Biology Notes for Class 12
Chapter 2: Sexual Reproduction in Flowering Plants
Chapter Summary
     Flowers are the seat of sexual reproduction in angiosperms. In the flower, androecium consisting of stamens represents the male reproductive organs and gynoecium consisting of pistils represents the female reproductive organs.
     A typical anther is bilobed, dithecous and tetrasporangiate. Pollen grains develop inside the microsporangia. Four wall layers, the epidermis, endothecium, middle layers and the tapetum surround the microsporangium. Cells of the sporogenous tissue lying in the centre of the microsporangium, undergo meiosis (microsporogenesis) to form tetrads of microspores. Individual microspores mature into pollen grains.
     Pollen grains represents the male gametophytic generation. The pollen grains have a two-layered wall, the outer exine and inner intine. The exine is made up of sporopollenin and has germ pores. Pollen grains may have two cells (a vegetative cell and generative cell) or three cells (a vegetative cell and two male gametes) at the time of shedding.
     The pistil has three parts – the stigma, style and the ovary. Ovules are present in the ovary. The ovules have a stalk called funicle, protective integument(s), and an opening called micropyle. The central tissue is the nucellus in which the archesporium differentiates. A cell of the archesporium, the megaspore mother cell divides meiotically and one of the megaspores forms the embryo sac (the female gametophyte). The mature embryo sac is 7-celled and 8-nucleate. At the micropylar end is the egg apparatus consisting of two synergids and an egg cell. At the chalazal end are three antipodals. At the centre is a large central cell with two polar nuclei.
     Pollination is the mechanism to transfer pollen grains from the anther to the stigma. Pollinating agents are either abiotic (wind and water) or biotic (animals).
      Pollen-pistil interaction involves all events from the landing of pollen grains on the stigma until the pollen tube enters the embryo sac (when the pollen is compatible) or pollen inhibition (when the pollen is incompatible). Following compatible pollination, pollen grain germinates on the stigma and the resulting pollen tube grow through the style, enter the ovules and finally discharges two male gametes in one of the synergids. Angiosperms exhibit double fertilisation because two fusion events occur in each embryo sac, namely syngamy and triple fusion. The products of these fusions are the diploid zygote and the triploid primary endosperm nucleus (in the primary endosperm cell). Zygote develops into the embryo and the primary endosperm cell forms the endosperm tissue. Formation of endosperm always precedes development of the embryo.
     The developing embryo passes through different stages such as the proembryo, globular and heart-shaped stages before maturation. Mature dicotyledonous embryo has two cotyledons and an embryonal axis with epicotyl and hypocotyl. Embryos of monocotyledons have a single cotyledon. After fertilisation, ovary develops into fruit and ovules develop into seeds.
     A phenomenon called apomixis is found in some angiosperms, particularly in grasses. It results in the formation of seeds without fertilisation. Apomicts have several advantages in horticulture and agriculture.
     Some angiosperms produce more than one embryo in their seed. This phenomenon is called polyembryony.
FLOWER – A FASCINATING ORGAN OF ANGIOSPERMS
Flowers are objects of aesthetic, ornamental, social, religious and cultural value – they have always been used as symbols for conveying important human feelings such as love, affection, happiness, grief, mourning, etc. To a biologist, flowers are morphological and embryological marvels and the sites of sexual reproduction. Figure 2.1 will help you recall the parts of a typical flower.
PRE FERTILIZATION: STRUCTURE AND EVENTS:
Ø Hormonal and structural changes in plants leads to development of flower,
Ø Androecium consists of a whorl of stamens represents male sex organ.
Ø Gynoecium represents the female reproductive organ.
Stamen, Microsporangium and Pollen grain:
Ø Typical stamen consists of two parts, long and slender stalk called filament and terminal bilobed structure called anther.
Ø Atypical angiosperm anther is bilobed.
Ø Each lobe have two theca i.e. dithecous.
Ø Each anther contains four microsporangia located at the corners, two in each lobe.
Ø Microsporangia become pollen sacs and are packed with pollen grains.
Structure of microsporangium:
Ø Each microsporangium surrounded by four wall layers
- o   Epidermis
- o   Endothecium
- o   Middle layer.
- o   Tapetum.
Ø The innermost layer is tapetum which is multinucleated, with dense cytoplasm; it nourishes the developing pollen grain.
Ø The centers of each microsporangium contain homogenous cells called sporogenous tissues.
Microsporogenesis:
Ø The process of formation of microspores from pollen mother cell  through  meiosis  is called microsporogenesis.
