All flowering plants (angiosperms) show sexual reproduction. Flowers are the sites of sexual reproduction. Reproduction in flowering plants class 12 notes
PRE-FERTILISATION: STRUCTURES & EVENTS
- Several hormonal and structural changes result in the differentiation and development of the floral primordium.
- Inflorescences bear the floral buds and then the flowers.
STRUCTURE OF A FLOWER
A typical flower has 2 parts: Androecium & Gynoecium.
Androecium (whorl of Stamens)
It is the male reproductive part of the flower.
It consists of a whorl of stamens. Their number and length are variable in different species.
A stamen has 2 parts:
a. Filament: Long and slender stalk. Its proximal end is attached to the thalamus or the petal of the flower.
b. Anther: Terminal and typically bilobed. Each lobe has 2 thecae (dithecous). Often a longitudinal groove runs lengthwise separating the theca.
Transverse section of anther
- The anther is a tetragonal structure consisting of four microsporangia located at the corners.
- Each lobe consists of two microsporangia.
- The microsporangia develop into pollen sacs. They extend longitudinally all through the length of an anther and are packed with pollen grains.
Structure of a microsporangium:
- A typical microsporangium is near circular in outline. – It is surrounded by four wall layers– the epidermis, endothecium, middle layers & tapetum.
- The outer 3 layers give protection and help in the dehiscence of anther to release the pollen.
- The tapetum (innermost layer) nourishes the developing pollen grains for living.
- – Cells of the tapetum contain dense cytoplasm and generally have more than one nucleus.
When the anther is young, a group of compactly arranged homogenous cells (sporogenous tissue) occupies the center of each microsporangium.
- As the anther develops, each cell of sporogenous tissue undergo meiotic divisions to form microspore tetrads (microspores are arranged in a cluster of four cells).
- Each one is a potential pollen (microspore mother cell).
- The formation of microspores from a pollen mother cell (PMC) through meiosis is called microsporogenesis.
- As the anthers mature and dehydrate, the microspores dissociate from each other and develop into pollen grains.
- Each microsporangium contains thousands of pollen grains.
They are released with the dehiscence of anther.
Pollen grain (male gametophyte):
Generally spherical, 25-50 micrometer in diameter . Cytoplasm surrounded by a plasma membrane.
A pollen grain has a two-layered wall: exine and intine.
o Exine: The hard outer layer. Made up of sporopollenin (highly resistant organic material).
It can withstand high temperatures and strong acids and alkali. Enzymes cannot degrade sporopollenin.
Exine has apertures called germ pores where sporopollenin is absent.
Pollen grains are preserved as fossils due to the presence of sporopollenin. Exine exhibits patterns and designs.
o Intine: The inner wall. It is a thin and continuous layer made up of cellulose and pectin.
A matured pollen grain contains 2 cells:
o Vegetative cell: It is bigger, has abundant food reserve and a large irregularly shaped nucleus.
o Generative cell: It is small and floats in the cytoplasm of the vegetative cell. It is spindle-shaped with dense cytoplasm and a nucleus.
In over 60% of angiosperms, pollen grains are shed at the 2-celled stage. In others, the generative cell divides mitotically to give rise to the two male gametes before pollen grains are shed (3-celled stage).
- The shed pollen grains have to land on the stigma before they lose viability. The viability period of pollen grains is variable. It depends on temperature and humidity.
- The viability of pollen grains of some cereals (rice, wheat, etc.) is 30 minutes. Some members of Leguminosae, Rosaceae & Solanaceae have viability for months.
Economic importance of pollen grains:
o These are rich in nutrients. Pollen tablets are used as food supplements. Pollen tablets & syrups increase the performance of athletes and racehorses.
o Pollen grains can be stored for years in liquid nitrogen (-196 degree Celcius). They are used as pollen banks, similar to seed banks, in crop breeding programmes.
o Pollen grains of some plants (e.g. Parthenium or carrot grass) are allergic for some people. It leads to chronic respiratory disorders – asthma, bronchitis, etc.
