Bio Chapter 2
Bio Chapter 2
Structure of microsporangium:
Each microsporangium surrounded by four wall layers
o Epidermis
o Endothecium
o Middle layer.
o Tapetum.
The innermost layer is tapetum which is multinucleated, with dense cytoplasm;
it nourishes the developing pollen grain.
The centers of each microsporangium contain homogenous cells called
sporogenous tissues.
Microsporogenesis:
The process of formation of microspores from pollen mother cell through meiosis
is called microsporogenesis.
The sporogenous tissue of microsporangium differentiated into microspore
mother cell or pollen mother cell.
Each microspore mother cell undergoes meiosis and gives rise to haploid
microspore tetrad.
On dehydration microspore tetrad dissociated to form four microspores.
Each microspore developed into a pollen grain.
Pollen grain:
Pollen grain represents the male gametophytes.
It is spherical and measuring about 25-50 micrometer in diameter.
It is covered by two layers.
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The hard outer layer called the exine is made up of sporopollenin, which is one
of the most resistant organic materials known. It can withstand high temperature
and strong acids and alkali. No enzyme can degrades sporopollenin is so far
known.
The exine has prominent apertures called germ pore where sporopollenin is
absent.
The inner wall of pollen grain is called intine. It is thin and continuous layer made
of cellulose and pectin.
On maturity the pollen grain contains two cells, the vegetative cell and
generative cell.
The vegetative cell is bigger, has abundant food reserve and a large irregularly
shaped nucleus.
The generative cell is small and floats in the cytoplasm of vegetative cell.
In 60% of angiosperms, pollen grains are shed at this 2-celled stage.
In others the generative cell divides mitotically to form two male gametes before
pollen grain are shed (3-celled stage).
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Hilum is the junction between the funicle and ovule.
Each ovule has one or two protective envelops called integuments.
Integument covered the ovule except an opening at the top called micropyle.
Opposite of the micropylar end, is the chalaza, representing the basal part of the
ovule?
Megasporogenesis:
The process of formation of megaspores from the megaspore mothercell is
called Megasporogenesis.
In the centre of the ovule there is a mass of tissue called nucellus.
Cells of nucellus have abundant reserve food materials.
One cell of the nucellus towards micropylar end differentiated into megaspore
mother cell (MMC).
It is a large diploid cell, dense cytoplasm with prominent nucleus.
The MMC undergo meiotic division resulting four haploid megaspores.
Female gametophyte:
Out of four megaspores, one megaspore is functional and other three degenerates.
The functional megaspore developed into the female gametophyte.
Female gametophyte is known as the embryo sac.
Development of embryo sac from a single megaspore is called as monosporic
type of embryo sac.
The nucleus of the functional megaspore divided by mitotic division to form two
nuclei which move to the opposite pole, 2-nucleated embryo sac.
Two successive mitotic division leads to formation of 4-nucleate and later 8-
nucleate stages of the embryo sac.
All mitotic divisions are free nuclear type; karyokinesis is not followed by
cytokinesis.
Six of the eight nuclei are surrounded by cell walls and organized into cells.
Three cells are grouped together at the micropylar end, constitute the
eggapparatus.
The egg apparatus, in turn consists of two synergids and one egg cell.
Synergids have special filiform apparatus, which play an important role in
guiding the entry of pollen tube into the synergids.
Three cells arranged towards chalazal end are called antipodal cells.
The large central cell has two polar nuclei.
A typical angiosperm embryo sac at maturity is 8- nucleated and 7-celled.
Pollination:
Transfer of pollen grains from the anther to the stigma of a pistil is termed as
pollination.
Both male and female gametes are non-motile.
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Kinds of pollination:
Autogamy:
Pollination within same flower.
In open and exposed anthers and stigma autogamy is rare.
Viola, Oxalis and Commelina produce two types of flowers:
o Chasmogamous: exposed anther and stigma
o Cleistogamous: closed anther and stigma.
Cleistogamous flower is invariably autogamous and assured seed set even in the
absence of the pollinator.
Geitonogamy:
Pollination between two flowers of the same plant.
Pollination by pollinating agent.
Genetically similar to the autogamy.
Xenogamy:
Transfer of pollen grains from the anther to the stigma of different plant.
It is commonly called as cross-pollination.
It brings genetically different types of pollen grains to the stigma.
Agents of pollination:
Plant use two abiotic agent i.e. wind and water for pollination.
One biotic agent for pollination such as animals.
Majority of plant use biotic agent for pollination.
Few plant use abiotic pollinating agent.
Anemophily:
Pollinating agent is wind.
