The below mentioned article provides a study-note on photoperiodism.

Photoperiodism:

The plants in order to flower require a certain day length i.e., the relative length of day and night which is called as photoperiod. The response of plants to the photoperiod expressed in the form of flowering is called as photoperiodism.

The phenomenon of photoperiodism was first discovered by Garner and Allard (1920, 22) who observed that the Biloxi variety of Soybeans (Glycine max) and ‘Maryland Mammoth’ variety of tobacco (Nicotiana tabacum) could be made to flower only when the daily exposure to the light was reduced below a certain critical duration and after many complex experiments concluded that ‘the relative length of the day is a factor of the first importance in the growth and development of plants’. Depending upon the duration of the photoperiod, they classified plants into three categories.

(1) Short Day Plants (SDP):

These plants require a relatively short day light period (usually 8-10 hours) and a continu­ous dark period of about 14-16 hours for subsequent flowering (Fig. 18.1A). Some examples of these plants which are also known as long-night-plants are Maryland Mammoth variety of to­bacco (Nicotiana tabacum) Biloxi variety of Soybeans (Glycine max), Cocklebur (Xanthium pennsylvanicum).

i. In short day plants the dark period is critical and must be continuous. If this dark period is interrupted even with a brief exposure of red light (660-665 mµ wavelength), the short day plant will not flower (Fig. 18.1B).

Effect of a brief exposure of red light

ii. Maximum inhibition of flowering with red light occurs at about the middle of critical dark period.

iii. However, the inhibitory effect of red light can be overcome by a subsequent exposure with far-red light (730-735 mu wavelengths).

iv. Interruption of the light period by dark does not have inhibitory effect on flowering in short day plants (Fig. 18.1 C).

v. Prolongation of the continuous dark period initiates early flowering in short day plants.

(2) Long Day Plants (LDP):

These plants require a longer day light period (usually 14-16 hours) in a 24 hours cycle for subsequent flowering. Some examples of these plants which are also called as short night plants are Hyoscyamus niger (Henbane) Spinacea (spinach) Beta vulgaris (Sugar beet).

i. In long day plants the light period is critical.

ii. A brief exposure in the dark period or the prolongation of the light period stimulates flowering in long day plants.

(3) Day Neutral Plants:

These plants flower in all photoperiods ranging from 5 hours to 24 hours continuous ex­posure. Some of the examples of these plants are tomato, cotton, sunflower, cucumber and certain varieties of peas and tobacco.

During recent years certain intermediate categories of plants have also been recognised. They are,

Long Short Day Plants:

These are short day plants but must be exposed to long days during early periods of growth for subsequent flowering. Some of the examples of these plants are certain species of Bryophyllum.

Short-Long Day Plants:

These are long day plants but must be exposed to short days during early periods of growth for subsequent flowering. Some of the examples of these plants are certain varieties of wheat (Triticum) and rye (Secale).

Photoperiodic Induction:

Plants may require one or more inductive cycles for flowering. An appropriate photo­period in 24 hours cycle constitutes one inductive cycle. If a plant which has received suf­ficient inductive cycles is subsequently placed under un-favourable photoperiods, it will still flower. Flowering will also occur if a plant receives inductive cycles after intervals of un-favourable photoperiods (i.e., discontinuous inductive cycles). This persistence of photo­periodic after effect is called as photoperiodic induction.

i. An increase in the number of inductive cycles results in early flowering of the plant. For instance Xanthium (a short day plant) requires only one inductive cycle and normally flowers after about 64 days. It can be made to flower even after 13 days if it has received 4-8 inductive cycles. In such cases the number of flowers is also increased.

ii. Continuous inductive cycles promote early flowering than discontinuous inductive cycles.

Some of the example of plants which require more than one inductive cycles for sub­sequent flowering are Biloxi soybean (SDP) —2 inductive cycles; Salvia occidentalis (SDP) — 17 inductive cycles; Plantago lanceolata (LDP)—25 inductive cycles.

Perception of the Photoperiodic Stimulus and Presence of a Floral Hormone:

It is now well established that the photoperiodic stimulus is perceived by the leaves. As a result, a floral hormone is produced in the leaves which is then trans located to the apical tip, subsequently causing the initiation of floral primordia.

That the photoperiodic stimulus is perceived by the leaves can be shown by simple ex­periments on cocklebur (Xanthium pennsylvanicum), a short day plant. Cocklebur plant will flower if it has previously been kept under short-day conditions (Fig. 18.2 A). If the plant is defoliated and then kept under short day condition, it will not flower (Fig. 18.2 B). Flowering will also occur even if all the leaves of the plant except one leaf have been removed (Fig. 18.2 C).

Experiment on cocklebur plants

If a cocklebur plant whether intact of defoliated, is kept under long day conditions it will not flower (Fig. 18.2 D, E). But, if even one of its leaves is exposed to short day condition and the rest are under long day photoperiods, flowering will occur (Fig. 18.2 F).

