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DIATOMS.

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Anatomy↗

Ageing and the influx of water into radish root-hair cells.

A micropotometric device previously described by the writer was used to determine quantitatively the velocity of water influx in cubic microns per square micron of hair surface per minute of comparatively older and younger root hairs of radish seedlings in a humid atmosphere at 29 degrees +/- 1 degrees C. when the micropotometers were filled with Hoagland solution at pH 6.8. In each experiment, measurements were made on two hairs of different length and different age on a given root and the hairs were inserted into the micropotometers a sufficient distance so that the area of immersion, 13,200micro(2), was the same in each instance. The range of velocities of water influx through the immersed surface was 4.46 to 1.16micro(3)/micro(2)/min. for the younger and shorter hairs which varied in length from 280 to 460 microns. The range of velocities of water influx through the immersed surface of the older hairs which varied from 661 to 2300 microns in length was 1.94 to 0.47micro(3)/micro(2)/min. The data indicate that water entry slows down in older hairs independent of root length. Estimations were made of the times to replace hair volumes based upon the mean velocities of water entry of the immersed areas. It was found that the time for the hairs to absorb an amount of water equivalent to their own volumes under the conditions specified was a matter of minutes or less; the range was 0.90 to 8.51 minutes.

Hair↗

Electroosmosis in Nitella.

The role of electroosmosis was studied directly in Nitella. The cells were mounted in a water-tight barrier between two chambers containing reversible electrodes for the application of potentials, and fitted with calibrated capillaries to measure water movement. No water movement was found when small existing bioelectric potentials were short-circuited through an external connection, nor when external potentials up to 1 or 2 volts were applied (producing currents up to 5 microa). Higher potentials (up to 10 volts) caused small movements of water, toward the negative pole. Larger and often irreversible water movements were produced by potentials up to 20 volts-sometimes persisting after current flow. A variety of evidence suggests that the effects are caused by injury at the cathodal end of the cell, allowing water to be attracted osmotically at the intact end and forced out at the injured end (transosmosis). This injury is reversible under small applied potentials, irreversible after large ones (100 to 200 times the natural bioelectric values). Such water flows persist in low salt concentrations (up to 0.09 M NaCl) but almost completely vanish in isotonic (0.26 M) mannitol. This confirms the osmotic, rather than the electroosmotic nature of the water movement. It is estimated that electroosmosis cannot account for more than 1 per cent of the water movement (or turgor) in Nitella cells. The dead cellulose walls display a small electroosmotic water flow at very high current densities (under 20 volts applied potential).

Electroosmosis↗