Low P (LP) levels in leaves can affect their photosynthetic N-use efficiency (PNUE), internal N allocation, and mesophyll conductance to CO2 (gm). The changes in leaf internal N allocation and gm in N-fixing trees and the consequent changes in PNUE under low soil P treatments are not well understood. In this study, we exposed seedlings of Dalbergia odorifera, Erythrophleum fordii (N-fixing trees), Castanopsis hystrix, and Betula alnoides (non-N-fixing trees) to three levels of soil P. The effects were not consistent among species, and LP had no specific effect on N-fixing species. Saturated net CO(2 )assimilation rate (A(sat)) values in D. odorifera and C. hystrix were remarkably lower under LP than under high P (HP) because Cc in D. odorifera and V-cmax and J(max) in C. hystrix were reduced. N-area values in D. odorifera and C. hystrix were also reduced under LP, and the degree of reduction of N-area was larger than that of A(sat), which resulted in decreased PNUE in these species. PR and gm in D. odorifera and PR, PB, and gm in C. hystrix significantly decreased under LP and were internal factors affecting the variation in PNUE in these two trees. PCW was significantly and linearly related to PR only in C. hystrix, indicating that more N was invested in the cell walls to resist the damage caused by low soil P, at the expense of Rubisco N. Our results showed that soil P deficiency affected leaf N utilization, photosynthetic efficiency, and seedling growth.

Plants grown under low magnesium (Mg) soils are highly susceptible to encountering light intensities that exceed the capacity of photosynthesis (A), leading to a depression of photosynthetic efficiency and eventually to photooxidation (i.e., leaf chlorosis). Yet, it remains unclear which processes play a key role in limiting the photosynthetic energy utilization of Mg-deficient leaves, and whether the plasticity of A in acclimation to irradiance could have cross-talk with Mg, hence accelerating or mitigating the photodamage. We investigated the light acclimation responses of rapeseed (Brassica napus) grown under low- and adequate-Mg conditions. Magnesium deficiency considerably decreased rapeseed growth and leaf A, to a greater extent under high than under low light, which is associated with higher level of superoxide anion radical and more severe leaf chlorosis. This difference was mainly attributable to a greater depression in dark reaction under high light, with a higher Rubisco fallover and a more limited mesophyll conductance to CO2 (gm). Plants grown under high irradiance enhanced the content and activity of Rubisco and gm to optimally utilize more light energy absorbed. However, Mg deficiency could not fulfill the need to activate the higher level of Rubisco and Rubisco activase in leaves of high-light-grown plants, leading to lower Rubisco activation and carboxylation rate. Additionally, Mg-deficient leaves under high light invested more carbon per leaf area to construct a compact leaf structure with smaller intercellular airspaces, lower surface area of chloroplast exposed to intercellular airspaces, and CO2 diffusion conductance through cytosol. These caused a more severe decrease in within-leaf CO2 diffusion rate and substrate availability. Taken together, plant plasticity helps to improve photosynthetic energy utilization under high light but aggravates the photooxidative damage once the Mg nutrition becomes insufficient.