Sexual Reproduction in Flowering Plants
Sexual Reproduction in Flowering Plants
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Chapter 1
1. Flower
4. Male gametogenesis
6. Megasporogenesis
7. Female gametogenesis
8. Pollination
Flower
Most fascinating organ of Angiosperms.
Flowers are Morphological marvels. (as they appear different than the whole plant body)
Flowers are Embryological marvels. (as flowers form fruits, which form seeds, which in turn form
new plants)
Parts of a Flower:
Sepal - Protect flower in bud stage. Also perform photosynthesis. (Accessory Whorl)
Group of Sepals - Calyx (denoted by letter ‘K’)
Stamen - Male Sex Organ. Made up of Anther & Filament. (Essential Whorl)
Carpel - Female Sex Organ. Made up of Stigma, Style & Ovary. (Essential Whorl)
Group of Carpels - Gynoecium (denoted by letter ‘G’)
💡 According to the scientist Goethe, flower is a modified shoot in which internodes do not
elongate, instead the axis of the internodes get condensed to form thalamus. While the 4
whorls of a flower are nothing but modified leaves.
Polycarpic: Flowering & fruiting takes place many times in their life span.
E.g. - Perennial Plants (life span - many years): Mango, Lichi, Guava etc.
Exceptions: Bamboo (50-100 years) and Strobilanthus kunthiana - Neela Kurengi (12 years) are
perennial but monocarpic.
1. Pre-fertilisation
Anther:
They are bilobed with each lobe having 2 theca (pollen sack), i.e., they are dithecous &
tetrasporangiate.
Often a longitudinal groove runs lengthwise the anther, separating the theca.
The two anther lobes are connected by a parenchymatous tissue.
Histology of Anther
Structure of Anther:
i. Epidermis - Single-celled outermost protective layer.
ii. Endothecium - Single-celled layer, the outer walls of which remain thin, but inner walls and
radial walls become thick due to thickening of α-cellulose fibres. The endothecium becomes
hygroscopic (moisture absorbing) in nature due to the presence of fibrous thickening.
Their main function is to help in
DEHISCENCE of anther.
iii. Middle Layers - 1-3 celled thick. Food is stored by Parenchymatous cells in this layer. It is
ephemeral (short-lived) in nature & is absent in mature anther.
iv. Tapetum - Single-celled thick. Innermost layer acts as a nutritive layer to Microspore mother
cells. Its cells have dense cytoplasm. Initially they are diploid but they become polyploid &
multi-nucleated due to endomitosis & free nuclear division respectively.
They have to become very efficient in their function & thus they increase the amount of their
DNA (polyploidy: 2n → 4n → 8n)
It disappears in mature anther.
FUNCTIONS:
Before degeneration, they form Proubisch bodies in cytoplasm where they get surrounded
by the sporopollenin produced earlier to form Ubisch bodies or Orbicules.
The Ubisch bodies (sporopollenin) participate in formation of outer cover of pollen grains
called Exine.
Microsporogenesis:
Microspore Mother Cells - Forms sporogenous tissue.
Microsporogenesis
Pollen grains have maximum fossils because the sporopollenin is resistant to decomposition.
💡 Fun fact: If pollen grain fossils are found while digging there might be plants buried
nearby i.e. fossil fuel.
Structure of a mature (2-celled) pollen grain. Formed by 1 meiosis & 1 mitosis. Also called
partially developed male gametophyte.
2. Intine - It is flexible as it is made up of pectin and cellulose. It bulges out slightly at germ
pores and later in pollination forms pollen tube through the germ pores.
The Period for which pollen grains remain viable is highly variable and to some extent
depends on prevailing temperature and humidity.
Pollen Banks
Cryopreservation - It is possible to store pollen grains of a large number of species for years in
liquid nitrogen (-196℃). Such stored pollen can be used as pollen banks, similar to seed banks,
in crop breeding programmes.
1. Bigger 1. Smaller
Carpel
Anatropous Ovule. Embryo Sac is 7 celled but 8 nucleated as Central Cell is binucleated. Nucellus.
Questions related to position of different cells would be answered according to Orthotropous ovule.
ARIL is a type of 3rd integument which develops from funicle at the base of the ovule.
Megasporogenesis
Process of formation of megaspores from MMC or megaspore mother cells (one cell of nucellus)
is called megasporogenesis.
💡 Only 1 out of 4 Megaspore formed by meiosis survive, which is nearest to the Chalazal
end.
i. The nucleus divides into 2, then further divides into 4 & then 8 by free nuclear division.
ii. The 8 nuclei are located in groups of 4 on opposite ends - Micropylar end & Chalazal end.
iii. Then, 1 nucleus from each of the 2 groups come to the center, providing 2 Polar nuclei for
Central Cell.
iv. The rest nuclei, left in groups of 3 on each end get into cells of their own, making Egg
Apparatus on the Micropylar end & Antipodal Cells on the Chalazal end.
v. Thus, the mature embryo sac now contains 7 cells and 8 nuclei.
Flowering plants have evolved an amazing array of adaptations to achieve pollination. They make
use of external agents to achieve pollination.