Plants produces enormous amount of pollen when compared to the number of
ovules available for pollination to compensate the uncertainties of pollination.
Flowers with well exposed stamens.
Large feathery stigma to trap air-borne pollen grains.
Most wind pollinated flower contains single ovule in one ovary and numerous
flower packed into an inflorescence e.g. corn cob.
Pollen grains are light and non-sticky.
Hydrophily:
Pollination by abiotic agent like water.
This type of pollination is very rare, about 30 genera, mostly monocot.
Vallisneria,Hydrilla and Zostera are the common example for Hydrophily.
All aquatic plants are not Hydrophily.
Pollen grains released into the surface of water and carried to the stigma by air
current as in Vallisneria.
In sea grass the flowers remained submerged.
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Pollen grains are long, ribbon like and carried passively inside the water
Pollen grains are protected from wetting by mucilaginous covering.
Outbreeding Devices:
Majority of the flowering plants produce hermaphrodite flower and undergo
autogamy.
Continuous autogamy or self-pollination results in inbreeding depression.
Flowering plants have developed many devices to avoid self-pollination and to
encourage cross-pollination. Such devices are called Outbreeding devices.
o Pollen released and stigma receptivity is not synchronized.
o Spatial separation of anthers and stigmas
o Anther and stigma are placed at different positions.
o Self-incompatibility.
o Production of unisexual flowers.
Artificial hybridization:
One of the major approaches of crop improvement programme.
Only desired pollen grain used for pollination.
Stigma is protected from contamination (from unwanted pollen grain).
Removal of anthers from the flower bud before the anther dehisces is called
emasculation.
Emasculated flowers covered by bag generally made up of butter paper, to
prevent contamination of its stigma with unwanted pollen. This step is called
bagging.
If the female flower is unisexual there is no need of emasculation.
Double fertilization:
After entering one of the synergids, the pollen tube releases two male gametes
into the cytoplasm of the synergids.
Syngamy: one of the male gamete fused with egg cell, to form a diploid zygote.
Two polar nuclei of central cell fused to form a diploid secondary nucleus.
Triple fusion: The second male gamete fused with the secondary nucleus to form
a triploid primary endosperm nucleus.
Since two type of fusion, syngamy and triple fusion take place in the embryo sac
the phenomenon is termed as double fertilization.
The central cell after triple fusion becomes primary endosperm cell and
developed into the endosperm.
The zygote developed into an embryo.
Endosperm:
Development of endosperm takes place before the embryo development.
Primary endosperm cell divides repeatedly to form a triploid endosperm.
Cells are filled with reserve food material and are used for the nutrition of the
developing embryo.
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PEN undergoes successive nuclear division to give rise to free nuclei. This is
called free-nuclear endosperm.
Subsequently cell wall formation takes place and become cellular endosperm.
The coconut water is free nuclear endosperm and the white kernel is the cellular
endosperm.
Endosperm may be consumed completely during embryo developed or it may be
consumed during germination of seed.
Embryo:
Zygote formed and placed at the micropylar end of the embryo sac.
Zygote starts its development only after some amount of endosperm formed.
Embryo development takes place in following stages:
o Proembryo
o Globular stage
o Heart shaped
o Matured embryo.
Dicot embryo:
A typical dicotyledonous embryo consists of an embryonal axis and two
cotyledons.
Embryonal axis above the cotyledon is the epicotyls.
Terminal part of the epicotyls is the plumule (gives rise to the shoot).
Embryonal axis below the cotyledon is the hypocotyl.
The terminal part of the hypocotyl is called the radicle (root tip).
The root tip is covered by the root cap.
Monocot embryo:
Possesses only one cotyledon
In grass family the cotyledon is called scutellum.
Scutellum situated towards one side of the embryonal axis.
Radicle and the root cap enclosed by a sheath called coleorhiza.
The portion of the embryonal axis above level of attachment of scutellum is called
epicotyls.
Epicotyl has the shoot apex or plumule enclosed by hollow foliar structure called
coleoptile.
Seed is the final product of the sexual reproduction.
Seed consists of seed coat, cotyledon and an embryo axis.
Cotyledon stores the reserve food material for development and germination.
Matured seed without endosperm called non-albuminous. (Ground nut)
A part of the endosperm retained in matured seed is Albuminous.
Remainants of nucellus in the matured seed is called perisperm. E.g. black
peeper, beet.
The wall of the ovary develops into the wall of fruit called pericarp.
Fruit developed from the ovary is called true fruit.
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In apple, strawberry, cashew, the thalamus contributes in the fruit formation is
called false fruit.
Fruit developed without fertilization is called Parthenocarpic fruits.
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