Resurrection plants are a perennial fascination to botanists. The transformation, within a few hours (or even minutes) of supplying them with water, from a plant that has all the appearances of being dead -dry, brown, crisp and shrivelled -to a plant that is obviously living and functioning -turgid, green, pliable and growing -suggests the miraculous. Studies of the complex processes of restoration and repair have been made on a number of resurrection plants, and at many levels of organization from molecules through membranes, organelles and cells to the whole plant (Gaff, 1989). The woody South African shrub Myrothamnus is the most extreme example of such plants, in that it has the highest level of organization to be repaired. It is transformed from lifeless-looking sticks with a water content below 5 % to a flourishing bush in a day after its roots receive water. Two papers in this issue from Ulrich Zimmermann's group in Wu$ rzburg concentrate on the restoration of the functioning hydraulic systems of the stems (see pp. 221-238, and 239-255 Before the rehydration of the still-viable cells and tissues of the shoot, water has to be delivered to them through the non-living xylem pipelines, which have been emptied of water. The tracheary elements must be refilled and the water flow through them re-established. Two studies of these processes have already been published by a group in South Africa (Sherwin & Farrant, 1996 ; Sherwin et al., 1998). The present papers concentrate on the following questions :$ What is the spatial and temporal scale of the rise of water in the stems ? $ What forces, capillary or root pressure, are driving water movement ? $ Does the hydraulic system of Myrothamnus have special features or properties that distinguish it from plants that cannot rehydrate from dryness ?The text is less ' innocent ' than it appears. Contained within it is a subtext with linkages to several very contentious issues in current work on plant water relations.
Capillary forcesThe advance of water through dry stems was followed with dye tracers, by the changes in refraction shown by wet tissue, and by the recurving of dry appressed leaves. The measured rates were fitted to an elaborate model of the kinetics of capillary advance through narrow tubes. The important variables in the model are the tube diameter and the contact angle formed at the water-air-vessel-wall interface. The data point to an advance of the water through very narrow tubes (c. 1 µm) with large contact angles (c. 70 %) (i.e. hydrophobic walls). Rate of water advance decreased with time (distance) and the walls became less hydrophobic. Capillarity did not provide sufficient force to account for the rise of water to the height of the stems in a day.
Root pressureTo drive water up the dry 80-cm stems at the necessary rate required the application of pressures greater than 8 kPa. Although the South African group measured root pressures no higher than 2n4 kPa (which would not be enough to refill the stems completely), the Wu$ rzburg group found pressur...