Leaf anatomy does not explain apparent short‐term responses of mesophyll conductance to light and CO2 in tobacco

Mesophyll conductance to CO₂ (g_m), a key photosynthetic trait, is strongly constrained by leaf anatomy. Leaf anatomical parameters such as cell wall thickness and chloroplast area exposed to the mesophyll intercellular airspace have been demonstrated to determine g_m in species with diverging phylogeny, leaf structure and ontogeny. However, the potential implication of leaf anatomy, especially chloroplast movement, on the short‐term response of g_m to rapid changes (i.e. seconds to minutes) under different environmental conditions (CO₂, light or temperature) has not been examined. The aim of this study was to determine whether the observed rapid variations of g_m in response to variations of light and CO₂ could be explained by changes in any leaf anatomical arrangements. When compared to high light and ambient CO₂, the values of g_m estimated by chlorophyll fluorescence decreased under high CO₂ and increased at low CO₂, while it decreased with decreasing light. Nevertheless, no changes in anatomical parameters, including chloroplast distribution, were found. Hence, the g_m estimated by analytical models based on anatomical parameters was constant under varying light and CO₂. Considering this discrepancy between anatomy and chlorophyll fluorescence estimates, it is concluded that apparent fast g_m variations should be due to artefacts in its estimation and/or to changes in the biochemical components acting on diffusional properties of the leaf (e.g. aquaporins and carbonic anhydrase).     

Leaf responses to drought stress in Mediterranean accessions of Solanum lycopersicum: anatomical adaptations in relation to gas exchange parameters

In a previous study, important acclimation to water stress was observed in the Ramellet tomato cultivar (TR) from the Balearic Islands, related to an increase in the water‐use efficiency through modifications in both stomatal (g_s) and mesophyll conductances (g_m). In the present work, the comparison of physiological and morphological traits between TR accessions grown with and without water stress confirmed that variability in the photosynthetic capacity was mostly explained by differences in the diffusion of CO₂ through stomata and leaf mesophyll. Maximization of g_m under both treatments was mainly achieved through adjustments in the mesophyll thickness and porosity and the surface area of chloroplasts exposed to intercellular airspace (S_c). In addition, the lower g_m/S_c ratio for a given porosity in drought‐acclimated plants suggests that the decrease in g_m was due to an increased cell wall thickness. Stomatal conductance was also affected by drought‐associated changes in the morphological properties of stomata, in an accession and treatment‐dependent manner. The results confirm the presence of advantageous physiological traits in the response to drought stress in Mediterranean accessions of tomato, and relate them to particular changes in the leaf anatomical properties, suggesting specific adaptive processes operating at the leaf anatomical level.     

Leaf Factors Affecting Light-Saturated Photosynthesis in Ecotypes of Solidago virgaurea from Exposed and Shaded Habitats

Plants of Solidago virgaurea L. from exposed and shaded habitats differ with respect to the response of the photosynthetic apparatus to the level of irradiance during growth. An analysis was carried out on leaf characteristies which might be responsible for the differences established in the rates of Hght-saturated CO₂ uptake. The clones were grown in controlled environment chambers at high and low levels of irradiance. Light-saturated rates of photosynthesis and transpiration were measured at natural and lower ambient CO₂ concentrations. A low temperature dependence of light-saturated CO₂ uptake at natural CO₂ concentrations, and a strong response to changes in stomatal width, suggested that the rate of CO₂ transfer from ambient air towards reaetion sites in chloroplasts was mainly limiting the pholosynthetic rate. Resistances to transfer of CO₂ for different parts of the pathway were calculated. There was a weak but significant correlation between stomatal conductance and the product stomatal frequency ± pore length. Mesopbyll conductance and dry weight per unit area were highly correlated in leaves not damaged by high irradiance. This suggests that mesophyll conductance increases with increasing cross sectional area (per unit leaf area) of the pathways of CO₂ transfer in the mesophyll from cell surfaces to reaction sites. The higher light-saturated photosynthesis in clones from exposed habitats when grown at high irradiance than when grown at low irradiance was attributable mainly to a lower mesophyll resistance. In shade clones the effect upon CO₂ uptake of the increase in leaf thickness when grown at high irradiance was counteracted by the associated inactivation of the photosynthetic apparatus. The difference in CO₂ uptake present between clones from exposed and shaded habitats when preconditioned to high irradiance resulted from differences in both mesophyll and stomatal resistances. A few hybrid clones of an F₁-population from a cross between a clone from an exposed habitat and a clone from a shaded habitat reacted, on the whole, in the same way as the exposed habitat parent. When grown at high irradiance, the hybrid clones showed higher photosynthetic rates than either parent; this was largely attributable to the unusually low stomatal resistance of the hybrid leaves.     

