 10 Life Science Chapter 1 Important MCQs
Question 39. Substances that originate at the tip of the stem and control growth elsewhere are known as
Answer: 2. Hormones
Question 40. The following hormone is terpenoid in nature
Answer: 2. Gibberellin
Question 41. The hormone that is not a growth promoter
Answer: 3. Abscisic acid
Question 42. The hormone that helps in removing dwarfism is
Answer: 2. Gibberellin
Question 43. Name the hormone whose precursor is tryptophan.
Answer: 1. Auxin
Question 44. Name the hormone that induces apical dominance.
Answer: 1. Auxin
Question 45. The hormone that may act as an anti-auxin
Answer: 1. ABA
WBBSE Class 10 Life Science Chapter 1 Quiz
Question 46. Hormone primarily connected with cell division is
Answer: 2. Cytokinin
Question 47. Name the non-indole auxin.
Answer: 4. NAA
Question 49. Which hormone is responsible for the Richmond lang effect?
Answer: 3. Cytokinin
Question 50. Which one of the following is a rejuvenating hormone?
Answer: 3. Kinetin
Question 51. The hormone that is present in maize seed is
Answer: 2. Zeatin
Question 52. The following hormone induces the closure of stomata
Answer: 1. ABA
Question 53. Which is employed for the artificial ripening of banana fruit?
Answer: 4. Ethylene
WBBSE Class 10 Life Science Chapter 1 Quiz
Question 54. Apical dominance is caused by
Answer: 4. Auxin in shoot tip
Question 55. Flowering dependent on cold treatment is
Answer: 4. Vernalization
Question 56. The translocation/movement of auxin is largely
Answer: 4. Both 2 & 3
Question 57. Gibberellic acids induce flowering in
Answer: 2. Long-day plants under short-day conditions
Question 58. Differentiation of shoot is controlled by
Answer: 1. High cytokinin: auxin ratio
WBBSE Class 10 Life Science Chapter 1 Quiz
Question 59. Pruning helps in making hedges dense because
Answer: 3. It frees axillary buds from apical dominance
Question 60. Which one of the following pairs is not correctly matched?
Answer: 1. Ga-leaf fall
Question 61. Which of the following is a gaseous hormone?
Answer: 3. Ethylene
Question 62. Which of the following hormones is involved in counteracting apical dominance induced by auxin?
Answer: 1. Cytokinin
Question 63. Chemically hormones are
Answer: 4. All of these
Question 64. Response and coordination in animals involve the sense organs, nervous system, and chemicals called hormones.
Answer: 3. Messengers
Class 10 Life Science Chapter 1 MCQs With Answers
Question 65. Goosebumps are also called
Answer: 1. Cutis anserina
Question 66. Thermo receptors are responsive to change of
Answer: 1. Temperature
Question 67. An important hormone required for combatting stress is
Answer: 4. Adrenaline
Question 68. Hyperthyroidism results in
Answer: 4. Both (2) & (3)
Question 69. The thyroid hormones t3 and i4 are the main regulators of
Answer: 4. Bmr
Question 70. Estrogen and testosterone are
Answer: 2. Sex hormones
Question 71. It stimulates the pituitary gland to release the sex hormones.
Answer: 3. Hypothalamus
Question 72. Androgens are the hormones released by the
Answer: 1. Testis
Class 10 Life Science Chapter 1 MCQs With Answers
Question 73. Hormones are secreted by
Answer: 4. Both (2) & (3)
Question 74. An example of an amine hormone is
Answer: 3. Epinephrine
Question 75. Examples of steroid hormones are
Answer: 4. Both ‘2’ and ‘3’ are correct
Question 76. The chemical structure of a hormone enables it to combine with a receptor in the cells of its
Answer: 1. Target
Question 77. Neurosecretory cells are found in
Answer: 2. Hypothalamus
Question 78. Oxytocin and vasopressin are secreted by
Answer: 1. Posterior pituitary
Class 10 Life Science Chapter 1 MCQs With Answers
Question 79. The hormones t3 and t4 work together to regulate the body’s
Answer: 3. Metabolic rate
Question 80. The hormone epinephrine is produced from
Answer: 3. Adrenal cortex
Question 81. The release of puberty triggers the development of female secondary sex characteristics.
Answer: 4. Oestrogen
Question 82. During this time, the kidneys are unable to prevent the excretion of excess water.
Answer: 2. Diabetes insipidus
WBBSE Class 10 Life Science Chapter 1 MCQs
Question 83. Goitre is due to swelling of
Answer: 4. Thyroid
Question 84. Is known as the master gland.
Answer: 4. Hypothalamus
Question 85. Which one of the following is a local hormone?
Answer: 4. Gastrin
Question 86. Which hormone is not tropic?
Answer: 1. ADH
Question 87. Diabetes mellitus is associated with
Answer: 4. All of the these
Question 88. In A Neuron, the Conversion Of Electrical Signal To Chemical Signal Occurs At/In
Answer: 1. Axonal End
WBBSE Class 10 Life Science Chapter 1 MCQs
Question 89. The Nervous System Is Made Up Of Two Major Types Of Cells Known As
Answer: 3. Neurons And Neuroglia
Question 90. Axons Are
Answer: 2. Efferent
Question 91. Information From One Neuron Flows To Another Neuron Across A
Answer: 3. Synapse
Question 92. Brain And Spinal Cord Constitute The
Answer: 1. CNS
Question 93. The Largest Part Of The Brain Is
Answer: 2. Cerebrum
Class 10 Life Science Chapter 1 Multiple Choice
Question 94. Conditioned Reflexes Are
Answer: 4. Acquired
Question 95. The Thin, Transparent Tissue That Covers The Outer Surface Of The Eye Is
Answer: 1. Conjunctiva
Question 96. The Accommodation Is A Of The Eye.
Answer: 2. Reflex Action
Question 96. Near-sightedness problem Is Also Known As
Answer: 3. Myopia
Question 97. A Bipolar Neuron Has
Answer: 3. One Axon & One Dendron
Question 98. Motor Neurons Transmit Impulses
Answer: 4. Cns To Effector
Question 99. An Example Of Neurotransmitter Is
Answer: 2. Dopamine
Class 10 Life Science Chapter 1 Multiple Choice
Question 100. The First And Second Lateral Ventricles Of The Brain Are Connected To The Third Ventricle Through The
Answer: 2. Foramen Of Monro
Question 101. Which Is The Correct Sequence Of The Components Of A Reflex Arc?
Answer: 4. Receptors→ Sensory Neuron→ Spinal Cord→ Motor Neuron→ Muscle
Question 102. The part of the human brain associated with controlling body temperature is?
Answer: Hypothalamus.
Question 103. Which one of the following is the correct reflex arc?
Answer: Receptor → Afferent nerve → Nerve centre→ Efferent nerve → Effector
Class 10 Life Science Chapter 1 Important MCQs
Question 104. Determine the number of Cranial nerves in the human body —
Answer: 12 pairs.
Question 105. Amoeboid Locomotion Is Performed By
Answer: 4. Pseudopodia
Question 106. Biped A I Ism Is Found In
Answer: 4. Human
Question 107. Synovial Joints Are
Answer: 2. Movable
Question 108. Examples Of Hinge Joints Are
Answer: 3. Knee
Question 109. Myotomes Are Found In
Answer: 1. Fishes
Class 10 Life Science Chapter 1 Important MCQs
Question 110. Pseudopodium In Ameoba Is Formed At The Anterior End By The
Answer: 3. Conversion Of Plasmasol To Gel
Question 111. Tail Feathers And Wing Feathers Of Birds Are Known As
Answer: 2. Rectrices And Remiges
Question 112. Abductors Are Antagonists Of
Answer: 1. Adductors
Question 113. When A Joint Is Such That It Allows the Movement Of Bones In All Directions, It Is Known As A
Answer: 4. Ball And Socket Joint
Question 114. Elbow Joint Is
Answer: 2. Hinge Joint
Question 115. Synovial Fluid Is Secreted By
Answer: 3. Synovial Membrane
Class 10 Life Science Chapter 1 MCQs With Answers
Question 116. Which one is the largest synovial joint of the human body?
Answer: 3. Hip joint
Question 117. A sessile animal Is
Answer: 3. Coral
Question 118. Flight muscles of birds are attached to
Answer: 1. Keel of sternum
Question 119. Some flowers are open after sunrise and close after sunset. This is
Answer: 1. Photonasty
Question 120. The tentacles on the leaves of an insectivorous plant called sundew bend to trap the insect as soon as they come in contact with the insect’s body. This is
Answer: 4. Chemonasty
Question 121. Select which of the following statements is correctly related to tropic movement-
Answer: 1. It is an induced movement of curvature controlled by the direction of the stimulus
Answer to all questions is compulsory
Write the answer in a complete sentence by choosing the correct answer for each question with the respective serial number.
Question 1. Select the correct pair-
Answer: 3. Lens-Causes refraction of light and accomplishes accommodation
Question 2. Identify which of the following statements is not true regarding Adrenaline-
Answer: 2. Helps in the production of spermatozoa during adolescence
Question 3. Select which of the following is the feature of tropic movement-
Answer: 1. Induced movement of curvature of particular parts of the plant controlled by the direction of the stimulus
Question 4. Match the words of Column-A with that of Column-B and select which of the following options is correct—
Answer: table-
Answer: 2. A-1,B-3,C-2
WBBSE Class 10 Life Science Model Question Paper 2023
Question 5. Decide which of the following sequence is correct-
Answer: 3. Receptor→Sensory Nerve→Nerve Centre→Motor Nerve→Effector
Question 6. Select the correct pair-
Answer: 4. Telophase- Reappearance of Nuclear Membrane and Nucleolus
Question 7. The name of the terminal parts of the Chromosome is—
Answer: Telomere
Question 8. Identify which of the following statements is not true regarding cross-pollination-
Answer: 3. Maintains the purity of species
Question 9. Consider the differences between asexual and sexual reproduction and select which of the options is/are correct-
Answer:

Answer: Correct option is not provided
Question 10. Select the correct pair in the case of humans:
Answer: 3. Normal pattern of the chromosome of ovum — 22A + X
WBBSE Class 10 Life Science Model Question Paper 2023
Question 11. 1.11Determine which of the following genotypes is homozygous for both the loci
Answer: 4. bbrr
Question 12. Identify the genotype of guineapig having white coat colour and rough hair-
Answer: 3. bbRR, bbRr
Question 13. Decide which of the following two were selected by Mendel as dominant traits—
Answer: 1. Length of stem — Long, Shape of seed — Round
Question 14. Determine the nature of the pea plant germinated from the seed produced as a result of pollination between a hybrid tall (Tt) and a pure dwarf (tt) pea plant—
Answer: 2. 50% Tall, 50% Dwarf
Question 15. Decide which of the following diseases can be prevented by taking suggestions from pre-marital genetic counselling-
Answer: 3. Thalassaemia
2. Answer 21 questions out of 26 questions given below as instructed. Fill in the blanks with proper words in the following sentences (any five):
Question 1. The hormone is found in very high amounts in the ripe seeds of plants.
Answer: Gibberellin
Question 2. Reflex action is fast, spontaneous and
Answer: Involuntary
Question 3. In cell division spindle fibres are not formed.
Answer: amitosis
Question 4. is an entomophilous flower.
Answer: Sunflower
WBBSE Class 10 Life Science Model Question Paper 2023
Question 5. The gene having the power of the rolling tongue is.
Answer: dominant
Question 6. As the gene responsible for hemophilia is recessive, the symptoms of this disease are only manifested in
condition.
Answer: X-linked inheritance
Decide whether the following statements are true or false (any five):
Question 7. The focal length of the lens increases in case of seeing distant objects.
Answer: True
Question 8. Each nucleoside contains a nitrogenous base and phosphoric acid.
Answer: False
Question 9. There is no role of females in determining the sex of humans.
Answer: True
Question 10. If any pea plant contains either TT or tt trait, then the pea plant becomes heterozygous with respect to such alleles.
Answer: False
Question 11. As the flowers of the pea plant are unisexual, so self-pollination and if needed, cross-pollination can be performed.
Answer: True
Question 12. The daughter cells are changed and modified in different ways during cell differentiation phase to form tissue, organ and system.
Answer: True
WBBSE Class 10 Life Science Model Question Paper 2023
Match the words in Column-A with those which are most appropriate in Column-8 and re-write the correct pair mentioning the serial no. of both columns (any five) :

Answer: 2.13 – (2), 2.14- (3) 2.15- (4), 2.16- (5), 2.17- (6), 2.18- (1)
Answer in a single word or in a single sentence (any six):
Question 19. Choose the odd one and write it: Olfactory nerve, Vagus nerve, Optic nerve, Auditory nerve
Answer: Vagus nerve
Question 20. What is the fate of hormones in the animal body after its function is over ?
Answer: Hormones are destroyed and excreted immediately after their functions are over.
Question 21. A pair of related terms is given below. On the basis of the relationship in the first pair write the suitable word in the I gap of the second pair. Purine : Adenine :: Pyrimidine :
Answer: Cytosine
Question 22. What happens if the functions of checkpoints in the cell cycle get hampered?
Answer: Genomic instability and/or tumorigenesis
Question 23. What is hybridization?
Answer: Process of interbreeding individuals from genetically distinct populations to produce hybrids.
Question 24. What is a dominant trait?
Answer: A trait produced by a dominant allele in individuals who have one copy of the allele which can come from just one parent.
Class 10 Life Science Model Question Paper With Answers
Question 25. Among the following four terms, one includes the other three. Find it out and write it :
Increase in Basal Metabolic Rate, Thyroxine, Gradual maturation of Red Blood Corpuscle, Exophthalmic Goitre.
Answer: Exophthalmic Goitre
Question 26. In which phase of Interphase are the proteins essential for the formation of spindle fibres in synthesized?
Answer: G2 – phase.
Extensor muscle:
to increase the angle between two body parts.
Abductor’s muscle:
to move limbs away from the midline.
Rotator muscle:
To move limbs around their long axis.
Question 27. Prepare a list of functions controlled by Auxin related to the growth of plants.
Answer:
Major Plant Hormones Auxin
Auxins are a class of nitrogenous phytohormones & the most important growth regulators produced from the growing regions of plant tissue including roots, shoots, and leaves.
These promote cell division, stem and root growth. These can also drastically affect plant orientation by promoting cell division on one side of the plant in response to sunlight & gravity.
The term auxin was first used by Frits Went.
Chemical composition:
Auxins generally occur as complexes, usually found with an amino acid or sugar. These are composed of carbon, hydrogen, oxygen, and nitrogen.
The amino acid Tryptophan and many other Indole compounds serve as precursors of auxins.
Class 10 Life Science Model Question Paper With Answers
Chemical composition:
Auxins generally occur as complexes, usually found with an amino acid or sugar. These are composed of carbon, hydrogen, oxygen, and nitrogen.
The amino acid Tryptophan and many other Indole compounds serve as precursors of auxins.
Types: They are classified into two types as detailed below:
Natural Auxin:
They are Indole compounds like Indole 3-Acetic Acid (IAA) and Non-Indole compounds like Naphthalene Acetic Acid. Indole 3-Acetic Acid was the first plant hormone identified.
It is manufactured primarily in the shoot tips (in leaf primordia and young leaves), in embryos, and in parts of developing flowers and seeds.
Synthetic Auxin:
These are synthetic compounds similar to natural auxin and they include 2,4-D (2,4-Dichlorophenoxy Acetic Acid) or 2, 4, 5-T (2,4,5- Trichlorophenoxy Acetic Acid).
Translocation:
The transport of IAA from cell to cell through the parenchyma surrounding the vascular tissues requires the expenditure of ATP energy.
IAA moves in one direction only i.e., the movement is polar and in this case, downward.
Such downward movement in shoots is said to be basipetal (apex to base) and in roots it is acropetal (outwards towards the root apices from the base).
Synthetic auxins move in all directions inside plants.
Function:
Apical Growth:
Auxins bring about apical dominance and thereby induce apical growth of the shoot.
Tropic movements:
These are deposited unequally on the shoot or root surface and thus cause phototropic curvature and geotropism

Cell enlargement:
Auxin helps to increase the size and volume of the cells.
Cell enlargement is caused by the solubilization of carbohydrates, loosening of wall microfibrils, synthesis of more wall materials, increased membrane permeability, and respiration.
Metabolism:
Auxin stimulates respiration by increasing the availability of respiratory substrate. Thus it enhances metabolism by mobilizing plant resources.
Cambial activity:
The degree of cambial activity is directly proportional to auxin concentration. Auxin also controls xylem differentiation.
Cell division:
It initiates the cell division of the parenchymatous cells at the site of wounded tissue causing healing of wounds after mechanical injury in plants.
Class 10 Life Science Model Paper WBBSE 2023 Set 2
Root formation:
Auxin promotes root initiation at a concentration that is inhibitory for the growth of intact roots.
Parthenocarpic fruit Development:
Pollen contains a lot of auxin, it acts as a signal indicating the completion of pollination and transformation of the ovary to fruit.
Thus the application of synthetic auxin induces the development of fruit without the act of fertilization i.e. parthenocarpic fruit development.
Synthetic auxin (2,4-D) initiates rootings in stem cuttings.
(x)Synthetic auxin can act as a weedicide by killing dicotyledonous weeds preventing the division of cambial tissue.
As monocotyledonous plants are devoid of cambium, they are not destroyed by auxin compounds.
Anti-auxin:
Auxins have an inhibitory effect on the abscission of leaves and fruits, i.e., shedding of mature leaves and ripe fruits from the plant.
It has been found that the abscission zone does not form when the concentration of auxins is high in the leaves or fruits.
On the contrary, Abscisic acid (ABA) is a major hormone in plants that induces the formation of an abscission zone in the leaf stalk or petiole and brings about the shedding of leaves.
It acts as an antiauxin because it counteracts the auxin activity by initiating abscission.
In Plants Hormones Gibberellin
Gibberellins are one of the longest-known classes of non-nitrogenous phytohormones that regulate various developmental processes including stem elongation, germination, dormancy, flowering, and leaf and fruit senescence.
Gibberellic acid or gas can be of more than 100 types and the most common being 3- Gibberellic Acid (GA3).
Gibberellin was discovered by Kurosawa (1926) from rice plants suffering from Bakanae (foolish seedling) disease caused by Gibberella.
Gibberellins are naturally synthesized in maturing seeds, germinating seedlings, growing tissues of expanding cotyledons, growing leaves, apical buds, root tips, etc.
Class 10 Life Science Model Paper WBBSE 2023 Set 2
Chemical composition:
Gibberellins are tetracyclic diterpene acids. These consist of carbon, hydrogen, and oxygen.
Acetate is the precursor for the synthesis of all kinds of gibberellins.
The gibberellins are named GAj through GAn in the order of discovery.
Translocation:
All known gibberellins are synthesized in plastids and then modified in endoplasmic reticulum and cytosol until they reach their biologically active form.
The transport of gibberellin is not polar. These are transported in all directions from the site of formation through the xylem, phloem, or by cell tq cell.
Functions:
Elongation of internode:
It brings about the growth of the internode and thereby brings about apical growth along with auxin.
Flowering:
It modifies the apical bud to the floral bud, by bringing about the development of floral tissue through modification of the apical meristem.
Breaks seed dormancy:
It breaks seed dormancy and induces germination of seed through denovo synthesis of a-amylase.
Leaf growth:
It helps in the development of young leaves through stimulation of the leaf meristem
It promotes fruit growth and development. It also influences parthenocarpy.
Question 28. Distinguish between the mitosis of plant cells with the mitosis of animal cells on the basis of the following features—
Answer:
Basic Differences Between Mitosis Of Animal Cell And Plant Cell


