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BIOLOGY
BOTANY
Content Creation
The wise
possess all
II
BIOLOGY: BOTANY
Annexure
References 220
English – Tamil Terminology 222
Competitive Examination Questions 225
Botany Practicals 239
III
Competitive
Model questions to face various competitive exams
Exam questions
IV
Specializations available for botany are: Plant biochemist: Biochemists study the
chemical and physical principles of living
Cytology Genetics
things and of biological processes, such as cell
Lichenology Economic botany
development, growth, heredity, and disease.
Palynology Palaeobotany
Bryology Ethnobotany Molecular biologist: Molecular biologists
conduct research and academic activities.
Phycology Phytochemistry
The research component involves the study
Forestry Plant morphology
of biological structures in well-equipped
Phytopathology Plant anatomy
laboratories with advanced technology to help
Plant physiology Plant genetics them explore complex molecular structures
Agronomy Horticulture and their particular functions. The equipment
Plant ecology Plant systematic may include microscopes, lab centrifuges,
computers with specific software that allows
Veterinary Science
them to analyze obtained data, and many more.
Bachelor of Veterinary Science or B.V.Sc. is an
undergraduate program in veterinary
VI
Epiphyllous
young plant buds
growing from roots (f) Reproduction
by leaf
Bryophyllum
Node
Internode
(g) Runner
Centella asiatica
Runner
(b) Rhizome – Zingiber officinale
Terminal bud
(Daughter plant)
Root
Stolon
(c) Corm – Colocasia (h) Stolon
Fragaria
Offset
Naked scale
leaves
Bulbil
Stock Stock
Stock Scion
(ii) Approach (iii) Tongue
(i) Bud grafting (iv) Crown grafting (v) Wedge grafting
grafting grafting
a) Types of Grafting
Figure 1.2(a): Artificial methods of vegetative reproduction in plants
i. Bud grafting: A T- shaped incision is made c. Layering: In this method, the stem of
in the stock and the bark is lifted. The scion bud a parent plant is allowed to develop roots
with little wood is placed in the incision beneath while still intact. When the root develops,
the bark and properly bandaged with a tape. the rooted part is cut and planted to grow as
a new plant. Examples: Ixora and Jasminum.
ii. Approach grafting: In this method both
Mound layering and Air layering are few types
the scion and stock remain rooted. The stock
of layering (Figure 1.2 b).
is grown in a pot and it is brought close to
the scion. Both of them should have the same i. Mound layering: This method is applied for
thickness. A small slice is cut from both and the the plants having flexible branches. The lower
cut surfaces are brought near and tied together branch with leaves is bent to the ground and
and held by a tape. After 1-4 weeks the tip of part of the stem is buried in the soil and tip of
the stock and base of the scion are cut off and the branch is exposed above the soil. After the
detached and grown in a separate pot. roots emerge from the part of the stem buried
in the soil, a cut is made in parent plant so that
iii. Tongue grafting
the buried part grow into a new plant.
A scion and stock having the same thickness is
cut obliquely and the scion is fit into the stock
and bound with a tape.
iv. Crown grafting.
When the stock is large in size scions are cut
(i) Mound layering
into wedge shape and are inserted on the slits
or clefts of the stock and fixed in position
using graft wax.
v. Wedge grafting
In this method a slit is made in the stock or the Polythene
Bark tissue Moist soil
bark is cut. A twig of scion is inserted and tightly removed tied to retain
bound so that the cambium of the two is joined. moisture
(ii) Air layering
(a) Anther primordium (b) Differentiation of (c) Formation of parietal and (d) Formation of wall layers
archesporial cell sporogenous cell
Epidermis
Epidermis Endothecium
Middle layers Middle layer
Tapetum Tapetum
Sporogenous cell Microspores
Pollen tetrad
Stomium
Connective
(e) Sporogenous stage (f) Pollen tetrad stage (g) Microspore stage
Connective
Epidermis
Endothecium Activity
Middle layer
Pollen grain Collect buds and opened flowers of Datura
Stomium metel. Dissect the stamens, separate the
anthers and take thin transverse sections and
observe the structure under the microscope.
Record the various stages of anther
development from your observations.
(h) Pollen grain stage
(a) Orthotropous (b) Anatropous (c) Hemianatropous (d) Campylotropous (e) Amphitropous (f) Circinotropous
Figure 1.8 Types of ovule
Archesporial cell
Synergid
Egg
polar nucleus
Antipodal
Nucellus
Megaspore Functional 2-nucleate stage
megaspore 4-nucleate stage 8-nucleate stage
mother cell
Contrivances of cross-pollination
The flowers of the plants have also several
mechanisms that promote cross-pollination
which are also called contrivances of cross-
pollination or outbreeding devices. It
includes the following.
1. Dicliny or Unisexuality
Chasmogamous flower
When the flowers are unisexual only cross-
pollination is possible. There are two types.
i. Monoecious: Male and female flowers
on the same plant. Coconut, Bitter gourd.
Cleistogamous flower
In plants like castor and maize, autogamy is
prevented but geitonogamy takes place.
Figure 1.11 Commelina with Cleistogamous
Figure 2.8 Commelina with cleistogamous and chasmogamous flower ii. Dioecious : Male and female flowers on
and Chasmogamous flowers different plants. Borassus, Carica papaya
and date palm. Here both autogamy and
2. Homogamy: When the stamens and
geitonogamy are prevented.
stigma of a flower mature at the same time
it is said to be homogamy. It favours self- 2. Monocliny or Bisexuality
pollination to occur. Example: Mirabilis jalapa, Flowers are bisexual and the special adaptation
Catharanthus roseus of the flowers prevents self-pollination.
3. Incomplete dichogamy: In dichogamous i. Dichogamy: In bisexual flowers anthers
flowers the stamen and stigma of a flower and stigmas mature at different times, thus
mature at different time. Sometimes , the time of checking self-pollination. It is of two types.
maturation of these essential organs overlap so a. Protandry: The stamens mature earlier
that it becomes favourable for self-pollination. than the stigmas of the flowers. Examples:
B. Cross - pollination Helianthus, Clerodendrum (Figure 1.12 a).
It refers to the transfer of pollens on the stigma b. Protogyny: The stigmas mature earlier than
of another flower. The cross-pollination is of the stamens of the flower. Examples: Scrophularia
two types: nodosa and Aristolochia bracteata (Figure 1.12 b).
Stigma
Style Stamens Long style Short style
Style
a) Distyly - Primula
i) Pin-eyed flower ii) Thrum-eyed flower
Self-Pollination Cross-Pollination
(Autogamy) (Xenogamy or Allogamy)
Abiotic Agencies
1. Anemophily (Wind) Biotic Agencies
2. Hydrophily (Water)
• Flowers are brightly coloured. The adjacent by pushing its head into the corolla. During
parts of the flowers may also be brightly the entry of the bee into the flower the body
coloured to attract insect. For example strikes against the sterile end of the connective.
in Poinsettia and Bougainvillea the bracts This makes the fertile part of the stamen to
become coloured. descend and strike at the back of the bee.
• Flowers are scented and produce nectar. The pollen gets deposited on the back of the
bee. When it visits another flower, the pollen
• Flowers in which there is no secretion of
RECURRENTgets rubbed against the stigma and completes
nectar, the pollen is either consumed as
APOMIXISthe act of pollination in Salvia (Figure 1.17).
food or used in building up of its hive by the
honeybees. Pollen and nectar are the floral
Pistil
rewards for the visitors. Anther Pollen gets dusted
on the body of
the insect
• Flowers pollinated byVegetative flies and beetles
Agamospermy
produce foul odour toreproduction
attract pollinators.
(i) (ii)
Antipodal (n)
Secondary
nucleus (2n)
Vegetative
Egg (n)
tube nucleus (n)
Embryo
Petal
Stigma
Style
Shrivelling
petal & sepal
Ovary
Ovule
Fruit
Sepal
Seed
Seed
Plumule
Cotyledon
Testa
Radicle
More to Know
• The calyx may persist and • The funiculus develops Ricinus - Caruncle
enlarge (Solanum melongena) into a fleshy structure
or may cover the fruit which is often very colourful and called aril.
(Physalis minima) (Myristica and Pithecellobium)
Physalis - Persistent calyx
• The flower stalk or axis
below the gynoecium
enlarges into a juicy pear Aril
shaped body which is edible
Myristica Pithecellobium
(Anacardium occidentale).
