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.     

Ca2+ transient induced by extracellular changes in osmotic pressure in Arabidopsis leaves: differential involvement of cell wall-plasma membrane adhesion

We investigated the mechanism underlying the perception of extracellular changes in osmotic pressure in Vallisneria gigantea Graebner and transgenic Arabidopsis thaliana (L.) Heynh. expressing cytoplasmic aequorin. Hypertonic and hypotonic treatments of A. thaliana leaves each rapidly induced a Ca2+ transient. Both responses were essentially dependent on the presence of extracellular Ca2+ and were sensitive to Gd3+ a potential blocker of stretch-activated Ca2+ channels. Immediately after plasmolysis caused by hypertonic treatment and subsequent deplasmolysis caused by hypotonic treatment, the cells did not respond to a second hypertonic treatment and exhibited an impaired adhesion of the plasma membrane (PM) to the cell wall (CW). Recovery of the responsiveness required about 6 h. By contrast, no refractory phenomenon was observed in response to hypotonic treatment. Pretreatment with cellulase completely inhibited the Ca2+ transient induced by hypertonic treatment, but it did not affect the response to hypotonic treatment. V. gigantea mesophyll cells pretreated with cellulase exhibited an impaired adhesion of the PM to the CW. The leaf cells of multicellular plants can respond to both hypertonic and hypotonic treatments through the stretch-activated Ca2+ channels, whereas cellulase-sensitive adhesion of the PM to the CW is involved only in the response to hypertonic treatment.     

Aquaporins and plant water balance

The impact of aquaporin function on plant water balance is discussed. The significance of these proteins for root water uptake, water conductance in the xylem, including embolism refilling and the role of plant aquaporins in leaf physiology, is described. Emphasis is placed on certain aspects of water stress reactions and the correlation of aquaporins to abscisic acid as well as on the relation of water and CO₂ permeability in leaves.     

高山植物叶片δ13C的海拔响应及其机理

植物 1 3C的分辨研究已成为植物生态学和全球碳循环研究的核心问题之一。植物 1 3C的分辨是环境和生物因子共同作用的综合结果 ,海拔梯度变化不仅可以造成植物生存环境的变化 ,而且还可以造成植物形态和生理特征的变化 ,因此 ,高山植物 1 3C分辨随海拔的变化为深入揭示植物 1 3C分辨的环境和生物因子的作用机理提供了非常理想的研究条件。在简单介绍植物 1 3C分辨基本理论的基础上 ,对目前国际上高山植物 1 3C分辨的海拔响应研究进行了述评。重点介绍了随海拔变化的大气 1 3C组成、温度、气压、水分等环境因子和植物叶片的气孔导度、羧化效率、氮含量和叶肉细胞导度等生物因子对高山 C3植物 1 3C分辨的影响 ,指出高山植物 1 3C分辨的海拔响应机理仍存在一些不确定性 ,为国内相关研究的开展提供了一定参考     

盐胁迫下芦苇叶肉细胞超微结构的研究

对青藏高原柴达木盆地柯柯盐湖边盐碱地上生长的芦苇叶肉细胞的超微结构进行了研究,并以西宁地区非盐碱地上生长的芦苇作对照。结果表明：西宁地区的芦苇叶肉细胞的叶绿体呈椭圆形,其膜系统完整,基粒片层和基质片层发育良好。在盐碱地上生长的芦苇叶肉细胞的叶绿体呈圆形,叶绿体内出现较大的淀粉粒,并发现有线粒体嵌入叶绿体的现象。叶绿体的类囊体膨大,线粒体的嵴也有膨大的现象。在盐湖水中生长的芦苇叶肉细胞,叶绿体的类囊体排列紊乱、扭曲、松散。类囊体膜局部被破坏,部分类囊体膜解体,空泡化,甚至消失,一些溶解了的类囊体流进细胞质中。综上所述,芦苇叶肉细胞超微结构的变化是该植物适应柯柯盐湖地区盐渍、低温、低气压、强辐射等环境因子的结果。     

Structural and Functional Grounds for Ephedra sinica Expansion in Mongolian Steppe Ecosystems

Morphological and structural characteristics of photosynthetic organs, diurnal changes in photosynthetic and transpiration rates, and the efficiency of water use were studied in three plant species from mountain-steppe ecosystems in Mongolia, Ephedra sinica Stapf, Stipa glareosa P. Smirn., and Allium polyrhizum Furcz. ex Regel. The species studied differed in the structural and functional mechanisms for the adaptation of photosynthetic apparatus to arid conditions. E. sinica has thick, vertical assimilating shoots, which are characterized by a high density (620 mg/cm³) and a small proportion of photosynthetic tissues (13%). The proportion of meso-phyll in the leaves of A. polyrhizum and S. glareosa was two and three times higher, respectively. The low content of phototrophic tissues in E. sinica shoot was compensated for by a high photosynthetic activity of single chloroplasts (25 mg CO₂/(10⁹ chloroplast h)), which was six times higher, than in two other species. Daily course of photosynthesis and transpiration inE. sinica differed from those of A. polyrhizum and S. glareosa by the absence of the midday depression. E. sinica had the highest efficiency of water use (45 mg CO₂/g H₂O) due to a low transpiration rate (0.25 g/g fr wt h). It is concluded that, in E. sinica, the main strategy for adaptation to arid stress is to develop in the shoot a few photosynthesizing cells of high assimilation activity. Such structural organization of photosynthetic organs in ephedra contributes to its higher efficiency of water use and stability of physiological characteristics under changing environmental conditions. These specific features of the structure of assimilating organs and their functional features contribute to a greater expansion of E. sinica with increasing climate aridization in Mongolia.     

