tree to its weight, there being increased transpiration and general loss of turgor at high temperature. I shall, however, show that the diurnal movement persists in the absence of transpiration.
Diurnal movement in absence of transpiration: Experiment 5.—In the leaf of Arenga saccharifera, I found that the petiole was the organ of movement. I cut off the transpiring lamina and covered the cut end with collodion flexile. The plant was now placed in a chamber saturated with moisture. The petiole continued to give records of its diurnal movement in every way similar to the record of the intact leaf. In another experiment with the water plant, Ipoemia reptans, immersed in water, the normal diurnal movement was given by the plant, where there could be no question of variation of turgor due to transpiration. (See also Expt. 7.)
In the diurnal movement of the 'Praying' Palm the concave curvature of the rigid neck in the morning, became flattened or slightly convex in the afternoon. The force necessary to cause this is enormously great, and could on no account result from the passive yielding to the weight of the upper part of the tree.
From the facts given above it will be seen that the diurnal movement is not brought about by variation in transpiration. I now turn to another phenomenon which appeared at first to have some connection with the movement of the tree. Kraus found that the tissue tensions of a shoot exhibit a daily periodicity. He, however, found that between 10°C. and 30°C., variation of temperature had no effect on the daily period. But as regards the diurnal movement of the tree, it is the temperature which is the principal factor. Kraus also found a daily variation of bulk in different plant-organs; this variation of bulk is connected with transpiration, for the removal of the