The Perianth becomes • The nucellar tissue is either absorbed completely
Anacardium -
fleshy as in Jack fruit. pedicel (edible) by the developing embryo sac and embryo or
small portion may remain as storage tissue. Thus
• The cells present at the tip of the outer
the remnant of nucellar tissue in the seed is called
integument around the micropyle develop
perisperm. Example: Black pepper and beet root
Embryonal mass
Hypophysis
Terminal cell
Suspensor
Basal cell
Cotyledon
Plumule
Embryonal mass
Hypophysis
Hypophysis Cotyledons
Radicle
Suspensor Radicle
Root cap
Suspensor Root cap
(f) Heart shaped embryo (g) Mature embryo (h) Mature embryo in a seed
Testa Radicle
Root cap
Coleorhiza
Seed entire
L.s. of fruit
Plumule
Cotyledon
Figure
b) 1.23(b)
Monocot Monocot seed
seed (Oryza - Oryza sativa
sativa)
A short Figure
axis with
2.25plumule
Structureand radicle protected
of seed
Testa
by the root cap is present. The plumule is
Radicle surrounded by a protective sheath called
Seed cut opened
coleoptile. The radicle including root cap
Figure 1.23(a) Dicot
a) Dicot seed seed - Cicer arientinum
(Cicer arientinum)
is also covered by a protective sheath called
26 Asexual and Sexual Reproduction in Plants
Fruit (Caryopsis) entire
Flower
Microspore
mother cell
Anther
is
os
ei
M
Megaspore Megaspore
mother cell Pollen (n)
(n)
Sporophyte (2n)
Embyo sac
Embryo (2n)
Endosperm Endosperm
(3n) nucleus (3n) Syngamy
Zygote
Double fertilization
(2n)
Glossary
Apospory: The process of embryo sac formation
from diploid cells of nucellus as a result of
mitosis
2 Classical Genetics
Classical Genetics 33
34 Classical Genetics
•
The pairs of contrasting characters which 3LVWLO 3ROOHQRIZKLWH
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Classical Genetics 35
6HHG
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knowledge of cellular mechanism, DNA, genes,
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and meticulous work into the mechanism of
Figure 2.4: Mendel’s seven characters in Garden
inheritance played an important role which led
Peas, shown on the plant’s seven chromosomes
36 Classical Genetics
Classical Genetics 37
t tall plant
t 2. 3.2 Test cross
(TT)
Heterozygous Heterozygous Test cross is crossing an individual of unknown
tall plant tall plant genotype with a homozygous recessive.
(Tt) (Tt)
Homozygous In Mendel’s monohybrid cross all the plants
dwarf plant
(tt)
are tall in F1 generation. In F2 tall and dwarf
Offspring (F2)
plants were in the ratio of 3:1.Mendel self
genotypes TT Tt tt pollinated dwarf F2 plants and got dwarf plants
in F3 and F4 generations. So he concluded that
Genotypic Ratio 1 : 2 : 1
the genotype of dwarf was homozygous (tt). The
Phenotypes Tall Dwarf genotypes of tall plants TT or Tt from F1and F2
Phenotypic Ratio 3 : 1 cannot be predicted. But how we can tell if a
tall plant is homozygous or heterozygous? To
Figure 2.6: Monohybrid Cross determine the genotype of a tall plant Mendel
The gene for plant height has two alleles: Tall crossed the plants from F2 with the homozygous
(T) x Dwarf (t). The phenotypic and genotypic recessive dwarf plant. This he called a test
analysis of the crosses has been shown by cross. The progenies of the test cross can be
easily analysed to predict the genotype of the
Checker board method or by Forkline method.
plant or the test organism. Thus in a typical
2.3.1 Mendel’s analytical and empirical test cross an organism (pea plants) showing
approach dominant phenotype (whose genotype is to be
Mendel chose two contrasting traits for each determined) is crossed with the recessive parent
character. So it seemed logical that two distinct instead of self crossing. Test cross is used to
identify whether an individual is homozygous
factors exist. In F1 the recessive trait and its
or heterozygous for dominant character.
factors do not disappear and they are hidden
38 Classical Genetics
Gametes T T t t
Tall pea plants Dwarf pea plant
Offspring (F1)
Tt Tt (Le Le / Le le) (le le)
genotypes
Gibberellin GA1 Gibberellin Gibberellins
Phenotypes Tall Tall
Active are not
All tall plants Precursor Precursor produced
molecule gibberellins molecule
T t
Le allele codes for le allele codes for
gametes Heterozygous gametes
functional enzyme GA1 nonfunctional enzyme
tall plant
T (Tt)
t Figure 2.8: Gene for plant height in Peas
Heterozygous
Heterozygous
tall plant 2.3.3 Back cross
tall plant
(Tt)
(Tt)
• Back cross is a cross of F1 hybrid with any
Heterozygous
tall plant
one of the parental genotypes. The back
(Tt) cross is of two types; they are dominant
back cross and recessive back cross.
Figure 2.7: Test cross • It involves the cross between the F1 offspring
with either of the two parents.
Classical Genetics 39
40 Classical Genetics
Haploid
F1 gametes
RY Ry rY ry RY Ry rY ry Round Peas & Wrinkled Peas
F1 gametes RR rr
1/4 1/4 1/4 1/4 Dominant allele RR Active enzyme SBE - I
F2 Generation RY Ry rY ry Linear
Branched
unbranched Round
1/4
starch
starch Converted peas
amylopectin
RY RR YY RR Yy Rr YY Rr Yy amylose to
1/4
Recessive allele rr Inactive enzyme
F1 RR Yy RR yy Rr Yy Rr yy
Ry
gametes Linear Linear
1/4
unbranched unbranched
No Wrinkled
Rr YY Rr Yy rr YY rr Yy starch starch peas
rY conversion
amylose amylose
1/4
ry
Rr Yy Rr yy rr Yy rr yy
Figure 2.11: Molecular explanation of
Phenotypic Ratio 9:3:3:1
round and wrinkled peas.
Figure 2.10: Dihybrid Cross in Garden peas
Classical Genetics 41
42 Classical Genetics
Classical Genetics 43
44 Classical Genetics
Classical Genetics 45
46 Classical Genetics
Classical Genetics 47
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F1 Dark Green F1 Pale Green Figure 2.21: A cellular explanation of the variegated
leaved leaved
phenotype of the leaves in Mirabilis jalapa
Figure 2.19: Chloroplast inheritance
48 Classical Genetics
Classical Genetics 49
50 Classical Genetics
Classical Genetics 51
52 Classical Genetics
3 Chromosomal Basis of
Inheritance
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RF =
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4
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A B A B Its importance is
A B a b
�
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a b A B
a b A b
frequency of crossing over.
a b a B � Crossing over helps to understand the
nature and mechanism of gene action.
2
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X100 = 50% � If a useful new combination is formed it
Four strand double cross over can be used in plant breeding.
A B a B
A B
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a B
a b A b
Crossing over results in the formation of new
a b A b combination of characters in an organism
4
called recombinants. In this, segments of DNA
RF = X100 = 100%
4 are broken and recombined to produce new
Figure 3.11: T
ypes of crossing over and its combinations of alleles. This process is called
Recombination Frequency (RF) Recombination. (Figure 3.12)
Heteroduplex region
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Ploidy
Aneuploidy Euploidy
Hyperploidy Hypoploidy
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Example: 2 Triticale, the successful first man When two plants (A and B) belonging to the
made cereal. Depending on the ploidy level same genus but different species are crossed,
Triticale can be divided into three main groups. the F1 hybrid is viable and has more ornate
flowers. Unfortunately, this hybrid is sterile
(i).
Tetraploidy: Crosses between diploid and can only be propagated by vegetative
wheat and rye. cuttings. Explain the sterility of the hybrid
(ii). Hexaploidy: Crosses between tetraploid wheat and what would have to occur for the sterility
Triticum durum (macaroni wheat) and rye of this hybrid to be reversed.
A Duplications
B A A A A A
B
B B B B
C Deletion of Deletion of B
segment C segment C C C C
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From the above figure identify the type of Self incompatibility: A genetic mechanism
mutation and explain it. which prevent self fertilization thus encourage
outcross.
18. Write the salient features of Sutton and
Boveri concept. Synapsis: The pairing of two homologous
19. Explain the mechanism of crossing over. chromosomes that occurs during meiosis.
Glossary
Branch Migration: The process in which base
pairs on homologous strands are consequently
exchanged at a Holliday junction, moving the
branch up or down the DNA sequence.
Biotechnology is the
Learning Objectives science of applied
biological process. In
The learner will be able to other words it is science
Apply the knowledge of traditional of development and
and modern biotechnology in day to utilization of biological
day life. processes, forms and
Appreciate the uses of fermentation systems for the benefit of Karl Ereky
process. mankind and other life
Acquire the knowledge on the process forms. The term biotechnology was coined
of genetic engineering by Karl Ereky, a Hungarian Engineer in 1919.
Biotechnology has been extended to include
Analyse the uses
any process in which organisms, tissues,
and limitations of
cells, organelles or isolated molecules such as
genetically modified
enzymes are used to convert biological or other
plants
raw materials to products of greater value.