Seasonal changes in the effects of elevated CO2 on rice at three levels of nitrogen supply: a free air CO2 enrichment (FACE) experiment

Over time, the stimulative effect of elevated CO₂ on the photosynthesis of rice crops is likely to be reduced with increasing duration of CO₂ exposure, but the resultant effects on crop productivity remain unclear. To investigate seasonal changes in the effect of elevated CO₂ on the growth of rice (Oryza sativa L.) crops, a free air CO₂ enrichment (FACE) experiment was conducted at Shizukuishi, Iwate, Japan in 1998–2000. The target CO₂ concentration of the FACE plots was 200 µmol mol^?1 above that of ambient. Three levels of nitrogen (N) were supplied: low (LN, 4 g N m^?2), medium [MN, 8 (1998) and 9 (1999, 2000) g N m^?2] and high N (HN, 12 and 15 g N m^?2). For MN and HN but not for LN, elevated CO₂ increased tiller number at panicle initiation (PI) but this positive response decreased with crop development. As a result, the response of green leaf area index (GLAI) to elevated CO₂ greatly varied with development, showing positive responses during vegetative stages and negative responses after PI. Elevated CO₂ decreased leaf N concentration over the season, except during early stage of development. For MN crops, total biomass increased with elevated CO₂, but the response declined linearly with development, with average increases of 32, 28, 21, 15 and 12% at tillering, PI, anthesis, mid‐ripening and grain maturity, respectively. This decline is likely to be due to decreases in the positive effects of elevated CO₂ on canopy photosynthesis because of reductions in both GLAI and leaf N. Up to PI, LN‐crops tended to have a lower response to elevated CO₂ than MN‐ and HN‐crops, though by final harvest the total biomass response was similar for all N levels. For MN‐ and HN‐crops, the positive response of grain yield (ca. 15%) to elevated CO₂ was slightly greater than the response of final total biomass while for LN‐crops it was less. We conclude that most of the seasonal changes in crop response to elevated CO₂ are directly or indirectly associated with N uptake.     

Changes in Morphology,Anatomy, and Photosynthetic Capacity of Needles of Japanese Larch (Larix kaempferi) Seedlings Grown in High CO2 Concentrations

Photosynthetic traits of two-year-old Japanese larch seedlings (Larix kaempferi Carr.) grown at elevated CO₂ concentrations were studied in relation to structural changes in the needles. Seedlings were grown at two CO₂ concentrations, 360 (AC) and 720 (EC) mol mol^–1 at high and low nutrient supply rates, high N (HN) and low N (LN). The photosynthetic capacity fell significantly in EC+LN, but increased significantly in EC+HN. Since the mesophyll surface area exposed to intercellular space per unit leaf area (A^mes/A) is correlated with the photosynthetic rate, we measured A^mes/A for larch needles growing in EC. Changes of A^mes/A in both EC+HN and EC+LN were very similar to the changes in photosynthetic capacity. This suggests that the changes of A^mes/A in EC probably caused the changes in the photosynthetic capacity. The changes of A^mes/A in EC were attributed to changes in the mesophyll cell size and mesophyll cell number. The photosynthetic capacity in EC can be explained by taking morphological and structural adaptations into account as well as biochemical factors.     