- It represents the female reproductive part of the flower.
- It may consist of a single pistil (monocarpellary) or more than one pistil (multicarpellary).
- In multicarpellary, the pistils may be fused (syncarpous) or free (apocarpous).
Each pistil has three parts:
o Stigma: It is a landing platform for pollen grains.
o Style: It is an elongated slender part beneath the stigma.
o Ovary: It is the basal bulged part of the pistil. Inside the ovary is the ovarian cavity (locule) in which the placenta is located. Arising from the placenta are the ovules (megasporangia). The number of ovules in an ovary may be one (wheat, paddy, mango etc.) to many (papaya, water melon, orchids etc.).
- It is a small structure attached to the placenta through a stalk (funicle). The junction where the body of the ovule and funicle fuse is called the hilum.
- Each ovule has one or two protective envelopes called integuments. Integuments encircle the ovule except at the tip where a small opening (micropyle) is present.
- Opposite the micropylar end is the chalaza (basal part).
- Enclosed within the integuments, there is a mass of cells called nucellus. Its cells contain reserve food materials.
- Located in the nucellus is the embryo sac (female gametophyte). An ovule generally has a single embryo sac formed from a megaspore through meiosis.
It is the formation of megaspores from the megaspore mother cell (MMC).
– Ovules generally differentiate a single megaspore mother cell in the micropylar region of the nucellus.
It is a large cell containing dense cytoplasm and a prominent nucleus.
– The MMC undergoes meiotic division. It results in the production of 4 megaspores.
Female gametophyte (embryo sac):
In a majority of flowering plants, one of the megaspores is functional while the other three degenerate.
– The functional megaspore develops into the female gametophyte. This method of embryo sac formation from a single megaspore is termed monosporic development.
Formation of the embryo sac:
The nucleus of the functional megaspore divides mitotically to form two nuclei. They move to the opposite poles, forming a 2-nucleate embryo sac.
– The nuclei again divide two times forming 4-nucleate and 8-nucleate stages of the embryo sac.
These divisions are strictly free nuclear, i.e. nuclear divisions are not followed immediately by cell wall formation.
– After the 8-nucleate stage, cell walls are laid down leading to the organization of the typical female gametophyte or embryo sac.
– 6 of the 8 nuclei are surrounded by cell walls and organized into cells.
Remaining 2 nuclei (polar nuclei) are situated below the egg apparatus in the large central cell.
Distribution of the cells within the embryo sac: A typical mature embryo sac is 8-nucleate and 7-celled.
o 3 cells are grouped at the micropylar end and form egg apparatus. It consists of 2 synergids and one egg cell.
o Synergids have special cellular thickenings at the micropylar tip called filiform apparatus. It helps to guide the pollen tubes into the synergid.
o 3 cells at the chalazal end are called the antipodals.
o The large central cell has two polar nuclei.
- It is the transfer of pollen grains from the anther to the stigma of a pistil.
- Some external agents help the plants for pollination. Depending on the source of pollen, pollination is 3 types.
a. Autogamy |self pollination
In this, pollen grains transfer from the anther to the stigma of the same flower.
In flowers with exposed anthers & stigma, complete autogamy is rare.
Autogamy in such flowers requires synchrony in pollen release and stigma receptivity. Also, anthers & stigma should lie close to each other.
Plants like Viola (common pansy), Oxalis & Commelina produce 2 types of flowers:
• Chasmogamous flowers: They are similar to flowers of other species with exposed anthers and stigma.
• Cleistogamous flowers: They do not open at all. Anthers & stigma lie close to each other.
They are autogamous. When anthers dehisce in the flower buds, pollen grains come in contact with the stigma for pollination.
Cleistogamous flowers produce assured seed-set even in the absence of pollinators.
In this, pollen grains transfer from the anther to the stigma of another flower of the same plant.
It is functionally cross-pollination involving a pollinating agent. But it is genetically similar to autogamy since the pollen grains come from the same plant.
c. Xenogamy |cross pollination
In this, pollen grains transfer from anther to the stigma of a different plant. It brings genetically different pollen grains to the stigma.