Cognize the terms
of bio prospecting 4.1 Development of Biotechnology
and bio piracy. Biotechnology has developed by leaps
and bounds during the past century. The
Chapter outline development of the biotechnology can be well
understood under two main heads namely
conventional or traditional biotechnology
4.1 Development of Biotechnology
and modern biotechnology
4.2 Historical Perspective
1. Conventional or traditional
4.3 Traditional Biotechnology biotechnology: This is the kitchen technology
4.4 Advancements in Modern developed by our ancestors, it is as old as
Biotechnology human civilization. This technology uses
4.5 Tools for Genetic Engineering bacteria and other microbes in the daily usage
4.6 Methods of Gene transfer for preparation of dairy products like curd,
ghee, cheese and in preparation of foods
4.7 Screening for Recombiants
like idli, dosa, nan, bread and pizza. This
4.8 Transgenic Plants / Genetically conventional biotechnology also extends to
Modified Crops preparation of alcoholic beverages like beer,
4.9 Applications of Biotechnology. wine, etc.
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binding site
translated.
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repressor that
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replication from a phage. pBluescript SK (+/–) is an example
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7HORPHUH 7HORPHUH
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KLV
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Endocytosis endosome DNA-coated
gold particles
Lipoplex
DNA
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lipid mixing by screen
DNA-pcoated
Lipoplex Endosomal gold particles
Endosome maturation
DNA
DNA
Liposome fragmentation
Plant cell
Ti 1 2 3 3
plasmid Recombinant
Insertion of Ti plasmid Introduction The plant cells
gene into plasmid into plant Regeneration
T DNA are grown in Plant with
using restriction cells of plant
culture new trait
Restriction enzyme and DNA ligase
cleavage site
Ori
Figure 4.18: a. Plasmid vector designed for
Sterile velvet on a block Imprints of all colonies
blue-white screening b. Blue-white colony
selection method Figure 4.19: Replica plating technique
Weight Membrane
Glass plate DNA
4.7.6 Bioassay for Target Gene Effect mitochondrial genome or plastid genome.
Target gene is target DNA, foreign DNA, Genome of many plants contain both functional
passenger DNA, exogenous DNA, gene of and non-expressive DNA proteins. Genome
interest or insert DNA that is to be either project refer to a project in which the whole
cloned or specifically mutated. Gene targeting genome of plant is analysed using sequence
experiments have been targeting the nuclei analysis and sequence homology with other
and this leads to ‘gene knock-out’. For this plants. Such genome projects have so far
purpose, two types of targeting vectors are used. been undertaken in Chlamydomonas(algae),
They are insertion vectors and replacement or Arabidopsis thaliana, rice and maize plants.
transplacement vectors. Genome content of an organism is expressed in
1. Insertion vectors are entirely inserted into terms of number of base pairs or in terms of the
targeted locus as the vectors are linearized content of DNA is expressed in c-value.
within the homology region. Initially, these
Genome sequencing: The location of genes
vectors are circular but during insertion,
on the entire diploid chromosome of an
become linear. It leads to duplication of
organism.
sequences adjacent to selectable markers.
2 The replacement vector has the homology
region and it is co-linear with target. This Barcode: You might have
vector is linearized prior to transfection seen in all books barcoding
outside the homology region and then and also in items you buy
consequently a crossing over occurs to in supermarket. This will
replace the endogenous DNA with the reveal the identity of the book or item as well
incoming DNA. the details like prize. Similarily, Barcode in
genetic term refer to the identify of the taxon
Transfection: Introduction of foreign based on its genetic makeup. In practice, it
nucleic acids into cells by non-viral methods. is an optical, machine-
readable representation
4.7.7. Genome Sequencing and Plant
of data which describes
Genome Projects
about the characters
The whole complement of gene that determine
of any plants or any
all characteristic of an organism is called
objects.
genome. The genome may be nuclear genome,
Bioleaching
• is the use of microorganisms Protien
Residue
in solution to recover metal pollutants from
contaminated sites. Sun Energy
Composting
• is the process by which the Algae
(Renewable resource)
solid waste is composted by the use of
microbes into manure which acts as a CO2
nutrient for plant growth. Glycerin
products
Rhizofiltration
• is the uptake of metals
or degradation of organic compounds by Existing Renewable
Technology Fuel
rhizosphere microorganisms.
Figure 4.31: Algal Biofuel
Rhizostimulation is the stimulation of plant
•
Biological hydrogen production by algae
growth by the rhizosphere by providing
The biological hydrogen production with
better growth condition or reduction in
algae is a method of photo biological water
toxic materials.
splitting. In normal photosynthesis the alga,
Limitations Chlamydomonas reinhardtii releases oxygen.
• Only biodegradable contaminants can When it is deprived of sulfur, it switches to the
be transformed using bioremediation production of hydrogen during photosynthesis
processes. and the electrons are transported to ferredoxins.
• Bioremediation processes must be [Fe]-hydrogenase enzymes combine them into
specifically made in accordance to the the production of hydrogen gas.
conditions at the contaminated site. CO2 Fixation H2 Production
O2 + 4H+ + 4e-
4.8.12 Biofuel: Algal Biofuel 2H2O
Algal fuel, also known as algal biofuel, or algal Figure 4.32: Hydrogen production by algae
oil is an alternative to liquid fossil fuels, the 4.8.13 Bioprospecting
petroleum products. This use algae as a source
Bioprospecting is the process of discovery and
of energy-rich oils. Also, algal fuels are an
commercialization of new products obtained
alternative to commonly known biofuel sources
obtained from corn and sugarcane. The energy from biological resources. Bioprospecting
crisis and the world food crisis have initiated may involve biopiracy, in which indigenous
interest in algal culture (farming algae) for knowledge of nature, originating with
making biodiesel and other biofuels using land indigenous people, is used by others for profit,
unsuitable for agriculture. Botryococcus braunii without authorization or compensation to the
is normally used to produce algal biofuel. indigenous people themselves.
Cleave: To break phosphodiester bonds of Taq polymerase: A heat stable DNA polymerase
dsDNA, usually with a restriction enzyme. isolated from a thermophilic bacterium Thermus
aquaticus.
Cloning site: A location on a cloning vector
into which DNA can be inserted. Vectors: Vehicles for transferring DNA from
one cell to another.
Cloning: Incorporation of a DNA molecule
into a chromosomal site or a cloning vector. Biofuel: Fuels like hydrogen, ethanol and
methanol produced from a biological source by
Cloning Vector: A small, self-replicating DNA the action of microorganisms.
inserted in a cloning gene.
Bioleaching: Process of using microorganisms
COS sites: The 12-base, single strand, to recover metals from their ores or contaminant
complementary extension of phage lambda (l) environment
DNA.
Bioremediation: Process of using organisms
DNA Polymerase: An enzyme that catalyses the to remove or reduce pollutants from the
phosphodiester bond in the formation of DNA. environment.
Endonucleases: An enzyme that catalyses the Green Technology: Pollution-free technology
cleavage of DNA at internal position, cutting in which pollution is controlled at source.
DNA at specific sites.
Phytoremediation: Use of certain plants to
Genome: The entire complement of genetic remove contaminants or pollutants from the
material of an organism. environment (soil, water or air).
Insert DNA: A DNA molecule incorporated Recombinant: Cell / Organism formed by a
into a cloning vector. recombination of genes.
Ligase: An enzyme used in genetic engineering Transformation: Process of transferring
experiment to join the cut ends of dsDNA. a foreign DNA into a cell and changing its
M-13: AssDNA bacteriophage used as vector genome.
for DNA sequencing. Vector: Agent used in recombinant DNA
Phagemid: A cloning vector that contains technique to carry new genes into foreign cells.
components derived from both phage DNA and Wild Type: Natural form of organisms.
plasmid.
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biotechstudyapp
cultured plant cells in artificial condition produced calli and free cells in tissue
called in vitro (inside glass) in culture culture of Tradescantia reflexa.
medium (Knop’s salt solution) containing
glucose and peptone and developed callus Guha and Maheshwari (1964)
(unorganized growth of cells and tissue) and
proposed the concept Totipotency, it means developed in vitro production of haploid
the development of whole plant from isolated embryos from anthers of Datura.
cells or tissue in in vitro condition.
Vasil and Hildbrandt (1965)
P.R.White (1934) achieved differentiation of tobacco
developed root cultures, used Knop’s solution plants from single, isolated cells in micro
along with three vitamins like pyridoxine, propagation.
thiamine and nicotinic acid
Takebe et al. (1971)
F.C. Steward (1948) regenerated tobacco plants from isolated
used coconut water in plant tissue culture mesophyll protoplasts.
work and obtained cell proliferation from
carrot explants (Cellular totipotency ). Carlson
and co-workers obtained protoplast fusion
Morel and Martin (1952, 1955)
between Nicotiana glauca and Nicotiana
developed virus-free Dahlia and potato longsdorffii and developed first interspecific
plants using shoot meristem culture. somatic hybrid in 1971.
