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Ascent of Sap

(1) The document discusses the path, mechanism, and theories of ascent of sap in plants. (2) It explains that ascent of sap occurs through the xylem tissue and discusses experiments that demonstrate this. (3) The most widely supported theory is the transpiration pull and cohesion theory, which states that transpiration in leaves creates tension that pulls water upward through the plant, aided by the cohesive and adhesive properties of water.

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DRMEHUL DAVE
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138 views6 pages

Ascent of Sap

(1) The document discusses the path, mechanism, and theories of ascent of sap in plants. (2) It explains that ascent of sap occurs through the xylem tissue and discusses experiments that demonstrate this. (3) The most widely supported theory is the transpiration pull and cohesion theory, which states that transpiration in leaves creates tension that pulls water upward through the plant, aided by the cohesive and adhesive properties of water.

Uploaded by

DRMEHUL DAVE
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Ascent of SAP: Path, Mechanism and

Theories
Let us make an in-depth study of the ascent of SAP. After reading
this article you will learn about (A) Path of Ascent of Sap (B)
Mechanism of Ascent of Sap and Theories of Ascent of Sap.
Ascent of SAP:
The water after being absorbed by the roots is distributed to all parts
of the plant (excess of which is lost through transpiration). In order to
reach the topmost parts of the plant, the water has to move upward
through the stem. This upward movement of water is called as Ascent
of Sap.

Ascent of sap can be studied under the following two heads:


(A) Path of Ascent of Sap, and

(B) Mechanism of Ascent of Sap.

(A) Path of Ascent of Sap:


It is well established that the ascent of sap takes place through xylem.

It can be shown by the following experiments:


(i) A leafy twig of balsam plant (it has semi- transparent stem) is cut
under water (to avoid entry of air-bubbles through the cut end) and
placed in a beaker containing water with some eosin (a dye) dissolved
in it. After sometime coloured lines will be seen moving upward in the
stem. If sections of stem are cut at this time, only the xylem elements
will appear to be filled with coloured water.

(ii) Ringing Experiment:


A leafy twig from a tree is cut under water and placed in a beaker
filled with water. A ring of bark (all the tissues outer to vascular
cambium) is removed from the stem. After sometime it is observed
that the leaves above the ringed part of the stem remain fresh and
green (Fig. 6.1). It is because water is being continuously supplied to
the upper part of the twig through xylem.
(B) Mechanism of Ascent of Sap:
In small trees and herbaceous plants the ascent of sap can be
explained easily, but in tall trees like Australian Eucalyptus, some
conifers such as mighty Sequoias (Sequoia, Sequoia Dendron,
Metasequoia are the tallest and thickest trees of the present day flora,
sometimes reaching a height of 300-400′) where the water has to rise
up to the height of several hundred feet, the ascent of sap, in fact,
becomes a problem. Although the mechanism of ascent of sap is not
well understood, a number of theories have been put forward to
explain it.

Theories of Ascent of SAP:


(A) Vital Theories:
Supporters of vital theories think that the ascent of sap is under the
control of vital activities in the stem.

Two such theories are common but they are not very convincing:
(1) According to Godlewski (1884) ascent of sap takes place due to the
pumping activity of the cells of xylem parenchyma which are living.
The cells of the medullary rays which are also living, in some way
change their O.P. When their O.P. becomes high they draw water from
the lower vessel and their O.P. becomes low. Now due to the low O.P.,
water from the cells of xylem parenchyma is pumped into the above
vessel. This process is repeated again and again and water rises
upward in the xylem.
This theory seemed only hypothetical, and was further discarded by
the experiments of Strasburger. (1891, 1893) who demonstrated that
ascent of sap continues even in the stems in which living cells have
been killed by the uptake of poisons.

(2) According to Bose (1923) upward translocation of water takes


plate due to the pulsatory activity of living cells of inner most cortical
layer just outside the endodermis. This theory was also rejected
because many workers could not repeat his experiment and many
others found no correlation between pulsatory activity and the ascent
of sap.

(Bose, in his experiment used an electric probe which was connected


to a galvanometer. When the needle of the electric probe was inserted
into the stem slowly and slowly, the needle of the galvanometer
showed some oscillations but when the electric probe needle reached
the innermost layer of cortex, the needle of galvanometer showed
violent oscillations. He attributed this to the pulsating activity of these
cells.)