Ø The   sporogenous   tissue   of  microsporangium   differentiated   into microspore   mother cell or pollen mother cell.
Ø Each microspore mother cell undergoes meiosis and gives rise to haploid microspore tetrad.
Ø On dehydration microspore tetrad dissociated to form four microspores.
Ø Each microspore developed into a pollen grain.
Pollen grain:
Ø Pollen grain represents the male gametophytes.
Ø It is spherical and measuring about 25-50 micrometer in diameter.
Ø It is covered by two layers.
Ø 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.
Ø The exine has prominent apertures called germ pore where sporopollenin is absent.
Ø The  inner  wall  of  pollen  grain  is  called intine. It   is  thin  and  continuous  layer   made of cellulose and pectin.
Ø On maturity the pollen grain contains two cells, the vegetative cell and generative cell.
Ø The vegetative cell is bigger, has abundant food reserve and a large irregularly shaped nucleus.
Ø The generative cell is small and floats in the cytoplasm of vegetative cell.
Ø In 60% of angiosperms, pollen grains are shed at this 2-celled stage.
Ø In others the generative cell divides mitotically to form two male gametes before pollen grain are shed (3-celled stage).
Economic importance of pollen grain:
Ø Pollen grain may cause severe allergies and bronchial afflictions.
Ø It may cause chronic respiratory disorders – asthma, bronchitis, etc.
Ø Pollen grain of Parthenium or carrot grass causes pollen allergy.
Ø Pollen grains are rich in nutrients hence used as pollen tablets for food supplements.
Ø Pollen consumptions increase performance of athletes and race horses.
Ø After shedding the viability depends on temperature and humidity.
Ø In wheat and rice the pollen grain lose viability within 30 min. of their release.
Ø In Rosaceae, Leguminoseae and Solanaceae they remain viable for months.
Ø Pollen grain can be preserved for years in liquid nitrogen (-196oC).
The Pistil, Megasporangium (ovule) and Embryo Sac:
Ø The Gynoecium represents the female reproductive part of the flower.
Ø The Gynoecium may contain single pistil (monocarpellary) or may have more than one pistil (multicarpellary).
Ø Fused pistils are called syncarpous and free pistils are called apocarpous.
Ø Each pistil has three parts the stigma, style and ovary.
Ø Inside the ovary is the ovarian cavity (locule).
Ø The placenta located inside the ovarian cavity.
Ø Megasporongia or ovules arise from the placenta.
Ø The number of ovule inside the ovary may be single or many.
The Megasporangium (Ovule):
Ø Ovule is a small structure attached to the placenta of locule with a stalk called funicle.
Ø The body of the ovule fused with the funicle in the region called hilum.
Ø Hilum is the junction between the funicle and ovule.
Ø Each ovule has one or two protective envelops called integuments.
Ø Integument covered the ovule except an opening at the top called micropyle.
Ø Opposite of the micropylar end, is the chalaza, representing the basal part of the ovule?
Megasporogenesis:
Ø The     process     of     formation     of megaspores from     the megaspore     mother cell is called Megasporogenesis.
Ø In the centre of the ovule there is a mass of tissue called nucellus.
Ø Cells of nucellus have abundant reserve food materials.
Ø One cell of the nucellus towards micropylar  end  differentiated  into megaspore mother cell (MMC).
Ø It is a large diploid cell, dense cytoplasm with prominent nucleus.
Ø The MMC undergo meiotic division resulting four haploid megaspores.
Female gametophyte:
Ø Out of four megaspores, one megaspore is functional and other three degenerates.
Ø The functional megaspore developed into the female gametophyte.
Ø Female gametophyte is known as the embryo sac.
Ø Development of embryo sac from a single megaspore is called as monosporic type of embryo sac.
Ø The nucleus of the functional megaspore divided by mitotic division to form two nuclei which move to the opposite pole, 2-nucleated embryo sac.
Ø Two successive mitotic division leads to formation of 4-nucleate and later 8-nucleate stages of the embryo sac.
Ø All mitotic divisions are free nuclear type; karyokinesis is not followed by cytokinesis.
Ø Six of the eight nuclei are surrounded by cell walls and organized into cells.
Ø Three cells are grouped together at the micropylar end, constitute the egg apparatus.
Ø The egg apparatus, in turn consists of two synergids and one egg cell.
Ø Synergids have special filiform apparatus, which play an important role in guiding the entry of pollen tube into the synergids.
Ø Three cells arranged towards chalazal end are called antipodal cells.
Ø The large central cell has two polar nuclei.