The photoperiodic stimulus can be transmitted from one branch of the plant to another branch. For example, if in a two branched cocklebur plant one branch is exposed to short day and other to long day photo period, flowering occurs on both the branches (Fig. 18.3 A).

Flowering also occurs if one branch is kept under long day conditions and other branch from which all the leaves except one have been removed is exposed to short day condition (Fig. 18.3 B). However, if one branch is exposed to long photoperiod and the other has been defoliated under short day condition, flow­ering will not occur in any of the branches (Fig. 18.3 C).

Experiments on cocklebur plants

Nature of the Floral Hormone:

Although there are firm evidences for the existence of a floral hormone but it has not yet been isolated. Therefore, the nature of this hormone which has been named as florigen is not very clear. But it is quite evident that this hormone is a material substance which can be trans located from leaves to the apical tips situated at other parts of the plant resulting in flowering.

Recent researches are indicative of ‘florigen’ to be a macromolecule unlike other plant growth hormones which are rather small molecules. This macromolecule may possibly be a RNA or protein molecule which is trans located from the leaf to the apical tips (or meristems) via phloem in photo-induced plants (Corbesier and Coupland, 2005).

Grafting experiments in cocklebur plants have even proved that the floral hormone can be trans located from one plant to another. For example, if one branched cocklebur plant (Fig. 18.4 A) which has been exposed to short day conditions is grafted to another cocklebur plant kept under long day conditions, flowering occurs on both the plants (Fig. 18.4 B).

Obviously the flo­ral hormone has been transmitted to the receptor plant through graft union. But if a cocklebur plant is grafted to another similar plant both of which have been kept under long day condi­tions, flowering will not occur on either of the two plants (Fig. 18.4 C).

Grafting experiments in cocklebur plants

It has also been indicated that the floral hormone may be identical in short-day and long- day plants. For example, grafting experiments between certain long-day plants and short-day plants have shown that flowering occurs on both the plants even if one of them has been kept under non-inductive photoperiods.

Phytochrome:

It has already been seen that a brief exposure with red light during critical dark period inhibits flowering in short-day plants and this inhibitory effect can be reversed by a subse­quent exposure with far-red light. Similarly, the prolongation of the critical light period or the interruption of the dark period stimulates flowering in long-day plants. This inhibition of flowering in short-day plants and the stimulation of flowering in long-day plants involves the operation of a proteinaceous pigment called as phytochrome.

i. The pigment phytochrome exists in two different forms:

(i) Red light absorbing from which is designated as PR and

(ii) Far-red light absorbing form which is designated as PFR.

ii. These two forms of the pigment are photo chemically inter convertible.

iii. When PR form of the pigment absorbs red light (660-665mp), it is converted into PFR form.

iv. When PFR form of the pigment absorbs far-red light (730-735mp), it is converted into PR form.

v. The PFR form of the pigment gradually changes into PR form in dark.

Darkness

It is considered that during the day the PFR form of the pigments is accumulated in the plant which is inhibitory to flowering in short-day plants but is stimulatory in long–day plants. During critical dark period in short-day plants, this form gradually changes into PR form result­ing in flowering.

A brief exposure with red light will convert this form again into PR form thus inhibiting flowering. Reversal of the inhibitory effect of red light during critical dark period in SDP by subsequent far-red light exposure is because the PFR form after absorbing far-red light (730-735mµ) will again be converted back into PR form.

Prolongation of the critical light period or the interruption of the dark period by red-light in long-day plants will result in further accumulation of the PPR form of the pigment, thus stimu­lating flowering in long-day plants.

Successful purification of intact native phytochrome (from etiolated oat seedlings) was first re­ported by Vierstra and Quail in 1983. The native phytochrome is a soluble protein with a molecular weight of about 250 kDa. It’s a homodimer of two identical polypeptides each with a molecular weight of about 125 kDa.

Each polypeptide has a prosthetic group called as chromophore which is covalently linked to the polypeptide via a sulphur atom (Thioether Linkage) in the cysteine residue of the polypeptide. The protein part of the phytochrome is called as apoprotein. Apoprotein along with chromophore constitute holoprotein.

The chromophore of phytochrome is an open tetrapyrrole which is related to phycocyanobilin in structure and therefore, more recently this chromophore has been called as phytochromobilin. The structures of chromophores or the prosthetic groups of PR and PFR fomis of phytochrome which are cis and trans isomers of each other respectively, are given in Fig 18.5. The cis-trans isomerization occurs at carbon-15 in response to red and far-red light.

Apart from absorbing red and far-red light, the phytochrome also absorbs blue light. The PR form of phytochrome is blue while PFR form is olive-green in colour. But owing to very low conc. of phytochrome, the colour of this pigment is not visible in plant tissues. (Phytochrome accounts for less than 0.2 % of the total extractable protein in etiolated seedlings).

