+2 BIO-ZOO-EM - Vol-1 (1-6 Lessons)
+2 BIO-ZOO-EM - Vol-1 (1-6 Lessons)
+2 BIO-ZOO-EM - Vol-1 (1-6 Lessons)
BIO-ZOOLOGY
REVISED EDITION (Q & A) – 2020-21
( PART –I )
1. Reproduction in Organisms
2. Human Reproduction
3. Reproductive Health
4. Principles of Inheritance and Variation
5. Molecular Genetics
6. Evolution
P.SENGUTTUVAN. M.Sc.,M.Ed.,M.Phil.
P.G.T-Zoology –GHSS –Thoppur.
DHARMAPURI -DIST .
&
C.VALARMATHI. M.Sc.,M.Ed.,M.Phil.
P.G.T-Zoology.GHSS-Palayampudur
DHARMAPURI –DIST.
7) Name the phenomenon where the female gamete directly develops into a new organism with an avian
example.
Phenomenon - Parthenogenesis.
In some organisms female gamete (ovum) is directly develop into a complete individual by physical or
chemical induction. e.g., Turkey, Chicken, Pigeon.
10) The unicellular organisms which reproduce by binary fission are considered immortal. – Justify ?.
Most unicellular organisms reproduce by cell division.
The whole parent body act as reproductive unit and disappears after new daughter cells are formed.
Whole parent body converted into daughter cell thus, there is no death for unicellular organisms hence
they are called immortal.
2. What are the stages at which multiple fission of plasmodium takes place?
In Plasmodium, multiple fission occurs in the Schizont and in the oocyte stages.
3. What is strobilation ?
In some metazoans, several transverse fissions occur simultaneously giving rise to a number of individuals.
E.g. Aurelia.
Viviparous Oviparous
It is the type of development in which the young The young hatch from eggs laid outside the mother‟s
ones are born alive after being nourished in the body. Eg: Reptiles and Birds.
uterus through placenta . Eg :Mammals.
7. Define Gemmules :-
Gemmules are formed by internal buds through a sexual reproduction.
It is a hard ball, consisting og food laden archaeocytes.
Eg.In sponges during unfavourable conditions
19) At what stage of development are the gametes formed in new born male and female?
1. Male - Spermatogenesis starts at the age of puberty. It is initiated by the release of Gonadotropin.
2. Female - At puberty secondary oocyte and ovum is formed from primary oocytes by miotic division.
30) Describe the structure of the human ovum with a neat labelled diagram?
Human ovum is microscopic, non - cleidoic and alecithal.
It‟s cytoplasm is called Ooplasm. Ooplasm contains large nucleus called
germinal vesicle.
It has outer thick coat of follicular cells called corona radiata.
The middle thick layer is called zona pellucida.
The inner thin transparent layer is called vitelline membrane.
Between the vitelline membrane and zona pellucida is a narrow space called
perivitelline space.
31) Give a schematic representation of spermatogenesis and Oogenesis in humans?
33) Explain the role of oxytocin and relaxin in parturition and lactation?
1. Relaxin :-
It relaxes pelvic joints and by dilation of the cervix with continued powerful contractions.
The amnion ruptures and amniotic fluid flows through vagina.
The placenta and the remains of the umbilical cord is called „after birth‟ is expelled out after delivery.
2. oxytocin :-
It causes the ejection of milk from the alveoli of mammary glands.
During lactation, it stimulates the contraction of the empty uterus. Now uterus return to prepregnancy size.
34) Identify the given image and label its parts marked as a,b,c and d
a. Vitelline Membrane
b. Nucleus.
c. Zona Pellucida.
d. Corona radiata.
ADDITIONAL QUESTIONS
2. What are the accessory glands in female reproductive system and its function ?
1) The Bartholin’s gland - is posterior to the left and right of the opening of the vagina. Its secrete mucus to
lubricate the vagina.
5) The Skene’s glands - are located on the anterior wall of the vagina and around the lower end of
the urethra. They secrete a lubricating fluid.
8. Monozygotic (Identical) :- twins are produced when a single fertilized egg splits into two during the first
cleavage. They are of the same sex, look alike and share the same genes.
9. Dizygotic (Fraternal) :- twins are produced when two separate eggs are fertilized by two separate sperms.
The twins may be of the same sex or different sex and are non-identical.