Knop’s solution: Nutrient solution used in growth experiments of plants which contains:
Calcium nitrate 3.0 g Potassium nitrate 1.0 g Sucrose 50.0 g (optimal)
Magnesium sulfate 1.0 g Dibasic Potassium phosphate 1.0 g Deionized water 1000.0 ml
Explant
5.3.1 Laboratory Facilities for PTC
For PTC, the laboratory must have the following
facilities:
Explant in
Nutrient medium
Callus
Plantlet
Early
Late
Embryo
Embryo
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The culture of any plant meristematic tissue on ii. Fusion of protoplast: It is done through the
culture media. use of a suitable fusogen. This is normally PEG
(Polyethylene Glycol). The isolated protoplast
are incubated in 25 to 30% concentration of
PEG with Ca++ ions and the protoplast shows
agglutination (the formation of clumps of cells)
and fusion.
<RXQJSODQW
(SLGHUPLV Production of Secondary
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Biosynthesis and isolation of indole
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plant cell culture.
Figure 5.8: Protoplast Culture The process of production
of secondary metabolites can be
iii. Culture of protoplast: MS liquid medium is
scaled up and automated using bio-reactors
used with some modification in droplet, plating
for commercial production. Many strategies
or micro-drop array techniques. Protoplast
such as biotransformation, elicitation and
viability is tested with fluorescein diacetate immobilization have been used to make cell
before the culture. The cultures are incubated in suspension cultures more efficient in the
continuous light 1000-2000 lux at 25°C. The cell production of secondary metabolites. Few
wall formation occurs within 24-48 hours and examples of industrially important plant
the first division of new cells occurs between secondary metabolites are listed below in the
2-7 days of culture. table:
iv. Selection of somatic hybrid cells: The Secondary Plant source Uses
fusion product of protoplasts without nucleus of metabolites
different cells is called a cybrid. Following this Digoxin Digitalis purpuria Cardiac tonic
Codeine Papaver sominiferum Analgesic
nuclear fusion happen. This process is called
Capsaicin Capsicum annum Rheumatic
somatic hybridization. pain
4. Cell Suspension Culture treatment
Vincristine Catharanthus roseus Anti-
The growing of cells including the culture carcinogenic
of single cells or small aggregates of cells Quinine Cinchona officinalis Antimalarial
in vitro in liquid medium is known as cell Table 5.1: Secondary metabolites
suspension culture. The cell suspension is and its plant resources
prepared by transferring a portion of callus to
c) capacity to generate hybrid protoplasts. a) Agar is not extracted from marine algae
d) recovery of healthy plants from diseased such as seaweeds.
plants. b) Callus undergoes differentiation and
2. Micro propagation involves produces somatic embryoids.
a)
vegetative multiplication of plants by c) Surface sterilization of explants is done
using micro-organisms. by using mercuric bromide
d) PH of the culture medium is 5.0 to 6.0
b)
vegetative multiplication of plants by
6. Select the incorrect statement from given
using small explants. statement
c)
vegetative multiplication of plants by a) A tonic used for cardiac arrest is obtained
using microspores. from Digitalis purpuria
d) Non-vegetative multiplication of plants b) Medicine used to treat Rheumatic pain
by using microspores and megaspores. is extracted from Capsicum annum
8QGLIIHUHQWLDWHG
Organogenesis: The process of initiation and
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development of shoot or root though in vitro
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6 Principles of Ecology
nin m
n
to n
rmatio
e s
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ing
ts
od
nn
no
en
os
uc
Cl
fo
er
em
tio
n
Tuber
ov
Floweri
n
in
M
rm
Ge
ou
Tre
Co
Clouds
Figure 6.8: Latitudinal and Altitudinal Vegetation
Height above the sea level forms the
altitude. At high altitudes, the velocity of wind
remains high, temperature and air pressure
Moist
decrease while humidity and intensity of light Rain winds
increases. Due to these factors, vegetation at
tation
zonation.
hv
eg
Poor
eta
b. Direction of Mountain
t
ion
Sea
North and south faces of mountain or hill possess
different types of flora and fauna because they
differ in their humidity, rainfall, light intensity,
light duration and temperature regions. Figure 6.9: Steepness of mountain
a) b)
Marginal Stem
spines
Leaf
Succulent c d)
c) Petiole
leaves 3
2
Leaves
Scale
leaves 1
Rhizome Stipular
Roots spines
Stem 4 Phyllode
Figure 6.21: a)Succulent xerophyte – Aloe 1,2,3 and 4 the gradual development
Spine
b) Non succulent perennial - Ziziphus of phyllodes in Acacia
Palisade parenchyma
Epiphytes
Spongy parenchyma Epiphytes are plants which grow perched on
Lower epidermis other plants (Supporting plants). They use
Figure 6.24: A Succulent leaf of Pepromia (T.S.) the supporting plants only as shelter and not
(lateral wing portion only) for water or food supply. These epiphytes
21. Sticky glands of Boerhaavia and Cleome 36. List any two adaptive features evolved in
support parasites enabling them to live successfully
a) Anemochory b) Zoochory on their host?
c) Autochory d) Hydrochory 37.
Mention any two significant roles of
predation plays in nature.
22. Define ecology.
38.
How does an orchid ophrys ensures its
23.
What is ecological hierarchy? Name the pollination by bees ?
levels of ecological hierarchy.
39. Water is very essential for life. Write any
24. What are ecological equivalents? Give one three features for plants which enable them
example . to survive in water scarce environment.
25. Distinguish habitat and niche 40.
Why do submerged plants receive weak
26.
Why are some organisms called as illumination than exposed floating plants
eurythermals and some others as in a lake?
stenohaline ? 41.
What is vivipary? Name a plant group
27. ‘Green algae are not likely to be found in the which exhibits vivipary.
deepest strata of the ocean’. Give at least one
reason.
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EnvironmentalStudies
7 Ecosystem
Learning Objectives Have you seen lakes, ponds and pools in your
surroundings? They are all called water bodies
with many components in them. Can you list
Learning objectives
out the things which are found in water bodies?
The learner will be able to, Mud, nutrients, clay, dissolved gases, planktons,
Describe the Structure, functions and microorganisms, plants like algae, Hydrilla,
types of ecosystems Nelumbo, Nymphaea and animals like snake,
small fish, large fish, frog, tortoise and crane are
Draw ecological pyramids by means the components in the water bodies which are
of number, biomass and energy all together form an ecosystem. Further, we all
Interpret carbon and phosphorus know that plants and animals are prominent
cycle living components in the environment. They
interact with nonliving components such as air,
Recognise pond ecosystem as a self- water, soil, sunlight, etc. For example, you have
sufficient and self-regulating system studied in class XI, one of the life processes,
Analyse ecosystem services and its photosynthesis which utilize sunlight , water,
management carbondioxide, nutrients from the soil and
release oxygen to the atmosphere. From this, we
Discuss about the importance and
understand that the exchange of materials takes
conservation of ecosystem
place between living and nonliving components.
Explain the types of plant succession Likewise, you can study the structure, function
and types of ecosystem in this chapter. The
term ‘ecosystem’ was proposed by A.G.
Tansley (1935), who defined it as ‘the system
Chapter outline resulting from the integration of all the living
and nonliving factors of the environment’.
Whereas, Odum (1962) defined ecosystem ‘as
7.1 Structure of the structural and functional unit of ecology’.
ecosystem
7.2 Functions of Parallel terms for ecosystem coined by
ecosystem various ecologists
• Biocoenosis – Karl Mobius
7.3 Plant succession • Microcosm – S.A. Forbes
• Geobiocoenosis – V. V. Dokuchaev, G.F. Morozov
• Holocoen - Friederichs
• Biosystem – Thienemann
• Bioenert body – Vernadsky
148 Ecosystem
Ecosystem 149
150 Ecosystem
occupying the first trophic level (T1) are Figure 7.3: Diagrammatic
called producers. The energy produced by representation of energy flow
the producers is utilized by the plant eaters Laws of thermodynamics
(herbivores) they are called primary consumers
and occupies the second trophic level (T2). The storage and loss of energy in an ecosystem
is based on two basic laws of thermo-dynamics.
Fourth Trophic level (T4) Secondary
(Tertiary consumers) carnivore - Eagle i. First law of thermodynamics
Third Trophic level (T3) Primary It states that energy can be transmitted from
(Secondary consumers) carnivore - Snake
one system to another in various forms. Energy
Second Trophic level (T2)
(Primary consumers)
Herbivore - Rabbit Omnivore
- crow
cannot be destroyed or created. But it can be
First Trophic level (T1) transformed from one form to another. As
Autotrophs - Plants
(Producers) a result, the quantity of energy present in the
Figure 7.2: Diagrammatic universe is constant.
representation of trophic levels Example:
Herbivores are eaten by carnivores, which occupy In photosynthesis, the product of starch
the third trophic level (T3). They are also called (chemical energy) is formed by the combination
secondary consumers or primary carnivores. of reactants (chlorophyll, H2O, CO2). The
Carnivores are eaten by the other carnivores, energy stored in starch is acquired from the
which occupy the fourth trophic level (T4). They external sources (light energy) and so there is
are called the tertiary consumers or secondary
Ecosystem 151
152 Ecosystem
Ecosystem 153
T3 T3 T2
T2
T2 T2
T1
T1 T1
T1
A B C D
T1 - Producers | T2 - Herbivores | T3 - Secondary consumers | T4 - Tertiary consumers
Figure 7.8: Pyramids of numbers ( individuals per unit area) in different types of ecosystems.