Leaf hydraulic conductance and mesophyll conductance are not closely related within a single species

Stomata represent one resistor in a series of resistances for carbon and water exchange between the leaf and the atmosphere; the remaining resistors occurring within the leaf, commonly represented as mesophyll conductance to CO₂, g_m, and leaf hydraulic conductance, k_Leaf. Recent studies have proposed that g_m and k_Leaf may be coordinated across species because of shared pathways. We assessed the correlation between g_m and k_Leaf within cotton, under growth CO₂ partial pressure and irradiance treatments and also with short‐term variation in irradiance and humidity. g_m was estimated using two isotopic techniques that allowed partitioning of total g_m (Δ¹³C‐g_m) into cell wall plus plasma membrane conductance (Δ¹⁸O‐g_m) and chloroplast membrane conductance (g_cm). A weak correlation was found between Δ¹³C‐g_m and k_Leaf only when measured under growth conditions. However, Δ¹⁸O‐g_m was related to k_Leaf under both short‐term environmental variation and growth conditions. Partitioning g_m showed that g_cm was not affected by short‐term changes in irradiance or correlated with k_Leaf, but was strongly reduced at high growth CO₂ partial pressure. Thus, simultaneous measurements of g_m, k_Leaf and g_cm suggest independent regulation of carbon and water transport across the chloroplast membrane with limited coordinated regulation across the cell wall and plasma membrane.     

Mesophyll conductance in land surface models: effects on photosynthesis and transpiration

The CO₂ transfer conductance within plant leaves (mesophyll conductance, g_m) is currently not considered explicitly in most land surface models (LSMs), but instead treated implicitly as an intrinsic property of the photosynthetic machinery. Here, we review approaches to overcome this model deficiency by explicitly accounting for g_m, which comprises the re‐adjustment of photosynthetic parameters and a model describing the variation of g_m in dependence of environmental conditions. An explicit representation of g_m causes changes in the response of photosynthesis to environmental factors, foremost leaf temperature, and ambient CO₂ concentration, which are most pronounced when g_m is small. These changes in leaf‐level photosynthesis translate into a stronger climate and CO₂ response of gross primary productivity (GPP) and transpiration at the global scale. The results from two independent studies show consistent latitudinal patterns of these effects with biggest differences in GPP in the boreal zone (up to ~15%). Transpiration and evapotranspiration show spatially similar, but attenuated, changes compared with GPP. These changes are indirect effects of g_m caused by the assumed strong coupling between stomatal conductance and photosynthesis in current LSMs. Key uncertainties in these simulations are the variation of g_m with light and the robustness of its temperature response across plant types and growth conditions. Future research activities focusing on the response of g_m to environmental factors and its relation to other plant traits have the potential to improve the representation of photosynthesis in LSMs and to better understand its present and future role in the Earth system.     

Mesophyll conductance in leaves of Japanese white birch (Betula platyphylla var. japonica) seedlings grown under elevated CO2 concentration and low N availability

To test the hypothesis that mesophyll conductance (g_m) would be reduced by leaf starch accumulation in plants grown under elevated CO₂ concentration [CO₂], we investigated g_m in seedlings of Japanese white birch grown under ambient and elevated [CO₂] with an adequate and limited nitrogen supply using simultaneous gas exchange and chlorophyll fluorescence measurements. Both elevated [CO₂] and limited nitrogen supply decreased area‐based leaf N accompanied with a decrease in the maximum rate of Rubisco carboxylation (V_c,max) on a CO₂ concentration at chloroplast stroma (C_c) basis. Conversely, only seedlings grown at elevated [CO₂] under limited nitrogen supply had significantly higher leaf starch content with significantly lower g_m among the treatment combinations. Based on a leaf anatomical analysis using microscopic photographs, however, there were no significant difference in the area of chloroplast surfaces facing intercellular space per unit leaf area among treatment combinations. Thicker cell walls were suggested in plants grown under limited N by increases in leaf mass per area subtracting non‐structural carbohydrates. These results suggest that starch accumulation and/or thicker cell walls in the leaves grown at elevated [CO₂] under limited N supply might hinder CO₂ diffusion in chloroplasts and cell walls, which would be an additional cause of photosynthetic downregulation as well as a reduction in Rubisco activity related to the reduced leaf N under elevated [CO₂].     