3. Answer any 12 questions in 2-3 sentences out of 17 questions given below:
Question 1. Prepare a list of hormones that control the following functions—
Causes an increase in the length of bones through mineralization of the matrix of cartilage located at the terminal parts of long bones.
Answer: GH or STH
Transforms ruptured follicle into a temporary endocrine gland namely Corpus Luteum and provides necessary stimulation for the secretion of Progesterone hormone from that gland.
Answer: LH
Inhibits the production of glucose in the liver from protein and lipids.
Answer: Insulin
Causes contraction of uterine muscles during parturition
Answer: Relaxin
Class 10 Life Science Model Paper WBBSE 2023 Set 2
Question 2. Explain the causes of Myopia and Hyperopia
Answer:
Endocrine disorders or hormonal disorders are typically an endocrine disease that results when a gland produces too much (hyper-secretion) or too little (hypo-secretion) of an endocrine hormone, called a hormone imbalance.
Some important hormonal disorders of humans are—
Dwarfism:
Pituitary dwarfism is decreased bodily growth due to hormonal problems (hyposecretion of STH) in childhood.
Causes:
Pituitary dwarfism, or growth hormone deficiency, is a condition in which the pituitary gland does not make enough growth hormone (hypo-function of STH).
Pituitary gland dysfunction can be congenital, which means that the child is born with the abnormality, or can be acquired during or after birth. It tends to run in families.
Symptoms:
The main symptom of pituitary dwarfism is below-average growth, although body proportions will be normal. Other characteristics might include an immature appearance, a chubby body build, a prominent forehead, and an underdeveloped bridge of the nose.

Diabetes insipidus (Dl) is a condition in which the kidneys are unable to prevent the excretion of water due to the hyposecretion of ADH leading to the excretion of an abnormally large amount of urine from the body.
Causes:
During the day, our kidneys filter the blood many times. Normally, most of them are reabsorbed and only a small amount of concentrated urine is excreted.
Dl occurs when the kidneys cannot concentrate the urine normally due to a decrease in the reabsorption of water in the renal tubules and a large amount of dilute urine is excreted.
The amount of water excreted in the urine is controlled by antidiuretic hormone (ADH). Dl caused by a lack of ADH is called central diabetes insipidus.
Excessive thirst that may be intense or uncontrollable, usually with the need to drink large amounts of water.
Excessive urine volume,
Excessive urination, often needing to urinate every hour throughout the day and night.
Goitre:
Goitre is a swelling (hypertrophy) of the thyroid gland in the neck due to hypothyroidism.
Causes:
Iodine deficiency, leading to hypothyroidism, is the major cause of endemic goiter. The thyroid gland needs iodine in order to manufacture thyroid hormones, which regulate the body’s rate of metabolism.

Hypothyroidism is the result of an underactive thyroid gland, and this causes goiter. Because the gland produces too little thyroid hormone, it is stimulated to produce more, leading to swelling.

Symptoms:
The main symptom of goiter is swelling of the thyroid gland, which causes a lump to develop in the front of the neck.
The following are the main symptoms that can result from neck swelling- symptoms of tightness, cough, and hoarseness; Trouble swallowing (dysphagia), dry & rough skin, hair loss, excessive fatigue, etc.
Class 10 Life Science Model Paper WBBSE 2023 Set 2
Diabetes mellitus:
Diabetes mellitus is a chronic, lifelong condition that affects the body’s ability to use the energy found in food.
There are two major types of diabetes:
Type-1 diabetes is also called insulin-dependent diabetes. It used to be called juvenile-onset diabetes because it often begins in childhood.
Type-2 diabetes used to be called adult-onset diabetes, but with the epidemic of obese and overweight kids, more teenagers are now developing type-2 diabetes.
Type-2 diabetes is also called non-insulin-dependent diabetes.
Causes:
All types of diabetes mellitus have something in common. Normally, our body breaks down the sugars and carbohydrates we eat into glucose.
Glucose fuels the cells in our body. But the cells need insulin, a hormone, in the bloodstream in order to take the glucose and use it for energy.
With diabetes mellitus, either the body doesn’t make enough insulin or it can’t use the insulin it produces or a combination of both.
In Type-2 diabetes, the pancreas usually produces some insulin. But either the amount produced is not enough for the body’s needs, or the body’s cells are resistant to it.
Symptoms:
Since the cells cannot take in the glucose, it builds up in the blood. High levels of FuncIaivientaIs of UFe Sconce
blood glucose can damage the tiny blood vessels in the kidneys, heart, eyes, or nervous system.
That is why diabetes – especially if left untreated – can eventually cause heart disease, stroke, kidney disease, blindness, and damage to nerves in the feet.
The early symptoms of untreated diabetes are related to elevated blood sugar levels and loss of glucose in the urine. The high amount of glucose in the urine can cause increased urine output and leads to dehydration.
This condition is called Polyuria. Dehydration causes increased thirst and water consumption. This condition is known as polydipsia.
The inability of insulin to perform normally has effects on protein, fat, and carbohydrate metabolism. A relative or absolute insulin deficiency eventually leads to weight loss despite an increase in appetite.
This condition is called polyphagia. Some untreated diabetes patients also complain of fatigue, nausea, and vomiting. Fluctuations in blood glucose levels can lead to blurred vision.
Extremely elevated glucose levels can lead to lethargy and coma.

The Common Hormonal Disorders Are Summarised In The Following Table:


Question 3. Explain what phenomena happen when the following muscles contract :
Answer:
Flexor muscle :
To decrease the angle between two body parts.
Extensor muscle :
To increase the angle between two body parts.
Abductor’s muscle :
To move limbs away from the midline.
Rotator muscle :
To move limbs around their long axis.
WBBSE Life Science Class 10 Question Paper Set 2
Question 4. Prepare a list of functions controlled by Auxin related to the growth of plants.
Answer:
Major Plant Hormones Auxin
Auxins are a class of nitrogenous phytohormones & the most important growth regulators produced from the growing regions of plant tissue including roots, shoots, and leaves.
These promote cell division, stem and root growth. These can also drastically affect plant orientation by promoting cell division on one side of the plant in response to sunlight & gravity.
The term auxin was first used by Frits Went.
Chemical composition:
Auxins generally occur as complexes, usually found with an amino acid or sugar. These are composed of carbon, hydrogen, oxygen, and nitrogen.
The amino acid Tryptophan and many other Indole compounds serve as precursors of auxins.
Chemical composition:
Auxins generally occur as complexes, usually found with an amino acid or sugar. These are composed of carbon, hydrogen, oxygen, and nitrogen.
The amino acid Tryptophan and many other Indole compounds serve as precursors of auxins.
Types: They are classified into two types as detailed below:
Natural Auxin:
They are Indole compounds like Indole 3-Acetic Acid (IAA) and Non-Indole compounds like Naphthalene Acetic Acid. Indole 3-Acetic Acid was the first plant hormone identified.
It is manufactured primarily in the shoot tips (in leaf primordia and young leaves), in embryos, and in parts of developing flowers and seeds.
Synthetic Auxin:
These are synthetic compounds similar to natural auxin and they include 2,4-D (2,4-Dichlorophenoxy Acetic Acid) or 2, 4, 5-T (2,4,5- Trichlorophenoxy Acetic Acid).
Translocation:
The transport of IAA from cell to cell through the parenchyma surrounding the vascular tissues requires the expenditure of ATP energy.
IAA moves in one direction only i.e., the movement is polar and in this case, downward.
Such downward movement in shoots is said to be basipetal (apex to base) and in roots it is acropetal (outwards towards the root apices from the base).
Synthetic auxins move in all directions inside plants.
Function:
Apical Growth:
Auxins bring about apical dominance and thereby induce apical growth of the shoot.
Tropic movements:
These are deposited unequally on the shoot or root surface and thus cause phototropic curvature and geotropism

Cell enlargement:
Auxin helps to increase the size and volume of the cells.
Cell enlargement is caused by the solubilization of carbohydrates, loosening of wall microfibrils, synthesis of more wall materials, increased membrane permeability, and respiration.
Metabolism:
Auxin stimulates respiration by increasing the availability of respiratory substrate. Thus it enhances metabolism by mobilizing plant resources.
Cambial activity:
The degree of cambial activity is directly proportional to auxin concentration. Auxin also controls xylem differentiation.
Cell division:
It initiates the cell division of the parenchymatous cells at the site of wounded tissue causing healing of wounds after mechanical injury in plants.
Root formation:
Auxin promotes root initiation at a concentration that is inhibitory for the growth of intact roots.
Parthenocarpic fruit Development:
Pollen contains a lot of auxin, it acts as a signal indicating the completion of pollination and transformation of the ovary to fruit.
Thus the application of synthetic auxin induces the development of fruit without the act of fertilization i.e. parthenocarpic fruit development.
Synthetic auxin (2,4-D) initiates rootings in stem cuttings.
(x)Synthetic auxin can act as a weedicide by killing dicotyledonous weeds preventing the division of cambial tissue.
As monocotyledonous plants are devoid of cambium, they are not destroyed by auxin compounds.
Anti-auxin:
Auxins have an inhibitory effect on the abscission of leaves and fruits, i.e., shedding of mature leaves and ripe fruits from the plant.
It has been found that the abscission zone does not form when the concentration of auxins is high in the leaves or fruits.
On the contrary, Abscisic acid (ABA) is a major hormone in plants that induces the formation of an abscission zone in the leaf stalk or petiole and brings about the shedding of leaves.
It acts as an antiauxin because it counteracts the auxin activity by initiating abscission.
WBBSE Life Science Class 10 Question Paper Set 2
Question 5. Distinguish between the mitosis of plant cells with the mitosis of the animal cell on the basis of the following features—
Answer:
Basic Differences Between Mitosis Of Animal Cell And Plant Cell


Question 6. Explain how Bryophyllum undergoes vegetative propagation with the help of an adventitious bud.
Answer:
Vegetative Reproduction
Vegetative reproduction is basically a special type of asexual reproduction where a vegetative part of the plant body, separated from the original plant body, develops and grows into a new plant by simple cell division.
The Vegetative Reproduction Is Of Two Kinds:
It occurs naturally through budding, fission, fragmentation, etc. Artificially this reproduction can be carried out by cutting, grafting, etc.
Parthenogenesis or parthenocarpy
Parthenogenesis is a form of asexual reproduction in which the growth and development of the embryo occur without fertilization.
In animals, parthenogenesis means the development of an embryo from an unfertilized egg cell. It is common in rotifers, aphids, bees, and crustaceans.
Some vertebrates like lizards also reproduce by parthenogenesis. Parthenogenesis may be natural or artificial.
Natural parthenogenesis occurs regularly in the life cycle of some animals. It is of two types:
Complete and incomplete parthenogenesis.
Complete parthenogenesis:
It is also called obligatory partheno-genesis.
In this case, the males are completely absent and the females develop from the unfertilized eggs as is found in aphids, phyllopods, and rotifers.
It is also found in some vertebrates.
A lizard Lacerta Mexico Americana reproduces exclusively by parthenogenesis with no males, in the population.
Incomplete parthenogenesis:
In this case sexual generation alternates with parthenogenesis generation.
For example, in bees and wasps, some eggs develop without fertilization and produce males, while those eggs that are fertilized develop into females.
In Gall fly, the larvae may lay eggs which develop parthenogenetically into a new generation of larvae. This is called paedogenetic parthenogenesis or paedogenesis.
In many sexually reproducing animals, the egg can be activated by artificial methods to start the development without fertilization.
This is called artificial parthenogenesis. Eggs of Sea urchins can be made to develop successfully if treated with weak salt solutions, weak organic acids, electric shock or shaking in seawater, or by pricking the egg with a glass needle.
In higher plants, the process of formation of fruits without pollination and fertilization is called parthenocarpy. Parthenocarpy is a form of asexual reproduction seen in flowering plants.
The fruits are generally seedless. During cultivation, parthenocarpy is introduced along with other plant hormones including gibberellin and it results in maturing of the ovaries without the process of fertilization and produces bigger and pulpy fruits.
Pineapples, bananas, cucumber, grapes, watermelon, oranges, pears,s, etc are some examples of parthenocarpy. In some plants, pollination or another stimulation is required for parthenocarpy. This is termed stimulative parthenocarpy.
Plants that do not require pollination or other stimulation to produce parthenocarpic fruits have vegetative parthenocarpy.
Seedless cucumbers are an example of vegetative parthenocarpy and seedful watermelon is an example of stimulative parthenocarpy.
WBBSE Life Science Class 10 Question Paper Set 2
Question 7. Tabulate which changes occur in a chromosome during the Anaphase of Karyokinesis.
Answer:
Changes occur in a chromosome during the Anaphase of Karyokinesis
1. Splitting into daughter chromosomes.
2. Poleward anaphase movement of daughter chromosomes.
3. V, L, or I shaped the appearance of daughter chromosomes.
Question 8. Describe how Yeast completes the process of budding.
Answer:
Yeast completes the process of budding
The asexual reproduction of yeast occurs by budding.
The parent nucleus divides into two daughter nuclei by mitosis.
During budding, the daughter cell first appears as an outgrowth since one daughter nucleus migrates to a corner of the parent cell. Both haploid and diploid cells can undergo budding. The outgrowth enlarges, matures, and detaches from the parent cell.
Question 9. Prepare a list of changes that occur during the adolescence phase of human development
Answer:
Changes that occur during the adolescence phase of human development
Question 10. Explain the following two significances of meiotic cell division—
Maintains the constant number of chromosomes in a species Origin of variation in an organism
Answer:
Significance Of Meiosis
1. Gametogenesis:
It is a necessary part of the life cycle of sexually reproducing animals since it leads to the formation of gametes (sex cells) through meiosis.
2. Maintenance Of Constant Chromosome Number Of A Species:
The gametes produced as a result of meiosis are haploid (n) and the zygote formed by their fusion is diploid (2n).
Thus, it is the only means for restoring the constancy in chromosome number, which is a characteristic of the species from generation to generation.
3. Production Of Variation In Organisms:
Meiosis results in new combinations of genetic material. During crossing over, the hereditary factors from male and female parents get mixed due to the breakage and exchange of chromatids.
This brings in genetic variation within the species. The variations are important raw materials for evolution and also help in the improvement of races.
4. Alternation of generation:
Meiosis causes conversion from sporophytic generation to gametophytic generation in plants, i.e. causes the alternation of generation through prezygotic, post-zygotic, or sporadic meiosis.
Meiosis occurs in sporogenous cells (micro and megaspore mother cells) of the sporophyte-producing haploid spores. The spores on germination form gametophytes (male and female).
Cells of the gametophyte form gametes. Fusion of these gametes again leads to diploid or sporophytic generation and in this way, the alternation of generation between gametophytic and sporophytic generations keeps on going.
Question 11. State Mendel’s second law of heredity.
Answer:
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.
Question 12. Prove the authenticity of the statement- “The phenotypic and genotypic ratio remain identical in case of Incomplete Dominance”.
Answer:
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.
WBBSE Life Science Class 10 Question Paper Set 2
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.
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.
Question 13. Write two causes behind Mendel’s success in conducting experiments on heredity.
Answer:
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.
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.
Question 14. “Dispersal of animals is one of the driving forces of locomotion”— Judge the statement with the help of proper examples.
Answer:
Reasons And Motivations Behind Locomotion
Animals move for a variety of reasons, such as to find food, a mate, a suitable microhabitat, or to escape from predators.
Hunt For Food & Water:
Since animals can not prepare food, they are to perform locomotion to find out suitable area with plenty of food & water.
To seek shelter & escape from predators:
Locomotion increases the chances of survival of an organism by allowing the organism to seek shelter in favorable habitat, and to escape dangerous situations by avoiding predators.
Dispersal for mating or breeding:
Locomotion enables members of the species to disperse to find suitable mates to coordinate breeding activity and the survival of the young.
Search for a new & favorable environment:
Animals, especially birds, migrate from areas of low or decreasing resources to areas of high or increasing resources. The two primary resources being sought are food and nesting locations. Escaping from cold is also a factor.
Basic differences between movement and locomotion:
Though, in the case of animals, we often use the terms movement and locomotion, interchangeably, there are definite differences between the two.
Locomotion takes place at the organism level while movement can take place at any biological level from cellular to organisms.
In simple words, locomotion is movement from one place to another and involves shifting of the entire body parts (e.g. a person moving or running) and movement involves a change in shape, size, or direction of various body parts (e.g. shaking of your hands).
All kinds of locomotion are movements but all kinds of movements are not locomotion.
Movement is the motion that occurs in an organism or a body with or without the involvement of any change in the position or location of the organism or the body,
while locomotion is defined as the voluntary movement of an organism from one place to another either in search of food or shelter or mate or to escape from the predators.
Therefore, the differences between movement and locomotion may be summarized in a tabular form as below:

Question 15. Show the chemical constituents of chromosomes with the help of a table.
Answer:

Question 16. Compare DNA and RNA on the basis of the following features
Answer:

Question 17. “Some phenotypes may have multiple genotypes and some other phenotypes may have a single genotype” justify the statement from the results derived from the dihybrid experiment in the case of the pea plant.
Answer:
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.
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.
WBBSE Class 10 Life Science Previous Year Papers
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.
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


4. Write the 6 questions or their alternatives given below. Sightless candidates have to answer a question no. 4.1 A instead of question no 4.1. The marks allotted for each question is 5 (the division of marks is either 3+2, 2+3, or 5) :
Question 1. Draw a scientific diagram of a neuron and label the following parts :
Answer:

Draw a scientific diagram of the morphological structure of a eukaryotic chromosome and label the following parts—
Answer:

Write the Functions of the following structural parts of a eukaryotic chromosome :
Answer:

Question 2. Compare the antagonistic functions of the following three pairs of hormones in the human body:
Explain the relationship between the hindbrain and the function of control of the breathing mechanism.
Antagonistic functions of insulin and glucagon :
1. Insulin increases cellular oxidation of glucose, stimulates the formation and storage of glycogen in the liver & muscles and inhibits the formation of glucose from non-carbohydrates. All these activities result in the maintenance of optimum levels of blood sugar.
Glucagon stimulates liver glycogen to undergo breakdown to be converted to glucose which increases blood sugar levels.
2. Insulin increases protein synthesis in the body. Glucagon hydrolyzes protein into amino acids.
3. Insulin decreases lipid & cholesterol levels in the blood. Glucagon stimulates the increase of fat & cholesterol level in the blood. Antagonistic functions of estrogen and progesterone :
1. Estrogen is secreted by ovaries prior to ovulation. Progesterone is secreted by ovaries after ovulation.
2. During pregnancy, estrogen induces enlargement of breasts and uterus. During pregnancy, progesterone reduces the contractility of the uterus and stimulates the growth of mammary glands.
Antagonistic features of FSH and LH :
1. FSH helps in the maturation of immature follicles into mature Graafian follicles. In the presence of FSH, LH ruptures Graafian follicles causing ovulation.
2. FSH stimulates the secretion of estrogen from Graafian follicles. LH stimulates the secretion of progesterone from the corpus luteum.
3. In males, FSH induces the development of seminiferous tubules and spermatogenesis. In males, LH stimulates the secretion of testosterone in the testis.
The breathing movements (ie., taking in oxygen and taking out carbon dioxide) are initiated in response to the ratio of carbon dioxide and oxygen within the body. High levels of C02 and low levels of 02 collectively influence the body to exhale C02 and take in 02.
This is regulated by the medulla oblongata of the hindbrain. In response to C02 and 02 ratios, medulla oblongata signals the heart and diaphragm accordingly to facilitate respiration.
The respiratory center of the medulla oblongata is concerned with controlling the depth and rate of respiration.
OR
The following physiological functions of a person wounded in an accident are found hampered. Write the name of the parts of the brain attached to those functions :
Explain the mechanism of feedback control of the function of hormones with the help of a suitable example.
Movement of tongue and swallowing of food – Medulla oblongata
Answer:
Feedback control:
The secretion of most, if not all, hormones is regulated by some type of closed-loop control system known as a feedback mechanism
(because the amount released or secreted is sensed and that information is relayed back to the secretory cell by a variety of ways). Feedback control is mostly negative, rarely positive.
In a negative feedback control, the synthesis of a hormone slows down or halts when its level in the blood rises above the normal or threshold limit.
In the less common positive feedback mechanism, one hormone further stimulates the production of another hormone instead of diminishing it. Some examples of feedback control are given below.
Hypothalamus, in response to some external stimulus, produces a thyrotropin-releasing hormone for the secretion of thyrotropic hormone.
The thyrotropin-releasing hormone (TRH) stimulates the anterior pituitary lobe to secrete thyrotropic hormone. The latter in turn stimulates the thyroid gland to produce thyroxine.
If thyroxine is in excess, it exerts an influence on the hypothalamus and anterior pituitary lobe, which then secrete a lesser amount of releasing hormone and thyroid-stimulating hormone (TSH) respectively.
A rise in the TSH level in the blood may also exert a negative feedback effect on the hypothalamus and retard the secretion of TRH. This restores the normal blood-thyroxine level.

Sometimes, the accumulation of a biochemical increases its own production. For example, uterine contraction at the onset of labor stimulates the release of the hormone oxytocin, which intensifies uterine contractions.
The contractions further stimulate the production of oxytocin. This is a positive feedback control.
WBBSE Class 10 Life Science Previous Year Papers
Mode Of Transport Of Animal Hormones:
Most hormones are secreted into the general circulation to exert their effects on appropriate distant target tissues. Water-soluble hormone molecules circulate in watery blood plasma in a free state, (i.e. not attached to other molecules).
Steroid and thyroid hormones are less soluble in aqueous solution and over 90% circulate in blood as complexes bound to specific transport proteins like plasma globulins or albumin.
The transport proteins make the lipid-soluble hormones temporarily water-soluble and act as a ready reserve of hormones.

Functioning And Fate Of Hormones:
The chemical structure of a hormone enables it to combine with a receptor in the cells of its target. The receptor may be present on the plasma membrane of the cell or inside the cytoplasm or nucleus.
Only a hormone’s “target” cells, which have receptors for that hormone, will respond to its signal. When the hormone binds to its receptor, it forms a receptor-hormone complex.
This complex undergoes changes and enters into the nucleus of the target cell. Within the nucleus, it increases the synthesis of cell protein and takes part in the metabolic process of the cell.
All hormones diminish within the body at differing rates based on their chemical half-life. Once hormones have served their function on their target organs/tissues, these are destroyed.
These are either destroyed by the liver or the tissues of the target organs and excreted out of the body.
Role Of Hormones As Biochemical Messenger And Regulators:
Hormones are informational molecules that carry the message of metabolic change from the endocrine glands to the target cells or organizer
These are released into the extracellular fluid, where they are diffused into the bloodstream. The latter carries them from the site of production to the site of action.
Hormones stimulate or inhibit one or more Physiological processes for the welfare of the body.
Maintenance of the internal chemical environment of the body to a constant is called homeostasis. Hormones play a major role in maintaining homeostasis through their integrated action.
These also play a leading role in the chemical coordination of the living body. Thus hormones are known as chemical messengers.
Question 3. Prepare a list of the role of artificial plant hormones in agriculture and horticulture. What are the influences of Insulin hormone on the absorption and metabolism of glucose in the human body?
Answer:
Pancreas:
The pancreas is a large elongated gland located in the abdominal cavity just inferior and posterior to the stomach.
Hormonal Secretions:
The pancreas is considered to be a heterocrine or mixed gland as it contains both endocrine and exocrine tissue. The endocrine function consists primarily of the secretion of the two major hormones, insulin, and glucagon.
The endocrine cells of the pancreas are found in small groups throughout the pancreas called islets of Langer Within these islets are two major types of cells alpha and beta cells.
The alpha cells produce the hormone glucagon and the beta cells produce the hormone insulin.
Insulin:
It is an antidiabetogenic protein hormone that lowers blood sugar levels.
Functions:
Effect on carbohydrate metabolism:
Insulin increases the oxidation of glucose in the cells, stimulates the formation & storage of glycogen in the liver & muscle, inhibits the formation of glucose from non-carbohydrates in the liver, and increases the permeability of glucose through the cell membrane from blood to the cells.
All these activities result in the maintenance of optimum levels of blood sugar.
Effect on protein metabolism:
It increases protein synthesis in the body.
Effect on fat metabolism:
It also decreases lipid & cholesterol levels in the blood & prevents the formation of harmful ketone bodies in the liver.
Glucagon:
It is anti-insulin in nature. Together with insulin, it maintains a steady level of blood sugar in the body.
Functions:
Effect on carbohydrate metabolism: It stimulates liver glycogen to undergo breakdown to be converted into glucose which increases blood sugar levels.
WBBSE Class 10 Life Science Previous Year Papers
Effect on protein metabolism:
Glucagon hydrolyses protein into amino acids and increases nitrogen excretion through urine.
Effect on fat metabolism:
It stimulates the increase of fat & cholesterol level in the blood.
Gonads:
The gonads and ovaries in females and testes in males are responsible for producing the sex hormones of the body.
Testes:
The testes are a pair of ellipsoid Fun(Iami iniaIs of Lifi Sell no organs found in the scrotum of males that produce the androgen testosterone in males after the start of puberty.
Testosterone:
It has effects on many parts of the body, including the muscles, bones, sex organs (both primary & secondary), and hair follicles,
During puberty, testosterone controls the growth and development of the sex organs and secondary sex characteristics like muscular growth, breaking of voice, growth of hair on the face, chest, etc.
Ovaries:
The ovaries are a pair of almond-shaped glands located in the pelvic body cavity lateral and superior to the uterus in females. The ovaries produce the female sex hormones progesterone and estrogens. It also secretes another hormone called relaxin.
Estrogen:
Oestrogen stimulates the growth, development, and functional activities of primary and secondary sex organs in females during puberty.
It regulates the menstrual cycle and stimulates breast development.
It enhances the deposition of fat in the female body.
Progesterone:
In the presence of estrogen, progesterone stimulates the complete development of the primary & secondary female sex organizer
It is most active during ovulation & pregnancy. It helps the embedding of embryos in the uterus and stimulates the development & maintenance of pregnancy.
It also regulates the menstrual cycle & breast development at puberty.
Relaxin:
It is secreted from the uterus at the terminal stage of pregnancy. It facilitates the expulsion of the fetus from the uterus by causing relaxation of the pelvic ligaments.
OR
Write three differences between binocular vision with that of monocular vision on the following three aspects :
Write differences between inborn and acquired reflex actions on any two of the following aspects-
Answer:

Mention the differences between conditioned and unconditioned reflex actions.

Question 4. Show the alternation of generation in fern with the help of a word diagram.
Answer:


OR
Show the process of sexual reproduction in flowering plants with the help of a word diagram :
Answer:

Question 5. Distinguish between Mitosis and Meiosis on the basis of the following three aspects-
Explain the following phenomena related to meiotic cell division—
Answer:
Important features of meiosis
WBBSE Class 10 Life Science Previous Year Papers
1. Homologous Chromosomes:
These are chromosome pairs of approximately the same length and centromere position. Note that diploid cells have two sets or one pair of homologous chromosomes.
Out of the pair, one is inherited from the mother (maternal) and one from the father (paternal).

2. DNA replication:
Replication of DNA takes place during the interphase preceding meiosis. DNA replication generates sister chromatids from each chromosome. Sister chromatids are two identical copies of a chromatid that remain closely aligned.
Although DNA replication occurs in interphase, no longitudinal doubleness of chromosomes is visibly evident in Leptotene of Prophase I owing to contraction.
3. Synopsis:
The movement of chromosomes initiates in the zygotene stage and this movement results from an attracting force that brings the homologous pair of chromosomes together.
The chromosomes become shorter and thicker due to compaction.
When they come closer, homologous chromosomes pair and align at the equatorial plate of the cell for equal qualitative and quantitative distribution. The pairing takes place throughout the length.
This process of pairing is known as synapsis Pairing takes place not only between the homologous chromosomes but also between homologous regions of the chromosomes. Chromosome pairs undergoing synapsis have approximately the same length and centromere position.
Out of the pair, one is inherited from the mother (maternal) and one from the father (paternal). Non-sister chromatids belong to homologs.
WBBSE Class 10 Life Science Model Question Paper 2023
These are chromosome pairs having the same length, staining pattern, centromere position as well as the same characteristics of genes at particular loci.
A homologous pair of chromosomes consists of one chromosome from each parent and they are known as bivalents. Each chromosome of a bivalent is found to have two chromatids. Thus the four chromatids of a bivalent are together known as a tetrad.
4. Crossing Over:
The pachytene subphase of Prophase I is marked by a process called Crossing over that happens after both the homologous chromosomes in a pair join up to form a structure called a tetrad through synapsis.
Once a tetrad is formed, a portion of each homologous chromosome breaks off transversely and is re-attached to the same part of its homolog. Crossing over occurs between non-sister chromatids of homologous Sister Chiasma chromatids chromosomes.
This mixes up the traits that are found in each of the chromosomes, thus resulting in genetic recombination due to the exchange of segments between two non-sister chromatids belonging to a bivalent tetrad.
As a result of crossing over, X like structure is formed between the non-sister chromatids. The point of attachment at the crossing-over is called chiasma. It occurs during Diplotene.
The number of chiasmas may be one, two, or more depending on the length of the chromosomes.

5. Terminalization Of Chiasmata:
Chiasmata are generally pushed to the terminal ends of the chromosomes and this process is known as the terminalization of chiasmata (singular: chiasma).
The pair of homologous chromosomes begin to separate in the diplotene subphase of prophase I and chiasmata are fully terminalized in the diakinesis subphase of prophase.
Reduction in chromosome number:
During metaphase I, the tetrads line up on the plate. During anaphase I, the homologous chromosomes separate from one another i.e. one homologous chromosome with its two sister chromatids move to opposite poles.
Thus each pole has a haploid (n) number of chromosomes i.e. a reduction in chromosome number is achieved at this stage.
Telophase results in the formation of two haploid (n) daughter nuclei with each chromosome having two chromatids. For this reason, the first meiotic division is known as the reductional or heterotypic cell division.
7. Equational division:
Meiosis II or the second meiotic division has four phases similar to mitosis and is the second round of cell divisions during meiosis whereby the cells formed during Meiosis I divide again to form four haploid (n) gametes.
Between these two stages, the interkinesis or interphase is either quite short or skipped, unlike normal mitosis. Because of this, the S phase does not occur and so the DNA in these cells is not copied, making the resulting cells from this phase haploid.

OR
Distinguish between the cytokinesis of plant cells with the cytokinesis of animal cells on the basis of the following aspects :
Answer:
The longest phase of mitosis:
Prophase
The shortest phase of mitosis:
Anaphase
WBBSE Class 10 Life Science Model Question Paper 2023

Establish the interrelationships among genes, DNA, and chromosome.
Answer:
Inter-Relationship Among Chromosome, DNA, And Gene
The eukaryotic cells contain a membrane-bound nucleus which is designated as the ‘Director of the cell’.
The nucleus contains many thread-like, coiled, and elongated structures called chromatin fibers or chromatin reticulum, or nuclear reticulum.
The fibers of chromatin are uniformly distributed in the nucleoplasm. Chromatin fibers are observed only during the interphase or the preparatory phase of the cell cycle.
Just prior to cell division, chromatin fibers condense, become thick, and wrap up very tightly to form ribbon-like structures called chromosomes.

The number of particular species. They are usually found in pairs. Human beings have 23 pairs of chromosomes in each body cell.
The chromosome consists of a proteinaceous matrix and two spirally coiled chromonemata, each one of which contains a single DNA molecule.
The nucleus of an average human cell is only 6m in diameter, yet it contains 1.8 m of DNA which is distributed amongst the 23 pairs or 46 chromosomes each consisting of a single DNA molecule of about 40 mm.
Thus, Chromatin represents long-thin strands of the DNA-protein complex. It is unfolded and uncondensed form of DNA, while chromosomes are condensed DNA and protein.
The function of chromatin is to store DNA in the nucleus. Chromosomes are the bearers of hereditary instructions and regulate cellular processes.
DNA (or deoxyribonucleic acid) is the molecule that carries the genetic information in all cellular forms of life and some viruses.
It belongs to a class of molecules called nucleic acids, which are polynucleotides that is, long chains of nucleotides. Nucleotides are made up of a base, a sugar, and a phosphate. The four bases
chromosomes are constant in the nucleus for adenine (A), guanine (G), cytosine (C), and thymine (T) pair with each other (A with T and G with C).
WBBSE Class 10 Life Science Model Question Paper 2023
It is the order or sequence of these base pairs that provides the information needed for the growth and development of our bodies.
Specific parts of DNA carry the code for producing specific proteins which ultimately lead to the expression of different characters in an organism.
Each of these parts of DNA is termed a gene. Thus gene is the fundamental physical and functional unit of heredity that carries information from one generation to the next.
It is a segment of DNA, composed of a transcribed region and a regulatory sequence, that makes possible transcription. A series of genes are present in each DNA.
The coordinated interaction of two or more genes produces a given phenotypic trait. A complete set of chromosomal genes is inherited by the offspring as a unit from the parent.
Question 6. Predict what would be the hereditary results in the following cases :
What are the symptoms of Thalassaemia?
Answer:

OR
Tabulate three pairs of opposite traits regarding the seed of the pea plant as selected by Mendel. Show the process of sex determination in men with the help of a checkerboard.
Answer:


Answer to all questions is compulsory
1. Write the answer in complete sentences by choosing the correct answer for each question with the respective serial number.
Question 1. Select the correct pair-
Answer: The correct Pair is- Medulla Oblongata—Control of heartbeat and swallowing of food.
Question 2. Identify which of the following statements is not true regarding Insulin-
Answer: The statement which is not true regarding Insulin is—Helps in the conversion of fat and protein into glucose.
Question 3. Match the words of Column-A with that of Column-B and select which of the following options is correct-

