The water relations and hydraulic architecture of growing grass tillers (Fe
stuca arundinacea Schreb,) are reported. Evaporative Aux density, E (mmol s
(-1) m(-2)), of individual leaf blades was measured gravimetrically by cove
ring or excision of entire leaf blades. Values of E were similar for mature
and elongating leaf blades, averaging 2.4 mmol s(-1) m(-2). Measured axial
hydraulic conductivity, K-h (mmol s(-1) mm MPa-1), of excised leaf segment
s was three times lower than theoretical hydraulic conductivity (K-t) calcu
lated using the Poiseuille equation and measurements of vessel number and d
iameter. K-t was corrected (K-t*) to account for the discrepancy between K-
h and K-t and for immature xylem in the basal expanding region of elongatin
g leaves, From base to tip of mature leaves the pattern of K-t* was bell-sh
aped with a maximum near the sheath-blade joint (approximate to 19 mmol s(-
1) mm MPa-1). In elongating leaves, immature xylem in the basal growing reg
ion led to a much lower K-t*. As the first metaxylem matured, K-t* increase
d by 10-fold, The hydraulic conductances of the whole roof system, L-proot
(mmol s(-1) MPa-1) and leaf blades, L-pblade (mmol s(-1) MPa-1) were measur
ed by a vacuum induced water flow technique. L-proot and L-pblade were line
arly related to the leaf area downstream. Approximately 65% of the resistan
ce to wafer flow within the plant resided in the leaf blade. An electric-an
alogue computer model was used to calculate the leaf blade area-specific ra
dial hydraulic conductivity, L-pr (mmol s(-1) m(-2) MPa-1), using L-pblade,
K-t* and wafer flux values. L-pr values decreased with leaf age, from 21.2
mmol s(-1) m(-2) MPa-1 in rapidly elongating leaf to 7.2 mmol s(-1) m(-2)
MPa-1 in mature leaf. Comparison of L-pblade and L-pr values showed that ap
proximate to 90% of the resistance to wafer flow within the blades resided
in the liquid extra-vascular path. The same algorithm was then used to comp
ute the xylem and extravascular water potential drop along the liquid water
path in the plant under steady state conditions. Predicted and measured wa
ter potentials matched well. The hydraulic design of the mature leaf result
ed in low and quite constant xylem water potential gradient (approximate to
0.3 MPa m(-1)) throughout the plant. Much of the water potential drop with
in mature leaves occurred within a tenth of millimetre in the blade, betwee
n the xylem vessels and the site of water evaporation within the mesophyll.
In elongating leaves, the low K-t* in the basal growth zone dramatically i
ncreased the local xylem water potential gradient (approximate to 2.0 MPa m
(-1)) there. In the leaf elongation zone the growth-induced water potential
difference was approximate to 0.2 MPa.