Ascent of Sap
In the
last chapter, we studied about water absorption from roots to xylem in a
lateral direction and here we will learn about the mechanism of distribution of
water inside the plant. Like tributaries join together to form a river,
millions of root hairs conduct a small amount of water and confluence in xylem,
the superhighway of water conduction. Xylem handles a large amount of water to
conduct to many parts in an upward direction.
The water
within the xylem along with dissolved minerals from roots is called sap and its upward transport is called ascent of sap.
There is
no doubt; water travels up along the vascular tissue. But vascular tissue has
two components namely Xylem and Phloem. Of these two, which is responsible for
the ascent of sap? The following experiment will prove that xylem is the only
element through which water moves up.
Cut a
branch of balsam plant and place it in a beaker containing eosin (red colour dye) water. After some time, a red streak appears
on the stem indicating the ascent of water. Remove the plant from water and cut
a transverse section of the stem and observe it under the microscope. Only
xylem element is coloured red, which indicates the path of water is xylem.
Phloem is not colored indicating that it has no role in the ascent of sap
(Figure 11.12).
In ascent
of sap, the biggest challenge is the force required to lift the water to the
top of the tallest trees. A number of theories have been put forward to explain
the mechanism of the ascent of sap. They are, A. Vital force theories, B. Root
pressure theory, and C. Physical force theory.
According
to vital force theories, living cells are mandatory for the ascent of sap.
Based on this the following two theories derived:
Periodic
changes in osmotic pressure of living cells of the xylem parenchyma and
medullary ray act as a pump for the movement of water.
Bose
invented an instrument called Crescograph,
which consists of an electric probe
connected to a galvanometer (Figure 11.13). When a probe is inserted
Bose believed a rhythmic pulsating movement of inner cortex like a pump
(similar to the beating of the heart) is responsible for the ascent of sap. He
concluded that cells associated with xylem exhibit pumping action and pumps the
sap laterally into xylem cells.
Objections to vital force theories
i. Strasburger (1889) and Overton (1911) experimentally proved
that living cells are not mandatory for the ascent of sap. For this, he
selected an old oak tree trunk which when immersed in picric acid and
subjected to excessive heat killed all
the living cells of the trunk. The trunk when dipped in water, the ascent of
sap took place.
ii.
Pumping action of living cells should be in between two xylem elements
(vertically) and not on lateral sides.
If a
plant which is watered well is cut a few inches above the ground level, sap
exudes out with some force. This is called sap
exudation or bleeding. Stephen Hales, father of plant physiology observed
this phenomenon and coined the term ‘ Root
Pressure’. Stoking (1956) defined root
pressure as “a pressure developing in
the tracheary elements of the xylem
as a result of metabolic activities of the root”. But the following objections have been raised
against root pressure theory:
i. Root
pressure is totally absent in gymnosperms, which includes some of the tallest
plants.
ii.
There is no relationship between the ascent of sap and root pressure. For
example, in summer, the rate of the ascent of sap is more due to transpiration
in spite of the fact that root pressure is very low. On the other hand, in
winter when the rate of ascent of sap is low, a high root pressure is found.
iii.
Ascent of sap continues even in the absence of roots
iv. The
magnitude of root pressure is about 2atm, which can raise the water level up to
few feet only, whereas the tallest trees are more than 100m high.
Physical
force theories suggest that ascent of sap takes place through the dead xylem
vessel and the mechanism is entirely physical and living cells are not
involved.
Boehm (1809) suggested that the xylem vessels work like a capillary tube.
This capillarity of the vessels under normal atmospheric pressure is
responsible for the ascent of sap. This theory was rejected because the
magnitude of capillary force can raise water level only up to a certain height.
Further, the xylem vessels are broader than the tracheid which actually
conducts more water and against the capillary theory.
This
theory was first proposed by Unger
(1876) and supported by Sachs
(1878). This theory illustrates, that water is imbibed through the cell wall
materials and not by the lumen. This theory was rejected based on the ringing
experiment, which proved that water moves through the lumen of the cell and not
by a cell wall.
Cohesion
-tension theory was originally proposed by Dixon
and Jolly (1894) and again put
forward by Dixon (1914, 1924). This
theory is based on the following features:
Water
molecules have the strong mutual force of attraction called cohesive force due to which they cannot be easily separated from one another. Further, the attraction between a
water molecule and the wall of the xylem element is called adhesion. These cohesive and adhesive force works together to form an unbroken continuous water column
in the xylem. The magnitude of the cohesive force is much high (350 atm) and is
more than enough to ascent sap in the tallest trees.
An
important factor which can break the water column is the introduction of air
bubbles in the xylem. Gas bubbles expanding and displacing water within the
xylem element is called cavitation
or embolism. However, the overall
continuity of the water column remains undisturbed since water diffuses into
the adjacent xylem elements for continuing ascent of sap.
The unbroken water column from leaf to root is just like a rope. If the rope is pulled from the top, the entire rope will move upward. In plants, such a pull is generated by the process of transpiration which is known as transpiration pull.
Water
vapour evaporates from mesophyll cells to the intercellular spaces near stomata
as a result of active transpiration. The water vapours are then transpired
through the stomatal pores. Loss of water from mesophyll cells causes a
decrease in water potential. So, water moves as a pull from cell to cell along
the water potential gradient. This tension, generated at the top (leaf) of the
unbroken water column, is transmitted downwards from petiole, stem and finally
reaches the roots. The cohesion theory is the most accepted among the plant
physiologists today.
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