The temporal dynamics of partitioning and rhizodeposition of recent photosynthate in wheat (Triticum aestivum) roots were quantified in situ in solution culture. After a 30-min pulse of (14)CO(2) to a single intact leaf, (14)C activities of individual carbon fluxes in the root, including exudation, respiration, and root content, were measured continuously over the next 20 h concurrently with (14)C efflux from the leaf. Immediately after the end of the (14)CO(2) pulse, (14)C activity was detected in the root, the hydroponic solution, and in root respiration. The rate of (14)C exudation from the root was maximal after 2 to 3 h, and declined to one-third of maximum after a further 5 h. Completion of the rapid phase of (14)C efflux from the leaf coincided with peak (14)C exudation rate. Thus, exudation flux is much more rapidly and dynamically coupled to current photosynthesis than has been appreciated. Careful cross-calibration of (14)C counting methods allowed a dynamic (14)C budget to be constructed for the root. Cumulative (14)C exudation after 20 h was around 3% of (14)C fixed in photosynthesis. Partitioning of photosynthate between shoot and root was manipulated by partial defoliation before applying the (14)CO(2) pulse to the remaining intact leaf. Although the rate of photosynthesis was largely unaffected by partial defoliation, the proportion of new photosynthate subsequently partitioned to and exuded from the root was substantially reduced. This clearly indicates that exudation depends more on the rate of carbon import into the root than on the rate of photosynthesis.