Upright-A) Grassland ecosystem B) Pond ecosystem , Spindle shaped -C) Forest ecosystem,
Inverted-D) Parasite ecosystem
starts with a single tree. Therefore there is However, in pond ecosystem, the bottom of
gradual increase in the number of organisms the pyramid is occupied by the producers, which
in successive tropic levels from producer to comprise very small organisms possessing
tertiary consumers. the least biomass and so, the value gradually
2 Pyramid of biomass increases towards the tip of the pyramid.
Therefore, the pyramid of biomass is always
A graphical representation of the amount of inverted in shape.
organic material (biomass) present at each
successive trophic level in an ecosystem is called 3. Pyramid of energy
pyramid of biomass. A graphical representation of energy flow at
In grassland and forest ecosystems, there each successive trophic level in an ecosystem is
is a gradual decrease in biomass of organisms called pyramids of energy. The bottom of the
at successive trophic levels from producers to pyramid of energy is occupied by the producers.
top carnivores (Tertiary consumer). Therefore, There is a gradual decrease in energy transfer
these two ecosystems show pyramids as upright at successive tropic levels from producers to the
pyramids of biomass. upper levels. Therefore, the pyramid of energy is
always upright.
B T4 C T3
A T4
T2
T3
T3
T2 T2
T1
T1
T1
154 Ecosystem
Senescence
Leaching
Absorption
by plants
Mineralisation Humification
Figure 7.11: Diagrammatic representation – Process of decomposition and cycling of nutrients.
Ecosystem 155
156 Ecosystem
Fe
rti
rti
Fe
I
Mining
Phosphate PO
rocks Guano Dead Uptake the organisms and degradation
organic
PI
Death matter Soil by the action of decomposers, the
Excretion PI
Bacteria phosphorus is released back into
Decomposition
Sediments Mineralization the lithosphere and hydrosphere
Po = Organic phosphates
PI = Inorganic phosphates to maintain phosphorus cycle.
Ecosystem 157
158 Ecosystem
The varieties of benefits obtained from the ecosystem are generally categorized into the following four types
Ecosystem services
Ecosystem 159
160 Ecosystem
Adayar Poonga
Ecosystem 161
162 Ecosystem
Generally, This succession takes less time than Since, green plants dominate
the time taken for primary succession. in the beginning of this
Example: The forest destroyed by fire and succession, there is a gradual
excessive lumbering may be re-occupied by increase in organic matter
herbs over period of times. and subsequently the energy
flow in the ecosystem.
3. Autogenic succession
6. Heterotrophic succession
Autogenic succession occurs as a result of
biotic factors. The vegetation reacts with If heterotrophic organisms like bacteria, fungi,
its environment and modifies its own actinomycetes, and animals are dominant
environment causing its own replacement by during the early stages of succession it is
new communities. This is known as autogenic called heterotrophic succession. Such a
succession. succession takes place in organic habitats. Since
Example: In forest ecosystem, the larger trees heterotrophs dominate in the beginning of such
produce broader leaves providing shade to the succession, there will be a gradual decrease in
forest floor area. It affects the shrubs and herbs the energy content.
which require more light (heliophytes) but
7.3.3 Classification of plant succession
supports the shade tolerant species (sciophytes)
to grow well. Detailed study of Hydrosere and Lithosere are
discussed below:
4. Allogenic succession
Plant succession
Allogeneic succession occurs as a result of
abiotic factors. The replacement of existing Hydrosere Mesosere Xerosere
community is caused by other external factors (Succession (Succession (Succession
(soil erosion, leaching, etc.,) and not by existing starts in starts in starts in
organisms. regions where regions regions where
water is
where moisture
Example: In a forest ecosystem soil erosion plenty)
Example: moisture is present
and leaching alter the nutrient value of the soil condition in minimal
Ponds, lakes,
leading to the change of vegetation in that area. is amount with
stream ,
5. Autotrophic succession swamps adequate) water
If the autotrophic organisms like green plants are Lithosere Halosere Psammosere
dominant during the early stages of succession it (Initiating on (Initiating in (Initiating on
is called autotrophic succession, this occurs in a barren rock) saline water) a sand)
the habitat which is rich in inorganic substances.
Figure 7.20: Classification of plant succession
Ecosystem 163
Forest stage
pond, begins with colonization of the pioneers
like phytoplankton and finally ends with the
formation of climax community like forest
stage. It includes the following stages Fig 7.21.
1. Phytoplankton stage - It is the first stage
of succession consisting of the pioneer
community like blue green algae, green algae,
164 Ecosystem
166 Ecosystem
Ecosystem 167
Food chain: Refers movement of energy from Guano: It is a accumulated excrement of sea
producers up to top carnivores birds and bats.
Food web: Interlocking pattern of food chain Phosphorus cycle: Circulation of Phosphorus
among organisms and environments
Pyramid of number: Refers number of
organisms in a successive trophic level Succession: Successive replacement of one type
of plant communities by other on barren or
Pyramid of biomass: Refers to quantitative
disturbed area.
relationship of the standing crops
Pioneers: Invaded plants on barren area
Pyramid of energy: Refers transformation of
energy at successive trophic levels Primary succession: Plants colonising on
barren area
Ten per cent law: refers only 10 per cent of
energy is stored in each successive trophic levels Secondary succession: Plants colonising on
disturbed area.
Bio geo chemical cycle: Exchange of nutrients
between organisms and environments Climax communities: Final establishment of
plant communities which are not replaced by
Carbon cycle: Circulation of carbon among
others.
ICT Corner
ECO SYSTEM
Let us know about the
Ecosystem in detail through
this activity.
Steps
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Introduction page will open.
• Click on the Learn icon in the introduction page to know in detail.
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• Click on the Test icon to write a quiz test finally it displays the marks we scored.
168 Ecosystem
8 Environmental Issues
169
Environmental Issues
• Natural from organic matter, volcanoes, Just above the atmosphere there are two
warm oceans and sediments. layers namely troposphere (the lower layer)
and stratosphere (the upper layer). The ozone
Methane
layer of the troposphere is called bad ozone
Methane is 20 times as effective as CO2 at and the ozone layer of stratosphere is known as
trapping heat in the atomosphere. Its sources good ozone because this layer acts as a shield
are attributed paddy cultivation, cattle rearing, for absorbing the UV radiations coming from
bacteria in water bodies, fossil fuel production, the sun which is harmful for living organisms
ocean, non-wetland soils and forest / wild fires.
N2O (Nitrous oxide)
Ozone is a colourless gas, reacts readily with
It is naturally produced in Oceans from biological air pollutants and cause rubber to crack, hurt
sources of soil and water due to microbial actions plant life, damages lung tissues. But ozone
and rainforests. Man-made sources include nylon absorbs harmful ultra violet β (uv-β) and UV –
and nitric acid production, use of fertilizers in α radiation from sunlight.
agriculture, manures cars with catalytic converter
What is Dobson Unit? DU is the unit of
and burning of organic matter.
measurement for total ozone. One DU (0.001
Global Warming Effects on Plants atm. cm) is the number of molecules of ozone
• Low agricultural productivity in tropics that would be required to create a layer of pure
• Frequent heat waves (Weeds, pests, fungi ozone 0.01 millimetre thick at a temperature of
need warmer temperature) 0° C and a pressure of 1 atmosphere (atm = the
• Increase of vectors and epidemics air pressure at the surface of earth). Total ozone
• Strong storms and intense flood damage layer over the earth surface is 0.3 centrimetres
• Water crisis and decreased irrigation (3 mm) thick and is written as 300 DU.
• Change in flowering seasons and pollinators The false colour
• Change in Species distributional ranges view of total ozone
• Species extinction - The purple and
blue colours are
8.1.3 Strategies to deal with Global
Warming where there is the
• Increasing the vegetation cover, grow more least ozone, and the
trees yellows and reds are
• Reducing the use of fossil fuels and green where there is more
Figure 8.3: The false
house gases ozone.
colour view of total ozone
171
Environmental Issues
173
Environmental Issues
175
Environmental Issues
Bio-diversity Conservation
In-situ Ex-situ
Sacred groves
Biosphere Wildlife
Sacred lakes National parks
Reserves Sanctuaries
Terrestial Marine
Figure 8.6: Flow chart on biodiversity conservation
177
Environmental Issues
179
Environmental Issues
181
Environmental Issues
183
Environmental Issues
ICT Corner
Environmental Issues
Steps
• Type the URL or scan the QR code to open the activity page.
• Click on the satellite it displays the shape and activities of the satellite.