10. Siamese (United) :- twins are the conjoined twins who are joined during birth.
5-MARK QUESTION
2. Yolk Sac :-
10) Select the correct term from the bracket and complete the given branching tree
A. Barriers
B. Lactational amonerrhoea
C. Tubectomy
D. CuT
14) What are the strategies to be implemented in India to attain total reproductive health?
1. Family Planning programme since 1951 and is periodical assessed every decade.
2. Reproductive and child Health care (RCH) programmes.
3. Creating awareness and providing medical assistance to build a healthy society.
4. Introducing sex education in schools to provide information about adolescence.
5. Educating couples and those in the marriageable age groups about the available birth control methods.
6. Awareness about care for pregnant women post natal care of mother and child.
7. Encouraging the government and non-governmental agencies to identify new birth control methods.
19) The procedure of GIFT involves the transfer of female gametes into the fallopain tube, can gametes be
transferred to the uterus to achieve the same result? Explain.
This is a procedure (IUI) to treat infertile men with low sperm count.
The semen is collected either from the husband or from a healthy donor.
And it is introduced into the uterus through the vagina by a catheter.
After stimulating the ovaries to produce more ova.
The sperms swim towards the fallopian tubes to fertilize the egg, resulting in normal pregnancy.
10. Foetoscope :-
It is used to monitor the foetal heart rate and other functions during late pregnancy and labour.
The average foetal heart rate is between 120 and 160 beats per minute.
An abnormal foetal heart rate or pattern may mean that the foetus is not getting enough oxygen and it
indicates other problems.
A hand-held doppler device is often used during prenatal visits to count the foetal heart rate.
During labour, continuous electronic foetal monitoring is often used.
ONE WORD
1. It is known as anti-sterility vitamin as it helps inthe normal functioning of reproductive structures –Vitamin E
2. Sex hormones were discovered by - Adolf Butenandt.
3. World Population Day - 11th July .
4. World AIDS Day - 1st December .
5. NACO (National AIDS Control Organisation) was established in - 1992.
6. They are commonly called as international diseases - Syphilis and gonorrhoea.
7. The world to initiate the „Family planning programme‟ since - 1951.
8. It is refers to „aborting the female in the mother‟s womb - Female foeticide.
9. It is „killing the female child after her birth - infanticide .
10. Prevention of children from sexual offences act is - POCSO Act.
11. This delay in ovarian cycles is called - lactational amenorrhoea.
12. All women are born with ovaries, but some do not have functional uterus it is called Mayer-Rokitansky
syndrome.
-: GOD GRACE :-
24) Which of the following is incorrect regarding ZW-ZZ type of sex determination?
b) Females are homogametic and males are heterogametic
28) What is criss-cross inheritance?.OR ( colour blind man X normal visioned woman ) (Annual -2020)
OR ( Sex linked characters in human being )
A marriage between a colour blind man and a normal visioned
woman.
It will produce normal visioned male and female individuals in F1
generation but the females are carriers.
The marriage between a F1 normal visioned carrier woman and a
normal visioned male will produce:
1. one normal visioned female,
2. one carrier female,
3. one normal visioned male and
4. one colour blind male.
Colour blind trait is inherited from the male parent to his grandson
through carrier daughter.Which is an example of criss-cross
pattern of inheritance.
“ This type of inheritance of recessive sex linked character from
father to daughter and then from the daughter to her sons” is
known as criss cross inheritance.
29) Why are sex linked recessive charactersmore common in the male human beings?
The X–linked genes have no corresponding alleles in the Y chromosome.
The Y linked genes have no corresponding allele in X chromosome.
The Y linked genes inherit along with Y chromosome and they phenotypically express only in the male.
Sex linked inherited traits are more common in males than females because, males are hemizygous and
therefore express the trait when they inherit one mutant allele.
1. Wiener Hypothesis :-
Wiener proposed the existence of eight alleles (R1, R2, R0, Rz, r, r1, r11, ry) at a single Rh locus.
All genotypes carrying a dominant „R allele‟ (R1, R2 ,R0 ,Rz).
Will produce Rh+positive phenotype and double recessive genotypes (rr, rr1, rr11, rry) will give rise to
Rh-negative phenotype.
2. Kin Selection :-
All other females in honey bees which are diploid having developed from fertilized eggs help to raise the
queen‟s eggs.