Ø A typical angiosperm embryo sac at maturity is 8- nucleated and 7-celled.
Pollination:
Ø Transfer of pollen grains from the anther to the stigma of a pistil is termed as pollination.
Ø Both male and female gametes are non-motile.
Kinds of pollination:
i. Autogamy:
Ø Pollination within same flower.
Ø In open and exposed anthers and stigma autogamy is rare.
Ø Viola, Oxalis and Commelina produce two types of flowers:
- Chasmogamous: exposed anther and stigma
- Cleistogamous: closed anther and stigma.
Ø Cleistogamous flower is invariably autogamous and assured seed set even in the absence of the pollinator.
ii. Geitonogamy:
Ø Pollination between two flowers of the same plant.
Ø Pollination by pollinating agent.
Ø Genetically similar to the autogamy.
iii. Xenogamy:
Ø Transfer of pollen grains from the anther to the stigma of different plant.
Ø It is commonly called as cross-pollination.
Ø It brings genetically different types of pollen grains to the stigma.
Agents of pollination:
Ø Plant use two abiotic agent i.e. wind and water for pollination.
Ø One biotic agent for pollination such as animals.
Ø Majority of plant use biotic agent for pollination.
Ø Few plant use abiotic pollinating agent.
Anemophily:
Ø Pollinating agent is wind.
Ø Plants produces enormous amount of pollen when compared to the number of ovules available for pollination to compensate the uncertainties of pollination.
Ø Flowers with well exposed stamens.
Ø Large feathery stigma to trap air-borne pollen grains.
Ø Most wind pollinated flower contains single ovule in one ovary and numerous flower packed into an inflorescence e.g. corn cob.
Ø Pollen grains are light and non-sticky.
Hydrophily:
Ø Pollination by abiotic agent like water.
Ø This type of pollination is very rare, about 30 genera, mostly monocot.
Ø Vallisneria, Hydrilla and Zostera are the common example for Hydrophily.
Ø All aquatic plants are not Hydrophily.
Ø Pollen grains released into the surface of water and carried to the stigma by air current as in Vallisneria.
Ø In sea grass the flowers remained submerged.
Ø Pollen grains are long, ribbon like and carried passively inside the water
Ø Pollen grains are protected from wetting by mucilaginous covering.
Pollination by biotic agent:
Ø Majority of flowering plants use a range of animals as pollinating agents.
Ø Among the animal, insect particularly bees are the dominant biotic agents for pollination.
Ø Insect pollinating flowers are very large, colorful, fragrant and rich in nectar.
Ø Small flowers present in cluster to make them conspicuous.
Ø Flower pollinated by flies and beetles secrete foul odours.
Ø Nectar and pollen grains are the usual floral rewards for insects.
Ø In some species floral rewards are in providing safe places to lay eggs: e.g. Amorphophallus.
Ø A species of moth and Yucca plant cannot complete their life cycle without each other. The moth deposits its eggs in the locule of the ovary and the flower in turn get pollinated by the moth.
Ø Many insects may consume pollen or nectar without bring about pollination. Such floral visitors are referred as pollen/nectar robbers.
Outbreeding Devices:
Ø Majority of the flowering plants produce hermaphrodite flower and undergo autogamy.
Ø Continuous autogamy or self-pollination results in inbreeding depression.
Ø Flowering plants have developed many devices to avoid self pollination and to encourage cross- pollination. Such devices are called Outbreeding devices.
- Pollen released and stigma receptivity is not synchronized.
- Spatial separation of anthers and stigmas
- Anther and stigma are placed at different positions.
- Self incompatibility.
- Production of unisexual flowers.
Pollen pistil Interaction:
Ø All the events – from pollen deposition on the stigma until pollen tubes enter the ovule – are together referred as pollen-pistil interaction.
Ø Pollination does not guarantee the transfer of the right type of pollen grain to the right type of stigma.
Ø The pistil has the ability to recognize the pollen whether it is compatible or incompatible.
Ø If it is right type the stigma allow the pollen to germinate.
Ø If it is wrong type the stigma rejects the pollen, preventing germination.
Ø The ability of the pistil to recognize the pollen by continuous dialogue mediated by chemical like Boron, Inositol and sucrose level.
Ø Following compatible pollination, the pollen grain produce pollen tube through one of the germ pore.
Ø Content of the pollen grain move into the pollen tube.
Ø Pollen tube grows through the tissues of the stigma and style and reaches the ovary.
Ø If the pollen grain is in 2-celled stage the generative cell divides and forms two male gametes inside the pollen tube.
