Water‐use efficiency in response to climate change: from leaf to ecosystem in a temperate steppe

Water‐use efficiency (WUE) has been recognized as an important characteristic of ecosystem productivity, which links carbon (C) and water cycling. However, little is known about how WUE responds to climate change at different scales. Here, we investigated WUE at leaf, canopy, and ecosystem levels under increased precipitation and warming from 2005 to 2008 in a temperate steppe in Northern China. We measured gross ecosystem productivity (GEP), net ecosystem CO₂ exchange (NEE), evapotranspiration (ET), evaporation (E), canopy transpiration (T_c), as well as leaf photosynthesis (P_max) and transpiration (T_l) of a dominant species to calculate canopy WUE (WUE_c=GEP/T), ecosystem WUE (WUE_gep=GEP/ET or WUE_nee=NEE/ET) and leaf WUE (WUE_l=P_max/T_l). The results showed that increased precipitation stimulated WUE_c, WUE_gep and WUE_nee by 17.1%, 10.2% and 12.6%, respectively, but decreased WUE_l by 27.4%. Climate warming reduced canopy and ecosystem WUE over the 4 years but did not affect leaf level WUE. Across the 4 years and the measured plots, canopy and ecosystem WUE linearly increased, but leaf level WUE of the dominant species linearly decreased with increasing precipitation. The differential responses of canopy/ecosystem WUE and leaf WUE to climate change suggest that caution should be taken when upscaling WUE from leaf to larger scales. Our findings will also facilitate mechanistic understanding of the C–water relationships across different organism levels and in projecting the effects of climate warming and shifting precipitation regimes on productivity in arid and semiarid ecosystems.     

Water-use efficiency and carbon isotope discrimination in two cultivars of upland rice during different developmental stages under three water regimes

A pot experiment was conducted in a glasshouse to clarify and quantify the effect of plant part, water regime, growth period, and cultivar on carbon isotope discrimination (CID), and to analyze the relationship between CID, stomatal behavior and water-use efficiency (WUE). The experiment was comprised of two upland rice (Oryza sativa L.) cultivars and three water regimes (100, 70, and 40% of saturation moisture) in a completely randomized design. Plants were harvested at tillering, flowering, and maturity. No significant cultivar differences in above-ground dry matter-based WUE (WUE_A) and total dry matter-based WUE (WUE_T) were observed. WUE_A (and WUE_T) increased with water stress up to tillering, but decreased with water stress after tillering. Significant cultivar differences in CID in all the analyzed plant parts were observed at all harvest times. Reduction in CID with water stress was greatest at tillering, and the effect was less pronounced at flowering and at maturity. At each harvest, the effect was most pronounced in newly developed plant parts. Root and grain tended to have the lowest CID values, and stem the highest, at all harvest times. A negative relationship was observed between CID measured at tillering and WUE_A (and WUE_T) measured over the period from seedling to tillering, whereas a reverse relationship was obtained between CID measured at flowering and WUE_A (and WUE_T) measured over the period from tillering to flowering, and an unclear relationship between CID measured at maturity and WUE_A (and WUE_T) measured over the period from flowering to maturity. The ratio of the intercellular and atmospheric concentration of CO₂ (C_i/C_a) were closely associated with CID throughout the water regimes when one cultivar was considered, however, cultivar differences in CID were not related to variations in C_i/C_a. The results indicate that significant cultivar difference existed in CID in all the analyzed plant parts at all harvest times, while corresponding difference in WUE_A (and WUE_T) between the cultivars was not necessarily consistent. Abbreviations: WUE – water-use efficiency; WUEi – instantaneous WUE (or leaf transpiration efficiency); ADM – above-ground dry matter; TDM – total dry matter; WUE_A– ADM-based WUE; WUE_T– TDM-based WUE} CID – carbon isotope discrimination; NL – the newest leaves; FEL – recently fully expanded leaves; FL – flag leaves; P – photosynthesis rate; g – leaf stomatal conductance to water vapor; C_i– intercellular CO₂ concentration; C_a– atmospheric CO₂ concentration; T – transpiration rate; gs – total conductance of CO₂     

