Just as a soggy paper straw is prone to yielding under the applied suction of a thirsty drinker, the xylem tracheids in leaves seem prone to collapse as water potential declines, impeding their function. Here we describe the collapse, under tension, of lignified cells peripheral to the leaf vein of a broad-leaved rainforest conifer, Podocarpus grayi de Laub. Leaves of Podocarpus are characterized by an array of cylindrical tracheids aligned perpendicular to the leaf vein, apparently involved in the distribution of water radially through the mesophyll. During leaf desiccation the majority of these tracheids collapsed from circular to flat over the water potential range 21.5 to 22.8 MPa. An increase in the percentage of tracheids collapsed during imposed water stress was mirrored by declining leaf hydraulic conductivity (K leaf ), implying a direct effect on water transport efficiency. Stomata responded to water stress by closing at 22.0 MPa when 45% of cells were collapsed and K leaf had declined by 25%. This was still substantially before the initial indications of cavitation-induced loss of hydraulic conductance in the leaf vein, at 23 MPa. Plants droughted until 49% of tracheids had collapsed were found to fully recover tracheid shape and leaf function 1 week after rewatering. A simple mechanical model of tracheid collapse, derived from the theoretical buckling pressure for pipes, accurately predicted the collapse dynamics observed in P. grayi, substantiating estimates of cell wall elasticity and measured leaf water potential. The possible adaptive advantages of collapsible vascular tissue are discussed.Leaves employ the strong cohesive properties of water to do the work of pulling water from the soil to prevent leaf desiccation during gas exchange (Dixon and Joly, 1895). Of course this mode of water transport does not come without attendant costs, the most profound of which is the generation of hydraulic tension or negative pressure in the plumbing of vascular plants. The magnitude of this tension is generally large due to subzero soil water potential and substantial resistances to hydraulic flow through the vascular system of plants (Jeje and Zimmermann, 1979;Pockman et al., 1995). As such, it is common to measure hydraulic tensions (negative water potentials) of the order of 22 MPa in plants exposed to moderate water stress. In nonliving xylem cells conducting dilute sap, such tension will exert a large mechanical force on cell walls wherever they are bordered by air spaces. To place this force into perspective, if it were possible to reproduce a tension of 22 MPa inside a stainless steel tube it would be capable of crushing a pipe of 60 mm radius and 2 mm wall thickness.To resist megapascals of crushing pressure across the cell wall, xylem conduits have evolved thick secondary walls incorporating lignin as a means of fortifying their tangential elastic modulus against collapse (Raven, 1977). However, given that both lignin and celluloses are costly to synthesize, it is likely that plants minimize xylem wal...