So contribute to the queen‟s (honey bees) reproductive success and indirectly to their own, a phenomenon
known as Kin Selection.
3. Haemophilia :-
Haemophilia is commonly known as bleeder‟s disease, which is more common in men than women.
This hereditary disease was first reported by John Cotto in 1803.
Haemophilia is caused by a recessive X-linked gene.
A person with a recessive gene for haemophilia lacks a normal clotting substance (thromboplastin)
in blood, hence minor injuries cause continuous bleeding, leading to death.
The females are carriers of the disease and would transmit the disease to 50% of their sons even if the
male parent is normal.
Haemophilia follows the characteristic criss - cross pattern of inheritance.
4. Karyotyping – Idiogram :-
It is a technique through which a complete set of chromosomes is separated from a cell and the
chromosomes are arranged in pairs.
The individual chromosomes are cut from the photograph and are arranged in an orderly fashion in
homologous pairs. This arrangement is called a karyotype.
An Idiogram refers to a diagrammatic representation of chromosomes.
5. Pedigree analysis :-
Pedigree is a “family tree”, drawn with standard genetic symbols, showing the inheritance pathway for
specific phenotypic characters.
Pedigree analysis is the study of traits as they have appeared in a given family line for several past
generations.
6. Thalassemia :-
Thalassemia is an autosomal recessive disorder.
It is caused by gene mutation resulting in excessive destruction of RBC‟s due to the formation of abnormal
haemoglobin molecules resulting in anaemia.
Normally haemoglobin is composed of four polypeptide chains, two alpha and two beta globin chains.
Thalassemia is classified into alpha and beta based on which chain of haemoglobin molecule is affected.
It is controlled by two closely linked genes HBA1 and HBA2 on chromosome 16.
Mutation or deletion of one or more of the four alpha gene alleles causes Alpha Thalassemia.
In Beta Thalassemia, production of beta globin chain is affected.
It is controlled by a single gene (HBB) on chromosome
P.Senguttuvan. M.Sc., M.Ed.,M.Phil. & C.Valarmathi. M.Sc., M.Ed.,M.Phil. TNHSPGTA.–Dharmapuri. Page 21
7. Phenylketonuria :-
It is an inborn error of Phenylalanine metabolism caused due to a pair of autosomal recessive genes.
It is caused due to mutation in the gene PAH located on chromosome12.
This enzyme is essential for the conversion of phenylalanine to tyrosine.
Lacks this enzyme, so phenylalanine accumulates and gets converted to phenylpyruvic acid .
It is characterized by severe mental retardation, light pigmentation of skin and hair. Phenylpyruvic acid is
excreted in the urine.
8. Albinism :-
o It is an inborn error of metabolism, caused due to an autosomal recessive gene.
o Melanin pigment is responsible for skin colour. Absence of melanin results in a condition called albinism.
o A person with the recessive allele lacks the tyrosinase enzyme system, which is required for the
conversion of dihydroxyphenyl alanine (DOPA) into melanin pigment inside the melanocytes.
o In an albino peoples have lack of melanin pigments in their skin, hair, iris, etc.
-: GOD GRACE :-
16) Name the parts marked „A‟ and „B‟ in the given transcription unit :-
A - Promoter
B - Coding strand
19) Mention any two ways in which single nucleotide polymorphism (SNPs) identified in human genome can
bring revolutionary change in biological and medical science.?
Scientists have identified about 1.4 million locations where single base DNA differences
(SNPs – Single nucleotide polymorphism – pronounce as „snips‟) occur in humans.
Identification of „SNIPS‟ is helpful in finding chromosomal locations for disease associated sequences
and tracing human history.
21) In E.coli, three enzymes β- galactosidase, permease and transacetylase are produced in the presence of lactose.
Explain why the enzymes are not synthesized in the absence of lactose.
A repressor protein binds to the operator region of the operon and prevents translation, as a result,
β-galactosidase is not produced.
In the absence of preferred carbon source such as glucose, if lactose is available as an energy source for
the bacteria then lactose enters the cell as a result of permease enzyme.
Lactose acts as an inducer and interacts with the repressor to inactivate it.
The repressor protein binds to the operator of the operon and prevents RNA polymerase from
transcribing the operon.
In the presence of inducer, such as lactose or allolactose, the repressor is inactivated by interaction
with the inducer.