Ø If the pollen grain is in 3- cell stage the pollen tube carry two male gametes from the beginning.
Ø Pollen tube enters into the ovule through micropyle and then into the embryo sac through synergids guided by filiform apparatus.
Artificial hybridization:
Ø One of the major approaches of crop improvement programme.
Ø Only desired pollen grain used for pollination.
Ø Stigma is protected from contamination (from unwanted pollen grain).
Ø Removal of anthers from the flower bud before the anther dehisces is called emasculation.
Ø 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.
Ø If the female flower is unisexual there is no need of emasculation.
Double fertilization:
Ø After entering one of the synergids, the pollen tube releases two male gametes into the cytoplasm of the synergids.
Ø Syngamy: one of the male gamete fused with egg cell, to form a diploid zygote.
Ø Two polar nuclei of central cell fused to form a diploid secondary nucleus.
Ø Triple fusion: The second male gamete fused with the secondary nucleus to form  a triploid primary endosperm nucleus.
Ø Since two type of fusion, syngamy and triple fusion take place in the embryo sac the phenomenon is termed as double fertilization.
Ø The central cell after triple fusion becomes primary endosperm cell and developed into the endosperm.
Ø The zygote developed into an embryo.
POST- FERTILIZATION : STRUCTURE AND EVENTS
Events of endosperm and embryo development, maturation of ovule into seed and ovary into fruit, are collectively termed as post-fertilization events.
Endosperm:
Ø Development of endosperm takes place before the embryo development.
Ø Primary endosperm cell divides repeatedly to form a triploid endosperm.
Ø Cells are filled with reserve food material and are used for the nutrition of the developing embryo.
Ø PEN undergoes successive nuclear division to give rise to free nuclei. This is called free-nuclear endosperm.
Ø Subsequently cell wall formation takes place and become cellular endosperm.
Ø The coconut water is free nuclear endosperm and the white kernel is the cellular endosperm.
Ø Endosperm may be consumed completely during embryo developed or it may be consumed during germination of seed.
Embryo:
Ø Zygote formed and placed at the micropylar end of the embryo sac.
Ø Zygote starts its development only after some amount of endosperm formed.
Ø Embryo development takes place in following stages:
- Proembryo
- Globular stage
- Heart shaped
- Matured embryo.
Dicot embryo:
Ø A typical dicotyledonous embryo consists of an embryonal axis and two cotyledons.
Ø Embryonal axis above the cotyledon is the epicotyls.
Ø Terminal part of the epicotyls is the plumule (gives rise to the shoot).
Ø Embryonal axis below the cotyledon is the hypocotyl.
Ø The terminal part of the hypocotyl is called the radicle (root tip).
Ø The root tip is covered by the root cap.
Monocot embryo:
Ø Possesses only one cotyledon.
Ø In grass family the cotyledon is called scutellum.
Ø Scutellum situated towards one side of the embryonal axis.
Ø Radicle and the root cap enclosed by a sheath called coleorhiza.
Ø The portion of the embryonal axis above level of attachment of scutellum is called epicotyls.
Ø Epicotyl has the shoot apex or plumule enclosed by hollow foliar structure called coleoptile.
Ø Seed is the final product of the sexual reproduction.
Ø Seed consists of seed coat, cotyledon and an embryo axis.
Ø Cotyledon stores the reserve food material for development and germination.
Ø Matured seed without endosperm called non-albuminous. (Ground nut)
Ø A part of the endosperm retained in matured seed is Albuminous.
Ø Remainants of nucellus in the matured seed is called perisperm. E.g. black peeper, beet.
Ø The wall of the ovary develops into the wall of fruit called pericarp.
Ø Fruit developed from the ovary is called true fruit.
Ø In apple, strawberry, cashew, the thalamus contributes in the fruit formation is called false fruit.
Ø Fruit developed without fertilization is called Parthenocarpic fruits.
APOMIXIS AND POLYEMBRYONY:
Ø Apomixis is very common in Asteraceae and grasses.
Ø Seeds are produced without fertilization.
Ø Apomixis is a type of asexual reproduction which mimics the sexual reproduction.
Ø Diploid egg cell is formed without meiosis and develops into seed without fertilization.
Ø In Citrus and Mango the nucellar cells starts dividing, protrude into the embryo sac and develop into embryo.
Ø Ovule having more than one embryo is termed as polyembryony.
Ø Hybrid plants are developed by apomixis to maintain the genetic identity.
Disclaimer: All contents are originally prepared by Shri K C Meena Ji, Principal, KVS.Â
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