Drought response of mesophyll conductance in forest understory species – impacts on water‐use efficiency and interactions with leaf water movement

Regulation of stomatal (g_s) and mesophyll conductance (g_m) is an efficient means for optimizing the relationship between water loss and carbon uptake in plants. We assessed water‐use efficiency (WUE)‐based drought adaptation strategies with respect to mesophyll conductance of different functional plant groups of the forest understory. Moreover we aimed at assessing the mechanisms of and interactions between water and CO₂ conductance in the mesophyll. The facts that an increase in WUE was observed only in the two species that increased g_m in response to moderate drought, and that over all five species examined, changes in mesophyll conductance were significantly correlated with the drought‐induced change in WUE, proves the importance of g_m in optimizing resource use under water restriction. There was no clear correlation of mesophyll CO₂ conductance and the tortuosity of water movement in the leaf across the five species in the control and drought treatments. This points either to different main pathways for CO₂ and water in the mesophyll either to different regulation of a common pathway.     

Effects of irradiance and leaf water deficit on net carbon dioxide assimilation and mesophyll and transport resistances

Rate of net CO₂ assimilation by soil-grown soybean plants were studied over a range of relative leaf water contents at each of four levels of irradiance. There was a large interaction between light level and leaf water deficit on the rate of CO₂ assimilation. The effect of leaf water deficit on assimilation became larger as irradiance increased. Both stomatal resistance to CO₂ transport and mesophyll resistance to CO₂ assimilation increased as leaf-water deficit increased. The increase in both resistance with changing leaf-water content was largest at high irradiance and became smaller as irradiance decreased. Relief of soil-moisture stress by watering induced large oscillations of CO₂ assimilation, stomatal resistance, and mesophyll resistance. The oscillation of the mesophyll resistance occurred in the absence of changes in relative water content and appeared to be related to oscillations in leaf temperature. The observed increase in mesophyll resistance with decreasing leaf-water content under nonoscillative conditions may be caused by changes in leaf temperature rather than leaf water content.     

基于FvCB模型的叶片光合生理对环境因子的响应研究进展

为提高叶片光合速率并更好地理解叶片光合生理对环境因子变化的响应机制,FvCB模型(C_3植物光合生化模型)常用于分析不同环境条件下CO_2响应曲线并预测叶片活体内光合系统的内在变化状况。系统介绍了FvCB模型的建立、发展过程和拟合方法等基本理论,综述了该模型在叶片光合生理对光、CO_2、水、温度和N营养等环境因子变化的响应机制中的应用研究。为进一步完善FvCB模型并更好地理解叶片活体内光合系统对环境因子变化的响应机制,未来拟加强以下研究:1)羧化速率与光合电子传递速率之间的联系;2)叶肉导度的具体组分及其对FvCB模型参数估计的影响;3)叶片气孔导度和叶肉导度对环境因子变化的调控机制。     

Morpho-anatomical and physiological leaf traits of two alpine herbs, Podophyllum hexandrum and Rheum emodi in the Western Himalaya under different irradiances

Morpho-anatomical leaf traits and photosynthetic activity of two alpine herbs, Podophyllum hexandrum (shade-tolerant) and Rheum emodi (light-requiring), were studied under field (PAR>2 000 μmol m⁻² s⁻¹) and greenhouse (PAR 500 μmol m⁻² s⁻¹) conditions. Mesophyll thickness, surface area of mesophyll cells facing intercellular spaces (S_mes), surface area of chloroplasts facing intercellular spaces (S_c), intercellular spaces of mesophyll cells (porosity), photon-saturated rate of photosynthesis per unit leaf area (P _Nmax), and ribulose-1,5-bisphosphate carboxylase/oxygenase activity decreased in the greenhouse with respect to the field and the decreases were significantly higher in R. emodi than in P. hexandrum. P. hexandrum had lower intercellular CO₂ concentration than R. emodi under both irradiances. The differences in acclimation of the two alpine herbs to low irradiance were due to their highly unlikely changes in leaf morphology, anatomy, and P _Nmax which indicated that the difference in radiant energy requirement related to leaf acclimation had greater impact under low than high irradiance.     