This allows RNA polymerase to bind to the promotor site and transcribe the operon to produce lac
mRNA which enables formation of all the required enzymes needed for lactose metabolism.
23) A low level of expression of lac operon occurs at all the windows for treatment of various genetic disorders.
Justify the statement. ?
Lactose present in the external medium can enter the bacterium only when the bacterium contain the
enzyme permease.
So, formation of permease require a low level expression of lac – operon.
25) From their examination of the structure of DNA, What did Watson and Crick infer about the probable
mechanism of DNA replication, coding capability and mutation?
Semi-conservative replication was proposed by Watson and Crick in 1953.
This mechanism of replication is based on the DNA model.
They suggested that the two polynucleotide strands of DNA molecule unwind and start separating at one
end. During this process, covalent hydrogen bonds are broken.
The separated single strand then acts as template for the synthesis of a new strand.
Subsequently, each daughter double helix carries one polynucleotide strand from the parent molecule that
acts as a template and the other strand is newly synthesised and complementary to the parent strand.
27) What are the three structural differences between RNA and DNA ?
no DNA RNA
1. It is double stranded It is single stranded
2. Deoxy ribose sugar is present Ribose sugar is present
3. Adenine, guanine, cytosine and thyamine Adenine, guanine, cytosine & Uracil
4. Chemically & Structurally less stable Chemically & Structurally more stable
DNA REPLICATION
c) Write the source of energy for this replication and name the enzyme involved in this process.
Deoxy nucleotide triphosphate acts as substrate and also provides energy for polymerization reaction.
DNA helicase, DNA ligase, DNA polymerase – these enzymes are involved in this process.
d) Mention the differences in the synthesis of protein, based on the polarity of the two template strands.
1. If both the strands act as a template, they would code for RNA with different sequences. This in turn would
code for proteins with different amino acid sequences. This would result in one segment of DNA coding for
two different proteins, hence complicate the genetic information transfer machinery.
2. If two RNA molecules were produced simultaneously, double stranded RNA complementary to each other
would be formed. This would prevent RNA from being translated into proteins.
1. Transcription - It is the process of copying genetic information from one strand of DNA into RNA .
This process takes place in presence of DNA dependent RNA polymerase.
2. Translation – transcribed mRNA canbe translated into Proteins.
6. What is operon?
Operon is defined as a cluster of genes with related functions
5. Wobble Hypothesis :-
It is a hypothesis proposed by Crick (1966) which states that tRNA
anticodon has the ability to wobble at its 5‟ end by pairing with even
non-complementary base of mRNA codon.
According to this hypothesis, in codon-anticodon pairing the third base
may not be complementary.
The third base of the codon is called wobble base and this position is
called wobble position.
The number of tRNAs required for a polypeptide synthesis.
In the above example though the codon and the anti codon do not match perfectly, yet the required amino acid
is brought perfectly.
This enables the economy of tRNA, GUU, GUC, GUA and GUG code for the amino acid - Valine.
7. What are Operons ? How many operon groups are present in E.coli ? ( March -2020)
The clusters of gene with related functions are called operons.
75 different operons present in E.coli.
-: GOD GRACE :-
************************************************************************************
15) List out the major gases seems to be found in the primitive earth.
Ammonia, methane, hydrogen and water vapour.
The atmosphere was oxygen free and the combination of CO2, NH3 .
2. Petrification
When the animal die the original parts of their body may be replaced molecule minerals and the orginal
substance being lost through disintegration.This method of fossilization is called petrifaction.
The principle minerals involved in this type fossilization are iron pyries, silica, calcium carbonate and
bicarbonates of calcium and magnesium.
18. How does Hardy-Weinberg‟s expression (p2+2pq+q2=1) explain that genetic equilibrium is maintained in a
population? List any four factors that can disturb the genetic equilibrium.
The allele frequencies in a population are stable and are constant from generation to generation in the
absence of gene flow, genetic drift, mutation recombination and natural selection.
Evolution is a change in the allele frequencies in a population over time. Hence population in hardy
Weinberg is not evolving
Explain the equilibrium :-
A large population of beetles appear in two colours dark grey(black) and light grey and their colour is
determined by „A‟ gene „AA‟ and „Aa‟ beetles are light grey.
