Abstract

Vessels with simple perforation plates, found in the majority of angiosperms, are considered the evolutionarily most advanced conduits, least impeding the xylem sap flow. Nevertheless, when measured, their hydraulic resistivity (R, i.e., inverse value of hydraulic conductivity) is significantly higher than resistivity predicted using Hagen-Poiseuille equation (RHP). In our study we aimed (i) to quantify two basic components of the total vessel resistivity - vessel lumen resistivity and end wall resistivity, and (ii) to analyze how the variable inner diameter of the vessel along its longitudinal axis affects resistivity. We measured flow rates through progressively shortened stems of hop (Humulus lupulus L.), grapevine (Vitis vinifera L.), and clematis (Clematis vitalba L.) and used elastomer injection for identification of open vessels and for measurement of changing vessel inner diameters along its axis. The relative contribution of end wall resistivity to total vessel resistivity was 0.46 for hop, 0.55 for grapevine, and 0.30 for clematis. Vessel lumen resistivity calculated from our measurements was substantially higher than theoretical resistivity - about 43% for hop, 58% for grapevine, and 52% for clematis. We identified variation in the vessel inner diameter as an important source of vessel resistivity. The coefficient of variation of vessel inner diameter was a good predictor for the increase of the ratio of integral RHP to RHP calculated from the mean value of inner vessel diameter. We discuss the fact that we dealt with the longest vessels in a given stem sample, which may lead to the overestimation of vessel lumen resistivity, which consequently precludes decision whether the variable vessel inner diameter explains fully the difference between vessel lumen resistivity and RHP we observed.

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