Answer: 3. 1-3, 2-1, 3-2
Question 4 Determine from the answers given below in which phases of karyokinesis during mitotic cell division following two incidents happen- 1. Daughter chromosomes tend to move apart from each other towards their own poles Nuclear membrane and nucleolus disappear
Answer: 2. During mitotic cell division—
Question 5. Select which of the following is the feature of cross-pollination-
Answer: The feature of cross-pollination is— More wastage of pollen grains.
WBBSE Class 10 Life Science Model Question Paper 2023
Question 6. Determine the number of DNA molecules that get coiled to form each chromosome in a newly formed daughter cell produced by mitotic cell division in the human body-
Answer: 2. The number of DNA molecules that get coiled to form each chromosome in a newly formed daughter cell produced by mitotic cell division in the human body is 1.
Question 7. Identify the genotype of guineapig having black colour and rough hair-
Answer: 1. The genotype guineapig having black colour and rough hair are—BbRr, BBRr.
Question 8. Decide which of the following two were selected by Mendel as recessive traits-
Answer: 2. Length of stem—dwarf and Form of ripe seed—wrinkled were two recessive traits selected by Mendel.
Question 9. Asses from the following, the probable genotype of parents having a haemophilic son and normal daughter-
Answer: 3. The probable genotype of parents having a haemophilic son and normal daughter are- H || H, h![]()
Question 10. Parthenium is an exotic species in our country. Other indigenous species cannot survive in such places where it grows. This establishes one of the postulates of Darwin’s theory. Identify the postulate-
Answer: 2. The correct postulate is Interspecific struggle.
Question 11. Miller and Urey, in their experiment, were able to synthesize some preliminary constituents necessary for the creation of life. Identify the ones which were amino acids among them-
Answer: The amino acids were—Glycine and Alanine.
WBBSE Class 10 Life Science Model Question Paper 2023
Question 12. Decide for which of the following purposes bees demonstrate waggle dance-
Answer: 2. Bees demonstrate waggle dance to-^ Inform other worker bees about the direction and the distance of the source of food from the bee hive.
Question 13. Identify which of the following is the correct information related to biosphere reserve-
Answer: 1. The correct information related to biosphere reserve is- conservation is promoted to local people and other biotic communities along with the conservation of the ecosystem.
Question 14. Decide which of the following pair is not correct-
Answer: The wrong pair is—A greenhouse gas— Eutrophication
Question 15. Decide which of the following Project Tiger is located within our state-
Answer: Sunderbans Project Tiger is located within our state.
WBBSE Class 10 Life Science Model Question Paper 2023
2. Answer any 21 questions out of the 26 questions given below instructed.
Fill in the blanks with proper words in the following sentences (any five):
Question 1. Acharya Jagadish Chandra Bose proved the property of __________ by sending electrical impulses in Mimosa and Desmodium plants.
Answer: Sensitivity
Question 2. If gametes in humans were produced by mitosis instead of meiosis then the number of autosomes in a somatic cell of an offspring would have been __________.
Answer: 88
Question 3. A disease in the human population caused by a recessive gene located in the ‘X’ Chromosome is __________.
Answer: Haemophilia
Question 4. The hoof of modern horse is the transformation of the digit number __________ of their ancestors.
Answer: 3
Question 5. At the __________ phase of the nitrogen cycle, ammonia is converted into nitrite and nitrate by the action of some bacteria.
Answer: Nitrification
Question 6. To produce the bottled cold drinks widely sold in the market, a lot of __________ water is wasted.
Answer: 2.6 Fresh
Decide whether the following statements are true or false (any five):
Question 7. Tropic movement is the movement of growth in plants.
Answer: True
WBBSE Class 10 Life Science Model Question Paper 2023
Question 8. Crossing over takes place during mitotic cell division.
Answer: False
Question 9. Mendel used the term gene while describing his experiments related with heredity.
Answer: False
Question 10. The leaf of the Cactus is modified into the spine for the reduction of the rate of transpiration.
Answer: True
Question 11. Rhododendron is an endangered plant species conserved in the Eastern Himalaya hotspot.
Answer: True
Question 12. Choroid helps in the accommodation of the eye by changing the curvature and shape of the lens.
Answer: False
Match the words in Column-A with those which are most appropriate in Column-B and re-write the correct pair mentioning the serial no. of both Columns (any five):

Answer: 13. D, 14. G, 15. A, 16. E, 17. B, 18. C
Answer in a single word or in a single sentence (any six):
Question 19. Choose the odd one and write it: Cerebrum, Hypothalamus, Pons, Thalamus
Answer: Pons
Class 10 Life Science Model Paper WBBSE 2023
Question 20. Where the Schwann cells are located?
Answer: Schwann cells are found in close contact with axons in the peripheral nerves.
Question 21. A pair of related terms is given below. On the basis of the relationship in the first pair write the suitable word in the gap of the second pair. Mitosis: Radicle :: Meiosis: __________.
Answer: Spore mother cell
Question 22. Which law did Mendel conclude from his dihybrid cross experiment?
Answer: Law of Independent Assortment
Question 23. Give an example of a variation found among healthy persons which is transmitted through generations.
Answer: Rolling tongue and non-rolling tongue
Question 24. How do Chimpanzees break open the hard shells for eating the nuts?
Answer: Chimpanzees put the nut on the flat surface of a hard stone and use another stone or tough piece of wooden branch as a hammer to break the shell of nut.
Question 25. Among the following four terms, one includes the other three. Find it out and write it: SPM, Air Pollution, Greenhouse gas, Lung disease.
Answer: Air pollution
Question 26. Name the practice which jointly the local peoples and forest department maintain for the reclamation of a forest.
Answer: Joint Forest Management (JFM)
3. Answer any 12 questions in 2-3 sentences out of the 17 questions given below.
Question 1. Distinguish between the functions of hormones and the nervous system on the following parameters:
Answer:
Differences between the endocrine system and nervous system

Question 2. ‘A person can see distant objects distinctly but is unable to visualize near objects in a perfect way’-Predict what would be the probable cause and suggest the corrective measure for such a problem.
Answer:
Defects Of Visions And Corrective Measures
A person with normal eyes can, by virtue of accommodation, see clearly all objects that are at a distance greater than about 25 cm from the eye.
If due to certain abnormalities the eye is unable to accommodate itself to various distances, then the eye is said to be defective.
Some common defects of the eye are—
1. Myopia:
Near-sightedness, also called myopia is the common name for impaired vision in which a person sees near objects clearly while distant objects appear blurred.
In such a defective eye, the image of a distant object is formed in front of the retina and not at the retina itself. Consequently, a nearsighted person cannot focus clearly on an object farther away than the far point of the defective eye.
Class 10 Life Science Model Paper WBBSE 2023
Causes:
This defect arises because the power of the eye is too great due to the decrease in the focal length of the crystalline lens.
This may arise due to either-
Excessive curvature of the cornea, or
Elongation of the eyeball.
Correction:
This defect can be corrected by using a concave (diverging) lens. A concave lens of appropriate minus (-) power or focal length is able to bring the image of the object back to the retina itself.

2. Hyperopia or hypermetropia:
Far-sightedness, also called hyperopia or hypermetropia, is the common name for a defect in vision in which a person sees near objects with blurred vision, while distant objects appear in sharp focus.
In this case, the image is formed behind the retina.
Causes:
This defect arises because either
the focal length of the eye lens is too great, or
the eyeball becomes too short so that light rays from the nearby object cannot be brought to focus on the retina to give a distinct image.
Correction:
This defect can be corrected by using a convex (converging) lens of appropriate focal length. Eyeglasses with converging lenses supply the additional focusing plus (+) power required for forming the image on the retina.
3. Presbyopia:
Presbyopia is a progressive form of farsightedness that affects most people by their early 40s. The power of accommodation of the eye decreases with aging.
Most people find that the near point gradually recedes.
Causes:
It arises due to the gradual weakening of the ciliary muscles and diminishing flexibility of the crystalline lens.
Correction:
Simple reading eyeglasses with convex lenses correct most cases of presbyopia.
Sometimes, a person may suffer from both myopia and hypermetropia. Such people often require bifocal lenses.
In the bifocal lens, the upper portion of the bifocal lens is a concave lens, used for distant vision. The lower part of the bi-focal lens is a convex lens, used for reading purposes.
Class 10 Life Science Model Paper WBBSE 2023
Cataract:
Generally, this defect can be found in aged or old people. Persons with this defect get blurred vision which sometimes even lead to total blindness.
The reason for this defect is that the lens loses its transparency and become opaque due to the deposition of protein material and calcium mineral in the lens.
This opaque condition of the lens does not allow the light rays from an object to pass through the lens. This defect can be rectified by surgically removing the lens and it has to be replaced by a highly convex lens.
Before intraocular lenses (lOLs) were developed, people had to wear very thick eyeglasses or special contact lenses to be able to see after cataract surgery.
Now, with cataract lens replacement by phacoemulsification or phaco surgery, several types of IOL implants are available to help people enjoy improved vision.
Question 3. Analyze the role of synthetic plant hormones in increasing production and solving the problem of weeds in agriculture.
Answer:
Role of synthetic hormones:
Synthetic hormones are successfully used in agriculture and horticulture. The roles of these synthetic hormones are mentioned below.
1. Developing new plants from stem cuttings:
Cuttings are used for artificial vegetative propagation of different plants like roses, Hibiscus, marigold, Chrysanthemum, ‘etc. After cutting the twigs from a mother plant, a solution of synthetic auxin or auxin powder is applied at the cut end.
Then, these cuttings are planted in moistened soil. By the action of this hormone, adventitious roots grow from the cut end and the cutting grows as an individual daughter plant.
2. Preventing shedding of immature fruits:
Sometimes, immature fruits shed off from the plant if these plants are sprayed with synthetic auxin solution for a few times during ear y developmental phase of the fruits, the rate of immature shedding declines sharply.
Horticulturists spray auxin solution on mango, litchi, grapes, banana, and several other fruit plants to prevent immature shedding of fruits. Synthetic gibberellin and synthetic cytokinin are also effective.
Class 10 Life Science Model Question Paper With Answers
3. Destroying weeds:
Weeds growing in crop fields share water and nutrients with agricultural crops. This affects the quality of production. Scientists have revealed that the application of certain phytohormones destroys dicotyledonous herbs and shrubs.
Application of a synthetic auxin named 2, 4-D effectively kills dicotyledonous weeds from monocot crop (paddy, wheat, etc.) fields.
4. Production of parthenocarpic fruits:
Fruits, produced from the ovary without fertilization do not contain seeds and become larger. These are called parthenocarpic fruits. A treatment of auxin solution before the maturation of flowers triggers the development of the ovary.
As a result, seedless fruits are produced before fertilization. Synthetic auxin is successfully applied on the plants of guava, grapes, banana, watermelon, etc. to produce seedless fruits.
Synthetic gibberellin is comparatively more effective on tomato plants. These two synthetic phytohormones are used to produce parthenocarpic fruits.
Question 4. LH and ICSH control the secretion of hormones of the reproductive glands of the human body’-judge the validity of the statement.
Answer:
In the female body, Lutenising Hormone (LH) stimulates ovule secretion and the formation of corpus luteum from the Graafian follicle. It also helps in the secretion of progesterone hormone from the corpus luteum.
In the male body, Interstitial Cell Stimulating Hormone (ICSH) stimulates the interstitial cells of Leydig of testes to secrete testosterone.
Question 5. How can you distinguish between the mitosis of plant cells and that of animal cells on the basis of the formation of spindle fiber and the process of cytokinesis?
Answer:
Distinguish between the mitosis of plant cells and that of animal cells are-

Question 6. Establish the relationship between the formation of malignant tumors in the human body with the loss of control in the cell cycle.
Answer:
The relationship between the formation of malignant tumors in the human body with the loss of control in the cell cycle
Checkpoints prevent uncontrolled cellular growth and thereby cancer. It mainly checks the genetic as well as physical integrity, if they found any genetic defect, they immediately arrest the cell from going to cellular division.
All cells will be checked in three stages. But if the genes which are responsible for the synthesis of checkpoints are mutated then they lost their control over cell division and the cells are going to divide in an uncontrolled way.
This uncontrolled cellular division gives rise to a cellular lump, called a tumor.
Class 10 Life Science Model Question Paper With Answers
Question 7. ‘The adventitious leaf bud plays a significant role in natural vegetative propagation of plant’-Evaluate the validity of the statement with a proper example.
Answer:
Natural Vegetative Propagation
Different plant parts are variously modified for vegetative propagation.

Natural vegetative propagation in higher plants:
Root:
The storage root acts as a structure for perpetuation, they help the organism to survive during unfavorable conditions and also germinate to produce a new plant body. e.g. Root tuber of sweet potato, Dahlia.

Stem:
The stem may also act as a parenting organ, which can grow and propagate on land and water and when separated, produces a new plant body. e.g. Offset of Water Hyacinth.
The propagation of stem in terrestrial plants is brought about by runner and stolon, e.g. There are various artificial methods like strawberries and grasses. Rhizomes are cutting, grafting, micropropagation, etc.

underground horizontally growing stems having nodes, internodes, and axillary buds. Branches grow from these buds.
Tuber is a modified underground stem tip.
The eyes or buds present on the tuber grow into new plants. The bulb is a modified shoot that has short stems and apical & axillary buds that grow to form shoots.
Leaf:
The leaf may become a propagating organ with the presence of storage food in the lamina and adventitious buds present at the edge of the lamina may germinate to produce a new plant body. e.g. Leaf of Bryophyllum.

Question 8. Show with the help of a cross, who is more important among parents in determining the sex of their offspring.
Answer:
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 in reference to 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.
Class 10 Life Science Model Question Paper With Answers
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.
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.
WBBSE Class 10 Life Science Previous Year Papers
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.

Question 9. ‘Different genotypes produce the same phenotype’-Justify the statement in the form of a table by taking an example from the result of the dihybrid cross of the Pea plant.
Answer:
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—

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.
Question 10. Give your opinion about probable suggestions which can be given to a pair of contenders before marriage in order to prevent the spread of a genetic disease from the society already known to you.
Answer:
Genetic Counselling
Thalassemia mutations and various abnormal hemoglobins interact to produce a wide range of disorders of varying degrees of severity.
Hemoglobin disorders are the most common worldwide inherited conditions. They are common in populations of tropical Africa, Asia, and the Mediterranean region and are spreading by migration throughout the world.
WBBSE Class 10 Life Science Previous Year Papers
A stem cell transplant is the only treatment that can cure thalassemia. But only a small number of people who have severe thalassemias are able to find a good donor match and have the risky as well as expensive procedure.
Genetic counseling, therefore, plays the most important part in thalassemia prevention programs considering the diversity and severity of the problem.
Genetic counseling is defined as the process by which patients or relatives at risk of a disorder that may be hereditary are advised of the consequences of the disorder and the probability of developing and transmitting it and the ways in which this may be prevented.
It Involves The Followings:
A correct diagnosis using genetic tests after evaluation of family history and medical records Explanation of the nature of disorder & the treatment available Estimation of genetic risk for parents and family members.
Communication of genetic risks and the options for avoiding them to avoid undue complications in an unbiased manner Support in making the right decision Accessibility for long-term contact and counseling.
Premarital screening for thalassemia and sickle cell should be made mandatory to decrease at-risk marriages.
The objective is to make people aware of the consequences of thalassemia on health and socio-economics so that they voluntarily ask for screening, and prevention and change their reproductive plans when a possible risk is found.
If the risk is found before marriage, the options are to remain single, not to marry another carrier or to marry irrespective of carrier status.
If the risk is found after marriage, the options are to separate and find a non-carrier partner, to have a few or no children, selective termination of pregnancy, or to take a chance and have children as usual.
There are therefore challenges involved in genetic counseling because all the available choices involve difficult moral and social problems and in most cases, there appears to be no right answer.
But on the other hand, once people understand the risk, they can not escape from making a choice even if the decision ‘not to choose’ is a choice.
Question 11. A good number of Tilapia fishes are released in a pond having only different indigenous fish species grown naturally. Think and write which types of the struggle for existence Tilapia fishes have to face in order to survive.
Answer:
The Tilapia fishes have to face three types of struggle for existence in the pond where they are released.
These are
Intra-specific struggle:
It is the struggle among all the newly released tilapia fishes for food and habitat
Inter-specific struggle:
It is the struggle between Tilapia and other naturally grown indigenous fishes for food and habitat.
Struggle with the environment:
The Tilapia fishes struggle with the condition of the pond where they are newly released. Water content, Temperature of water, amount of dissolved oxygen, poisonous substances present in that pond water, etc. are the obstacles that they struggle, to overcome.
Question 12. Prepare a list of roles air sacs of pigeons play to fly in the air.
Answer:
Importance of air sacs in pigeons:
Pigeon is a primary volant animal. It has nine non-vascular and non-muscular air sacs, emerging from the bronchioles, typically helping in flight.
The importance of air sacs in pigeons is-
Importance of air bladder in rohu fish:
WBBSE Class 10 Life Science Previous Year Papers
Question 13.
Based on the above two features establish the concept of the analogous organ with the help of a proper example.
Answer:
Analogous organs are those organs that are different in structure and origin but perform similar functions.
Analogous organs indicate convergent evolution. For example, the wings of birds, wings of insects, and patagium of bats perform the same function, i.e., they help the organisms to fly but they have different structures.
Wings of birds are modifications of forelimbs, wings of insects are an outgrowth of insects’ exoskeleton and the patagium of the bat is actually a fold of skin between forelimbs and hind limbs.
All these structures point toward the fact that in the same environment, different structures may evolve to perform the same function. This further points toward convergent evolution.
Question 14. Relate the following phenomena with the trend of disturbance in the Nitrogen Cycle resulting from different human activities:
Answer:
Global warming:
Around 40% increase of N20 (nitrous oxide) in the environment is due to human activities. N20 is released in the environment as a result of the combustion of fossil fuel and the overuse of nitrogen-rich fertilizers.
This N2O is a greenhouse gas that absorbs infrared radiation or heat of the sunlight which reflects on the earth and facilitates the greenhouse effect and global warming.
Acidification of soil and water of rivers and lakes:
Oxides of nitrogen get dissolved in rainwater and form nitric acid, which is a major component of acid rain. Acid rain destroys aquatic plants and animals and disrupts the ecological equilibrium of rivers lakes, ponds, etc.
Apart from this, the destruction of forest resources and harm to architecture and monuments take place due to acid rain.
Question 15. Hilsa, Bee, Penguin, Rauwolfia- Assess which are the causes of the endangeredness of the above-mentioned organisms.
Answer:
Hilsa:
Facing threat due to overexploitation of this population.
Bee:
Loss of habitat, and excessive use of cell phones that project electromagnetic waves, damage the ability of bees to return to their colony. In that way, it destroys the navigation system of bees.
Penguin:
Penguin faces threats from geological events like a volcanic eruption, pollution, climatic changes, and severe weather.
Rauwolfia:
This type of medicinal plant faces threats due to overexploitation.
WBBSE Class 10 Life Science Model Question Paper 2023
Question 16. Discuss any two roles of the People’s Biodiversity Register (PBR) in conserving local biodiversity.
Answer:
Joint Forest Management or JFM:
The proper management of biodiversity by the joint action of local people and the forest department of the state government which is approved by the Indian government, is known as Joint Forest Management or JFM.