• Click on the Vital Signs to see the global Climate data including surface air
temperature, Carbondioxide, Ozone, etc.,
URL:
https://play.google.com/store/apps/details?id=gov.nasa.jpl.earthnow.activity
9 Plant Breeding
es ta
in centre of crop plant means the
rsi
Babylon
B abylon
on places of agricultural origin
Mediter Syrian Desert SUMER of the crop plants. The non-
ranean sea Palestine Jordan
J dan R
Jord
centre denotes the place where
Jerusalem Dead
Sea Arabian Desert Gulf agriculture of the crop was
Isreal
Sakara
Nile
Red
ed
d Sea with each other.
Figure 9.1: Map shows Fertile crescent region
5
3
1
a. D
r. M. S. Swaminathan – He is pioneer
4
7 2
mutation breeder.
6 2a
8
8b b. S
ir. T.S. Venkataraman – An eminent
8a
Vavilov’s Centers of Crop Origin
sugarcane breeder.
Figure 9.2: V
avilov’s centres of crop origin c. D
r. B.P. Pal – Famous wheat breeder,
developed superior disease resistant
and crops domesticated
varieties of wheat.
Vavilov’s Centre of
Crops domesticated d. D
r. K. Ramiah – Eminent rice breeder,
Crop Origin
Foxtail millet, soybean, developed several high yielding
1 China varieties of rice.
bamboo, onion, crucifers.
Rice, sugarcane, mango, e. N
.G.P. Rao – An eminent sorghum
2 India
orange, eggplant, sesame. breeder, developed world’s first hybrid
Rice, banana, coconut,
2a South East Asia of Sorghum (CSH-1).
clove , hemp.
3 Central East Wheat, pea, hemp, cotton etc. f. C
.T. Patel – Who developed world’s
Wheat, rye, many subtropical first cotton hybrid.
4 The Near East
and tropical fruits.
Olive, vegetables, oil
g. C
houdhary Ram Dhan – Wheat
5 Mediterranean breeder, who is famous for C-591
yielding plants, wheats
6 Ethiopia Wheat, barley, sesame, variety of wheat, which is made Punjab
(Abyssinian) castor, coffee. as wheat granary of India.
7 Mesoamerica Maize, bean,
(South Mexican sweet potato, papaya, 9.5.1. Biofertilizers
& Central guava, tobacco. Biofertilizers are defined as preparations
American containing living cells or latent cells of
Centre) efficient strains of microorganisms that
8 South America Tomato, pine-apple help crop plants uptake of nutrients by
8a The Chiloe Potato their interactions in the rhizosphere when
Centre applied through seed or soil. Biofertilizers
8b The Brazilian Groundnut, cashew nut, could be also called as microbial cultures,
–Paraguayan pine apple, peppers, bioinoculants, bacterial inoculants or
Centre rubber. bacterial fertilizers.
9.5 Organic Agriculture They are efficient in fixing nitrogen,
Organic farming is an alternative agricultural solubilising phosphate and decomposing
system which originated early in the twentieth cellulose. They are designed to improve
century in reaction to rapidly changing farming the soil fertility, plant growth, and also the
practices. It is a production system that sustains number and biological activity of beneficial
the health of the soils, ecosystems and people. It microorganisms in the soil. They are eco-
relies on ecological processes, biodiversity and friendly organic agro inputs and are more
cycles adapted to local conditions rather than efficient and cost effective than chemical
the use of inputs with adverse effects. fertilizers.
C P Mobilizing Biofertilizers
Nutrient transfer
via AMF
PO43-
For 10,000 years, farmers and For 150 years, plant scientists and Today, farmers feed at least 10 times By 2050, we will need 50% more
breeders have been developing breeders have improved plant more people using almost same food to feed the rapid growing
and improving crops breeding on a scientific basis amount of lands as 100 years ago population
Cultivar register and Register and market (i) Multilocation yield trails
marketing the best pure lines with standard checks.
5th
Heterogenous cultivars Homogenous cultivars Year (ii) Best clone identified for
Seed release as a new variety
multiplication
Figure 9.12 : Mass selection vs Pureline selection
b. Pureline selection: Johannsen in 1903 Figure 9.13 Clonal Selection
coined the word pureline. It is a collection 9.7.3. Hybridization
of plants obtained as a result of repeated Hybridization is the method of producing new
self-pollination from a single homozygous crop varieties in which two or more plants
individual. Hence, a variety formed by this of unlike genetically constitution is crossed
method shows more homozygosity with together that result in a progeny called hybrid.
respect to all genes. The disadvantage of Hybridization offers improvement in crop and is
this type is that the new genotypes are never the only effective means of combining together
created and they are less adaptable and less the desirable characters of two or more varieties
stable to the environmental fluctuations. or species. The first natural hybridization was
c. Clonal Selection: In asexually propagated observed by Cotton Mather in maize.
crop, progenies derived from a plant
resemble in genetic constitution with the Steps in Hybridization
parent plant as they are mitotically divided. Steps involved in hybridization are as follows.
Based on their phenotypic appearance, 1. Selection of Parents: Male and female
clonal selection is employed to select plants of the desired characters are selected.
improved variety from a mixed population It should be tested for their homozygosity.
(clones). The selected plants are multiplied 2. Emasculation: It is a process of removal of
through vegetative propagation to give rise anthers to prevent self pollination before
to a clone. The genotype of a clone remains anthesis (period of opening of a flower)
unchanged for a long period of time. 3. Bagging: The stigma of the flower is
protected against any undesirable pollen
grains, by covering it with a bag .
Plant cell
1. Plasmid: 3. Vector: Restriction
Circular
enzyme cleaves plasmid.
DNA molecule is 2. DNA containing gene for
Second enzyme –
removed desired trait is removed
from cell. This from chromosome. Restriction DNA ligase – pastes gene
acts as vector to enzyme cuts gene into DNA molecule, making 4. Vector inserts gene into
carry gene from DNA recombinant vector chromosomes of plant cells
NEW BREEDING
ICT Corner
Plant Breeding
Let us know about the details of
Medicinal Plants in detail.
Steps
• Type the URL or scan the QR code to open the activity page then Introduction page will open.
• Click on ‘Plants’ it will display list of Medicinal Plants.
• Click on each plants individually on the next screen it displays the description, harvesting and
properties of the plants.
• Click the option on the top left side of the front page to see the preparation of oils, Powder etc.,
10 Economically
Useful Plants and
Entrepreneurial Botany
Mix 120g of hot Blend the Add the vegetable Pour the solution into a glass
chillies with 110 vegetables together paste to 500 ml of container and leave it undisturbed
g of garlic or manually or using warm water. Give the for 24 hours. If possible, keep the
onion. Chop them an electric grinder ingredients a stir to container in a sunny location. If
thoroughly. until it forms a thoroughly mix them not, at least keep the mixture in a
thick paste. together. warm place.
1 2 3 4
Strain the mixture. Pour the Pour the pesticide into a squirt Spray your plants with the
solution through a strainer, bottle. Make sure that the spray pesticide. Treat the infected
remove the vegetables and collect bottle has first been cleaned plants every 4 to 5 days with the
the vegetable-infused water and with warm water and soap solution. After 3 or 4 treatments,
pour into another container. This to get rid it of any potential the pest will be eliminated. If the
filtrate is the pesticide. Either contaminants. Use a funnel area is thoroughly covered with
to transfer the liquid into the
discard the vegetables or use it as the solution, this pesticide should
squirt bottle and replace the
a compost. keep bugs away for the rest of the
nozzle.
5 6 season. 7
Avoid spraying the plants during the sunny times of the day since it could burn plants. Many
other plants possess insect repellent or insecticidal properties. Combinations of these plants can
be fermented and used as biopesticide.
Figure 10.20: Preparation of organic pesticide
Steps
• Type the URL or scan the QR code to open the activity page then Introduction page will open.
• Select Package of Practices to know the various methods of agricultural crops breeding system.
• Click on Chat with expert helps the farmers to clarify their doubts.
• Click on Videos to know about the agricultural methods visually through videos.
Steps
• Type the URL or scan the QR code to open the activity page then Introduction page will open.
• Click on Agriculture it will display the approaches to cultivate the planted paddy, cotton and
sugarcane.
• Click on Horticulture it will display the approaches to cultivate the agricultural crops
like tea, coffee.
• Click on Organic Farming it will explain the Traditional method of farming and
Traditional Fertilizers.
• Click on Forestry it will explain the gardening methods about plants.
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221
222
223
224
225
226
227
228
229
4. Which of the following is not a feature of 10. Biolistics (gene-gun) is suitable for
the plasmids? (NEET-I 2016) (AIPMT Mains 2012)
a) Transferable b) Single-stranded a) disarming pathogen vectors
c) Independent replication b) transformation of plant cells
d) Circular structure c) constructing recombinant DNA by
joining with vectors
5. Which of the following is not required for
d) DNA fingerprinting.
nay of the techniques of DNA fingerprinting
available at present? (NEET-I 2016) 11. Genetic engineering is possible because
a) Restriction enzymes (CBSE 1998)
b) DNA-DNA hybridization a) phenomenon of transduction in bacteria
c) Polymerase chain reaction understood
d) Zinc finger analysis b) we can see DNA by electron microscope
c) we can cut DNA at specific sites by
6.