Altitudinal variation in photosynthetic capacity, diffusional conductance and δ13C of butterfly bush (Buddleja davidii) plants growing at high elevations

In this study, we have examined several physiological, biochemical and morphological features of Buddleja davidii plants growing at 1300 m above sea level (a.s.l.) and 3400 m a.s.l., respectively, to identify coordinated changes in leaf properties in response to reduced CO₂ partial pressure (P_a). Our results confirmed previous findings that foliar δ¹³C, photosynthetic capacity and foliar N concentration on a leaf area basis increased, whereas stomatal conductance (g_s) decreased with elevation. The net CO₂ assimilation rate (A_max), maximum rate of electron transport (J_max) and respiration increased significantly with elevation, although no differences were found in carboxylation efficiency of Rubisco (V_cmax). Consequently, also the J_max to V_cmax ratio was significantly increased by elevation, indicating that the functional balance between Ribulose‐1,5‐biphosphate (RuBP) consumption and RuBP regeneration changes as elevation increases. Our results also indicated a homeostatic response of CO₂ transfer conductance inside the leaf (mesophyll conductance, g_m) to increasing elevation. In fact, with elevation, g_m also increased compensating for the strong decrease in g_s and, thus, in the P_i (intercellular partial pressure of CO₂) to P_a ratio, leading to similar chloroplast partial pressure of CO₂ (P_c) to P_a ratio at different elevations. Because there were no differences in V_cmax, also A measured at similar PPFD and leaf temperature did not differ statistically with elevation. As a consequence, a clear relationship was found between A and g_m, and between A and the sum of g_s and g_m. These data suggest that the higher dry mass δ¹³C of leaves at the higher elevation, indicative of lower long‐term P_c/P_a ratio, cannot be attributed to changes either in diffusional resistances or in carboxylation efficiency. We speculate that because temperature significantly decreases as the elevation increases, it dramatically affects CO₂ diffusion and hence P_c/P_a and, consequently, is the primary factor influencing ¹³C discrimination at high elevation.     

Aquaporin plays an important role in mediating chloroplastic CO2 concentration under high‐N supply in rice (Oryza sativa) plants

Our previous studies demonstrated that chloroplastic CO₂ concentration (Cc) is not sufficient under high‐nitrogen (N) supply in rice plants. In this research, we studied how aquaporins‐ (AQPs) mediated Cc under different N‐supply levels. A hydroponic experiment was conducted in a greenhouse with three different N levels (low N, 0.71 mM; intermediate N, 2.86 mM; and high N, 7.14 mM) in a rice cultivar (Oryza sativa cv. Shanyou 63) and with an ospip1;1 mutant (Oryza sativa cv. Nipponbare). The photosynthetic nitrogen‐use efficiency (PNUE) decreased with increasing leaf‐N content. Under high‐N supply, the estimated Cc was significantly lower than the theoretical Cc and the specific Rubisco activity (carboxylation efficiency/Rubisco content, CE/Rubisco) decreased, because of a decrease of relative CO₂ diffusion conductance (total CO₂ diffusion conductance/leaf‐N content, g_t/N) in mesophyll cells. Real Time Quantitative PCR (Q‐RT‐PCR) showed that most OsPIP1s and OsPIP2s expression were downregulated under the high‐N supply. Furthermore, Cc and g_m decreased in the ospip1;1 mutant line compared with that of the wild‐type plant. It was concluded that under high‐N supply, the decreased PNUE was associated with non‐sufficient Cc, mediated by AQP in mesophyll conductance.     