Role of JFM in the conservation of biodiversity:
In the conservation of biodiversity, the role of JFM is as follows
People’s Biodiversity Register or PBR:
It is a ready reference prepared by the central forest department in accordance with the Biodiversity Law 2002. This document contains detailed information on the availability of local biodiversity, their habits and habitats, other behaviors, their ecological importance, etc.
Role of PBR in the conservation of biodiversity:
In the conservation of biodiversity, the role of PBR is as follows-
Question 17. Tabulate any of the four activities which are prohibited in a sanctuary following the provisions of the Wildlife Act.
Answer:
The four activities, that are prohibited in the sanctuary are-
WBBSE Class 10 Life Science Model Question Paper 2023
Answer 6 questions or their alternatives given below.
Question 1. Draw a neat diagram of the vertical section of the eyeball of the human eye and label the following parts:
In order to be able to learn about and/or solve problems presented to them by their environment, humans must be able to take in information from that environment;
process it quickly and accurately; decide when, how, and what action to take; and then perform or execute that action. In order to receive information from the environment we are equipped with sense organizer
A sense organ is a specialized bodily structure that receives or is sensitive to internal or external stimuli. It is composed of receptors. Human sense organs are the eyes, ears, tongue, skin, and nose.
The Eye As A Sense Organ-Its Location, Structure, And Function
The sense organ consisting of photosensitive receptors (the rod & cone cells) and which helps us in vision is known as the eye.
The two eyes are located in the deep cavities of the skull called orbits on the frontal part of the cranium.
The structure of different parts of the human eye and their corresponding functions are given below:

Or,
Explain the importance of the following parts of an eukaryotic chromosome:
Analyze the role of cell divisions in controlling growth, reproduction, and repair in an organism.
Answer:
The physical structure of eukaryotic chromosomes:
The morphological features of a chromosome appear ‘most distinctly under a microscope during the metaphase stage of cell division. From this study, we can find 5 parts of a chromosome. These parts are described below.
1. Chromatids:
In a metaphase chromosome, two identical and longitudinal strands are seen. These are chromatids. Two chromatids of the same chromosome are called sister chromatids, which remain attached to a constricted region or centromere.
Each chromatid carries one or a few very fine filaments along its length. These are called chromonemata (singular—chromonema). Each chromonema is composed of a longitudinally arranged coiled DNA.
Along each chromonema, several spherical linearly arranged bead-like structures are seen, which are called chronometers.
2. Primary constriction and centromere:
Each chromosome has a distinct constricted region at which the sister chromatids remain attached to each other. This is known as primary constriction.
At e primary constriction, a round plate-like and dense heterochromatin structure is seen, which is called the centromere. The centromere has a few adhesive points, called kinetochores, which attach to the spindle fibers during metaphase.
The DNA present in the .centromere is genetically inactive in nature.
WBBSE Class 10 Life Science Model Question Paper 2023
3. Secondary constriction:
Other than primary constriction, there are one or a few constricted regions in the chromosomes. These are called secondary constrictions. Generally, the nucleolus is seen affixed to the secondary constriction.
During the telophase of cell division, this region helps to reorganize the nucleolus. Therefore, secondary constriction is also known as nucleolar organizer region or NOR.
4. Satellite:
In a few chromosomes, a bulb-shaped terminal portion is seen beyond the secondary constriction. This is called a satellite or SAT body. The chromosomes with SAT body are called SAT chromosomes.
5. Telomere:
The terminal portions of a chromosome are called telomeres. These are genetically inactive regions of a chromosome. During interphase, telomeres help in DNA replication.
It also prevents the joining of a chromosome with another and controls the ageing and death of a cell.
Significance of cell cycle:
The significance of the cell cycle is mentioned below-
1. Controlling cell division:
Certain points of the cell cycle control cell division. These are known as checkpoints. In case of any functional disruption at any of those points, the cell division process becomes uncontrolled, which may lead to tumor formation.
Tumors are of two types-benign tumors and malignant tumors. Benign tumors are harmless but malignant tumor cells invade other tissues through blood or lymph and form tumors there.
This phenomenon is called metastasis, which is a characteristic feature of cancer cells.
2. Normal growth and wound healing:
Cell division helps an organism to grow in size. It also assists in wound healing.
Importance of cell division:
The importance of the cell cycle is given below.
1. Growth:
The number of cells in an organism increases due to cell division. The daughter cells produced by this process also grow in size. Therefore, the growth of any organism depends directly upon cell division.
2. Reproduction:
Amitosis, mitosis, and meiosis help in different types of reproduction processes. Simple unicellular organisms like Amoeba, reproduce by the amitosis process. Mitosis helps in asexual and vegetative reproduction in animals and plants.
By meiotic division, gametes and spores are formed. Therefore, meiosis helps in sexual and asexual reproduction.
3. Wound healing:
Mitosis helps in the repair of wounds and the regeneration of organs in plants and animals.
4. Transfer of genetic characters:
By cell division, the characters of the mother cell are transferred to the daughter cells. From a broader perspective, the newer characters in daughter cells help in adaptation and evolution.
Question 3. Tabulate three pairs of dominant-recessive traits of pea plants as selected by Mendel. State the first law of Mendel as deducted from the experiment of the Monohybrid cross.
Answer :
Three pairs of dominant-recessive traits of pea plant as selected by Mendel

Or,
A color-blind female married a normal male. Judge the probability of color blindness among their children in the first filial generation. Show with the help of a cross how the first law of Mendel deviates in the case of the Four-O clock plant in F2 generation.
Answer:
Inheritance of color blindness:
Sex-Linked Inheritance
The gene is located in the sex chromosome. Sex chromosomes may be X or Y chromosomes.
But, as the Y chromosome is more or less genetically inert (functionless or inactive) with respect to the X chromosome, we generally consider sex-linked genes and X-linked genes to be synonymous.
Some X-linked recessive characteristics are- color blindness, hemophilia, etc.
Haemophilia
Haemophilia is a rare disorder in which blood doesn’t clot normally because it lacks sufficient blood-clotting proteins (clotting factors) causing the sufferer to bleed severely even from a slight injury.
Symptoms:
The major signs and symptoms of hemophilia are excessive bleeding and easy bruising.
Children who have mild hemophilia may not have signs unless they have excessive bleeding from a dental procedure, an accident, or surgery,
Bleeding can occur on the body’s surface (external bleeding) or inside the body (internal bleeding)— blood in stool, blood in urine, bruising, nose bleeds, heavy or prolonged periods, etc.
Swollen joints and pain in the joints.
Causes:
A defect in one of the genes that determine how the body makes blood clotting factor VIII or IX causes hemophilia. These genes are located on the X chromosomes.
Chromosomes come in pairs. The two types of hemophilia are factor VIII deficiency (hemophilia A) and factor IX deficiency (hemophilia B, or Christmas disease).
The most common type of hemophilia is called hemophilia A in which the person does not have enough clotting factor VIII (factor eight).
A less common type is hemophilia B in which a person does not have enough clotting factor IX (factor nine). Females have two X chromosomes, while males have one X and one Y chromosome.
Only the X chromosome carries the genes related to clotting factors. Haemophilia usually occurs more in males than in females. About 1 in 5,000 males are born with hemophilia each year.
A male who has a hemophilia gene on his X chromosome will have hemophilia. When a female has a hemophilia gene on only one of her X chromosomes, she does not have symptoms of hemophilia, since at least one of the X- chromosomes have a factor VIII or IX gene that works to produce normal or near normal levels of factors.
Class 10 Life Science Model Paper WBBSE 2023
However, some women who carry this gene may have a bleeding tendency. They are called ‘symptomatic carriers’. They are recognized as having mild hemophilia.
In very rare cases, some women have particularly low factor levels causing them to have moderate or severe hemophilia. In such cases, both X chromosomes are affected or one is affected and the other is missing or inactive.
Inheritance Of Haemophilia:
In this example, the mother is a carrier of the hemophilia gene and the father does not have hemophilia There is a 50% chance that each son will have hemophilia.
There is a 50% chance that each daughter will be a carrier of the hemophilia gene.
In this example, the father has hemophilia and the mother does not carry the hemophilia gene:
None of the sons will have hemophilia All daughters will carry the hemophilia gene In this example, the father does not have hemophilia and the mother does not carry the hemophilia gene
None of the children (either daughters or sons) will have hemophilia or carry the gene.

A Royal Disease:
Haemophilia is sometimes referred to as “the royal disease,” because it affected the royal families of England, Germany, Russia, and Spain in the 19th and 20th centuries.
Queen Victoria of England, who ruled from 1837-1901, is believed to have been the carrier of hemophilia B, or factor IX deficiency. She passed the trait on to three of her nine children.
Her son Leopold died of a hemorrhage after a fall when he was 30. Her daughters Alice and Beatrice passed it on to several of their children.
Alice’s daughter Alix married Tsar Nicholas of Russia, whose son Alexei had hemophilia.
Their family’s entanglement with Rasputin, the Russian mystic, and their deaths during the Bolshevik Revolution have been chronicled in several books and films.
Haemophilia was carried through various royal family members for three generations after Victoria and then disappeared.
Treatment of hemophilia:
Treatment of hemophilia involves regular injections of clotting factor medicine.
Color Blindness
Though most of us share a common color vision sensory experience, some people have a color vision deficiency, which means that their perception of colors is different from what most of us see.
Color-blind people are able to see things as clearly as other people but they are unable to fully ‘see’ red, green, or blue light.
Color blindness is the inability or reduced ability to see colors or to perceive obvious differences between two colors under normal lighting.
Symptoms:
Common symptoms of color blindness include difficulty in distinguishing between colors and inability to see shades or tones of the same color,
Types:
Color blindness can be mild, moderate, or severe. Based on photo pigments defects in the three different kinds of cone cells that respond to blue, green & red light, color blindness can be of three types
Red-green color blindness:
People with this type of color blindness are unable to see some shades of red and green. Reds may appear brownish-yellow, and greens may look beige to some people.
Certain shades of orange, yellow, and green may appear yellow to others. Red may also appear black to some people. Red-green color blindness is sometimes called Daltonism after John Dalton, the famous scientist, who himself was red-green color blind.
Class 10 Life Science Model Paper WBBSE 2023
Blue-yellow color blindness:
People with this type of color blindness are unable to see some shades of blue and yellow. Blue may appear greener and it may be difficult to distinguish yellow and red from pink. Yellow may appear violet to some people.
Complete color blindness:
People with complete color blindness do not see any colors. Poor vision accompanies complete color blindness.
Red-green color blindness is the most common form of color vision deficiency in many parts of the world. It is also much more common in men than in women.
Blue-yellow color blindness affects men and women equally. Complete color blindness is rare.
Causes:
Color blindness is a genetic condition caused by a difference in how one or more of the light-sensitive cells found in the retina of the eye respond to certain colors.
Inherited forms of color blindness often are related to deficiencies in certain types of cones or outright absence of cones.
Usually, genes inherited from the parents cause the deficiency or are responsible for faulty photopigments.
Men are much more likely to be colorblind than women because the genes responsible for the most common, inherited color blindness are on the X chromosome.
Males only have one X chromosome, while females have two X chromosomes. In females, a functional dominant gene for normal vision on only one of the X chromosomes is enough to compensate for the loss on the other.
In X-linked inheritance, the mother carries the mutated gene on one of her X chromosomes and will pass on the mutated gene to 50 percent of her children.
Inheritance of colour blindness:
In X-linked inheritance, the mother carries the mutated gene on one of her X chromosomes and will pass on the mutated gene to 50 percent of her children.
Because females have two X chromosomes, the effect of a mutation on one X chromosome is offset by the normal gene on the other X chromosome.
In this case, the mother will not have the disease, but she can pass on the mutated gene and so is called a carrier.
If a mother is a carrier of an X-linked dis-ease (and the father is not affected), there is a, 1 in 2 chance that a son will have the disease, a 1 in 2 chance that a daughter will be a carrier of the disease, No chance that a daughter will have the disease.

Treatment:
In general, treatments include blood transfusions, bone marrow transplants, medications, and supplements, etc.
People who receive blood transfusions receive extra iron that the body can’t easily get rid of and iron can accumulate in tissues, which can be potentially fatal.
The human body has no active mechanism for the excretion of iron.
Excess iron in vital organs, even in mild cases of iron overload, increases the risk for liver disease (cirrhosis, cancer), heart attack or heart failure, diabetes mellitus, osteoarthritis, osteoporosis metabolic syndrome, hypothyroidism, etc.
Hence the treatment of blood transfusion is to be followed with Iron chelation which involves the removal of excess iron from the bloodstream.
Inheritance of thalassemia:
A child who inherits two thalassemia trait genes-one from each parent will have the disease.
A child of two carriers has a 25 percent chance of receiving two trait genes and developing the disease and a 50 per cent chance of being a thalassemia trait carrier.
As illustrated in marriages between two carriers (thalassemia minor) may result in – a 25% chance of thalassemia major children, a 50% chance of thalassemia minor children, and a 25% chance of normal children. Thus two thalassemia carriers should not get married.

Question 4. Evaluate the effects of the following pollutants on the environment and human health:
Answer:
Effects of Pollutants on the Environment and human health

Or,
Speculate the probable causes of each of the following phenomena:
Answer:
Probable causes of different phenomena

Question 5. ‘The ever-increasing population in the different cities of India is creating the crisis of ground water’-Support the statement with reasons on the basis of your experiences. Construct a concept map to show how the increase in human habitat is influencing the ecosystem of Sunderbans.
Answer:
Groundwater in aquifers below the surface of the earth is an important natural resource. It accounts for nearly 30% of all fresh water.
Class 10 Life Science Model Paper WBBSE 2023
Depletion of groundwater is caused due to the following reasons:
Overuse:
As the population continues to rise, frequent pumping of groundwater causes depletion since it does not have enough time to replenish itself. This has become a major cause in every big city and town.
Agricultural Needs:
Lack of adequate surface irrigation facilities leads to over-exploitation of groundwater to meet crop and livestock requirements. This is a persistent problem in Gangetic Plain and north India.
Anthropogenic pollution:
Groundwater contamination occurs due to the mixing of gas, oil, poisonous salts, and chemicals or pesticides rendering it unsafe.
The environmental effects of groundwater depletion include land subsidence, water shortage, loss of biodiversity, hampered precipitation rate, food shortage, etc.
(or)
Summarise which conservation measures have been adopted to increase the population of an endangered mammal exclusively found in the swampy grasslands under the foothills of the Eastern Himalayas. Discuss the role of biodiversity in maintaining the balance of the ecosystem of a river.
Answer:
Endangered mammal (Red panda) conservation measures:
Since river or lotic ecosystem refers to flowing water, hence biotic components are specialized to live with flow conditions. They include bacteria, primary producers, insects and other invertebrates, fish, and other vertebrates.
Bacteria decompose the organic matter, vegetation, and biofilm. They play a large role in energy recycling.
Primary producers:
These include phytoplanktons, mosses, liverworts, and many rooted plants. These are sources of energy and form microhabitats that shelter other fauna from predators and the water current.
Insects and other invertebrates act both as consumers and prey items in lotic systems.
Various species of fish and other vertebrates like salamanders, snakes, crocodiles, turtles, bird species, and mammals are part of the lotic ecosystem. They act as consumers and also as prey species to the larger vertebrates available.

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.
Read and Learn More WBBSE Solutions For Class 10 Life Science
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.
Heredity Class 10 Life Science
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.
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.
Heredity Class 10 Life Science
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.
Heredity Class 10 Life Science
Harmful variations:
These variations make organisms unfit for their environment.
Neutral variations:
These variations do not affect the organisms in any way.
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.
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.
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-
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.

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.
Mendel’s Laws Of Heredity Class 10
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.
Mendel’s Laws Of Heredity Class 10
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.
Heredity Class 10 Life Science
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.

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.

Mendel performed several mono-hybridization experiments on pea plants involving crosses between parents that differ in a single gene.
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—

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.
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.
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.

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.
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.
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


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.
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.
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.

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.

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.
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:
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.
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.
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.

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
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

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
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.
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.
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.
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
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
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.
Each cell copies its chromosome exactly and passes on an identical copy to each daughter cell by cell division. Offspring may resemble or look different from the parents in bewilderingly complex ways.
This happens because individuals in nature contain many genes and different versions (alleles) of each gene.

Modern Cell Theory Or Cell Doctrine States That:
All organisms are made up of cells, ie., cells are structural & functional units of life.
Cells arise from pre-existing cells (Omnis cellula e cellula)
All organisms start their life from a single-cell
The multiplication of cells and their growth leads to the growth of an organism.
Read and Learn More WBBSE Solutions For Class 10 Life Science
The eukaryotic cells contain a membrane-bound nucleus which is designated as the ‘Director of the cell’.
The nucleus contains many thread-like, coiled, and elongated structures called chromatin fibers or chromatin reticulum, or nuclear reticulum.
The fibers of chromatin are uniformly distributed in the nucleoplasm. Chromatin fibers are observed only during the interphase or the preparatory phase of the cell cycle.
Just before cell division, chromatin fibers condense, become thick, and wrap up very tightly to form ribbon-like structures called chromosomes.

The number of particular species. They are usually found in pairs. Human beings have 23 pairs of chromosomes in each body cell.
The chromosome consists of a proteinaceous matrix and two spirally coiled chromonemata, each one of which contains a single DNA molecule.
The nucleus of an average human cell is only 6m in diameter, yet it contains 1.8 m of DNA which is distributed amongst the 23 pairs or 46 chromosomes each consisting of a single DNA molecule of about 40 mm.
Thus, Chromatin represents long-thin strands of the DNA-protein complex. It is an unfolded and uncondensed form of DNA, while chromosomes are condensed DNA and protein.
Class 10 Life Science Cell Division Solutions
The function of chromatin is to store DNA in the nucleus. Chromosomes are the bearers of hereditary instructions and regulate cellular processes.
DNA (or deoxyribonucleic acid) is the molecule that carries the genetic information in all cellular forms of life and some viruses.
It belongs to a class of molecules called nucleic acids, which are polynucleotides that is, long chains of nucleotides. Nucleotides are made up of a base, a sugar, and a phosphate. The four bases
chromosomes are constant in the nucleus for adenine (A), guanine (G), cytosine (C), and thymine (T) pair with each other (A with T and G with C).
It is the order or sequence of these base pairs that provides the information needed for the growth and development of our bodies.
Specific parts of DNA carry the code for producing specific proteins which ultimately lead to the expression of different characters in an organism.
Each of these parts of DNA is termed a gene. Thus gene is the fundamental physical and functional unit of heredity that carries information from one generation to the next.
It is a segment of DNA, composed of a transcribed region and a regulatory sequence, that makes possible transcription. A series of genes are present in each DNA.
The coordinated interaction of two or more genes produces a given phenotypic trait. A complete set of chromosomal genes is inherited by the offspring as a unit from the parent.
Functionally there are two types of eukaryotic chromosomes-
A human somatic cell contains 23 pairs of chromosomes. Out of the 22 pairs are autosomes and 1 pair is allosomes. The identical male and female parent chromosomes occurring in a pair are known as homologous chromosomes.
Each chromosome of a homologous pair is known as a homolog.
Autosomes:
Autosomes are responsible for controlling all the somatic characteristics of the body (eg. height of the body, complexion, the texture of hair, etc) except sex determination.
There are 22 pairs of autosomes in humans.
The paired autosomes are numbered 1 through 22.
They are numbered according to size so that chromosome pair 1 is the longest, and chromosome pair 22 is the shortest. Each autosome contains a large number of genes arranged in a definite sequence.
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In these homologous pairs, the 2 chromosomes are of the same length. The position of the centromere is the same.
A diagram or photograph called a karyogram is often used to depict the chromosomes of a cell. In a karyogram, homologous chromosomes are placed next to each other.
For example, both homologs of chromosome pair 1 are put side by side. We get one homolog of each type of autosome pair from each of our parents.

