Contrasting strategies to cope with chilling stress among clones of a tropical tree, Hevea brasiliensis.

Eight Hevea brasiliensis Muell. Arg. clones (GT1, YUNYAN77-4, IRCA707, IRCA317, PB217, PB260, PR107 and RRIM600) were compared for their tolerance towards chilling stress. Net photosynthesis (Pn), stomatal conductance (Gs), optimal and effective photochemical efficiencies (F(v)/F(m) and ), non-photochemical quenching, cellular lysis and leaf necrosis were measured on trees chilled at 10 °C for 96 h, as well as upon recovery at 28 °C. In addition, ascorbate peroxidase, catalase, dehydroascorbate reductase, glutathione reductase, monodehydroascorbate reductase and superoxide dismutase activities were monitored. Clone RRIM600 appeared to be the most tolerant, because it showed no cellular lysis or leaf necrosis and the best recovery as revealed by Pn, Gs, F(v)/F(m) and . Its ability to sustain chilling stress seemed related in part to the fast closure of stomata, suggesting an 'avoidance strategy' for this clone. IRCA707, GT1 and YUNYAN77-4 were also tolerant to the cold treatment as only a few leaf injuries were observed. However, YUNYAN77-4 showed a particular behaviour with a large stomata opening during the first hour of chilling, some photosynthetic activity after 96 h at 10 °C, but the slowest recovery in Pn. The greatest cell or leaf damage was observed on PB260, IRCA317, PR107 and PB217 clones, thus classified as sensitive to chilling. These clones showed the strongest decrease in Pn, F(v)/F(m) and and the slowest recovery for F(v)/F(m) and , indicating a high sensitivity of photosystem II to cold temperatures. Punctual increases of various enzymatic activities were observed for all clones during chilling kinetics. During recovery, the strongest increases in enzymatic activity were observed for the most tolerant clones, suggesting that efficient reactive oxygen species elimination is a crucial step for determining chilling tolerance in Hevea although the enzymes implicated varied from one tolerant clone to another. This study points out contrasted strategies of the Hevea clones in copping with chilling stress and recovery.

Long-term drought results in a reversible decline in photosynthetic capacity in mango leaves, not just a decrease in stomatal conductance.

The negative effects of drought on plant growth, development of natural plant communities and crop productivity are well established, but some of the responses remain poorly characterized, particularly the effect of long-term drought on photosynthetic capacity. We hypothesized that long-term drought results in a decline in leaf photosynthetic capacity, and not just a decrease in diffusive conductance. To test this hypothesis, we studied the effect of drought, slowly developed over 3.5 months, in leaves of eight potted mango (Mangifera indica L.) trees. We found that photosynthesis was not only limited by stomatal closure, but was also downregulated as a consequence of a strong decrease in photosynthetic capacity assessed by the measurements of maximal net photosynthesis (A(max)) and the light-saturated rate of photosynthetic electron transport (J(max)). The rapid recovery of A(max) and J(max), after only 1 week of rewatering, the maintenance of a stable pool of leaf nitrogen throughout the trial, and the decrease in quantum efficiency of open centers of photosystem II, indicate that the photosynthetic machinery escaped photodamage in the drought-treated trees and was simply downregulated during drought. The hexose-to-sucrose ratio was higher in leaves from drought-treated trees than in control leaves, suggesting that photosynthetic capacity decreased as a consequence of sink limitation.

Interpreting the decrease in leaf photosynthesis during flowering in mango.

Little is known about the effect of flowering on leaf photosynthesis. To understand why net photosynthesis (A(net)) is lower in Mangifera indica L. leaves close to inflorescences than in leaves on vegetative shoots, we measured nitrogen and carbohydrate concentrations, chlorophyll a fluorescence and gas exchange in recently matured leaves on vegetative terminals and on floral terminals of 4-year-old trees. We used models to estimate photosynthetic electron fluxes and mesophyll conductance (g(m)). Lower A(net) in leaves close to developing inflorescences was attributable to substantial decreases in stomatal conductance and g(m), and also in photosynthetic capacity as indicated by the decrease in the light-saturated rate of photosynthetic electron transport (J(max)). The decrease in J(max) was the result of decreases in the amount of foliar nitrogen per unit leaf area, and may have been triggered by a decrease in sink activity as indicated by the increase in the hexose:sucrose ratio. Parameters measured on leaves close to panicles bearing set fruits were generally intermediate between those measured on leaves on vegetative shoots and on leaves close to inflorescences, suggesting that the changes in A(net) associated with flowering are reversible.

