Megasporogenesis and Megagametogenesis in Plants | Embryology | Biology

Read this essay to learn about the process of megasporogenesis and megagametogenesis in plants, explained with the help of suitable diagrams.

Development of Megaspore Mother Cell:

The ovule develops as multicellular placen­tal outgrowth including the epidermal and a number of hypodermal cells. With further deve­lopment, this gives rise to nucellus and one or two integuments from its basal region. In ovules, with two integuments, usually the inner one is formed first than the outer one. The inner one is more delicate and inconspicuously developed than the outer one.

One hypodermal cell of the nucellus becomes differentiated from the other by its bigger size, dense cytoplasm and conspicuous nucleus, called archesporial cell (Fig. 3.6A). The archesporial cell divides transversely and forms an inner primary sporogenous cell and an outer primary parietal cell (Fig. 3.6B).

The primary sporogenous cell functions as mega­spore mother cell (Fig. 3.6C) and the primary parietal cell undergoes repeated vertical divi­sions and forms layers of parietal cells (Fig. 3.6C). Sometimes, the archesporial cell does not divide and directly functions as megaspore mother cell.

Megasporogenesis (Development of Megaspores):

The megaspore mother cell is diploid (2n), which undergoes meiosis and forms four haploid (n) megaspores (Fig. 3.6D). The first divi­sion of megaspore mother cell is transverse, forming two cells. Both the cells again divide transversely and thus four (4) haploid mega­spores are formed.

The megaspores are then arranged in an axial row, called linear tetrad (Fig. 3.6D). Out of four megaspores, only one which remains towards the chalazal end behaves as functional megaspore and the other three which remain towards the micropylar end, gradually degenerate (Fig. 3.6E). The func­tional megaspore forms the female gameto­phyte i.e., the embryo sac.

Megagametogenesis (Formation of female gametophyte i.e., Embryo sac):

Megaspore (n) is the first cell of the female gametophyte (Fig. 3.7A). The functional mega­spore becomes enlarged at the expense of tape tum and the nucellus and thus forms the female gametophyte i.e., the embryo sac. Initially, the embryo sac is uninucleate and with further growth its nucleus divides by three successive divisions and forms eight nuclei (Fig. 3.7B, C and D).

Out of eight nuclei, initially four remain towards the micropyle end and the other four towards the chalazal end. One nucleus from each pole then moves towards the centre and forms a pair of polar nuclei (Fig. 3.7E). These nuclei fuse together and form 2n nucleus, the definitive nucleus. It is also known as polar fusion nucleus or secondary nucleus.

The three nuclei of the micropylar end form the egg appa­ratus and the rest three at the chalazal end are called antipodal cells. In the egg apparatus, each nucleus is surrounded by viscous mass of cyto­plasm without any wall, of which the middle one is the largest and called egg, ovum or oosphere and the rest two (one on each side of the egg) are the synergids or helping cells. The antipodal cells have viscous mass of cytoplasm, covered by cellulosic wall (Fig. 3.7F).

This type of embryo sac development is very common in angiosperms and is known as ordi­nary type or normal type or Polygonum type. This type is also known as monosporic type, because, out of four megaspores, only one remains functional and forms the embryo sac.

Other types of embryo sac development (Fig. 3.8):

Monosporic type:

1. Oenothera type:

In this type (like Polygonum type), usual linear tetrad of megaspores are formed, but instead of the innermost one, the outermost megaspore (which is present towards micropyle) remains functional and forms the embryo sac. The functional mega­spore undergoes two successive divisions and forms 4 nuclei.

All the nuclei remain towards the micropyle. Out of four nuclei, three nuclei form the egg apparatus (egg and two synergids) and the remaining one forms a sin­gle polar nucleus. Second polar nucleus and antipodal cells are absent, e.g., Oenothera and other members of Onagraceae.

Bisporic type:

2. Allium type:

The megaspore mother cell divides to form two cells, the upper one quickly degenerates. The lower one then divides and forms two nuclei, distributed in the two poles. Later on, both the nuclei undergo two successive divisions and form usual octant type of embryo sac, i.e., poly­gonum type. Here two megaspore nuclei take part in the development of embryo sac i.e., bisporic type, e.g., Allium, Scilla, Trillium etc., of Liliaceae.

Tetrasporic type:

3. Peperomia type:

The megaspore mother nucleus undergoes meiotic division and forms four nuclei which remain crosswise in the embryo sac without any wall. All the nuclei undergo two successive divisions and form 16 nuclei which remain dispersed inside the sac. Later on, out of 16 nuclei, egg and one synergid remain at the micropylar end, six antipodal cells towards the chalazal end, and the rest eight at the centre forming polar nuclei, e.g., Peperomia of Piperaceae etc.

4. Penaea type:

Like Peperomia type, 16 nuclei are formed, those remain crosswise in the embryo sac. Later on, the nuclei are dis­tributed in a different manner. The egg and two synergids remain at the micropylar end, three nuclei at the chalazal end, and four at the centre and three each on the two side walls, e.g., Penaea of Penaeaceae.

5. Drusa type:

Like Peperomia type, initially four megaspores are formed, these are distri­buted in different ways. One megaspore remains towards the micropyle, and the rest three at the chalazal end.

All the nuclei undergo two divisions and form 16 nuclei, out of which four nuclei remain towards the micropyle and the rest twelve at the chalazal end. In the mature embryo sac, egg and two synergids remain towards the micropyle, two (one from each pole) at the centre and the rest eleven at the chalazal end, e.g., Drusa oppositifolia of Apiaceae.

6. Fritillaria type:

Like Drusa type, out of four nuclei formed, one nucleus remains towards the micropyle, and the rest three at the chalazal end. The chalazal nuclei fused together and form 3n nucleus. Both the cells thus undergo one mitotic division and again form a tetrasporic stage. Out of four nuclei, two remain at each pole.

All the nuclei then undergo mitotic division and form eight nuclei. Out of four haploid nuclei at the micropyle, one egg and two synergids are formed, those remain at the micropylal end; three triploid nuclei at the chalazal end and one from each pole remain at the centre (one haploid and the other one triploid), e.g., Fritillaria, Tulipa and some other mem­bers of Liliaceae.

7. Plumbagella type:

It is like Fritillaria type which forms 1st and 2nd tetrasporic stage with two haploid nuclei at the micropyle and two triploid nuclei at the chalazal end of the embryo sac. Later on, the nuclei are distributed in such a way that the egg is at the micropyle, one triploid nucleus at the chalazal end and one triploid plus one hap­loid nuclei at the centre, e.g., Plumbagella of Plumbagellaceae.

8. Plumbago type:

It is like Penaea type where firstly four nuclei are formed followed by eight nucleated embryo sac. The two nuclei at each side (four sides) remain crosswise. Later on, four nuclei, one from each side, become aggregated in the centre. The nucleus at the micropylar end behaves as egg, e.g., Plumbago of Plumbaginaceae.

9. Adoxa type:

In this type, the megaspore mother nucleus divides meiotically into four nuclei arranged two at each end. Both the nuclei — further undergo mitotic division and thus eight nuclei are formed. Like the normal type i.e., Polygonum type, one egg and two synergids remain at the micropylar region, three antipodal cells at the chalazal end and two nuclei remain in the centre, e.g., Adoxa, Sambucus of Caprifoliaceae.