Allosomes Or Sex Chromosomes
Allosomes are primarily responsible for the sex determination of an organism.
Out of the 23 pairs of chromosomes in each human somatic cell, one pair is known as the sex chromosome.
Sex Chromosomes Are Of Two Types In Humans:
However, they pair and segregate into daughter cells during meiosis. Males have X and Y combinations. Females have X and X combinations in their body cells.
Therefore, the Karyotype Of Each Human Somatic Cell Is Depicted As Below:

The chromosome number is the precise number of chromosomes typical for a given species. In any species, the chromosome number is always the same and constant.
Therefore, the chromosome number is used in the identification of species and in tracing the relationship within the species.
In sexually reproducing organisms, the number of chromosomes in the body cells (or somatic cells = skin cell, blood cell, muscle cell, etc.) is diploid (2n; a pair of each chromosome),
since the nucleus of the somatic cell contains two homologs of each homologous pair of chromosomes-one is the paternal set (from the father) & the other is the maternal set (from the mother).
It may however be noted that the number of chromosomes does not correlate with the apparent complexity of an animal or a plant:
In humans, for example, the diploid number is 2n = 46 (that is, 23 pairs), compared with 2n = 78, or 39 pairs, in the dog and 2n = 36 (18 pairs) in the common earthworm.
The number of chromosomes in the sex cells (or germ cells or gametes) is haploid (n) since a single set of unpaired chromosomes is present in the nucleus of such cells.
Cell Cycle And Its Phases Class 10 Notes
In man, sperm and ova possess 23 chromosomes (n) each.
Thus the diploid (2n) number of chromosomes in somatic cells is just the double haploid (n) number of chromosomes in games. The haploid number is produced during meiosis.
In the nucleus of each cell, the DNA molecule is packaged into thread-like structures called chromosomes. Each chromosome is made up of DNA tightly coiled many times around proteins called histones that support its structure. A small amount of RNA is also present.
Chromosomes are not visible in the cell’s nucleus not even under a microscope when the cell is not dividing.
However, the DNA that makes up chromosomes becomes more tightly packed during cell division and is then visible under a microscope.
Chromosomes (Gr., chrom=colour, soma= body) are rod-shaped, dark-stained bodies seen during the metaphase stage of mitosis when cells are stained with a suitable basic dye and viewed under a light microscope.
Chromosomes were first described by Strasburger (1815), and the term ‘Chromosome’ was first used by Waldeyer in 1888.
During metaphase, a chromosome appears to possess two threads called chromatids, which become intertwined in the matrix of chromosomes.
These chromatids are spirally coiled chromonemata (sing., chromonema) at metaphase. Chromatin is composed of DNA, RNA, and protein.
Purified chromatin isolated from interphase nuclei consists of about 30-40% DNA, 50-65% protein, and 0.5-10% RNA; but there is a considerable variation due to species and tissues of the same species.
Each chromosome has a constriction point called the centromere, which divides the chromosome into two sections, or “arms”.
The location of the centromere on each chromosome gives the chromosome its characteristic shape and can be used to help describe the location of specific genes.

The DNA double helix is bound to proteins called histones. The histones have positively charged (basic) amino acids to bind the negatively charged (acidic) DNA.
The DNA is wrapped around the histone core of eight protein subunits, forming the nucleosome. Now all of this DNA and protein organization, all the DNA rolled around the histone proteins, is called chromatin.
Chromomeres are serially aligned, small bead-like accumulations of chromatin material that are visible along the length of the chromosome, especially during prophase.
Cell Cycle And Its Phases Class 10 Notes
Chromosome morphology changes with the stage of cell division, and at mitotic metaphase, it is most suitable to study a eukaryotic chromosome morphology When the following structural features can be seen under a light microscope.



The material of the chromosomes is the chromatin.
Chromatin is composed of DNA, RNA, and protein.
Purified chromatin isolated from interphase nuclei consists of about 30-40% DNA, 50-65% protein, and 0.5-10% RNA, but there is a considerable variation due to species and species.
DNA: DNA (Deoxyribonucleic acid) is up of molecules nucleotides.
Each nucleotide contains a phosphate group (phosphoric acid), a sugar group, and a nitrogen base.
Nucleotides are arranged in two long strands that form a spiral called a double helix, tissues of the same The structure of the double helix is somewhat like a ladder, with the base pairs forming the ladder’s rungs and the sugar and phosphate molecules forming the vertical side pieces of the ladder.
Cell Cycle And Its Phases Class 10 Notes
There are two classes of nitrogen bases called purines (Adenine = A, Guanine = G) and pyrimidines (Cytosine = C, Thymine = T).
Each base pair is formed from two complementary nucleotides (purine with pyrimidine) bound together by hydrogen bonds. The base pairs in DNA are A with T and C with G.

The deoxyribose sugar in DNA is a pentose, a 5-carbon sugar (commonly we know of Hexose or 6- 6-carbon sugars as C6H12O6). The carbons are numbered 1′ to 5′(pronounced ” prime carbon”).
It is from this numbering system of the sugar group that DNA gets its polarity. The linkages between nucleotides occur between the 5′ and 3′ positions in the sugar group. One end has a free 5′ end and the other has a free 3′ end.
A phosphate group consists of a central phosphorous surrounded by four oxygen.
Protein:
RNA:
RNA (Ribonucleic acid) is helical single stranded having structural units called ribonucleotide.
Each ribonucleotide contains the pentose sugar called ribose, a molecule of a phosphate group, and a nitrogen base. The nitrogen base of RNA is two purine bases (Adenine, Guanine) and two pyrimidine bases (Cytosine, Uracil).
Depending on their staining properties during interphase the following two types of chromatin may be distinguished in chromosomes.
Euchromatin:
Portions of chromosomes that stain lightly are only partially condensed; this chromatin is termed euchromatin. Euchromatin contains structural genes and is considered genetically active chromatin since it has a role in the phenotype expression of the genes.
Cell Cycle And Its Phases Class 10 Notes
Heterochromatin:
In the dark-staining regions, the chromatin remains condensed and is called heterochromatin.
Heterochromatin is characterized by its especially high content of repetitive DNA sequences and contains very few if any, structural genes.
It is late replicating (i.e., it is replicated when the bulk of DNA has already been replicated) and is not transcribed.
However, heterochromatin helps in gene regulation and the protection of chromosome integrity. Centromeric regions invariably contain heterochromatin.
The distribution of euchromatin and heterochromatin portions in a typical chromosome.

All cells have within them a variety of different organelles. Organelles are cell parts that are adapted and specialized to perform various vital activities of the cell like the organs of the human body.
The cell organelles directly associated with cell division are—
Nucleus:
The nucleus is the seat of the chromosomes that are to be divided. A unique feature of the nucleus is that it disassembles and re-forms each time most cells divide.
At the beginning of cell division, the chromosomes condense, the nucleolus disappears, and the nuclear envelope breaks down, resulting in the release of most of the contents of the nucleus into the cytoplasm.
At the end of cell division, the process is reversed. The interphase chromatin condenses approximately a thousandfold further to form the compact chromosomes as seen in dividing cells.

Centrosome and microtubules:
The centrosome is located in the cytoplasm of an animal cell usually close to the nucleus. It consists of two centrioles — oriented at right angles to each other.
It is duplicated duringthe S- phase of the cell cycle. Just before cell division, the two centrosomes move apart until they are on opposite sides of the nucleus.
As cell division proceeds, microtubules grow out from each centrosome with their ends growing toward the metaphase plate. Microtubules are thick, strong spirals of thousands of subunits.
Cell Division And Cell Cycle Class 10 WBBSE
Those subunits are made of a protein called tubulin. The microtubule spokes radiate from a central site occupied by the centrosome, which is the primary microtubule-organizing center (MTOC) in many interphase cells.
This cytoskeleton transports material within cells and coordinates cell division. These clusters of microtubules are called spindle fibers.

Microtubules are critical throughout the cell cycle – they organize chromosomal components and split them in two.
Spindle fibers have three destinations are attached to one kinetochore of a chromatid. Some bind to the arms of the chromosomes.
Still, others continue growing from the two centrosomes until they extend between each other in a region of overlap.
All three groups of spindle fibers participate in the assembly of the chromosomes at the metaphase plate at metaphase and the separation of the chromosomes at anaphase. In plant cells, however, the spindle is formed from cytoplasm and nucleoplasm.
Ribosome:
Ribosomes are the workbench of protein synthesis. Therefore, ribosomes play an important role in cell division. Several ribosomes become associated with Messenger RNA (mRNA) to form polyribosomes or polysomes. Polysomes act as sites for polypeptide synthesis.
A cell will not copy its DNA in preparation for cell division unless it knows that it has enough ribosomes to make new proteins because copying DNA requires a huge amount of proteins and energy.
This copying process happens during the interphase. Thus, the number of ribosomes in a cell is a form of regulating cellular homeostasis.

Mitochondria:
Cells require an ample amount of ATP (Adenosine triphosphate) to synthesize bioactive compounds such as lipids, proteins, and nucleotides for cell division.
Mitochondrial ATP production is also vital for cell division in addition to other basic functions in the cell including the regulation of cell volume, solute concentration, and cellular architecture.

Mitochondria are the fuel of the cell and act as a type of “driver” in cell division. The mitochondrial network fragments during mitosis to allow proper segregation of the organelles between daughter cells.
The fundamental and active biological process by which a cell produces its replica having similar structural, genetic, and physiological properties and thereby, brings upon continuity of life is called cell division.
Significance Of Cell Division:
The importance of cell division can be appreciated by realizing the following facts:
Continuity of life:
Cell division is a prerequisite for the continuity of life.
On one hand, it helps cells to maintain a favorable surface area to volume relationship and on the other, forms the basis of evolution to various life forms,
Cell Division And Cell Cycle Class 10 WBBSE
Means of reproduction:
In unicellular organisms, cell division is the means of asexual reproduction, which produces two or more new individuals from the mother cell.
In sexually reproducing organisms, the reduction division of meiosis helps to maintain constancy of the chromosome number of a species,
Growth:
In multicellular organisms, life starts from a single cell called a zygote (fertilized egg). The zygote transforms into an adult that is composed of millions of cells formed by successive divisions.
Thus, growth occurs by cell division,
Means of repair, healing & regeneration:
Cell division is the basis of the repair and regeneration of old and worn-out tissues. It causes healing of the injured regions of the body.
Plant & animal cells generally undergo three types of cell division-amitosis (direct cell division), mitosis (indirect equational cell division), and meiosis (indirect reduction division).
Amitosis occurs in prokaryotes and protozoans, while mitosis and meiosis occur in eukaryotes.
In the case of direct division, the nucleus and cell body undergo a simple mass division into two parts. During indirect division, the nucleus undergoes complicated changes before it is divided into two daughter nuclei.
Amitosis:
Amitosis, also known as binary fission, is a type of direct cell division in which both the nucleus and the cytoplasm undergo a simple mass division without going through complicated stages involving spindle or chromosome formation, maneuvers, and wall formation.
It is the means of asexual reproduction in unicellular organisms like bacteria & protozoans and also a method of multiplication or growth in fetal membranes of some vertebrates.
In amitosis, the splitting of the nucleus is followed by cytoplasmic constriction.
The nucleus elongates first & then assumes simple mass division without going through complicated stages involving spindle or chromosome formation, their maneuvers, and wall formation.
It is the means of asexual reproduction in unicellular organisms like bacteria & protozoans and also a method of multiplication or growth in fetal membranes of some vertebrates.
In amitosis, the splitting of the nucleus is followed by cytoplasmic constriction. The nucleus elongates first & then assumes a dumb-bell-shaped appearance.

The depression or constriction increases in size & ultimately divides the nucleus into two nuclei.
Next, the cytoplasmic constriction divides the cell into two equal or approximately similar halves. Therefore, without the occurrence of any nuclear events, two daughter cells are formed each of which can grow into a completely new organism.
Mitosis:
Mitosis producestwo genetically identical daughter cellsl. It means the two daughter cells have a similar genetic composition to their parents.
Meiosis:
Meiosis produces four haploid (n) daughter cells that come from diploid parents (2n). In this process, each of the daughter cells has half the chromosome of the parental cells.
During development from a zygote to a fully differentiated body, cells in the body alternately divide (mitosis) and “appear” to be resting (interphase).
Cell Division And Cell Cycle Class 10 WBBSE
The sequence of activities exhibited by cells in the period between the end of one division and the end of the next is termed the cell cycle.
Cell Cycle Constitutes Of Two Phases:
Interphase:
Interphase, which appears to be a long resting stage between cell divisions, is a period of diverse activities that are indispensable in making the next mitosis possible.
During this long period, the cell constantly synthesizes DNA, RNA & protein, stores up energy, and grows in size.
The volume of the cell decreases highly as a result. The nuclear membrane, however, remains intact and chromosomes remain as long thread-like chromatin fiber in the nucleoplasm.
By studying molecular events in cells, scientists have determined that interphase can be divided into four steps:
Gap 0 (G0), Gap 1 (G1), S (synthesis) phase, Gap 2 (G2).

Gap 0 (G0):
There are times when a cell will leave the cycle and quit dividing. This may be a temporary resting period or permanent.
An example of the latter is a cell that has reached an end stage of development and will no longer divide (e.g. neuron). After birth, the nerve cells in mammals do not divide and remain in the perpetual G0 phase throughout life.
Gap 1 (G1):
Cells increase in size in Gap 1, produce RNA, and synthesize protein.
An important cell cycle control mechanism that is activated during this period (G1 Checkpoint, also known as the restriction or start checkpoint) ensures that everything is ready for DNA synthesis.
If a cell meets the requirements for the G1 checkpoint, the cell will enter the S phase and begin DNA replication.
This transition, as with all of the major checkpoint transitions in the cell cycle, is signaled by cyclins and cyclin-dependent kinases (CDKs).
Cyclins are If a cell meets the requirements for the G1 checkpoint, the cell will enter the S phase and begin DNA replication.
This transition, as with all of the major checkpoint transitions in the cell cycle, is signaled by cyclins and cyclin-dependent kinases (CDKs). Cyclins are cell signaling molecules that regulate the cell cycle.The
G12 phase varies from 3-4 hours to serval days, months, or even years
S Phase:
To produce two similar daughter cells, the complete DNA instructions in the cell must be duplicated.
DNA replication and synthesis of histone occur during this S (synthesis) phase. As a result, chromosome duplication occurs in this phase. It lasts for 7-8 hours.
Gap 2 (G2):
During the gap between DNA synthesis and mitosis, the cell will continue to grow and produce new proteins.
At the end of this gap, there is another control checkpoint (G2 Checkpoint) to determine if the cell can now proceed to enter M (mitosis) and divide.
However, the most important role of the G2 checkpoint is to ensure that all of the chromosomes have been accurately replicated without mistakes or damage.
Cell Division And Cell Cycle Class 10 WBBSE
If the checkpoint mechanisms detect problems with the DNA, the cell cycle is halted and the cell attempts to either complete DNA replication or repair the damaged DNA. In this stage, diploid cells contain 4X times the amount of DNA.
It is then followed by mitosis.
Mitosis or M Phase:
Cell growth and protein production stop at this stage in the cell cycle. All of the cell’s energy is focused on the complex and orderly division into two similar daughter cells.
Mitosis is much shorter than interphase, lasting perhaps only for one to two hours.
As in both G1 and G2, there is a Checkpoint in the middle of mitosis (Metaphase checkpoint) that ensures the cell is ready to complete cell division.
The M checkpoint is also known as the spindle checkpoint because it determines whether all the sister chromatids are correctly attached to the spindle microtubules.
Because the separation of the sister chromatids during anaphase is an irreversible step, the cycle will not proceed until the kinetochores of each pair of sister chromatids are firmly anchored to at least two spindle fibers arising from opposite poles of the cell.
Uncontrolled cell division or propagation of damaged DNA can contribute to genomic instability and tumorigenesis.
If cell division is not regulated, a tumor will develop due to uncontrolled cell proliferation.
A tumor, also called neoplasm, is a mass of abnormal tissue that arises without obvious cause from pre-existing body cells, has no purposeful function, and is characterized by a tendency to autonomous and unrestrained growth.
The Abnormal Cells That Generally Makeup Tumors, Differ From Normal Cells In Having Undergone One Or More Of The Following Alterations:
Tumors may be-
Benign or Malignant type
Benign Or Non Cancerous Tumor:
The cells keep enlarging in size but are confined to the site of origin only.
They do not spread to the other parts of the body. The cells may cause pain, and discomfort and affect other organs due to their increased size, but their effect is not lethal. However, sometimes, benign tumors can also turn cancerous.
Cell Division Class 10 Life Science Pdf
Malignant Or Cancerous Tumor:
The tumor cells do not remain confined to the site of origin. They move & spread to other parts via blood or other tissue fluid of the body to form secondary tumors.
The moving and setting process is called metastasis. Metastasis is always fatal and these cells kill other cells or tissues.
Mitosis is a type of equational & indirect cell division in which chromosomes of the parent cell are equally distributed resulting in two genetically identical daughter cells.
The cells undergoing mitosis are called mitocytes. In plants, the myocytes are mostly meristematic cells. In animals, the myocytes are stem cells, germinal epithelium, and embryonic cells.
This division was first observed by Strassburger (1870) in plant cells and by Fleming (1882) in animal cells. The basic outline of mitosis remains the same in all living organisms.
Chromosomes replicated during mitosis are divided in such a way as to ensure that each daughter cell receives a copy of every chromosome of the parent cell.
The replicated chromosomes are attached to a ‘mitotic apparatus’ that aligns them and then separates the sister chromatids to produce an even partitioning of the genetic material.
This separation of the genetic material in a mitotic nuclear division (or karyokinesis) is followed by a separation of the cell cytoplasm in a cellular division (or cytokinesis) to produce two daughter cells. A mitosis division generally takes a time of 30 minutes to 3 hours.
Though Mitosis Is A Continuous Process, For a Better Understanding
The Whole Process Is Divided Into the Following Stages:
1. Prophase (Longest phase)
2. Prometaphase
3. Metaphase
4. Anaphase (shortest phase)
5. Telophase
C-Phase or Cytokinesis (a division of cell cytoplasm)
Karyokinesis (nuclear division):
It is the process by which the nucleus of the parent cell divides into two daughter nuclei.