Agents of Pollination
1.Abiotic agents (wind & water)
Pollination by wind (anemophily):
More common abiotic agent. – Wind pollinated flowers often have a single ovule in each ovary and numerous flowers packed into an inflorescence.
E.g. Corncob – the tassels are the stigma and style which wave in the wind to trap pollen grains. Wind-pollination is quite common in grasses.
Ways for effective pollination:
- The flowers produce an enormous amount of pollen.
- The pollen grains are light and non-sticky so that they can be transported in wind currents.
- They often possess well-exposed stamens (for easy dispersion of pollens into wind currents).
- Large, feathery stigma to trap air-borne pollen grains.
Pollination by water (hydrophily):
It is quite rare. It is limited to about 30 genera, mostly monocotyledons. E.g. Vallisneria & Hydrilla (freshwater), Zostera (marine sea-grasses), etc.
As against this, water is a regular mode of transport for the male gametes among the lower plants.
It is believed, particularly for some bryophytes & pteridophytes, that their distribution is limited because of the need for water for the transport of male gametes and fertilization.
In Vallisneria, the female flower reaches the surface of the water by the long stalk and the male flowers or pollen grains are released onto the surface of the water.
They are carried by water currents and reach the female flowers.
In seagrasses, female flowers remain submerged in water. Pollen grains are long and ribbon-like. They are carried inside the water and reach the stigma.
– The pollen grains of most of the water-pollinated species have a mucilaginous covering to protect from wetting.
Not all aquatic plants use hydrophily. In most aquatic plants (water hyacinth, water lily, etc.), the flowers emerge above the level of water for entomophily or anemophily.
– Wind and water pollinated flowers are not very colorful and do not produce nectar.
2.Biotic agents (animals)
- The majority of flowering plants use animals as pollinating agents. E.g. Bees, butterflies, flies, beetles, wasps, ants, moths, birds (sunbirds & hummingbirds) bats, primates (lemurs), arboreal (tree-dwelling) rodents, reptiles (gecko lizard & garden lizard), etc.
- Pollination by insects (Entomophily), particularly bees are more common.
- Often flowers of animal pollinated plants are specifically adapted for a particular species of animal.
Features of insect-pollinated flowers:
- Large, colorful, fragrant, and rich in nectar. Nectar & pollen grains are the floral rewards for pollination.
- When the flowers are small, they form inflorescence to make them visible.
- The flowers pollinated by flies and beetles secrete foul odors to attract these animals.
- The pollen grains are generally sticky.
- When the animal comes in contact with the anthers and the stigma, its body gets pollen grains. When it comes in contact with the stigma, it results in pollination.
- Some plants provide safe places as a floral reward to lay eggs.
E.g. Amorphophallus (It has the tallest flower of 6 feet).
A moth species and the plant Yucca cannot complete their life cycles without each other.
The moth deposits its eggs in the locule of the ovary. The flower gets pollinated by moths.
The larvae come out of the eggs as seeds start developing.
Many insects consume pollen or nectar without bringing about pollination. They are called pollen/nectar robbers.
Hermaphrodite flowers can undergo self-pollination. Continued self-pollination results in inbreeding depression.
To avoid self-pollination and encourage cross-pollination, there are some devices in plants:
a. Avoiding synchronization: Here, the pollen is released before the stigma becomes receptive or the stigma becomes receptive before the release of pollen. It prevents autogamy.
b. Arrangement of anther & stigma at different positions: This also prevents autogamy.
c. Self-incompatibility: It is a genetic mechanism to prevent self-pollen (from the same flower or other flowers of the same plant) from fertilization by inhibiting pollen germination or pollen tube growth in the pistil.
d. Production of unisexual flowers: If male & female flowers are present on the same plant (i.e., monoecious, e.g. castor & maize), it prevents autogamy but not geitonogamy.
In dioecious plants (e.g. papaya), male and female flowers are present on different plants (dioecy). This prevents both autogamy and geitonogamy.
