from a reduced duration of expansion. The magnitude of the responses as a function of the node position of Phosphorus deficiency generally decreases plant biomass accumuleaves were not considered. lation by limiting interception of photosynthetically active radiation (PAR) rather than reducing efficiency of conversion of PAR into dry Existing knowledge is not sufficient for modeling leaf matter. To document the role of P availability in leaf growth and expansion and decline in crops grown under varying P senescence dynamics in maize (Zea mays L.), a 3-yr field experiment conditions. Our objective was to study the effect of soil was conducted in southern France with very low, moderate, high, or P supply level, ranging from very low to very high, on very high soil test P levels. Leaf appearance rate, individual leaf area, maize leaf area development and senescence compoand green fraction changes were recorded at weekly intervals. Rates nent parameters. Leaf analysis has proved useful in unand duration of expansion and senescence processes were derived derstanding differences between maize cultivars in reindependently from fitted logistic functions. Phosphorus deficiency sponse to water stress (Dwyer and Stewart, 1986), slowed the rate of leaf appearance and reduced the final area of leaves temperature (Hesketh and Warrington, 1989; Zur et located below the main ear by 18 to 27%, depending on year. The al., 1989; Reid et al., 1990), and both factors combined reduction in leaf expansion rates accounted for most of the area reduction over leaf position and years. Senescence rates of the lower (Stewart and Dwyer, 1994a). These studies led Stewart leaves were reduced by 29%. The expansion and senescence dynamics and Dwyer (1994b) to model expansion and senescence of upper leaves were little affected by soil P level. The whole plantof maize leaves using temperature and water stress funcpeak green leaf area was lower under P-stressed conditions (16%), and tions. By using such a level of analysis, this work aims its date of occurrence was significantly delayed (6%). Plant senescence to provide modelers with relevant information to simurate was reduced by 15 to 33% during most of the grain filling period.late the evolution of LAI either with a leaf-to-leaf or a Leaf area duration from emergence to complete senescence was rewhole canopy approach, in varying P conditions. duced by 13.5%. The early effects of P deficiency on leaf dynamics accounted for most of the 7 to 10% reduction in the amount of MATERIALS AND METHODS absorbed PAR, observed as soon as canopy development allowed maximum light interception.