Prophase:
It is the longest stage of mitosis during which chromatin threads condense, shorten & thicken to form chromosomes followed by the disappearance of both the nucleolus & the nuclear membrane and the formation of the mitotic apparatus.
The observed changes are-Nucleus becomes spherical and the cytoplasm becomes more viscous.
The chromatin threads slowly condense due to dehydration, shorten & thicken to form well-defined chromosomes.

Since each chromosome is already doubled due to the doubling of DNA contents in interphase, each chromosome now appears as two sister chromatids joined at the centromere or kinetochore.
During early prophase, the chromosomes remain evenly distributed in the nucleoplasm but as prophase progresses, the chromosomes migrate towards the nuclear membrane.
The spindle fibers (microtubules) begin to form outside the nucleus.
In plants, the microtubule organizing center (MTOC) may be of plastid MTOC or nuclear envelope MTOC or may be organized from many of the microtubules that originate from the rigid cell wall.
In plants the spindle apparatus or mitotic spindle is ancestral.
In animals, the movement of centrioles occurs due to the pushing apart by the growth of the spindle fiber between them. Fibrils appear like spokes of a wheel around each centriole to form asters.
The asters are formed from the cytoplasm and the spindle fibers are formed mainly from the nuclear material. In animals and brown algae, the mitotic spindle is amphiastral which includes two asters in opposite poles of the spindle.
Each aster consists of two centrioles surrounded by astral rays.
Cell Division Class 10 Life Science Pdf
Prometaphase
At the end of prophase, ie. during a cell’s entry to the prometaphase, the major event that happens is the breakdown of the nuclear envelope into small vesicles.
The observed changes are
The nuclear envelope breaks down into membrane vesicles with the result that nucleoplasm and cytoplasm mix. The chromosomes are therefore set free into the cytoplasm.
Specialized protein complexes or Kine- to chores become fully matured on the centromeres of the chromosomes.
The disruption of the nuclear envelope allows the mitotic spindles to gain access to the mature into- chores.
As the microtubules of the mitotic spindle enter the nuclear region, some chromosomes are attached to spindle microtubules through kinetochores.
These are called kinetochore microtubules. The remaining microtubules are called non-kinetochore microtubules.
Once they have captured the chromosomes, the kinetochore microtubules begin to exert force on the chromosomes to move them.
Nucleolus disappears.
Some cell biologists consider the prometaphase stage as early metaphase and include it under metaphase i.e. no separate prometaphase stage is considered.


Metaphase:
Metaphase is marked by the appearance of the spindle and the arrangement of chromosomes on the equator of the spindle. The diamond-shaped spindle formation starts in prophase and gets completed in metaphase.
Two pointed ends of the spindle are called the poles and the central broad part is known as the equator or the equatorial plate. The spindle is formed of spindle fibers that are composed of tubulin protein. There are two types of spindle fiber.s
Short fiber discontinuous fiber or chromosomal fiber-these are extended from the pole to the equator.
Long fiber continuous fiber or chromosomal fiber-these are extended from one pole to another pole.
The main events during this phase are—
The chromosomes migrate toward the equator of the spindle.
Each chromosome becomes more compact and short and its two chromatids remain separate except at the centromere which has not divided so far.
Kinetochore microtubules align the chromosomes in one plane to form a metaphase plate or equatorial plate.
The process of formation of a metaphase plate is called congression.
In animal cells, larger chromosomes remain attached to the periphery of the metaphase plate and smaller ones are placed at the central part. In plant cells, however, the orientation of chromatids on the equatorial plate is random.
Centromeres lie on the equatorial plane while the chromosome arms are directed away from the equator through a process called auto orientation.
Anaphase:
It is the shortest stage of mitosis during which the centromeres and the daughter chromosomes separate and begin to move towards the opposite poles of the equatorial plate.
The following changes occur during anaphase-
Chromosomes split simultaneously at the centromeres so that the sister chromatids separate. They are now called daughter chromosomes, each one consisting of a single chromatid.
The separated sister chromatids move towards opposite poles. This is called the anaphase movement.
The Poleward anaphase movement of daughter chromosomes occurs due to the shortening of kinetochore microtubules, the appearance and elongation of interzonal fibers, and the consequent pulling, pushing & repulsive forces.
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Daughter chromosomes may appear as V-shaped (metacentric) L-shaped (sub-metacentric), and L-shaped (telocentric).
The arms of daughter chromosomes remain directed towards the equator and centromere towards the pole of the spindle apparatus.

Telophase:
At the end of the polar migration of the daughter chromosomes, the telophase is marked by the uncoiling & deserialization of chromosomes followed by the reappearance of the nuclear membrane and nucleolus.
The main events during this phase are as follows-
Chromosomes reach the poles of the spindle and form two groups
Chromosomes begin to uncoil, undergo hospitalization, and form the chromatin network.
Kinetochore microtubules disappear.
The nuclear membrane is formed around each mass of chromatin from the endoplasmic reticulum resulting in the formation of two daughter nuclei.
Both the nucleoplasm and the cytoplasm are rehydrated.
Finally, a nucleolus is reorganized in each daughter nucleus at the chromosomal organizer site.

Cytokinesis:
Cytokinesis is the division of cell-cytoplasm into two separate cells each having a nucleus along with the redistribution of various cell organelles (mitochondria, Golgi bodies, etc).
It usually occurs in telophase along with the formation of daughter nuclei after the nuclear division. If cytokinesis does not occur after karyokinesis, the cell will be a binucleate one.
The process of cytokinesis differs in plant and animal cells.
Cytokinesis in Animal Cells:
In animal cells, cytokinesis starts with the appearance of a shallow groove cleavage, or furrow in the cytoplasm at the equator of the spindle. Slowly and slowly it deepens and constricts the cytoplasm and divides the cell into two parts.

Cytokinesis In Plant Cells:
In plant cells, cytokinesis is accomplished by the formation of phragmoplast and cell plate at the equator of the dividing cell. Cell plate or phragmoplast is formed by the fusion of small vesicles of Golgi bodies called phragmosomes.
Cell Division Class 10 Life Science Pdf
Gradually more amount of materials like cellulose, hemicellulose, pectin, etc are deposited on both sides of the cell plate to form a complete cell wall that separates the cytoplasm of the two daughter cells.

Basic Differences Between Mitosis Of Animal Cell And Plant Cell


The Importance Of Mitosis For The Organisms Has Been Summarised As Follows:
1. Maintaining the same genetic constitution:
In mitosis cell division, the two resulting daughter cells always contain the same number of chromosomes as the parent cell from which they derive.
Thus, It maintains equilibrium in the amount of DNA and RNA contents through equational division.
2. Opportunity for growth & development:Itt provides an opportunity for the growth and development of organs and the body of organisms. The number of cells within an organism increases by mitosis and this is the basis of growth in multicellular organisms from a single-celled zygote.
3. Repair & Replacement:
Old, decaying, and dead cells are constantly dying and being replaced by mitosis. For example- our skin cells and blood cells regularly die off; they are replaced and repaired by mitosis.
4. Regeneration & Healing:
Regeneration is the ability to replace lost or damaged body parts. Plants can regenerate all body parts from precursor cells. Some animals can regenerate whole parts of their body i.e.
legs in crustaceans, arms in starfish, and tails in lizards. The production of these new cells involves mitosis. Similarly, the healing process of a wound involves mitosis. We can regenerate skin, a large amount of liver, and the very tips of fingers and toes.
Class 10 Life Science Cell Division Solutions
5. Asexual reproduction:
Mitosis helps the organisms in asexual reproduction. By cell division, one cell divides to become two. This process is used by some organisms, such as protozoans, most plants, and lower invertebrates to reproduce.
Meiosis is the form of reductional eukaryotic cell division comprising a heterotypic division followed by a homotype division that produces haploid sex cells or gametes [which contain a single copy (n) of each chromosome] from diploid germ mother cells
[which contains two copies (2n) of each chromosome] in which genetic recombination takes place by crossing over between the genes.
The process takes the form of one DNA replication followed by two successive nuclear and cellular divisions (Meiosis I and Meiosis II).
Let us illustrate cell division by taking the chromosome number of humans. The cells of human beings contain a constant diploid (2n) number of chromosomes (23 pairs or 46 numbers 44 + XY in males and 44 + XX in females).
Humans reproduce sexually in which male and female gametes fuse to form the zygote. Gametes should contain haploid (n) number of chromosomes.
(23 numbers 22 + X or 22 + Y)so thatt the chromosome number of the zygote remains constant at 46 from generation to generation.
This happens due to meiosis which reduces the chromosome number to half in gametes and prevents it to go on doubling with each generation. Vanbeneden (1883) first reported meiosis. Farmer and Moore (1905) coined the term meiosis.
The cells undergoing meiosis are known as meiocytes. In plants, the meiocytes are microsporocytes (pollen mother cell) of anthers and megasporocytes (megaspore mother cell) of ovules.
In animals, the meiocytes are primary spermatocytes in the testes and primary oocytes in the ovaries.
Meiosis consists of two cycles of nuclear division (Meiosis-I and Meiosis-II), usually accompanied by cell division
[especially in sexually reproducing multicellular forms, where it is generally used to produce gametes through gametogenesis], preceded by DNA replication inintermeioticc interphase.
The stages of meiosis are as follows:

The process takes the form of one DNA replication followed by two successive nuclear and cellular divisions (Meiosis I and Meiosis II).
Let us illustrate cell division by taking the chromosome number of humans. The cells of human beings contain a constant diploid (2n) number of chromosomes (23 pairs or 46 numbers 44 + XY in males and 44 + XX in females).
Humans reproduce sexually in which male and female gametes fuse to form the zygote. Gametes should contain a haploid (n) number of chromosomes (23 numbers 22 + X or 22 + Y) so that the chromosome number of the zygote to remain constant at 46 from generation to generation.
This happens due to meiosis which reduces the chromosome number to half in gametes and prevents it to go on doubling with each generation. Vanbeneden (1883) first reported meiosis. Farmer and Moore (1905) coined the term meiosis.
Class 10 Life Science Cell Division Solutions
The cells undergoing meiosis are known as meiocytes. In plants, the meiocytes are microsporocytes (pollen mother cell) of anthers and megasporocytes (megaspore mother cell) of ovules.
In animals, the meiocytes are primary spermatocytes in the testes and primary oocytes in the ovaries.
Meiosis consists of two cycles of nuclear division (Meiosis-I and Meiosis-II), usually accompanied by cell division [especially in sexually reproducing multicellular forms, where it is generally used to produce gametes through gametogenesis], preceded by DNA replication in iintermeioticinterphase.
The stages of meiosis are as follows:

Important features of meiosis
1. Homologous Chromosomes:
These are chromosome pairs of approximately the same length and centromere position. Note that diploid cells have two sets or one pair of homologous chromosomes.
Out of the pair, one is inherited from the mother (maternal) and one from the father (paternal).

2. DNA replication:
Replication of DNA takes place during the interphase preceding meiosis. DNA replication generates sister chromatids from each chromosome. Sister chromatids are two identical copies of a chromatid that remain closely aligned.
Although DNA replication occurs in interphase, no longitudinal doubleness of chromosomes is visibly evident in Leptotene of Prophase I owing to contraction.
3. Synopsis:
The movement of chromosomes initiates in the zygotene stage and this movement results from an attracting force that brings the homologous pair of chromosomes together.
The chromosomes become shorter and thicker due to compaction.
When they come closer, homologous chromosomes pair and align at the equatorial plate of the cell for equal qualitative and quantitative distribution. The pairing takes place throughout the length.
This process of pairing is known as synapsis Pairing takes place not only between the homologous chromosomes but also between homologous regions of the chromosomes. Chromosome pairs undergoing synapsis have approximately the same length and centromere position.
Out of the pair, one is inherited from the mother (maternal) and one from the father (paternal). Non-sister chromatids belong to homologs.
These are chromosome pairs having the same length, staining pattern, centromere position as well as the same characteristics of genes at particular loci.
A homologous pair of chromosomes consists of one chromosome from each parent and they are known as bivalents. Each chromosome of a bivalent is found to have two chromatids. Thus the four chromatids of a bivalent are together known as a tetrad.
4. Crossing Over:
The pachytene subphase of Prophase I is marked by a process called Crossing over that happens after both the homologous chromosomes in a pair join up to form a structure called a tetrad through synapsis.
Once a tetrad is formed, a portion of each homologous chromosome breaks off transversely and is re-attached to the same part of its homolog. Crossing over occurs between non-sister chromatids of homologous Sister Chiasma chromatids chromosomes.
This mixes up the traits that are found in each of the chromosomes, thus resulting in genetic recombination due to the exchange of segments between two non-sister chromatids belonging to a bivalent tetrad.
As a result of crossing over, X liX-liketructure is formed between the non-sister chromatids. The point of attachment at the crossing-over is called chiasma. It occurs during Diplotene.
The number of chiasmas may be one, two, or more depending on the length of the chromosomes.

5. Terminalization Of Chiasmata:
Chiasmata are generally pushed to the terminal ends of the chromosomes and this process is known as the terminalization of chiasmata (singular: chiasma).
The pair of homologous chromosomes begin to separate in the diplotene subphase of prophase I and chiasmata are fully terminalized in the diakinesis subphase of prophase.
Wbbse Life Science Class 10 Chapter 2 Questions And Answers
Reduction in chromosome number:
During metaphase I, the tetrads line up on the plate. During anaphase I, the homologous chromosomes separate from one another i.e. one homologous chromosome with its two sister chromatids move to opposite poles.
Thus each pole has a haploid (n) number of chromosomes i.e. a reduction in chromosome number is achieved at this stage.
Telophase results in the formation of two haploid (n) daughter nuclei with each chromosome having two chromatids. For this reason, the first meiotic division is known as the reductional or heterotypic cell division.
7. Equational division:
Meiosis II or the second meiotic division has four phases similar to mitosis and is the second round of cell divisions during meiosis whereby the cells formed during Meiosis I divide again to form four haploid (n) gametes.
Between these two stages, the interkinesis or interphase is either quite short or skipped, unlike normal mitosis. Because of this, the S phase does not occur and so the DNA in these cells is not copied, making the resulting cells from this phase haploid.

1. Gametogenesis:
It is a necessary part of the life cycle of sexually reproducing animals since it leads to the formation of gametes (sex cells) through meiosis.
2. Maintenance Of Constant Chromosome Number Of A Species:
The gametes produced as a result of meiosis are haploid (n) and the zygote formed by their fusion is diploid (2n).
Thus, it is the only means for restoring the constancy in chromosome number, which is a characteristic of the species from generation to generation.
3. Production Of Variation In Organisms:
Meiosis results in new combinations of genetic material. During crossing over, the hereditary factors from male and female parents get mixed due to the breakage and exchange of chromatids.
This brings in genetic variation within the species. The variations are important raw materials for evolution and also help in the improvement of races.
4. Alternation of generation:
Meiosis causes conversion from sporophytic generation to gametophytic generation in plants, i.e. causes the alternation of generation through prezygotic, post-zygotic, or sporadic meiosis.
Meiosis occurs in sporogenous cells (micro and megaspore mother cells) of the sporophyte-producing haploid spores. The spores on germination form gametophytes (male and female).
Wbbse Life Science Class 10 Chapter 2 Questions And Answers
Cells of the gametophyte form gametes. Fusion of these gametes again leads to diploid or sporophytic generation and in this way, the alternation of generation between gametophytic and sporophytic generations keeps on going.
The basic differences are—