Gas Exchange and Epidermal Characteristics of Miscanthus Populations in Taiwan Varying with Habitats and Nitrogen Application

Seventeen clones of C₄ grass Miscanthus spp. collected from different climatic regions and elevations of Taiwan were transplanted in pots. 15–16 months after collection the plants received 0, 1, and 2 g of nitrogen fertiliser (N₀, N₁, and N₂, respectively) per pot. All the measurements were done 10–12 d after N application. The relationships between net photosynthetic rate (P _N) and photon flux density (PFD) showed a saturated curve, with PFD saturation at about 1 000 µmol m^–2 s^–1. The ranges of PFD saturated P _N (P _sat) for all the tested clones with N₀, N₁, and N₂ were 8–16, 11–18, and 12–21 µmol m^–2 s^–1, respectively. The clones from southern Taiwan, a tropical region, showed the highest P _sat, followed by the clones from northern Taiwan, a subtropical region, while those from mountainous area showed the lowest P _sat. The clones collected from southern Taiwan showed the highest frequency of stomata on the adaxial surface, and those collected from the high mountainous area showed the lowest frequency. Also the adaxial surface of leaves from the higher mountainous area had more wax deposited than the leaves from the lowland. Thus the low P _sat in mountain clones is limited by both stomatal and non-stomatal factors. Further, the lower leaf conductance and different epidermal characteristics of mountain clones might prevent excessive loss of heat through transpiration and provide production against ultraviolet-B radiation.     

The use of low [CO2] to estimate diffusional and non-diffusional limitations of photosynthetic capacity of salt-stressed olive saplings

In this study it has been shown that increased diffusional resistances caused by salt stress may be fully overcome by exposing attached leaves to very low [CO₂] (～ 50 µmol mol^?1), and, thus a non‐destructive‐in vivo method to correctly estimate photosynthetic capacity in stressed plants is reported. Diffusional (i.e. stomatal conductance, g_s, and mesophyll conductance to CO₂, g_m) and biochemical limitations to photosynthesis (A) were measured in two 1‐year‐old Greek olive cultivars (Chalkidikis and Kerkiras) subjected to salt stress by adding 200 mm NaCl to the irrigation water. Two sets of A–C_i curves were measured. A first set of standard A–C_i curves (i.e. without pre‐conditioning plants at low [CO₂]), were generated for salt‐stressed plants. A second set of A–C_i curves were measured, on both control and salt‐stressed plants, after pre‐conditioning leaves at [CO₂] of ～ 50 µmol mol^?1 for about 1.5 h to force stomatal opening. This forced stomata to be wide open, and g_s increased to similar values in control and salt‐stressed plants of both cultivars. After g_s had approached the maximum value, the A–C_i response was again measured. The analysis of the photosynthetic capacity of the salt‐stressed plants based on the standard A–C_i curves, showed low values of the J_max (maximum rate of electron transport) to V_cmax (RuBP‐saturated rate of Rubisco) ratio (1.06), that would implicate a reduced rate of RuBP regeneration, and, thus, a metabolic impairment. However, the analysis of the A–C_i curves made on pre‐conditioned leaves, showed that the estimates of the photosynthetic capacity parameters were much higher than in the standard A–C_i responses. Moreover, these values were similar in magnitude to the average values reported by Wullschleger (Journal of Experimental Botany 44, 907–920, 1993) in a survey of 109 C₃ species. These findings clearly indicates that: (1) salt stress did affect g_s and g_m but not the biochemical capacity to assimilate CO₂ and therefore, in these conditions, the sum of the diffusional resistances set the limit to photosynthesis rates; (2) there was a linear relationship (r² = 0.68) between g_m and g_s, and, thus, changes of g_m can be as fast as those of g_s; (3) the estimates of photosynthetic capacity based on A–C_i curves made without removing diffusional limitations are artificially low and lead to incorrect interpretations of the actual limitations of photosynthesis; and (4) the analysis of the photosynthetic properties in terms of stomatal and non‐stomatal limitations should be replaced by the analysis of diffusional and non‐diffusional limitations of photosynthesis. Finally, the C₃ photosynthesis model parameterization using in vitro‐measured and in vivo‐measured kinetics parameters was compared. Applying the in vivo‐measured Rubisco kinetics parameters resulted in a better parameterization of the photosynthesis model.     

Structural Adaptation of the Leaf Mesophyll to Shading

Structural characteristics of the mesophyll were studied in five boreal grass species experiencing a wide range of light and water supply conditions. Quantitative indices of the palisade and spongy mesophyll tissues (cell and chloroplast sizes, the number of chloroplasts per cell, the total cell and chloroplast surface area per unit leaf surface area) were determined in leaves of each of the species. The cell surface area and the cell volume in spongy mesophyll were determined with a novel method based on stereological analysis of cell projections. An important role of spongy parenchyma in the photosynthetic apparatus was demonstrated. In leaves of the species studied, the spongy parenchyma constituted about 50% of the total volume and 40% of the total surface area of mesophyll cells. The proportion of the palisade to spongy mesophyll tissues varied with plant species and growth conditions. In a xerophyte Genista tinctoria, the total cell volume, cell abundance, and the total surface area of cells and chloroplasts were 30–40% larger in the palisade than in the spongy mesophyll. In contrast, in a shade-loving species Veronica chamaedris, the spongy mesophyll was 1.5–2 times more developed than the palisade mesophyll. In mesophyte species grown under high light conditions, the cell abundance and the total cell surface area were 10–20% greater in the palisade mesophyll than in the spongy parenchyma. In shaded habitats, these indices were similar in the palisade and spongy mesophyll or were 10–20% lower in the palisade mesophyll. In mesophytes, CO₂ conductance of the spongy mesophyll accounted for about 50% of the total mesophyll conductance, as calculated from the structural characteristics, with the mesophyll CO₂ conductance increasing with leaf shading.