Water use efficiency of two succulents with contrasting CO2 fixation pathways

Two succulents with similar growth forms but different types of photosynthesis, Cotyledon orbiculata (crassulacean acid metabolism, CAM) and Othonna opima (C₃ pathway), were investigated with respect to the modulation of water use efficiency (WUE) during the transition from the rainy season to subsequent drought. Environmental conditions were simulated in a controlled-environment experiment on the basis of data collected in the habitat of the two species in the southern Namib desert. Experiments included one or more periods of hot bergwind, which frequently occurs in this region. When water was readily available, daily net CO₂ fixation was similar in the two species. This result confirms that the daily CO₂ fixation of CAM plants is as high as that of morphologically similar C₃ plants adapted to the same habitat. As expected, both species reduced CO₂ fixation and water loss through transpiration during simulated hot bergwind periods and their WUE values increased. However, after the second hot bergwind period, nearly identical WUEs were recorded: 41.0 and 40.0 mmol mol^?1 for C. orbiculata and O. opima, respectively. Therefore the statement that a CAM plant is a better ‘water saver’ than a C₃ plant does not necessarily hold for CAM and C₃ plants with similar growth forms growing under the same environmental conditions.     

Water relations and photosynthesis of a barrel cactus,Ferocactus acanthodes,in the Colorado desert

Summary The structural characteristics, water relations, and photosynthesis of Ferocactus acanthodes (Lemaire) Britton and Rose, a barrel cactus exhibiting Crassulacean acid metabolism (CAM), were examined in its native habitat in the western Colorado desert. Water storage in its succulent stem permitted nighttime stomatal opening ot continue for about 40 days after the soil water potential became less than that of the stem, a period whe the plant would be unable to extract water from the soil. After 7 months of drought and consequent unreplenished water loss from a plant, diurnal stomatal activity was not observed and the stem osmotic pressure was 6.4 bars, more than double the value measured during wet periods with nighttime stomatal opening. F. acanthodes had a shallow root system (mean depth of 8 cm) which responded within 24 h to rainfall.When the nocturnal stem surface temperature was raised from 8.0° C to 35.0° C, the stomatal resistance increased 4-fold, indicating that cool nighttime temperatures are advantageous for gas exchange by F. acanthodes. Moreover, the optimal temperature for CO₂ uptake in the dark was only 12.6° C. CO₂ uptake at night became maximal for 3.0 mEinsteins cm^-2 of photosynthetically active radiation incident during the preceding day, and the minimum number of incident quanta absorbed per CO₂ fixed was 68. The transpiration ratio (mass of water transpired/mass of CO₂ fixed) had the relatively low value of 70 for an entire year, consistent with values obtained for other CAM plants. The total amount of water annually diverted to the floral structures was about 6% of the stem wet weight. The annual growth increment estimated from the net CO₂ assimilation corresponded to about 10% of the stem mass for barrel cacti 34 cm tall, in agreement with measured dimension changes, and indicated that such plants were about 26 years old.     

Day-Night Variations in Malate Concentration, Osmotic Pressure, and Hydrostatic Pressure in Cereus validus

Malate concentration and stem osmotic pressure concomitantly increase during nighttime CO₂ fixation and then decrease during the daytime in the obligate Crassulacean acid metabolism (CAM) plant, Cereus validus (Cactaceae). Changes in malate osmotic pressure calculated using the Van't Hoff relation match the changes in stem osmotic pressure, indicating that changes in malate level affected the water relations of the succulent stems. In contrast to stem osmotic pressure, stem water potential showed little day-night changes, suggesting that changes in cellular hydrostatic pressure occurred. This was corroborated by direct measurements of hydrostatic pressure using the Jülich pressure probe where a small oil-filled micropipette is inserted directly into chlorenchyma cells, which indicated a 4-fold increase in hydrostatic pressure from dusk to dawn. A transient increase of hydrostatic pressure at the beginning of the dark period was correlated with a short period of stomatal closing between afternoon and nighttime CO₂ fixation, suggesting that the rather complex hydrostatic pressure patterns could be explained by an interplay between the effects of transpiration and malate levels. A second CAM plant, Agave deserti, showed similar day-night changes in hydrostatic pressure in its succulent leaves. It is concluded that, in addition to the inverted stomatal rhythm, the oscillations of malate markedly affect osmotic pressures and hence water relations of CAM plants.     

Comparison of ecosystem water-use efficiency among Douglas-fir forest, aspen forest and grassland using eddy covariance and carbon isotope techniques

Comparisons were made among Douglas‐fir forest, aspen (broad leaf deciduous) forest and wheatgrass (C₃) grassland for ecosystem‐level water‐use efficiency (WUE). WUE was defined as the ratio of photosynthetic CO₂ assimilation rate and evapotranspiration (ET) rate. The ET data measured by eddy covariance were screened so that they overwhelmingly represented transpiration. The three sites used in this comparison spanned a range of vegetation (plant functional) types and environmental conditions within western Canada. When compared in the relative order Douglas‐fir (located on Vancouver Island, BC), aspen (northern Saskatchewan), grassland (southern Alberta), the sites demonstrated a progressive decline in precipitation and a general increase in maximum air temperature and atmospheric saturation deficit (D_max) during the mid‐summer. The average (±SD) WUE at the grassland site was 2.6±0.7 mmol mol^?1, which was much lower than the average values observed for the two other sites (aspen: 5.4±2.3, Douglas‐fir: 8.1±2.4). The differences in WUE among sites were primarily because of variation in ET. The highest maximum ET rates were approximately 5, 3.2 and 2.7 mm day^?1 for the grassland, aspen and Douglas‐fir sites, respectively. There was a strong negative correlation between WUE and D_max for all sites. We also made seasonal measurements of the carbon isotope ratio of ecosystem respired CO₂ (δ_R) in order to test for the expected correlation between shifts in environmental conditions and changes to the ecosystem‐integrated ratio of leaf intercellular to ambient CO₂ concentration (c_i/c_a). There was a consistent increase in δ_R values in the grassland, aspen forest and Douglas‐fir forest associated with a seasonal reduction in soil moisture. Comparisons were made between WUE measured using eddy covariance with that calculated based on D and δ_R measurements. There was excellent agreement between WUE values calculated using the two techniques. Our δ_R measurements indicated that c_i/c_a values were quite similar among the Douglas‐fir, aspen and grassland sites, despite large variation in environmental conditions among sites. This implied that the shorter‐lived grass species had relatively high c_i/c_a values for the D of their habitat. By contrast, the longer‐lived Douglas‐fir trees were more conservative in water‐use with lower c_i/c_a values relative to their habitat D. This illustrates the interaction between biological and environmental characteristics influencing ecosystem‐level WUE. The strong correlation we observed between the two independent measurements of WUE, indicates that the stable isotope composition of respired CO₂ is a useful ecosystem‐scale tool to help study constraints to photosynthesis and acclimation of ecosystems to environmental stress.     

Photosynthesis, water use efficiency and stable carbon isotope composition are associated with anatomical properties of leaf and xylem in six poplar species

Although fast‐growing Populus species consume a large amount of water for biomass production, there are considerable variations in water use efficiency (WUE) across different poplar species. To compare differences in growth, WUE and anatomical properties of leaf and xylem and to examine the relationship between photosynthesis/WUE and anatomical properties of leaf and xylem, cuttings of six poplar species were grown in a botanical garden. The growth performance, photosynthesis, intrinsic WUE (WUE_i), stable carbon isotope composition (δ¹³C) and anatomical properties of leaf and xylem were analysed in these poplar plants. Significant differences were found in growth, photosynthesis, WUE_i and anatomical properties among the examined species. Populus cathayana was the clone with the fastest growth and the lowest WUE_i/δ¹³C, whereas P. × euramericana had a considerable growth increment and the highest WUE_i/δ¹³C. Among the analysed poplar species, the highest total stomatal density in P. cathayana was correlated with its highest stomatal conductance (g_s) and lowest WUE_i/δ¹³C. Moreover, significant correlations were observed between WUE_i and abaxial stomatal density and stem vessel lumen area. These data suggest that photosynthesis, WUE_i and δ¹³C are associated with leaf and xylem anatomy and there are tradeoffs between growth and WUE_i. It is anticipated that some poplar species, e.g. P. × euramericana, are better candidates for water‐limited regions and others, e.g. P. cathayana, may be better for water‐abundant areas.     

Plant transpiration at high elevations: Theory,field measurements,and comparisons with desert plants

Summary The influence of elevational changes on plant transpiration was evaluated using leaf energy balance equations and well-known elevational changes in the physical parameters that influence water vapor diffusion. Simulated transpirational fluxes for large leaves with low and high stomatal resistances to water vapor diffusion were compared to small leaves with identical stomatal resistances at elevations ranging from sea level to 4 km. The specific influence of various air temperature lapse rates was also tested. Validation of the simulated results was accomplished by comparing actual field measurements taken at a low elevation (300 m) desert site with similar measurements for a high elevation (2,560 m) mountain research site. Close agreement was observed between predicted and measured values of transpiration for the environmental and leaf parameters tested.Substantial increases in solar irradiation and the diffusion coefficient for water vapor in air (D _wv) occurred with increasing elevation, while air and leaf temperatures, the water vapor concentration difference between the leaf and air, longwave irradiation, and the thermal conductivity coefficient for heat in air decreased with increasing elevation. These changes resulted in temperatures for sunlit leaves that were further above air temperature at higher elevations, especially for large leaves. For large leaves with low stomatal resistances, transpirational fluxes for low-elevation desert plants were close to those predicted for high-elevation plants even though the sunlit leaf temperatures of these mountain plants were over 10°C cooler. Simulating conditions with a low air temperature lapse rate (0.003° C m^-1 and 0.004° C m^-1) resulted in predicted transpirational fluxes that were greater than those calculated for the desert site. Transpiration for smaller leaves decreased with elevation for all lapse rates tested (0.003° C m^-1 to 0.010° C m^-1). However, transpirational fluxes at higher elevations were considerably greater than expected for all leaves, especially larger leaves, due to the strong influence of increased solar heating and a greater D _wv. These results are discussed in terms of similarities in leaf structure and plant habit observed among low-elevation desert plants and high-elevation alpine and subalpine plants.     

科尔沁草甸生态系统水分利用效率及影响因素

生态系统水分利用效率(WUE)是衡量碳水循环耦合程度的重要指标。利用科尔沁温带草甸草地碳水通量观测数据,对该生态系统总初级生产力水分利用效率(WUEGPP)的日季变化规律及对环境和生理因子的响应进行分析。结果表明:(1)WUEGPP日变化呈下降-稳定-上升的变化趋势,最大值出现在日出后1—2 h,阴天条件下WUEGPP高于晴天,生长中期WUEGPP高于生长初期和末期;(2)总初级生产力、总蒸散和WUEGPP季节变化均呈夏季高、春秋低的形式,生长季平均值分别为0.57 mg m-2s-1、0.08 g m-2s-1和5.97 mg/g,最大值分别为1.49 mg m-2s-1、0.16 g m-2s1和13.62 mg/g;(3)总初级生产力与饱和差、气温和叶面积指数均呈二次曲线关系,与冠层导度呈对数曲线关系;总蒸散与气温呈二次曲线关系,与饱和差、叶面积指数和冠层导度相关性均不显著;(4)WUEGPP与饱和差、气温和叶面积指数均呈二次曲线关系,与冠层导度呈对数曲线关系,饱和差、冠层导度和叶面积指数分别为2.0 k Pa、0.0015 m/s和4.2是控制WUEGPP增加的阈值;(5)净生态系统生产力水分利用效率(WUENEP)和净初级生产力水分利用效率(WUENPP)季节变化规律与WUEGPP一致,均值分别为3.47和5.47 mg/g。     

Stomata of the CAM plant Tillandsia recurvata respond directly to humidity

Summary Under controlled conditions, CO₂ exchange of Tillandsia recurvata showed all characteristics of CAM. During the phase of nocturnal CO₂ fixation stomata of the plant responded sensitively to changes in ambient air humidity. Dry air resulted in an increase, moist air in a decrease of diffusion resistance. The evaporative demand of the air affected the level of stomatal resistance during the entire night period. Due to stomatal closure, the total nocturnal water loss of T. recurvata was less at low than at high humidity. It is concluded that stomata respond directly to humidity and not via bulk tissue water conditions of the leaves. Such control of transpiration may optimize water use efficiency for this almost rootless, extreme epiphyte.     

Water use efficiency in C3 cereals under Mediterranean conditions: a review of physiological aspects

In this review, we will discuss physiological traits of C₃ cereals related to water use efficiency (WUE) in Mediterranean environments, from leaf (WUE_{instantaneous}) to crop level (WUE_yield or ‘water productivity’). First, we analyse the WUE_{instantaneous} and the possible trade‐off between improving this parameter and growth/yield performance. Ways to ameliorate WUE without penalties are discussed. We also analyse in what cases breeding by high or low WUE_{instantaneous} is a suitable criterion to maintain grain yield under drought (Mediterranean) conditions. This question is approached in the framework of carbon isotope discrimination, (Δ¹³C), the main indirect parameter used to integrate (at time and space scale) the WUE_{instantaneous} in C₃ plants. A negative correlation between these two parameters has been confirmed by several studies. The relationship between Δ¹³C and grain yield, however, is more complex, and may differ from one environment to another. In Mediterranean conditions with moderate or no water stress, a positive correlation between Δ¹³C and grain yield is found in barley and wheat, whereas in ‘stored‐water’ crops (such as in some regions of Australia), lower Δ¹³C (i.e. higher WUE_{instantaneous}) is associated with higher grain yield, particularly in more stressful conditions. These apparent inconsistencies and their possible implications for plant breeding are discussed. One physiological trait that has received minor attention in attempts to improve WUE_{instantaneous} is the role of ear photosynthesis. Ears of barley and durum wheat have a higher WUE_{instantaneous} than the flag leaf, both in well‐watered and in drought conditions. The underlying causes of the higher WUE_{instantaneous} of ears are not fully understood, but their refixation capacity (i.e. the capacity to re‐assimilate respired carbon dioxide) could be important. Although the genotypic variability of this trait has not been extensively studied, some data support the idea that variation in refixation capacity may be attributable to genetic factors. At the crop level, decreasing soil evaporation is a crucial factor in efforts to improve the WUE_yield in Mediterranean conditions, and fast initial growth of the crop (i.e. early vigour) seems to be relevant. In wheat, modern varieties with dwarfing genes (giberellic acid – insensitive) have higher yields but, concomitantly, they have lower initial growth performance. Recently, semi‐dwarf cultivars (giberellic acid – sensitive) with high grain yield and simultaneously high early vigour were found, opening new avenues to increase WUE_yield in wheat. The negative effects of futile water loss by cuticular and nocturnal transpiration are also commented. Finally, we discuss some agronomic practices (in particular, ‘deficit irrigation’ systems) linked to physiological traits that confer higher WUE_yield,, in particular, in the cases of Mediterranean regions.     

The relationship between the soil water storage and water-use efficiency of seven energy crops

The aim of this work was to determine two types of photosynthetic water-use efficiency in order to examine their utility as selection criteria for tolerance of energy crops to soil water deficit. Furthermore, effects of crop cultivation on soil water content and storage were investigated. Seven energy crops were examined: miscanthus, prairie cordgrass, willow, thorn-free rose, Virginia mallow, Bohemian knotweed, and topinambour. The highest values of instantaneous (WUE) and intrinsic (WUE_i) water-use efficiencies were found for miscanthus and prairie cordgrass. The reduction of WUE and/or WUE_i was caused mainly by a rapid rise in the transpiration rate and a greater stomatal conductance, respectively. Principal component analysis showed that neither WUE nor WUE_i could be recommended as universal selection criteria for the drought tolerance in different energy crops. The proper localization of soil with a good supply of water is most the important condition for energy crop plantations.     

PdEPF1 regulates water‐use efficiency and drought tolerance by modulating stomatal density in poplar

Water deficiency is a critical environmental condition that is seriously reducing global plant production. Improved water‐use efficiency (WUE) and drought tolerance are effective strategies to address this problem. In this study, PdEPF1, a member of the EPIDERMAL PATTERNING FACTOR (EPF) family, was isolated from the fast‐growing poplar clone NE‐19 [Populus nigra × (Populus deltoides × Populus nigra)]. Significantly, higher PdEPF1 levels were detected after induction by dehydration and abscisic acid. To explore the biological functions of PdEPF1, transgenic triploid white poplars (Populus tomentosa ‘YiXianCiZhu B385’) overexpressing PdEPF1 were constructed. PdEPF1 overexpression resulted in increased water deficit tolerance and greater WUE. We confirmed that the transgenic lines with greater instantaneous WUE had approximately 30% lower transpiration but equivalent CO₂ assimilation. Lower transpiration was associated with a 28% reduction in abaxial stomatal density. PdEPF1 overexpression not only strongly enhanced WUE, but also greatly improved drought tolerance, as measured by the leaf relative water content and water potential, under limited water conditions. In addition, the growth of these oxPdEPF1 plants was less adversely affected by reduced water availability than plants with a higher stomatal density, indicating that plants with a low stomatal density may be well suited to grow in water‐scarce environments. Taken together, our data suggest that PdEPF1 improves WUE and confers drought tolerance in poplar; thus, it could be used to breed drought‐tolerant plants with increased production under conditions of water deficiency.     

Stomatal Opening Mechanism of CAM Plants

Stomata usually open when leaves are transferred from darkness to light. However, reverse-phase stomatal opening in succulent plants has been known. CAM plants such as cacti and Opuntia ficus–indica achieve their high water use efficiency by opening their stomata during the cool, desert nights and closing them during the hot, dry days. Signal transduction pathway for stomatal opening by blue light photoreceptors including phototropins and the carotenoid pigment zeaxanthin has been suggested. Blue light regulated signal transduction pathway on stomatal opening could not be applied to CAM plants, but the most possible theory for a nocturnal response of stomata in CAM plants is photoperiodic circadian rhythm.     

Mycorrhizal association between the desert truffle Terfezia boudieri and Helianthemum sessiliflorum alters plant physiology and fitness to arid conditions

The host plant Helianthemum sessiliflorum was inoculated with the mycorrhizal desert truffle Terfezia boudieri Chatin, and the subsequent effects of the ectomycorrhizal relationship on host physiology were determined. Diurnal measurements revealed that mycorrhizal (M) plants had higher rates of photosynthesis (35%), transpiration (18%), and night respiration (49%) than non-mycorrhizal (NM) plants. Consequently, M plants exhibited higher biomass accumulation, higher shoot-to-root ratios, and improved water use efficiency compared to NM plants. Total chlorophyll content was higher in M plants, and the ratio between chlorophyll a to chlorophyll b was altered in M plants. The increase in chlorophyll b content was significantly higher than the increase in chlorophyll a content (2.58- and 1.52-fold, respectively) compared to control. Calculation of the photosynthetic activation energy indicated lower energy requirements for CO₂ assimilation in M plants than in NM plants (48.62 and 61.56 kJ mol⁻¹, respectively). Continuous measurements of CO₂ exchange and transpiration in M plants versus NM plants provided a complete picture of the daily physiological differences brought on by the ectomycorrhizal relationships. The enhanced competence of M plants to withstand the harsh environmental conditions of the desert is discussed in view of the mycorrhizal-derived alterations in host physiology.     