It is a process in which pistil recognizes compatible or incompatible pollen through the chemical components produced by them.
– If the pollen is compatible (right type), the pistil accepts it and promotes post-pollination events. Pollen grain germinates on the stigma to produce a pollen tube through one of the germ pores.
The contents of the pollen grain move into the pollen tube. The pollen tube grows through the tissues of stigma and style and reaches the ovary.
If the pollen is incompatible (wrong type), the pistil rejects pollen by preventing pollen germination on the stigma or the pollen tube growth in the style.
In some plants, pollen grains are shed at 2-celled conditions (a vegetative cell & a generative cell). In such plants, the generative cell divides and forms the two male gametes during the growth of the pollen tubes in the stigma.
In plants that shed pollen in the 3-celled condition, pollen tubes carry 2 male gametes from the beginning.
– Pollen tube reaches the ovary, then enters the ovule through the micropyle, and then enters one of the synergids through the filiform apparatus.
The filiform apparatus present at the micropylar part of the synergids guides the entry of the pollen tube.
A plant breeder can manipulate pollen-pistil interaction, even in incompatible pollinations, to get desired hybrids.
- It is a crop improvement programme in which desired pollen grains are used for pollination.
- This is achieved by the following techniques:
o Emasculation: Removal of anthers from the bisexual flower bud of a female parent before the anther dehisces.
o Bagging: Here, emasculated flowers are covered with a suitable bag (made up of butter paper) to prevent contamination of its stigma with unwanted pollen.
When the stigma attains receptivity, mature pollen grains collected from anthers of the male parent are dusted on the stigma.
Then the flowers are rebagged and allowed to develop the fruits.
For unisexual flowers, there is no need for emasculation. 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.
DOUBLE FERTILISATION |Describe Double Fertilization In Plants
After entering one of the synergids, the pollen tube releases the 2 male gametes into the cytoplasm of the synergid.
One male gamete moves towards the egg cell and fuses with its nucleus (syngamy). This forms the zygote (a diploid cell).
The other male gamete moves towards the two polar nuclei located in the central cell and fuses with them to produce a triploid primary endosperm nucleus (PEN). As it involves the fusion of 3 haploid nuclei, it is called triple fusion.
Since 2 types of fusions (syngamy & triple fusion) take place in an embryo sac, it is called double fertilization.
It is an event unique to flowering plants.
The central cell after triple fusion becomes the primary endosperm cell (PEC) and develops into the endosperm while the zygote develops into an embryo.
POST- FERTILISATION: STRUCTURES & EVENTS |what are post-fertilization events
Post-fertilisation events: Endosperm & embryo development, maturation of ovule(s) into seed(s) & ovary into fruit.
The primary endosperm cell divides repeatedly and forms a triploid endosperm tissue.
Endosperm cells are filled with reserve food materials. They are used for the nutrition of the developing embryo.
In common endosperm development, the PEN undergoes successive nuclear divisions to give rise to free nuclei. This stage is called the free-nuclear endosperm. The number of free nuclei varies greatly.
The endosperm becomes cellular due to the cell wall formation. The tender coconut water is a free-nuclear endosperm (made up of thousands of nuclei) and the surrounding white kernel is the cellular endosperm.
The embryo develops at the micropylar end of the embryo sac where the zygote is situated.
– Most zygotes divide only after the formation of a certain amount of endosperm. This is an adaptation to provide nutrition to the developing embryo.
Though the seeds differ greatly, the embryogeny (early embryonic developments) is similar in monocots & dicots.
– The zygote gives rise to the proembryo and subsequently to the globular, heart-shaped, and mature embryo.
- It has an embryonal axis and 2 cotyledons.
- – The portion of the embryonal axis above the level of cotyledons is the epicotyl, which terminates with the plumule (stem tip).
- – The cylindrical portion below the level of cotyledons is hypocotyl that terminates with the radicle (root tip). The root tip is covered with a root cap.
They possess only one cotyledon.
In the grass family, the cotyledon is called the scutellum. – It is situated lateral to the embryonal axis.