Question 1. The series of cell division is prophase,___________, anaphase &___________.
Answer: Metaphase, Telophase
Question 2. The 4 bases of nucleic nucleotides of DNA are- adenine,___________, cytosine, and thymine.
Answer: Guanine
Question 3. ___________are long thread-like structures made of a DNA molecule and protein.
Answer: Chromosomes
Question 4. There are two types of chromosomes___________ and sex chromosomes or allosomes.
Answer: Autosomes
Question 5. The phenomenon of fast cell divisions in the cancerous cells leading to a stage when the cells start moving to different body parts is known as___________.
Answer: Metastasis
Wbbse Life Science Class 10 Chapter 2 Questions And Answers
Question 6. Several mitotic divisions of a mother cell required for the production of 64 cells are___________.
Answer: 6
Question 7. If meiosis II fails to occur after meiosis I, it is called___________.
Answer: Brachymeiosis
Question 8. The sequence of the cell cycle is___________.
Answer: G1.S.G2,M
Question 9. ___________protect the ends of the chromosomes.
Answer: Telomers
Question 10. Centromeric regions of chromosomes invariably contain ___________.
Answer: Hetrochormatin
Question 11. Organelles are specialized structures of the ___________ which perform specific functions.
Answer: Cell
Question 12. The___________ consists of two centrioles.
Answer: Centrosome
Question 13. As cell division proceeds,___________ grow out from each centrosome.
Answer: Microtubules
Question 14. Ribosomes are the workbench of___________ synthesis.
Answer: Protein
Question 15. Cell division is the basis of repair and___________ of old and worn-out tissues.
Answer: Regeneration
Question 16.___________ produces 4 haploid (n) daughter cells that come from diploid parents (2n).
Answer: Meiosis
Question 17. DNA replication occurs during___________ phase of interphase.
Answer: S
Question 18. The___________ checkpoint is also known as the spindle checkpoint.
Answer: M
Question 19. During the stage of cell division,___________ the chromosomes move towards the opposite poles.
Answer: Anaphase
Wbbse Life Science Class 10 Chapter 2 Questions And Answers
Question 20. In plant cells, Cytokinesis is accomplished by the formation of___________ and cell-plate.
Answer: Phragmoplast
Question 21. The cells undergoing meiosis are known as___________
Answer: Meiocytes
Question 22. If 2n = 8, the number of chromatids in each daughter cell after meiosis will be___________.
Answer: 8.
Question 23. Anastral mitosis can be traced in___________ .
Answer: Plant cells
Question 24.___________ is the shortest and is the longest phase of cell division.
Answer: Anaphase, prophase
Question 25. The pairing of homologous chromosomes in meiosis is known as___________.
Answer: Synapsis
Question 1. Genetic information is transferred from parents to offspring.
Answer: True
Question 2. The character of all living organisms results from the interaction of the environment and parents.
Answer: False
Question 3. The DNA molecule contains proteins.
Answer: False
Question 4. Nucleotides are made up of a base, a sugar, and a nitrate.
Answer: False
Question 5. Chromosomes are long thread-like structures made of a DNA molecule and protein.
Answer: True
Class 10 Life Science Cell Division Solutions
Question 6. The number of chromosomes increases with the growth of the apparent complexity of an organism.
Answer: False
Question 7. Chromatin is long strands of the DNA-protein complex.
Answer: True
Question 8. Human sex chromosomes are of 2 types- X and Y.
Answer: True
Question 9. A picture called a karyogram is often used to look at our chromosomes.
Answer: True
Question 10. Human females inherit the Y chromosome from their fathers.
Answer: False
Question 11. One arm is very long and the other is very short in the acrocentric chromosome.
Answer: True
Question 12. The chromosome region distal to the secondary constriction is called primary constriction.
Answer: False
Question 13. DNA is a polynucleotide structure.
Answer: True
Question 14. The base pairs in DNA are A-G and T-C.
Answer: False
Question 15. The deoxyribose sugar in DNA is a hexose.
Answer: False
Class 10 Life Science Cell Division Solutions
Question 16. Histones constitute about 80% of the total chromosomal protein.
Answer: True
Question 17. Nerve cells are postmitotic.
Answer: False
Question 18. Two ribosomes become associated with mRNA to form polyribosomes.
Answer: False
Question 19. The mitochondrial network fragments during mitosis to allow proper segregation of the organelles between daughter cells.
Answer: True
Question 20. Interphase is a period of no activities.
Answer: False
Question 21. Normally mitosis is much longer than interphase.
Answer: False
Question 22. Karyokinesis is the division of the nucleus.
Answer: True
Question 23. During telophase, the chromosomes reach the poles of the spindle and form two groups.
Answer: True
Question 24. Mitosis helps the organisms in asexual reproduction.
Answer: True
Question 25. Diploid cells are produced by meiosis.
Answer: False

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

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

Answer: 1-E,2-A,3-D,4-B
Question 1. What contains the information of a cell that is inherited by future cells?
Answer: Segments of DNA, composed of a transcribed region and a regulatory sequence, called genes.
Question 2. Which are the keepers of the genetic material in eukaryotic cells?
Answer: Chromosomes
Question 3. What are the components of a nucleotide?
Answer: Nucleotides are made up of a nitrogenous base, a pentose sugar, and a phosphate group.
Question 4. What are the components of chromosomes?
Answer: Chromosomes are long thread-like structures made up of chromatin which is composed of DNA (30-40%), RNA (0.5-10%), and protein (50-65%).
Question 5. What is chromatin reticulum?
Answer: Uncoiled chromosomes are called chromatin reticulum that remain twisted, fine, anastomosed, and uniformly distributed in the nucleoplasm of an interphase nucleus
Question 6. What are sex chromosomes?
Answer: Sex chromosomes or allosomes are primarily responsible for the sex determination of an organism which differs in males and females of the same species, viz. X and Y chromosomes of humans. Males have an X and Y combination. Females have an X and X combination.
Class 10 Life Science Cell Division Solutions
Question 7. What is a karyogram?
Answer: It is a diagram or photograph of homologous chromosomes from a cell, arranged according to their size.
Question 8. What is the diploid chromosome number of human beings?
Answer: It is 2n=46.
Question 9. Who first described chromosomes?
Answer: Chromosomes were first described by Strassburger (1815).
Question 10. What will be the chromosome number of mesophyll tissue cells and male gametes in a flowering plant where 2n = 18?
Answer: Mesophyll tissue cells (somatic cells) = 2n = 18 Male gametes = n = 9
Question 11. What are sub-metacentric chromosomes?
Answer: Chromosomes with a centromere slightly away from the mid-point so that the two arms are unequal are called sub-metacentric chromosomes.
Question 12. What are the functions of telomeres?
Answer: Telomeres protect the ends of the chromosomes from damage and stop them from becoming attached
Question 13. A pair of related terms are given below: Based on the relationship in the first pair, write the suitable word in the gap of the second pair.
Answer:
DNA pyrimidine:Thymine:: RNA pyrimidine Uracil.
Embryonic cell: monocytes:: Primary oocyte Meiocytes.
Nuclear division:: cytoplasmic division: cytokinesis Karyokinesis.
Animal cell: cleavage cytokinesis:: Plant cell: Cell plate cytokinesis.
Question 14. Write the characteristics of heterochromatin.
Answer: Heterochromatin is characterized by its especially high content of repetitive DNA sequences and contains very few if any, structural genes.
Question 15. Write the full form of MTOC.
Answer: Microtubule-organizing center.
Question 16. What is tubulin?
Answer: Microtubules are made up of protein subunits called tubulin.
Question 17. What are the sub-phases of interphase?
Answer: Interphase can be divided into 4 sub-phases: Gap 0 (G0), Gap 1 (G1), S (synthesis) phase, and Gap 2 (G2).
Question 18. What are the G0 phases?
Answer: The G0 phase is the time when a cell leaves the cell cycle either permanently or temporarily and quits division.
Question 19. Write the full form of CDK.
Answer: Cyclin-dependent kinase.
Question 20. During which stage of mitosis, do chromosomes get aligned on the equator?
Answer: Metaphase
Question 21. By which type of cell division, haploid sex cells are produced?
Answer: Meiosis
Class 10 Life Science Cell Division Solutions
Question 22. What is synapsis?
Answer: The lengthwise pairing of homologous chromosomes during the zygotene stage of the first meiotic prophase is known as synapsis.
Question 23. Among the following four terms, one includes the other three. Find out the term and write it:
Answer:
Synopsis, crossing over, meiosis cell division, reduction in chromosome number Meiosis cell division.
Sporocytes, microsporocytes, megas- porocytes, meiocytes Meiocytes
G1; S, cell cycle, G2 Cell cycle
Question 24. What is endomitosis?
Answer: In endomitosis the chromosomes and DNA duplicate but fail to separate which leads to polyploidy. It occurs notably in the salivary glands of Drosophila and other flies.
Question 25. How many mother cells will form 1000 microspores?
Answer: \(\frac{1000}{4}=250 \text { mother cells. }\)
Question 1. What is nucleic acid? How is it chemically composed?
Answer:
Nucleic acid:
The organic acid that is found predominantly within the nucleus and takes part in the formation of chromosomes is known as nucleic acid.
Example:
Ribonucleic Acid or RNA (single helical) and Deoxyribonucleic Acid or DNA (double helical).
Chemically nucleic acid is made up of nucleotides. Each nucleotide is composed of a nitrogen base, a pentose sugar, and a Phosphoric acid.
Question 2. DNA consists of two complementary nucleotide chains. If the sequence of nucleotides in one of the chains is AGCTTCGA, then find the nucleotide sequence in the other chain.
Answer:
The adenine(A) base of one strand of DNA is hydrogen bonded to a thymine (T) in the opposite strand; while the guanine (G) is hydrogen bonded to a cytosine (C). Hence the complementary nucleotide sequence in the other chain would be TCGAAGCT.
Question 3. Mention The Difference Between DNA and RNA.
Answer:
The Difference Between DNA and RN

Question 4. What are giant chromosomes? Give examples. Some cells at certain stages contain large nuclei with giant or large-sized chromosomes. These chromosomes are known as giant chromosomes.
Giant chromosomes are of two types:
Polytene Chromosome:
These are also called salivary gland chromosomes.
Example:
Drosophila melanogaster
Lampbrush Chromosome:
These chromosomes are found in yolk-rich amphibian oocytes.
Question 5. Write the differences between diploid and haploid.
Answer:
The differences between diploid and haploid

Question 6. Enumerate the difference between euchromatin and heterochromatin
Answer:
The difference between euchromatin and heterochromatin

Question 7. Which organisms have the least and the most number of chromosomes?
Answer:
The organism with the least number of chromosomes is the male Australian ant; Myrmecia pilosula with one chromosome per cell.
Ophioglossum reticulatum, a species of fern also known as Adderstongue, has the largest number of chromosomes with more than 1260 or 680 pairs per cell.
Cell Cycle And Its Phases Class 10 Notes
Question 8. What are aneuploidy and polyploidy?
Answer:
Aneuploidy
Aneuploidy refers to the random abnormal number of chromosomes in the cells due mostly to nondisjunction. It is a type of numerical change in the usual chromosomal count of the cell.
A condition in which organisms have more than two complete sets of chromosomes in their cells is called polyploidy.
Question 9. Write the differences between autosomes and allosomes.
Answer:
The differences between autosomes and allosomes

Question 10. Name two haploid organisms. In haploid organisms that undergo sexual reproduction, name the stage in the life cycle when meiosis occurs. Give reasons in support of your answer.
Answer:

Meiosis takes place during the post-zygotic stage in haploid organisms. Since the organism is haploid, meiosis cannot occur during gametogenesis.
Question 11. Give the differences between pro-mitosis and mitosis.
Answer:
The differences between pro-mitosis and mitosis

Question 12. Write the specific scientific term for each of the following:
The Period Between Two Successive Mitotic Divisions
Interphase
Point At Which Two Sister Chromatids Are Held Together
Centromere
Nuclear Division
Karyokinesis
Process Of Cell Division By Which Chromosome Number Is Halved
Meiosis
Question 13. Write about the role of mitochondria in cell division.
Answer:
The role of mitochondria in cell division can be summarised as :
Cells require an ample amount of ATP (Adenosine triphosphate) to synthesize bioactive compounds such as lipids, proteins, and nucleotides for cell division.
Mitochondrial ATP production is also vital for cell division in addition to other basic functions in the cell including the regulation of cell volume, solute concentration, and cellular architecture.
Mitochondria are the fuel of the cell and act as a type of “driver” in cell division.
The mitochondrial network fragments during mitosis to allow proper segregation of the organelles between daughter cells.
Mitochondria contributes to synthesizing, breaking down, and recycling biochemicals needed for the functioning of genetic materials.
Mitochondrial dysfunction is associated with tumor metabolic pathways.
Question 14. What are the stages of mitosis?
Mitosis is a continuous process and for better understanding, the whole process is divided into the following stages:
1. Prophase
2. Prometaphase
3. Metaphase
4. Anaphase
5. Telophase
6. C-Phase or Cytokinesis (a division of cell cytoplasm)
Question 15. What are the characteristics of mitotic telophase?
Answer:
The characteristics of mitotic telophase
At the end of the polar migration of the daughter chromosomes, the telophase is marked by the uncoiling & deserialization of chromosomes followed by the reappearance of the nuclear membrane and nucleolus.
The main events during this phase are as follows-
Chromosomes reach the poles of the spindle and form two groups.
Chromosomes begin to uncoil, undergo hospitalization, and form the chromatin network.
Kinetochore microtubules disappear.
The nuclear membrane is formed around each mass of chromatin from the endoplasmic reticulum resulting in the formation of two daughter nuclei.
Both the nucleoplasm and the cytoplasm are rehydrated.
Finally, a nucleolus is reorganized in each daughter nucleus at the chromosomal organizer site.
Cell Cycle And Its Phases Class 10 Notes
Question 16. Between a prokaryote and a eukaryote, which cell has a shorter cell division time? Given that the average duplication time of E. coli is 20 minutes, how much time will two E. coli cells take to become 32 cells?
A prokaryotic cell divides by amitosis and an eukaryotic cell divides by mitosis. Amitosis is the fastest cell division which, on average, takes 20-30 minutes to complete.
The time required for mitosis differs with species and environment. Normally mitosis takes around 3 hours to complete.
Since there are two E.coli cells at the beginning, let us calculate the time required for one cell to produce 16 cellsso thatt the final count of cells to become 32.
Each cell produces two cells through one division. Since 24 = 16, therefore there will be 4 divisions to produce 16 cells.
Time required = 4 x 20 min = 80 min = 1 hr. 20 min.
Question 17. Mention the advantages and disadvantages of amitosis.
Answer:
Advantages of amitosis:
Amitosis is the fastest cell division and takes minimum time to complete. Thus it is the major means of reproduction in lower organisms like yeast, bacteria, etc.
Disadvantages of amitosis: Amitosis may result in different daughter nuclei with unequally distributed chromosome numbers.
Moreover, in this process of cell division, there is no possibility of genetic recombination and there is a possibility of expression of unwanted recessive genes.
Question 18. State the phases of the cell cycle or cell division in which the following phenomena occur:
Answer:
Interkinesis
After telophase I & before meiosis II
Chromatin fibers are present
Interphase
Synaptonemal complex formation
Prophase I of meiosis I
Centriole replication taking place
S-phase
the lowest amount of cellular growth & synthesis taking place.
Mitosis or M-phase
the cell increases in size and produces new organelles
G1 phase
Question 19. Which factors might cause cell cycle growth arrest? The following are the factors for cell cycle growth arrest:
Answer:
DNA damage:
DNA damage activates pathways either to repair the damage or to activate apoptotic pathways if the damage cannot be fixed. This causes the arrest of the cell cycle at the G2 checkpoint.
Lack of appropriate growth factors:
This will keep the cell from progressing through the cell cycle. A prolonged lack of growth is referred to as G0 of the cell cycle and occurs when the cell cannot pass the G1 checkpoint.
Failure of the chromosomes to line up on the equatorial plate during mitosis:
This prevents the cell from activating pathways to degrade the cohesion that holds the sister chromatids together. This is called metaphase checkpoint and it ensures proper segregation of chromosomes.
Question 20. State The Consequence If Each Of The Following Irregularities occurs during Mitosis:
Nuclear membrane fails to disintegrate
Intranuclear mitosis or promitosis:
The spindle is formed inside the nucleus. This happens in some protozoa (amoeba) and yeast.
Duplication of DNA does not occur
The G1 checkpoint does not allow the cell to proceed to the S phase.
Cytokinesis does not occur
Coenocyte or syncytium:
A multinucleate condition arises as it happens in Rhizopus and Vaucheria etc.
Dinomitosis:
Chromosomes get attached to the nuclear membrane during the movement. The nuclear envelope persists and the microtubular spindle is not formed.
Question 1. Adenine is a ______________ type of nitrogenous base.
Answer: Purine
Question 2. During embryonic development and growth in vertebrates____________cell division takes place.
Answer: Mitosis
Question 3. Chromosome is the condensed coiled structure of_____________ molecule.
Answer: DNA & protein
Question 1. Ovum is only produced as a result of mitosis
Answer: False
Question 2. In DNA, Adenine is linked with Guanine by hydrogen bonds.
Answer: False
Question 1. A pair of related terms is given below.Based onf the relationship in the first pair write the suitable word in the gap of the second pair. Prophase: Disappearance of nuclear membrane and nucleolus:: ____________________: Reappearance of nuclear membrane and nucleolus.
Answer: Telophase.
Question 2. Mitosis : Radicle ::__________________ : Spore mother cell
Answer: Meiosis.
Question 1. Write two importance of the cell cycle.
Answer:
Importance of cell cycle:
The cell cycle plays an important part in the development of embryos and it is important for the growth & development of our bodies as well. The cell cycle produces new cells and also replaces cells that are old, lost, or damaged.
Cell cycles have checkpoints to detect abnormal mutations arising out of radiation, chemicals, carcinogens, etc.
Abnormal cells may either be identified or repaired through the cell cycle as it happens in case of repair by P53 protein during G1 to S stages.
Question 2. Distinguish Between DNA and RNA based On The Following Features:
Answer:

Question 3. Distinguish between autosome and sex chromosome of humans based on the following features:
Answer:

Question 4. “In case of Prophase and Telophase changes of opposite nature happen” — Write two such changes.
Answer:
Two Opposite Nature Of Changes That Take Place In Prophase And Telophase Are Shown Below:
Cell Cycle And Its Phases Class 10 Notes
Question 5. During the meiosis cell division, a reduction in the number of chromosomes and exchange of segments between chromatids take place — Analyse what are the significance of these two phenomena.
Answer:
Significances of the following phenomena in connection with meiosis cell division:
Reduction in the number of chromosomes:
During anaphase I, the homologous chromosomes separate from one another and move to opposite poles.
Telophase I results in the formation of two haploid (n) daughter nuclei with each chromosome having two chromatids. Meiosis II is an equational division.
Thus the gametes produced as a result of meiosis are haploid (n) while the zygote formed by their fusion is diploid (2n).
Hence, meiosis is the only means for restoring the constancy in chromosome number, which is a characteristic of the species from generation to generation.
Exchange of segments between chromatids:
During crossing over, the hereditary factors from male and female parents get mixed up due to the breakage and exchange of chromatids.
This brings in genetic variation within the species. The variations are important raw materials for evolution and also help in the improvement of races.
Question 6. Identify the stages ofKaryokinesis of mitotic cell division depending on the following features:
Answer:
Alignment of chromosomes along the equator of the cell and their arrangement in a definite pattern
Metaphase
The disintegration of spindle fibers
Anaphase
The disappearance of nuclear membrane and nucleolus
Prophase and prometaphase
Movement of daughter chromosomes to the opposite poles of the cell
Anaphase
Question 7.”Meiosis is characteristically different from mitosis”— how would you justify the statement?
Answer:
