In this paper four classes of co-operative root-shoot interations are addre
ssed. (I) Nitrogen concentrations in the xylem sap originating from the roo
t and in the phloem sap as exported from source leaves are much lower than
those required for growth by apices and developing organs. Enrichment of xy
lem sap N is achieved by xylem to xylem (X-X) transfer, by which reduced N,
but not nitrate, is abstracted from the xylem of leaf traces and loaded in
to xylem vessels serving the shoot apex. Nitrogen enrichment of phloem sap
from source leaves is enacted by transfer of reduced N from xylem to phloem
(X-P transfer). Quantitative data for the extent of the contribution of X-
X and X-P transfer to the nutrition of young organs of Ricinus communis L.
and for their change with time are presented. (II) Shoot and root cooperate
in nitrate reduction and assimilation. The partitioning of this process be
tween shoot and root is shifted towards the root under conditions of nitrat
e- and K-deficiency and under salt stress, while P deficiency shifts nitrat
e reduction almost totally to the shoot. All four changes in partitioning c
an be attributed to the need for cation-anion balance during xylem transpor
t and the change in electrical charge occurring with nitrate reduction. (II
I) Even maintenance of the specificity of ion uptake by the root may - in a
ddition to its need for energy - require a shoot-root interaction. This is
shown to be needed in the case of the maintenance of K/Na selectivity under
the highly adverse condition of salt stress and absence of K supply from t
he soil. (IV) Hormonal root to shoot interactions are required in the whole
plant for sensing mineral imbalances in the soil. This is shown and addres
sed for conditions of salt stress and of P deficiency, both of which lead t
o a strong ABA signalling from root to shoot but result in different patter
ns of response in the shoot.