At its lower end, the embryonal axis has the radicle and root cap enclosed in coleorhiza (an undifferentiated sheath).
– Portion of the embryonal axis above the level of attachment of the scutellum is the epicotyl.
It has a shoot apex and a few leaf primordia enclosed in coleoptile (a hollow foliar structure).
Seed from Ovule
- Seed is the fertilized ovule formed inside fruits. It is the final product of sexual reproduction. – It consists of seed coat(s), cotyledon(s) & an embryo axis.
- The cotyledons are simple, generally thick, and swollen due to storage food (as in legumes).
Mature seeds are 2 types:
- Non-albuminous seeds: have no residual endosperm as it is completely consumed during embryo development (e.g., pea, groundnut, beans).
- Albuminous seeds: retain a part of endosperm as it is not completely used up during embryo development (e.g., wheat, maize, barley, castor, coconut, sunflower).
Occasionally, in some seeds (black pepper, beet, etc.) remnants of nucellus are also persistent. It is called perisperm.
Integuments of ovules harden as tough protective seed coats. It has a small pore (micropyle) through which O2 & water enter into the seed during germination.
As the seed matures, its water content is reduced and seeds become dry (10-15 % moisture by mass). The general metabolic activity of the embryo slows down.
The embryo may enter a state of inactivity (dormancy). If favorable conditions are available (adequate moisture, oxygen, and suitable temperature), they germinate.
Fruit from Ovary
The ovary develops into a fruit. Transformation of ovules into seeds and ovary into fruit proceeds simultaneously.
– The wall of the ovary develops into the pericarp (wall of fruit).
The fruits may be fleshy (e.g. guava, orange, mango, etc.) or dry (e.g. groundnut, mustard etc.).
– Fruits are 2 types:
o True fruits : In most plants, the fruit develops only from the ovary and other floral parts degenerate and fall off. They called true fruits.
o False fruits : In this, the thalamus also contributes to fruit formation. E.g. apple, strawberry, cashew etc.
In some species, fruits develop without fertilization. Such fruits are called parthenocarpic fruits. E.g. Banana.
Parthenocarpy can be induced through the application of growth hormones. Such fruits are seedless.
Advantages of seeds:
- Since pollination and fertilisation are independent of water, seed formation is more dependable.
- Seeds have better adaptive strategies for dispersal to new habitats and help the species to colonize in other areas.
- They have food reserves. So young seedlings are nourished until they are capable of photosynthesis.
- The hard seed coat protects the young embryo.
- Being products of sexual reproduction, they generate new genetic combinations leading to variations
- Dehydration and dormancy of mature seeds are crucial for the storage of seeds. It can be used as food throughout the year and also to raise crops in the next season.
Viability of seeds after dispersal:
In a few species, the seeds lose viability within a few months. Seeds of many species live for several years.
Some seeds can remain alive for hundreds of years. The oldest is that of a lupine (Lupinus arcticus) excavated from Arctic Tundra. The seed germinated and flowered after an estimated record of 10,000 years of dormancy.
– 2000 years old viable seed is of the date palm (Phoenix dactylifera) discovered during the archeological excavation at King Herod’s palace near the Dead Sea.
APOMIXIS AND POLYEMBRYONY
Apomixis is the production of seeds without fertilization. E.g. Some species of Asteraceae and grasses.
- It is a form of asexual reproduction that mimics sexual reproduction.
Development of apomictic seeds:
In some species, the diploid egg cell is formed without reduction division and develops into the embryo without fertilization.
In many species (e.g. many Citrus & Mango varieties) some of the nucellar cells surrounding the embryo sac divide, protrude into the embryo sac, and develop into the embryos.
In such a species, each ovule contains many embryos. The occurrence of more than one embryo in a seed is called polyembryony.
Importance of apomixis in the hybrid seed industry
- If the seeds collected from hybrids are sown, the plants in the progeny will segregate and lose hybrid characters.
- Production of hybrid seeds is costly. Hence the cost of hybrid seeds is also expensive for the farmers.
- If the 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 crops year after year.