Which vector can clone only a small
endonuclease like DNAase I
fragment of DNA? (AIPMT 2014)
d) restriction endonuclease purified from
a) Bacterial artificial chromosome
bacteria can be used invitro
b) Yeast artificial chromosome
c) Plasmid d) Cosmid 12. Genetic Engineering is (BHU 2003)
a) Making artificial genes
7.
The colonies of recombinant bacteria
b) H ybridisation of DNA of one organism
appear white in contrast to blue colonies
to that of the others
of non-recombinant bacteria because of
c) Production of alcohol by using
(NEET 2013)
microorganisms
a) Insertional inactivation of alpha
d) Making artificial limbs, diagnostic
galactosidase in recombinant bacteria.
instruments such as ECG, EFG, etc.
b) Inactivation of glycosidase enzyme in
recombinant bacteria. 13. Ligase is used for (AMU 2006)
c) Non-recombinant bacteria containing a) Joining of two DNA fragments
beta galactosidase. b) Separating DNA
d) Insertional inactivation of alpha c) DNA polymerase reaction
galactosidase in non-recombinant bacteria. d) All of these
230
3YX,, 22.
Silencing of mRNA has been used in
producing transgenic plants resistant to
a) Ori-original restriction enzyme (AIPMT, 2011)
b) rop-reduced osmotic pressure a) Boll worms b) Nematodes
c) Hind III, EcoRI – selectable markers c) White rusts d) Bacterial blights
d) ampR, tetR – antibiotic resistance genes 23. Some of the characteristics of Bt cotton are
18.
A mixture containing DNA fragments (AIPMT,2010)
a,b,c,d with molecular weights of a+b=c, a) Long fibre and resistant to aphids
231
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234
28. The mass of living material at a trophic level 31. If 20 J of energy is trapped at producer level,
at a particular time is called (AIPMT 2015) then how much energy will be available to
a) Standing crop peacock as food in the following chain?
b) Gross primary productivity (AIPMT 2014)
c) Standing state Plant → Mice → Snake → Peacock
d) Net primary productivity a) 0.02 J b) 0.002 J
c) 0.2 J d) 0.0002 J
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INTRODUCTION
Laboratory is a place where ideas and concepts can be tested through experiments. Laboratory
investigations in biology increase the reasoning abilities, brings scientific attitude in a learner and also
helps in acquisition of skills of scientific processes. Hence, a biology student too, is obliged to attend
practical in laboratory with utmost sincerity, honesty and inquisitiveness. The practical work includes
GENERAL INSTRUCTIONS
In order to perform experiments successfully, a learner needs to go to the Biology Laboratory well
prepared. This includes the following.
1. Laboratory record book
2. Dissection box
3. Laboratory manual
4. A laboratory coat or apron
5. A hand towel
6. Drawing pencil (HB) and pencil eraser to record various experiments and to draw diagrams
7. Any item more as per the instructions of the teacher
While in the laboratory, a student should be very careful and methodical. One should listen carefully
to the instructions given by the teacher / instructor before performing an experiment. Maintain a
complete silence and working atmosphere in the laboratory. Record keeping is most important in
practical. Diagrams should be correctly drawn and well labelled. Always get the signature of the
teacher in the practical note book on each day after the practical class.
However, it is important that every student of Botany / Biology may pay proper attention to the
practical work and should try to acquire basic laboratory skills and develop a keen sense of observation
and acquire a sound training in the reporting of the work done.
If the material suggested for a particular experiment is not available, a suitable alternate material
may be used.
239
Total 7 ½ marks
Record 1 ½ marks
Skill 1 marks
240
Note: Teacher has to prepare a temporary slide using fresh specimen for demonstration. (During
examination permanent slides can be used if temporary slide preparation is not possible).
QUESTION No- II (B) - Fresh or preserved specimens and Models / Photographs / Charts
Economically important plant products and their uses:Sesame / Gingelly oil, Rubber, Aval
Exercise 18
(Flaked rice), Rose water, Henna powder,Aloe gel
241
Collect buds and opened flowers of Datura metel. Dissect the stamens, separate the
anthers and take thin sections and observe the structure under the microscope.
Record the various stages of anther from your observation.
Diagnostic Features
Connective
• A mature anther is bilobed (dithecous) and the two
Epidermis
lobes are joined by a connective.
Endothecium
• Each anther lobe has two pollen chambers in which Middle layer
pollen grains are produced. Pollen grain
Principle: In female reproductive part of a flower, the basal swollen part is ovary. The ovules are
present inside the ovary, later they develops to seed.
242
243
Aim: To study the adaptations in flowers for pollination by different agents (wind and insects)
Principle: The process of transfer of pollen grains from the anther to stigma of a flower is called
pollination.
Requirements: Fresh flowers of maize or any other cereal / gram, any insect pollination flowers
like Salvia, Calotropis, Ocimum and Asteraceae flowers.
Place the given flower on a slide and observe it with the help of hand lens. Note down the
adaptations of the flowers meant for pollination by the external agents.
Diagnostic Features
• The flowers are showy,
brightly coloured and scented.
Disc
• The flowers produce nectar or edible Retinaculum
Pollinium
pollen.
• Anthers and stigmas are commonly
inserted.
• Stigmas are usually unbranched and flat or lobed. Figure 4b: Calotropis
244
Soak the seeds of chick pea or gram in water for 2 – 3 hours. Drain the water and place the
seeds in a moist cotton cloth for 2 – 3 days. Observe for germination. Select some sprouted
seeds, observe under a dissection microscope and record the parts.
Aim: To study and identify the features of cloning vector – pBR 322
Principle: Vectors are used as carriers to deliver the desired foreign DNA into a host cell.
Endosperm
Requirements: Models/ Photographs / Pictures of E.coli Cloning vector pBR 322.
Scutellum
Coleoptile
Diagnostic Features (FR5, +LQG,,,
Shoot apex
• pBR 322 plasmid is a reconstructed plasmid containing 4361 base Radicle %DP+,
pairs and most widely used as cloning vector. DPSRoot
5 cap
WHW5
Coleorhiza
L.s. of fruit
• In pBR, p denotes plasmid and B and R respectively the notes S%5
of scientists Boliver and Rodriguez who developed the plasmid.b) Monocot seed (Oryza sativa)
RUL URS
The number 322 is the number of plasmids developed from theirFigure 2.25 Structure of seed
laboratory. 3YX,,
• It contains two different antibiotic resistance genes and recognition Figure 6: E-coli cloning
site for several restriction enzymes (Hind III, Eco R I, Bam H I, Sal vector (pBR 322)
I, Pvu II, Pst I, Cla I), Ori and antibiotic resistance genes (ampR and
tetR). Rop codes for the proteins involved in the replication of the plasmid.
245
Diagnostic Features
• Roots and shoots are differentiated from the callus. Figure 7: Callus with plantlets
8 A. Pyramid of numbers
Diagnostic Features T4
246
Diagnostic Features T2
8 C. Pyramid of energy
Diagnostic Features Tertiary
consumers
0.1 Joule
10 Joules
• The bottom of the pyramid of energy is occupied by the
producers. There is a gradual decrease in energy transfer Sunlight Primary consumers
1000 Joules
at successive trophic levels from producers to the upper 100 Joules
Producers
levels.
Figure 8 c: Pyramid of Energy
• Therefore pyramid of energy is always upright.
NOTE: Student have to work in pairs to perform this experiment and record the data in the
observation and record note book with the help of the teacher.
Need not consider this Monohybrid cross experiment for Board Practical Examination.
Aim:
To verify Mendel’s Monohybrid cross.
Principle:
When two purelines with contrasting traits of a particular character (phenotype) are crossed to produce
the next generation (F1 generation), all the members of the progeny are of only one phenotype, i.e.
of one of the two parents. The phenotype that appears is called dominant and the one that does not
appear is called recessive. When the F1 plants are selfed, the progeny i.e. the F2 generation, is in the
ratio of 3 dominant : 1 recessive (¾ : ¼ of 75% : 25%). This reappearance of the recessive phenotype in
F2 generation, verifies Mendel’s Monohybrid cross.
Requirements:
64 yellow and 64 green plastic beads, all of exactly same shape and size (when beads are not available,
pea seeds may be painted and used). Plastic beakers, petri dish and a napkin / hand towel.
247
YY yy
experiment. Follow the steps in given sequence.
1. Put 64 yellow beads in one beaker and 64 green Gametes Y Y y y
beads in the other to represent male and female
gametes respectively. Let the yellow bead be F1 generation Yy Hybrid Yellow seeds
Observation:
Record the result in the following table:
Total Number of Genotypes
Generation Phenotype(s)
individuals YY Yy yy
F1
Total
F2
Total
Phenotypic ratio : in F1
in F2
Genotypic ratio : in F1
in F2
Inference:
The results are so because when the F1 individuals are crossed together to raise the F2 generation, each
F1 individual produces two types of gametes: 50% having dominant allele and the remaining 50%
having recessive allele. These gametes undergo random fusion during fertilization to produce the F2
generation. According to simple probability of mixing of opposite sex gametes, offsprings of three
genotypes are likely to appear as follows:
Among these, proportion of dominant phenotype would be YY + Yy = yellow and recessive phenotype
yy = green, which occur in 3 : 1 or 75% : 25% ratio.
