Fig. 24.
After treatment with
salt solution.
Fig. 25.
Later stage of
the same.
Figs. 23-25.—Cells from beet treated with salt solution to
show osmosis and movement of the protoplasmic membrane.
34. Osmose in the cells of the beet.—We should now make a section of the fresh tissue of a red colored beet for examination with the microscope, and treat this section with the salt solution. Here we can see that the effect of the salt solution is to draw water out of the cell, so that the protoplasmic membrane can be seen to move inward from the cell wall just as was observed in the case of spirogyra.[4] Now treating the section with water and removing the salt solution, the diffusion current is in the opposite direction, that is inward through the protoplasmic membrane, so that the latter is pressed outward until it comes in contact with the cell wall again, which by its elasticity soon resists the pressure and the cells again become turgid.
35. The coloring matter in the cell-sap does not readily escape from the living protoplasm of the beet.—The red coloring matter, as seen in the section under the microscope, does not escape from the cell-sap through the protoplasmic membrane. When the slices are placed in water, the water is not colored thereby. The same is true when the slices are placed in the salt or sugar solutions. Although water is withdrawn from the cell-sap, this coloring substance does not escape, or if it does it escapes slowly and after a considerable time.
36. The coloring matter escapes from dead protoplasm.—If, however, we heat the water containing a slice of beet up to a point which is sufficient to kill the protoplasm, the red coloring matter in the cell-sap filters out through the protoplasmic membrane and colors the water. If we heat a preparation made for study under the microscope up to the thermal death point we can see here that the red coloring matter escapes through the membrane into the water outside. This teaches that certain substances cannot readily filter through the living membrane of protoplasm, but that they can filter through when the protoplasm is dead. A very important condition, then, for the successful operation of some of the physical processes connected with absorption in plants is that the protoplasm should be in a living condition.
37. Osmose experiments with leaves.—We may next take the leaves of certain plants like the geranium, coleus or other plant, and place them in shallow vessels containing water, salt, and sugar solutions respectively. The leaves should be immersed, but the petioles should project out of the water or solutions. Seedlings of corn or beans, especially the latter, may also be placed in these solutions, so that the leafy ends are immersed. After one or two hours an examination shows that the specimens in the water are still turgid. But if we lift a leaf or a bean plant from the salt or sugar solution, we find that it is flaccid and limp. The blade, or lamina, of the leaf droops as if wilted, though it is still wet. The bean seedling also is flaccid, the succulent stem bending nearly double as the lower part of the stem is held upright. This loss of turgidity is brought about by the loss of water from the tissues, and judging from the experiments on spirogyra and the beet, we conclude that the loss of turgidity is caused by the withdrawal of some of the water from the cell-sap by the strong salt solution.