Morphological and anatomical determinants of mesophyll conductance in wild relatives of tomato (Solanum sect. Lycopersicon,sect. Lycopersicoides; Solanaceae)

Natural selection on photosynthetic performance is a primary factor determining leaf phenotypes. The complex CO₂ diffusion path from substomatal cavities to the chloroplasts – the mesophyll conductance (g_m) – limits photosynthetic rate in many species and hence shapes variation in leaf morphology and anatomy. Among sclerophyllous and succulent taxa, structural investment in leaves, measured as the leaf dry mass per area (LMA), has been implicated in decreased g_m. However, in herbaceous taxa with high g_m, it is less certain how LMA impacts CO₂ diffusion and whether it significantly affects photosynthetic performance. We addressed these questions in the context of understanding the ecophysiological significance of leaf trait variation in wild tomatoes, a closely related group of herbaceous perennials. Although g_m was high in wild tomatoes, variation in g_m significantly affected photosynthesis. Even in these tender‐leaved herbaceous species, greater LMA led to reduced g_m. This relationship between g_m and LMA is partially mediated by cell packing and leaf thickness, although amphistomy (equal distribution of stomata on both sides of the leaf) mitigates the effect of leaf thickness. Understanding the costs of increased LMA will inform future work on the adaptive significance of leaf trait variation across ecological gradients in wild tomatoes and other systems.     

Integration of photosynthetic acclimation to CO2 at the whole-plant level

Primary events in photosynthetic (PS) acclimation to elevated CO₂ concentration ([CO₂]) occur at the molecular level in leaf mesophyll cells, but final growth response to [CO₂] involves acclimation responses associated with photosynthate partitioning among plant organs in relation to resources limiting growth. Source–sink interactions, particularly with regard to carbon (C) and nitrogen (N), are key determinants of PS acclimation to elevated [CO₂] at the whole-plant level. In the long term, PS and growth response to [CO₂] are dependent on genotypic and environmental factors affecting the plant's ability to develop new sinks for C, and acquire adequate N and other resources to support an enhanced growth potential. Growth at elevated [CO₂] usually increases N use efficiency because PS rates can be maintained at levels comparable to those observed at ambient [CO₂] with less N investment in PS enzymes. A frequent acclimation response, particularly under N-limited conditions, is for the accumulation of leaf carbohydrates at elevated [CO₂] to lead to repression of genes associated with the production of PS enzymes. The hypothesis that this is an adaptive response, leading to a diversion of N to plant organs where it is of greatest benefit in terms of competitive ability and reproductive fitness, needs to be more rigorously tested. The biological control mechanisms which plants have evolved to acclimate to shifts in source–sink balance caused by elevated [CO₂] are complex, and will only be fully elucidated by probing at all scales along the hierarchy from molecular to ecosystem. Use of environmental manipulations and genotypic comparisons will facilitate the testing of specific hypotheses. Improving our ability to predict PS acclimation to [CO₂] will require the integration of results from laboratory studies using simple model systems with results from whole-plant studies that include measurements of processes operating at several scales. Abbreviations: CAM, crassulacean acid metabolism; FACE, Free-Air CO₂ Enrichment; Pi, inorganic phosphate; LAR, leaf area ratio (m² g^-1); LWR, leaf weight ratio (g g^-1); NAR, net assimilation rate (g m^-2 d^{- 1}); PS, photosynthetic; RGR, relative growth rate (g g^-1 d^-1); R:S, root/shoot ratio; rubisco, ribulose bisphosphate carboxylase/oxygenase; RuBP, ribulose bisphosphate; SLA, specific leaf area (m² g^-1); SPS, sucrose phosphate synthase; WUE, water use efficiency (g biomass g H₂O^-1).     

The Péclet effect on leaf water enrichment correlates with leaf hydraulic conductance and mesophyll conductance for CO(2)

Leaf water gets isotopically enriched through transpiration, and diffusion of enriched water through the leaf depends on transpiration flow and the effective path length (L). The aim of this work was to relate L with physiological variables likely to respond to similar processes. We studied the response to drought and vein severing of leaf lamina hydraulic conductance (K_lamina), mesophyll conductance for CO₂ (g_m) and leaf water isotope enrichment in Vitis vinifera L cv. Grenache. We hypothesized that restrictions in water pathways would reduce K_lamina and increase L. As a secondary hypothesis, we proposed that, given the common pathways for water and CO₂ involved, a similar response should be found in g_m. Our results showed that L was strongly related to mesophyll variables, such as K_lamina or g_m across experimental drought and vein‐cutting treatments, showing stronger relationships than with variables included as input parameters for the models, such as transpiration. Our findings were further supported by a literature survey showing a close link between L and leaf hydraulic conductance (K_leaf = 31.5 × L^?0.43, r² = 0.60, n = 24). The strong correlation found between L, K_lamina and g_m supports the idea that water and CO₂ share an important part of their diffusion pathways through the mesophyll.     