Structure of the chromophores

None of the two components of phytochrome i.e., apoprotein and chromophore, can absorb light alone.

Phytochromes have been detected in wide range of plants in angiosperms, gymnosperms, bryophytes and algae. Dark grown etiolated seedlings are richest sources of phytochrome where this pigment is especially concentrated in apical meristems. (Etiolated seedlings have therefore been used extensively in this connection).

Phytochromes have directly been detected in different parts of seedlings, in roots, cotyledons, hypocotyls, epicotyls, coleoptile, stems, petioles, leaf blades, vegetative buds, floral receptacles, inflorescences, developing fruits and seeds. Presence of phytochrome has also been shown indirectly in other plant materials.

Within the cells, phytochrome exists in nucleus and throughout the cytosol.

The chromophore of phytochrme is synthesized in plastids while apoprotein is synthe­sized on nuclear genome. Assembly of these two components of phytochrome is autocatalytic and occurs in cytosol.

There are two major types of phytochromes in plants, (i) type I and (ii) type II. The type I predominates in etiolated seedlings while type II in green plants and seeds (such as oat seeds). There are minor differences in molecular weight and spectral properties of these two types of phytochromes.

Type I phytochrome is encoded by PHY A gene while type II is encoded by PHY B, PHY C, PHY D and PHY E genes.

The exact mechanism of the action of phytochromes is not very clear. They act probably (a) by controlling active transport of ions and molecules across membranes probably by regulating ATPase activity, (b) by controlling the activity of membrane bound hormones such as gibberellins (c) modulating the activity of membrane bound proteins and (d) by regulating tran­scription of numerous genes involving multiple signal transduction pathways.

(Besides photoperiodism, a large number of phytochrome mediated phtoresponses are known in plants. A list of some of these photoresponses is given at the end of this chapter. See Chapter 25 for more information regarding phytochrome and related phenomena).

Gibberellins and the Flowering Response:

It is now well known that the gibberellins can induce flowering in long-day plants even under non-inductive short days. It is also definite that the gibberellins alone do not constitute the ‘florigen’, but it is usually held that the gibberellins are in some way connected with the overall process of flowering.

According to a scheme proposed by Brian (1958), a gibberellin like hormone is produced in the leaves during the photoperiod somewhat as follows:

CO2 → Precursor (P) → Gibberellin-like hormone

The precursor may be slightly stimulatory or inactive or antagonistic to the gibberellin-like hormone. Red irradiations promote the conversion of the precursor to the gibberellin-like hor­mone. In the dark there is a slow reconversion of the gibberellin-like hormone to the precursor.

This reconversion is accelerated by far-red irradiations. It is further presumed that high concentration of the gibberellin-like hormone leads to the synthesis of florigen in long-day plants. In short-day plants the synthesis of florigen takes place when the level of gibberellin-like hormone is low. But, flowering eventually follows once the florigen synthesis has taken place in both the cases.

The whole scheme is diagrammatically shown below:

Whole scheme

Importance of Photoperiodism:

(i) The knowledge of the phenomenon of photoperiodism has been of great practical importance in hybridisation experiments.

(ii) Although the floral hormone ‘florigen’ has not yet been isolated, the isolation and characterization of this hormone will be of utmost economic importance.

(iii) The phenomenon of photoperiodism is an excellent example of physiological preconditioning (or after-effect) where an external factor (i.e., the photoperiodic stimulus) induces some physiological changes in the plant the effect of which is not immediately visible. It lingers on in the plant and prepares the latter for a certain process (i.e., flowering) which takes place at a considerably later stage during the life history of the plant.

Some Phytochrome Mediated Photo responses in Plants:

1. Photoperiodism.

2. Seed germination.

3. Elongation of leaf, petiole, stem.

4. Hypocotyl hook unfolding.

5. Unfolding of grass leaf. ,

6. Sex expression.

7. Bud dormancy.

8. Plastid morphology.

9. Plastid orientation.

11. Rhizome formation.

12. Bulb formation.

13. Leaf abscission.

14. Epinasty.

15. Succulency

16. Enlargement of cotyledons.

17. Hair formation along cotyledons.

18. Formation of leaf primordia.

19. Flower induction.

20. Differentiation of primary leaves.

21. Formation of tracheary elements.

22. Differentiation of stomata.

23. Change in rate of cell respiration.

24. Formation of phenylalanine deaminase.

25. Synthesis of anthocyanins.

26. Increases in protein systhesis.

27. Increase in RNA synthesis.

28. Changes in the rate of fat degradation.

29. Changes in the rate of degradation of reserve proteins.

30. Auxin catabolism.

31. Incorporation of sucrose into plumular tissue.

32. Permeability of cell membranes.

33. Lipoxygenase metabolism.

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