The anther and the stigma should lie close to each other
a. Monoecious Plants:
b. Dioecious Plants:
2. Homogamy - Synchrony (same time maturity) in pollen release and stigma receptivity. E.g. - Pea
3. Cleistogamy - Flowers that never bloom are called cleistogamous flowers. These are often
underground while the flowers above ground bloom.
ln some plants bisexual flowers are formed which never open throughout their life.
In such flowers, the anthers and stigma lie close to each other.
When anthers dehisce in the flower buds, pollen grains come in contact with the stigma to
effect pollination (syngamy).
Thus, cleistogamous flowers are invariably (w/o exceptions) autogamous as there is no chance
of cross-pollen landing on the stigma.
4. Bud Pollination - Pollination inside closed bud. E.g. - Pea, Wheat, Rice
2. Dichogamy - No synchrony (different time maturity) in pollen release and stigma receptivity. E.g. -
Ficus, Salvia & Sunflower
3. Chasmogamy - Flowers that bloom are called chasmogamous flowers. They have exposed stigma
and anther.
It is the primary requirement for cross pollination
Most flowers show Chasmogamy.
Heterostyly
5. Self sterility / Self incompatibility - This is a genetic mechanism to prevent self pollen (from the
same flower or other flower of the same plant) from fertilising the ovules by inhibiting pollen
germination or pollen tube growth in the pistil. E.g. - Petunia, Tobacco
Agents of Pollination:
Anemophily - By Wind
Hydrophily - By Water
Abiotic Agents:
Pollen grains coming in contact with stigma is a chance factor in both wind and water pollination.
To compensate for this uncertainties and associated loss of pollen grains, the flowers produce
enormous amount of pollen grains when compared to the number of ovules available for
pollination.
Both wind and water pollinated flowers are not very colourful and do not produce nectar.
b. The pollen grains are very small, light weight and dry (non-sticky).
c. They often possess well exposed stamens so that the pollens are easily dispersed into wind
currents.
e. Stigma is large, often hairy/feathery and mucilaginous (sticky), to easily trap air borne pollen
grains.
Other Features:
c. Generally unisexual.
d. Often have a single ovule in each ovary and numerous flowers are packed into an inflorescence.
E.g. - Corn cob.
Disadvantages of anemophily:
Not all aquatic plants show hydrophily. Most show anemophily or entomophily.
Pollination by water is quite rare in flowering plants and is limited to about 30 genera, mostly
monocotyledons.
Hydrophily is of 2 types:
Entomophily - By insects
Ornithophily - By birds
Chiropterophily - By bats
Malacophily - By Snail
Ophiophily - By Snake
Entomophily:
Among the animals, insects, particularly
bees (80% contribution) are the dominant biotic pollinating agents
Flowers are large, attractive, fragrant and with nectar glands.
In smaller flowers, a number of flowers are clustered together into an inflorescence to make them
conspicuous (visible).
Flies & Beetles pollinate foul-smelling flowers.
Night flowering plants are pollinated by Moths. They are highly scented and there flowers are generally
white coloured.
Pollen grains of insect pollinated flowers become sticky due to presence of pollen kitt.
Floral Rewards:
In some species floral rewards are in providing safe places to lay eggs.
e.g. Yucca, Amorphophallus (tallest flower : 6-7 feet height)
Yucca plant provide space to deposits eggs of moth in the locule of the ovary and the flower, in
turn, gets pollinated by the moth. (Essential - Obligatory symbiosis)
Fertilization
The fusion of male & female gamete is called fertilization.
Pollen-Pistil Interaction
All events from pollen deposition on stigma until the entry of pollen tube into ovule are together
referred as pollen-pistil interaction. (rapid/dynamic process)
If a pollen grain is suitable (compatible) for a stigma, then intine of vegetative (main) cell escapes
through germ pore in the form of pollen tube.
Every pollen tube carries 2 gametes. Generative cell undergoes mitosis to form 2 non-motile male
gametes carried by pollen tube.
There is chemotropic movement of pollen tube, mainly due to Boron, in Filiform Apparatus in
Synergid Cells. Other chemicals responsible - Calcium, Sugar, Inositol.
If it directly enters through Micropyle, its called Porogamy. E.g. - Most Angiosperms.
If it first enters the Chalaza and goes around the ovary to reach the micropyle, its called
Chalazogamy.
If it first enters the Funicle or Integument and goes around the ovary to reach the micropyle, its
called Mesogamy.
Pollen tube liberates its content into the Degenerating Synergid Cell.
2 male gametes are carried by the pollen tube for Double Fertilisation:
1. True Fertilisation (Syngamy) - The first one fuses with the egg/ovum in the Egg Cell to form
Zygote (2n - Diploid).
2. False Fertilisation (Triple Fusion) - The second one fuses with the 2 polar nuclei (or the polar
nuclei might have already fused forming a secondary nucleus) to form the Primary
Endosperm Nucleus (3n - Triploid).
Development of Endosperm:
The PEC (Primary Endosperm Cell) divides repeatedly and forms a triploid (3n) endosperm tissue.
The cells of this tissue are filled with reserve food materials and are used for nutrition of
developing embryo.