„A‟ allele has frequency (P) of 0.3 and „a‟ allele has a frequency (q) of 0.7 Then p + q = 1
If a population is in hardy Weinberg equilibrium, the genotype frequency can be estimated by hardy wein
berg equation
(P + q)2 = P2 + 2 pq + q2 (P=0.3, q = 0.7)
P2 = (0.3)2= 0.09 = 9% AA
2pq = 2 (0.3) (0.7)= 0.42 = 42% Aa
q2 = (0.7)2 = 0.49 = 49% aa
Hence the beetle population appears to be in Hardy Weinberg equilibrium,. Factors effecting the Hardy
Weinberg law : 1).Gene flow. 2).Mutation. 3).Crossing over. and 4). Natural selection.
19. Explain how mutations, natural selection and genetic drift affect Hardy Weinberg equilibrium.
1) No mutation – No new alleles are generated by mutation nor the genes get duplicated or deleted.
2) Random mating – Every organism gets a chance to mate and the mating is random with each other with
no preferences for a particular genotype.
3) No gene flow - Neither individuals nor their gametes enter or exit the population.
4) Very large population size - The population should be infinite in size.
5) No natural selection- All alleles are fit to survive and reproduce.
6) If any one of these assumptions were not met, the population will not be in Hardy- Weinberg equilibrium.
7) Only if the allele frequencies changes from one generation to the other, evolution will take place.
22. Taking the example of Peppered moth, explain the action of natural selection. What do you call the above
phenomenon?
Industrial melanism is a classical case of Natural selection exhibited by the moth, Biston betularia.
These were available in two colours, white and black.
Before industrialization peppered moth both white and black coloured were common in England.
Pre-industrialization witnessed white coloured background of the wall of the buildings hence the
white coloured moths escaped from their predators.
Post industrialization, the tree trunks became dark due to smoke and soot let out from the industries.
The black moths camouflaged on the dark bark of the trees and the white moths were easily identified
by their predators.
Hence the dark coloured moth population was selected and their number increased when compared
to the white moths.
Nature offered positive selection pressure to the black coloured moths.
Organisms that can adapt will survive and produce more progenies resulting in increase in population
through natural selection.
23. Darwin's finches and Australian marsupials are suitable examples of adaptive radiation – Justify the statement.
1. Darwin finches :-
Their common ancestor arrived on the Galapagos about 2 million
years ago.
During that time, Darwin's finches have evolved into 14 recognized
species differing in body size, beak shape and feeding behavior.
Changes in the size and form of the beak have enabled different
species to utilize different food resources such as insects, seeds,
nectar from cactus flowers and blood from iguanas, all driven by
Natural selection.
Genetic variation in the ALX1 gene in the DNA of Darwin finches
is associated with variation in the beak shape.
2. Marsupials :-
Marsupials in Australia and placental mammals in North America are separated from the common ancestor
more than 100 million year ago and each lineage continued to evolve independently.
Despite temporal and geographical separation, marsupials in Australia and placental mammals in North
America have produced varieties of species living in similar habitats with similar ways of life.
Their overall resemblance in shape, locomotory mode, feeding and foraging are superimposed upon different
modes of reproduction.
This feature reflects their distinctive evolutionary relationships.
Over 200 species of marsupials live in Australia along with many fewer species of placental mammals. Just
as the placental mammals have radiated across North America.
25. How does Mutation theory of De Vries differ from Lamarck and Darwin‟s view in the origin of new species.
Hugo de Vries proposed by Mutation theory are “ sudden random changes that occur in an organism that is
not heritable”.
His experiments in the Evening Primrose(O. lamarckiana)and observed variations in them due to mutation.
According to de Vries, sudden and large variations were responsible for the origin of new species.
Whereas Lamarck and Darwin believed in gradual accumulation of all variations as the causative factors in
the origin of new species.
ADDITIONAL QUESTIONS
3. Gene flow:-
Movement of genes through gamets or movements of individuals in and out of a population is referred to as
gene flow.
4. Mutation :-
Mutation is the original source of all genetic variation. Mutation rare for most organisms is low.
Hence new mutations on an allele frequencies from one generation to the next is usually not large.
6. Connecting link
The organisms which possess the characters of two different groups are called connecting links.
Example 1. Peripatus (Annelida and Arthropoda), 2. Archeopteryx (Reptiles and Aves).
-: GOD GRACE :-