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Precautions:
1. Take a sufficiently large number of seeds for analysis to minimise the error.
2. Observe the contrasting form of trait carefully.
To analyse seed sample of pea for Mendelian dihybrid Round yellow cotyledon X Wrinkled green cotyledon
ratio of 9 : 3 : 3 : 1.
RR YY rr yy
Principle:
F1 generation R r Yy
In a dihyrbid cross, the segregation of one gene pair
All round-yellow cotyledons
is independent of the segregation of the other pair.
It means that when the factors (genes) for different F1 Generation Round yellow cotyledon X Round yellow cotyledon
(selfed) R r Yy R r Yy
characters inherited from parents do not remain
linked in the offsprings, but their distribution in the RY Ry rY ry
gametes and in the progeny of subsequent generations R Y RR YY RR Yy Rr YY Rr Yy
rY Rr YY Rr Yy rr YY rr Yy
Requirement: r y Rr Yy Rr yy rr Yy rr yy
Plastic beakers, Pea seed samples or plastic beads, tray, Phenotypic Ratio 9:3:3:1
Teachers should select the Pea seed or plastic beads which represents the four types of traits such
as yellow round, yellow wrinkled, green round and green wrinkled in the ratio of 9:3:3:1
Procedure:
1. Take a lot of about 160 Pea seeds or plastic beads in a tray.
2. Separate out yellow round, yellow wrinkled, green round and green wrinkled and put them in
separate petridishes.
3. Note down the number of seeds in each plate and find out their approximate ratio.
Observation:
Present your finding in the form of a table.
Total Number of No. of yellow No. of yellow No. of green No. of green Approximate
seeds observed round seeds wrinkled seeds round seeds wrinkled seeds ratio
160 90 30 30 10 9 : 3:3:1
Inference:
The ratio of yellow round : yellow wrinkled : Green round : green wrinkled is approximately 9 : 3 : 3 : 1
which is exactly the same as obtained by Mendel for a dihybrid cross. This indicates that the contrasting
genes for seed colour and seed shape show an independent assortment in the population of pea seeds.
249
Aim:
To understand the unidirectional flow of energy 270 Joules
Tertiary
in an ecosystem and transfer of energy follows the consumers
Energy lost
30 Joules
10% law. 300 Joules
2700 Joules
Energy lost
Principle: Secondary consumers
The student studies about flow of energy and that 3000 Joules
27000 Joules
Energy lost
only about 10% of energy is made available to the
Sunlight Primary consumers
next trophic level. Large amount of energy about 270000 Joules
Energy lost
90% is lost at each trophic level in a food chain. 300000
Joules
30000 Joules
Producers
Requirements:
Problems to be given to students based on different Figure 11: Ten percent law
examples with alternating food chain and amount of energy.
The teacher must train the student by giving them various kinds of food chain with different
values.
Problem
Analyse the food chain given below and find out the amount of energy received by the organism in
third trophic level.
Sun
250
NOTE: Teachers can take the students to open space and teach them how to construct plot/
quadrats and to record the number of individuals of each plant species occurring in the quadrat.
The percentage frequency should be calculated and entered in the practical observation and
record note book. Examiner need not consider this experiment for Board Practical Examinations.
Aim:
To study population density and percentage frequency of different plant species of a given area by
quadrat method.
Principle:
The number of individuals in a population never remains constant. It may increase or decrease due
to many factors like birth rate, death rate, migration, etc. The number of individuals of a species
presents per unit area or space of a given time is called population density. The population density
and percentage frequency of different plant species can be determined by laying quadrats / segments
of suitable size and recording of the number of individuals of each species occurring in the quadrat.
Requirements:
Metre scale, string or cord, hammer, nails, paper, pencil, etc.
Procedure:
1. In the selected site of study, hammer the nails firmly in the soil without damaging the vegetation.
2. Fix four nails to make a square plot.
3. Tie each end of the nails using a thread, to make 1 m X 1 m plot.
4. If the number of plants in the plot is large, the plot can be divided into quadrats.
5. Count the number of individuals of a species “A” present in the first quadrat and record the data
in the table.
6. Similarly count the individuals of the species “A” in other quadrats respectively and record the data
in the table.
7. Count the number of individuals of a species “B” present in the all quadrats and record the data
in the table.
8. Repeat the same procedure for other species and record the data in the table.
Nail
Species No. 1 Species No. 3
String
per quadrat
individuals in quadrats in which Number of
S. No.
Density percentage
all the quadrats each species quadrats
I II III IV (N/B) (A/B) x 100
studied (N) occurred (A) studied (B)
1
2
3
4
5
Precautions:
1. The measurement of quadrat should be accurate.
2. The string or cord used should not be very thick.
252
Duplications
13 B. Chromosomal Aberration - Duplication A A A A
B B B B
Reasons: C C C C
E
B
C
C
B
D
C
to aberration, the genes B and C are duplicated and the sequence of genes
G G
H H H
I I
becomes A, B, C, B, C, D, E, F, G, H and I. (Refer figure 13b)
I
C C
Given below is the representation of a kind of chromosomal C C C
F
F
B B D
D
aberration. Identify it giving reasons for your identification. E E
E
E
E
Also mentions its significance. F F F
D
D
G G G
G
Identification: H H H H
I I I
I
The given genetic problem is identified as inversion type of a) Paracentric inversion b) Pericentric inversion
(does not include centromere) (includes centromere)
chromosomal aberration.
Figure: 13 c: Inversion
Reasons:
1. When the order of genes in a chromosomal segment is reversed due to rotation by an angle of 180°,
it is called inversion.
2. The order of genes in a chromosome is A, B, C, D, E, F, G, H and I. Due to aberration, the sequence
of genes become A, D, C, B, E, F, G, H and I (Refer figure 13c)
253
NOTE: Likewise the teacher can give different types of chromosomal aberrations with various
gene sequence to students for practise. The external examiner can also use the same technique
by giving different gene sequence.
B A C
20% 8%
Figure 14: Linkage Map
Reasons:
1. The frequency of crossing over is directly proportional to the relative distance of the genes on the
chromosomes.
2. More crossing over = More distance between two genes and
Less crossing over = Less distance between the two genes.
In the above problem, the sequence of the genes on the linkage map is B, A, C
NOTE: Teachers can give different crossing over percentage between its linked genes in a
chromosome and make the students construct the linkage maps. The external examiner can
also do the same for the Board Practical Examinations.
254
NOTE: Pollen germination can be studied by dusting some pollens from common flowers like
Crotalaria, Hibiscus, Pisum, etc. on a glass slide containing a drop of 10% sugar solution or
tender coconut water or any nutrient medium.
Observe the slide after about 10 – 15 minutes under the low power of compound microscope.
You will be able to observe the pollen tubes coming out of the pollen grains.
Requirements: Fresh seasonal flowers, cavity slide, cover slip, compound Generative cell
1. Prepare a nutrient solution by dissolving 1 gm. of sucrose / 1 gm. of boric Pollen tube
Tube nucleus
4. View the slide in the microscope after 5 minutes and then observe it
Tube nucleus
regularly for about half an hour.
Figure 15: Pollen
Observation: In nutrient medium, the pollen grains germinate. The tube cell germination
enlarges and comes out of the pollen grain through one of the germ pores to
form a pollen tube. The tube nucleus descends to the tip of the pollen tube. The
generative cell also passes into it. It soon divides into two male gametes.
Inference: Different stages of germinating pollens are observed. Some pollens are in their initial
stage of germination while others have quite long pollen tube containing tube nucleus and two
male gametes.
Precautions: 1. Flowers should be freshly plucked. 2. Use clean cavity slide to observe the pollen
grains. 3. The slides should not be disturbed, otherwise position of pollen grains will get changed.
255
DNA is one of the nucleic acids found in living systems. DNA acts as the genetic material in
most of the organisms.
Principle: Recombinant DNA technology has allowed breeders to introduce foreign DNA
in other organisms including bacteria, yeast, plants and animals. Such organisms are called
Genetically Modified Organisms (GMOs). Thus rDNA technology involves isolation of DNA
from a variety of sources and formation of new combination of DNA.
Aim: To isolate DNA from available plant materials such as spinach leaves, fresh green pea seeds,
green papaya, etc.
Requirements: Plant materials, mortar and pestle, beakers, test tubes, ethanol, etc.
Procedure: Take a small amount of plant material and grind it in a mortar with a little amount of
water and sodium chloride. Make it into a solution and filter it. To this filterate, add liquid soap
solution or any detergent solution and mix it with a glass rod. Then tilt the test tube and add
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Typist
S. Chitra, SCERT, Chennai
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