Anatomical variation of mesophyll conductance under potassium deficiency has a vital role in determining leaf photosynthesis

Leaves exposed to potassium (K) deficiency usually present decreased mesophyll conductance (g_m) and photosynthesis (A). The relative contributions of leaf anatomical traits in determining g_m have been quantified; however, anatomical variabilities related to low g_m under K starvation remain imperfectly known. A one‐dimensional model was used to quantify anatomical controls of the entire CO₂ diffusion pathway resistance within a leaf on two Brassica napus L. cultivars in response to K deficiency. Leaf photosynthesis of both cultivars was significantly decreased under K deficiency in parallel with down‐regulated g_m. The mesophyll conductance limitation contributed to more than one‐half of A decline. The decreased internal air space in K‐starved leaves was associated with the increase of gas‐phase resistance. Potassium deficiency reduced liquid‐phase conductance by decreasing the exposed surface area of chloroplasts per unit leaf area (S_c/S), and enlarging the resistance of the cytoplasm that can be interpreted by the increasing distance of chloroplast from cell wall, and between adjacent chloroplasts. Additionally, the discrepancies of A between two cultivars were in part because of g_m variations, ascribing to an altered S_c/S. These results emphasize the important role of K on the regulation of g_m by enhancing S_c/S and reducing cytoplasm resistance.     

Responses of photosynthesis to irradiance and temperature in soybean,Glycine max (L.) Merr

The response of photosynthesis to irradiance and temperature during growth was investigated in two soybean genotypes. Soybean is a species that can modify its structure and metabolism so as to adapt to differing light conditions; its responses to rapid changes in irradiance are characterized by their flexibility. However, the temperature during growth can change the response to irradiance: moreover, there may be a marked interaction with genotype.The response of photosynthesis to irradiance consists of changes in leaf thickness, which bring about variations in the mesophyll resistance to CO₂ transfer. The increase in net photosynthesis per unit of leaf area is due to the increase in the amount of assimilating material beneath unit of area, as corroborated by the stability of the net photosynthesis per unit volume. Moreover, the response of photosynthesis to temperature is due to the mesophyll diffusion constant which decreases with the growth temperature.     

Using tunable diode laser spectroscopy to measure carbon isotope discrimination and mesophyll conductance to CO₂ diffusion dynamically at different CO₂ concentrations

In C₃ leaves, the mesophyll conductance to CO₂ diffusion, g_m, determines the drawdown in CO₂ concentration from intercellular airspace to the chloroplast stroma. Both g_m and stomatal conductance limit photosynthetic rate and vary in response to the environment. We investigated the response of g_m to changes in CO₂ in two Arabidopsis genotypes (including a mutant with open stomata, ost1), tobacco and wheat. We combined measurements of gas exchange with carbon isotope discrimination using tunable diode laser absorption spectroscopy with a CO₂ calibration system specially designed for a range of CO₂ and O₂ concentrations. CO₂ was initially increased from 200 to 1000 ppm and then decreased stepwise to 200 ppm and increased stepwise back to 1000 ppm, or the sequence was reversed. In 2% O₂ a step increase from 200 to 1000 ppm significantly decreased g_m by 26–40% in all three species, whereas following a step decrease from 1000 to 200 ppm, the 26–38% increase in g_m was not statistically significant. The response of g_m to CO₂ was less in 21% O₂. Comparing wild type against the ost1 revealed that mesophyll and stomatal conductance varied independently in response to CO₂. We discuss the effects of isotope fractionation factors on estimating g_m.