2. Cellular Endosperm
Maize and tomato have mosaic endosperm in which patches of different colors are present.
The drinking portion (Coconut water) is Nuclear Endosperm an edible portion (white kernel) is
the Cellular Endosperm in coconut.
Embryo:
Embryo develops at the micropylar end of the embryo sac where the zygote is situated.
Most zygotes divide only after certain amount of endosperm is formed. This is an adaptation to
provide assured nutrition to the developing embryo.
Though the seeds differ greatly, the early stages of embryo development (embryogeny) are similar
in both monocotyledons and dicotyledons.
Cotyledon:
Epiblast - Remanent of the 2nd cotyledon proving that Monocots are advanced.
💡 Q) Why do you think Zygote is dormant for some time in a fertilised state?
A) Zygote requires nutrition to develop into embryo, which is provided by endosperm, so it
has to wait for the development of endosperm.
In other words, seed is a mature fertilized, integumented megasporangium (Ovule) formed inside
fruits.
Seed consists of -
4. Embryo -
b. Cotyledons - Simple structures, generally thick & swollen due to storage of food reserves
(as in legumes).
5. Endosperm - Triploid
Types of seeds:
Structure of Seed
Maize Grain = Caryopsis - Single seeded fruit in which fruit wall and seed coat are fused.
Advantages of Seed
Since reproductive processes such as pollination and fertilization are independent of water,
seed formation is more reliable.
Seed Viability
Some seed can remain alive for 100s of years. There are several records of very old viable
seeds.
E.g. – Lupine – Lupinus arcticus excavated from Artic Tundra (10,000 years of dormancy)
E.g. – Date Palm – Phoenix dactylifera discovered during the archaeological excavation at King
Herod’s palace near the Dead Sea. (2000 years old viable seed)
Generally equal to or less than the number of ovules (not all are fertilized) in an ovary.
Orchid fruit contains thousands of tiny seeds (dust seeds - very small) .
Parasitic species like Orobanche and Striga also have many seeds in a fruit.
Seed Dormancy
This facilitates entry of oxygen and water into the seed during germination.
As the seed matures, its water content is reduced, and seeds become relatively dry (10-15 per
cent moisture by mass). - DORMANT
The general metabolic activity of the embryo slows down. The embryo may enter a state of
inactivity called dormancy, or if favourable conditions are available (adequate moisture, oxygen
and suitable temperature), they germinate.
Seed Germination
3. Viviparous Germination - Germination of plant inside the fruit, when present on mother plant.
E.g. - Mangrove Plants, Rhizophora
Pericarp may be thick and fleshy or thick and hard or thin and soft.
1. Epicarp/Exocarp - Outermost
2. Mesocarp - Middle
3. Endocarp - Innermost
Fruits
Asexual Reproduction
2 types:
1. Vegetative Propagation
2. Apomixis/Agamospermy
Vegetative Propagation:
By Stem: Rhizome, Tuber, Corm, Bulb, Runner, Offset, Stolon, Sucker, Phylloclade of Opuntia
By Leaves: Bryophyllum
Although seeds, in general are the products of fertilisation, a few flowering plant such as some
species of Asteraceae and grasses, have evolved a special mechanism, to produce seeds without
fertilisation, called apomixis.
Agamospermy
Hybrid Varieties:
Hybrid varieties of several of our food and vegetable crops are being extensively cultivated.
Problems of Hybrids
Hybrid seeds have to be produced every year. If the seeds collected from hybrids are sown,
the plants in the progeny will segregate and do not maintain hybrid characters.
If these hybrids are made into apomicts, there is no segregation of characters in the hybrid
progeny. Then the farmers can keep on using the hybrid seeds to raise new crop year after
year and he does not have to buy hybrid seeds every year.
Because of the importance of apomixis in hybrid seed industry, active research is going on in
many laboratories around the world to understand the genetics of apomixis and to transfer
apomictic genes into hybrid varieties.
We can easily study pollen germination by dusting some pollen from flowers such as Pea,
Chickpea, Crotalaria, Balsam and Vinca on a glass slide containing a drop of sugar solution
After about 15–30 minutes, observe the slide under the low power lens of the microscope. We
can see pollen tubes coming out of the pollen grains.
Artificial hybridization
A breeder is interested in crossing different species and often genera to combine desirable
characters to produce commercially ‘superior’ varieties.
In such crossing experiments it is important to make sure that only the desired pollen grains are
used for pollination and the stigma is protected from contamination (from unwanted pollen).
If the female parent bears bisexual flowers, removal of anthers from the flower bud before the
anther dehisces using a pair of forceps is necessary. This step is referred to as emasculation.
Emasculated flowers have to be covered with a bag of suitable size, generally made up of
butter paper, to prevent contamination of its stigma with unwanted pollen. This process is
called bagging.
When the stigma of bagged flower attains receptivity, mature pollen grains collected from
anthers of the male parent are dusted on the stigma, and the flowers are rebagged, and the
fruits allowed to develop.
If the female parent produces unisexual flowers, there is no need for emasculation. The female
flower buds are bagged before the flowers open. When the stigma becomes receptive,
pollination is carried out using the desired pollen and the flower rebagged.