(B) Root Pressure Theory:


Although, root pressure which is developed in the xylem of the
roots can raise water to a certain height but it does not seem to
be an effective force in ascent of sap due to the following reasons:
(i) Magnitude of root pressure is very low (about 2 atms).

(ii) Even in the absence of root pressure, absent of sap continues. For
example, when a leafy twig is cut under water and placed in a beaker
full of water it remains fresh and green for sufficient long time.

(iii) In gymnosperms root pressure has rarely been observed.

(C) Physical Force Theories:


Various physical forces may be involved in the ascent of sap:—
(1) Atmospheric Pressure:
This does not seem to be convincing because:
(i) It cannot act on water present in xylem in roots,

(ii) In case it is working, then also it will not be able to raise water
beyond 34′.
(2) Imbibition:
Sachs (1878) supported the view that ascent of sap could take place
by imbibition through the walls of xylem. Now it is well known that
imbibitional force is insignificant in the ascent of sap because it takes
place through the lumen of xylem elements and not through walls.

(A leafy twig is cut under water and the cut end is dipped in melted
paraffin wax for some time. A thin section of stem near cut end is
removed to expose the cell walls. The twig is transferred to a beaker
containing water. The twig soon wilts because the lumens of xylem
elements have been plugged by wax).

(3) Capillary Force:


In plants the xylem vessels are placed one above the other forming a
sort of continuous channel which can be compared with long capillary
tubes and it was thought that as water rises in capillary tube due to
capillary force, in the same manner ascent of sap takes place in xylem.

There are many objections to this theory:


(i) For capillarity a free surface is required.

(ii) The magnitude of capillary force is low.

(iii) In spring when there is more requirement of water due to the


development of new leaves, the wood consists of broader elements.
While in autumn, when water supply decreases, the wood consists of
narrow elements. This is against capillarity.

(iv) In Gymnosperms usually the vessels are absent. Other xylem


elements do not form continuous channels.

(D) Transpiration Pull and Cohesion of Water Theory:


This theory was originally proposed by Dixon and Joly (1894) and
greatly supported and elaborated by Dixon (1914, 1924). This theory
is very convincing and has now been widely supported by many work-
ers.

It is based on the following features:


(i) Cohesive and Adhesive properties of water molecules to form a
continuous water column in the xylem.
(ii) Transpiration pull exerted on this water column.

Water molecules remain joined to each other due H-bonds between


water molecules, to the presence of H-bonds between them.
(Whenever a H-atom comes between two electro-negative atoms a
bond is established between the two which is called as H bond and is
represented by dotted lines. In case of water, the electropositive H-
atoms of one water molecule are connected with electronegative O-
atoms of other water molecules by H-bonds).

Although H-bond is very weak (containing about 5k. cal. energy) but
when they are present in enormous numbers as in case of water, a
very strong mutual force of attraction or cohesive force develops
between water molecules and hence they remain in the form of a
continuous water column in the xylem. The magnitude of this force is
very high (sometimes up to 350 atmos.), therefore the continuous
water column in the xylem cannot be broken easily due to the force of
gravity or other obstructions offered by the internal tissues in the
upward movement of water.

The adhesive properties of water i.e. the attraction between the water
molecules and the container’s walls (here the walls of xylem) further
ensure the continuity of water column in xylem.

When transpiration takes place in leaves at the upper parts of the


plant, water evaporates from the intercellular spaces of the leaves to
the outer atmosphere through the stomata. More water is released
into the intercellular spaces from the mesophyll cells. In turn, the
mesophyll cells draw water from the xylem of the leaf.

Due to all this, a tension is created in water in the xylem elements of


the leaves. This tension is transmitted downward to water in xylem
elements of the roots through the xylem of petiole and stem and the
water is pulled upward in the form of continuous unbroken water
column to reach the transpiring surfaces—up to the top of the plants.

According to some workers, the main objection against this theory is


that certain air bubbles present in the conducting channels will break
the continuity of the water column. This has been counteracted by
others who say that there are no air bubbles and if at all are present,
they will not break the water column which will remain continuous
through other elements of the xylem (Fig. 6.2).

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