INFLUENCE OF XYLEM VASCULAR ARCHITECTURE ON THE TRANSLOCATION OF PHOSPHORUS FROM NODAL ROOTS IN A GENOTYPE OF TRIFOLIUM-REPENS DURING UNDISTURBED GROWTH
Mjm. Hay et Nrs. Hamilton, INFLUENCE OF XYLEM VASCULAR ARCHITECTURE ON THE TRANSLOCATION OF PHOSPHORUS FROM NODAL ROOTS IN A GENOTYPE OF TRIFOLIUM-REPENS DURING UNDISTURBED GROWTH, New phytologist, 132(4), 1996, pp. 575-582
Our objective was to establish whether the xylem vascular connections
(architecture) of a genotype of Trifolium repens L. had implications f
or the intraplant allocation of recently assimilated phosphorus (P). O
ne nodal root of each plant was isolated and fed P-32-labelled nutrien
t solution for 24 h. The fed root was either on the parent axis (11-12
nodes proximal to the apex) or on a branch at the third or fourth nod
e along the branch when counting from the junction with the parent sto
len. Allocation patterns were obtained by dissecting plants and assayi
ng each dissected component for P-32. Under conditions of undisturbed
growth in a controlled environment xylem architecture was found to hav
e an important influence on the intraplant distribution of P-32 from n
odal roots. Allocation patterns of P-32 were consistent with those pre
dicted from knowledge of the xylem vascular architecture of the genoty
pe and a predominantly acropetal direction of the transpiration stream
. For instance, very little P-32 (< 1% of exported P-32 from the fed r
oot) was found in branches on the opposite side of the stolen to the f
ed root, and the strong acropetal direction of the transpiration strea
m resulted in little allocation of P-32 to leaves that had traces that
arose from axial bundles at positions proximal to that of the fed roo
t (the leaf subtending the fed root and the next distal leaf had low P
-32 content), to all plant organs proximal to the fed root (< 6%) and
to all other roots (< 4%). The high allocation of P-32 to the branch a
rising at the same node as the fed root (64%) reflects the numerous li
nks that the fed root has to vascular bundles in the branch (3-6, of w
hich two are axial bundles) against the single connection it has to th
e adjacent lower axial bundle in the parent stolen. Allocation of P-32
to the leaf and axillary bud at each node along the branch strongly f
avoured nodes on the adaxial side, a result consistent with the fact t
hat the root connections are to the upper and lower axial bundles on t
he adaxial side of the branch. Allocation to a particular node along t
he branch was also influenced by its nodal position relative to the fe
d root and the sink strength of its tissues for the transpiration stre
am.