Six-year time course of light-use efficiency, carbon gain and growth of beech saplings (Fagus sylvatica) planted under a Scots pine (Pinus sylvestris) shelterwood.

Two-year-old Fagus sylvatica L. saplings were planted under the cover of a Pinus sylvestris L. stand in the French Massif Central. The stand was differentially thinned to obtain a gradient of transmitted photosynthetically active radiation (PAR(t); 0-0.35). Eighteen Fagus saplings were sampled in this gradient, and their growth (basal stem diameter increment) was recorded over six years. Over the same period, morphological parameters (leaf area, number and arrangement in space) were monitored by 3D-digitization. Photosynthetic parameters were estimated with a portable gas-exchange analyzer. Photosynthesis was mainly related to light availability, whereas sapling morphology was mainly driven by sapling size. Annual stem diameter increment was related to the amount of light-intercepting foliage (silhouette to total leaf area ratio (STAR) x total sapling leaf area (LA)) and light availability above the saplings (PAR(t)). However, light-use efficiency, i.e., the slope of the relationship between STAR x LA x PAR(t) and stem diameter increment, decreased over time as a result of a relative decrease in the proportion of photosynthetic tissues to total sapling biomass.

Long-term drought modifies the fundamental relationships between light exposure, leaf nitrogen content and photosynthetic capacity in leaves of the lychee tree (Litchi chinensis).

Drought has dramatic negative effects on plants' growth and crop productivity. Although some of the responses and underlying mechanisms are still poorly understood, there is increasing evidence that drought may have a negative effect on photosynthetic capacity. Biochemical models of leaf photosynthesis coupled with models of radiation transfer have been widely used in ecophysiological studies, and, more recently, in global change modeling. They are based on two fundamental relationships at the scale of the leaf: (i) nitrogen content-light exposure and (ii) photosynthetic capacity-nitrogen content. Although drought is expected to increase in many places across the world, such models are not adapted to drought conditions. More specifically, the effects of drought on the two fundamental relationships are not well documented. The objective of our study was to investigate the effects of a long-term drought imposed slowly on the nitrogen content and photosynthetic capacity of leaves similarly exposed to light, from 3-year-old lychee trees cv. Kwaï Mi. Leaf nitrogen and non-structural carbohydrate concentrations were measured along with gas exchanges and the light-saturated rate of photosynthetic electron transport (J(max)) after a 5.5-month-long period of drought. Leaf nitrogen content on a mass basis remained stable, while the leaf mass-to-area ratio (LMA) increased with increasing water stress. Consequently, the leaf nitrogen content on an area basis (N(a)) increased in a non-linear fashion. The starch content decreased, while the soluble sugar content increased. Stomata closed and net assimilation decreased to zero, while J(max) and the ratio J(max)/N(a) decreased with increasing water stress. The drought-associated decrease in photosynthetic capacity can be attributed to downregulation of photosynthetic electron transport and to reallocation of leaf nitrogen content. It is concluded that modeling photosynthesis in drought conditions will require, first, the modeling of the effect of drought on LMA and J(max).

Spatial distribution of leaf nitrogen and photosynthetic capacity within the foliage of individual trees: disentangling the effects of local light quality, leaf irradiance, and transpiration.

There is presently no consensus about the factor(s) driving photosynthetic acclimation and the intra-canopy distribution of leaf characteristics under natural conditions. The impact was tested of local (i) light quality (red/far red ratio), (ii) leaf irradiance (PPFD(i)), and (iii) transpiration rate (E) on total non-structural carbohydrates per leaf area (TNC(a)), TNC-free leaf mass-to-area ratio (LMA), total leaf nitrogen per leaf area (N(a)), photosynthetic capacity (maximum carboxylation rate and light-saturated electron transport rate), and leaf N partitioning between carboxylation and bioenergetics within the foliage of young walnut trees grown outdoors. Light environment (quantity and quality) was controlled by placing individual branches under neutral or green screens during spring growth, and air vapour pressure deficit (VPD) was prescribed and leaf transpiration and photosynthesis measured at branch level by a branch bag technique. Under similar levels of leaf irradiance, low air vapour pressure deficit decreased transpiration rate but did not influence leaf characteristics. Close linear relationships were detected between leaf irradiance and leaf N(a), LMA or photosynthetic capacity, and low R/FR ratio decreased leaf N(a), LMA and photosynthetic capacity. Irradiance and R/FR also influenced the partitioning of leaf nitrogen into carboxylation and electron light transport. Thus, local light level and quality are the major factors driving photosynthetic acclimation and intra-canopy distribution of leaf characteristics, whereas local transpiration rate is of less importance.