北京山区元宝枫夜间液流活动特征及影响因素

树木夜间会维持部分气孔开放,从而能够在一定环境驱动因子的情况下进行夜间蒸腾。夜间液流作为储存水的重要来源,能够补充植物白天的水分亏缺,使其恢复水分储备,对植物生长发育有重要意义。采用TDP热探针法测定了位于八达岭林场的元宝枫树干液流密度,同步监测了主要环境因子,以深入揭示树木夜间蒸腾耗水规律和植被应对环境胁迫的调控机制,为山区植被建设、森林健康经营和挑选节水树种提供理论依据。结果表明:以0:00为界区分前半夜和后半夜,元宝枫夜间液流速率前半夜较后半夜活跃,且前半夜夜间累积液流量占夜间累积液流量的53.85%—64.10%,而后半夜夜间累积液流量占夜间累积液流量的35.9%—46.15%。5月的夜间累积液流量最大,平均夜间液流通量为5月6月8月9月7月。存在水分胁迫的条件下降雨之后夜间液流会增大,而当土壤水分条件较好,土壤水分不再是夜间液流的限制因子时,夜间液流通量并不高。不同树木形态的夜间液流通量有显著差异,在一定范围内,胸径树高冠幅越大的样木,夜间液流通量越大。用于夜间蒸腾的夜间液流通量与饱和水汽压差、温度、空气相对湿度、风速相关,其中夜间蒸腾存在于前半夜,表现为前半夜夜间液流通量与环境因子的相关性相较后半夜相关性较为显著,后半夜则以补水为主,补水量取决于土壤含水量和日蒸腾强度。存在干旱胁迫的条件下,夜间液流既用于夜间蒸腾,又有一部分用来补水;而土壤水分条件好时夜间液流则主要用于补水,此时夜间树干液流与环境因子相关性不高。元宝枫夜间液流通量的日蒸腾贡献率5、6月份大于7、8月份,即干季比湿季贡献率更高。夜间液流通量的日蒸腾贡献率与白天总蒸腾量相关性较高,并与累积太阳辐射成负相关。     

Relationships between gas-exchange characteristics and stomatal structural modifications in some desert grasses under high salinity

Two populations, one from lesser saline Derawar Fort (DF) and the other from highly saline Ladam Sir (LS) in the Cholistan desert, for each of the five grass species, Aeluropus lagopoides, Cymbopogon jwarancusa, Lasiurus scindicus, Ochthochloa compressa, and Sporobolus ioclados were examined to investigate the influence of salinity on structural and functional characteristics of stomata. Salinity tolerance in A. lagopoides mainly depended on controlled transpiration rate (E) and high water-use efficiency (WUE), which was found to be regulated by fewer and smaller stomata on both leaf surfaces as well as stomatal encryption by epidermal invaginations. C. jwarancusa had sunken stomata on the abaxial surface only, which largely reflected a reduced E, but less affected stomatal conductance (g _s) or WUE. L. scindicus had fewer but larger stomata along with hairs/trichomes which may function to avoid water loss through transpiration, and hence, to attain a high WUE. In O. compressa stomata were found only on the abaxial surface and these were completely encrypted by epidermal invaginations as well as a dense covering of microhairs, which was associated with a low E and high WUE under salinity stress. In S. ioclados, the traits of increased stomatal density and decreased stomatal area may be critical for stomatal regulation under salt-prone environments. High stomatal regulation depended largely on stomatal density, area, and degree of encryption under salinity, which is of great ecophysiological significance for plants growing under osmotic stresses.     

Nocturnal water storage in plants having Crassulacean acid metabolism

Measurements of water uptake and transpiration, during the dark period of plants having Crassulacean acid metabolism (CAM) allow calculation of leaf-volume changes (V). Nocturnal leaf-volume changes of CAM plants have also been reported in the literature on the basis of waterdisplacement measurements. A third way of estimation is from measurements of turgor changes and cellular water-storage capacity using the pressure probe, cytomorphometry and the Scholander pressure chamber. An extension of the interpretation of results reported in the literature shows that for leaf succulent CAM plants the three different approaches give similar values of V ranging between 2.3 and 10.7% (v/v). It is evident that nocturnal malic-acid accumulation osmotically drives significant water storage in CAM leaf tissue.Abbreviations and symbols C_c water-storage capacity - E transporation (evaporational water loss) - P turgor pressure - U water uptake - V cell volume - cell-wall elastic modulus - osmotic pressure - CAM Crassulacean acid metabolism     

CO2-Fixierungsreaktionen bei der Salzpflanze Mesembryanthemum crystallinum unter variierten Außenbedingungen

Summary The correlation of CO₂-fixation metabolism to various environmental conditions such as NaCl content of culture medium, air humidity and light intensity was investigated in the halophytic species Mesembryanthemum crystallinum. The data obtained demonstrate that a change in photosynthesis from C₃-pathway to crassulacean acid metabolism (CAM) is observed not only in NaCl treated plants as reported earlier but also in control plants grown in non-saline medium when environmental conditions (high light intensity, low air humidity) cause a water deficit in the leaves. It is suggested that water stress plays an important role in regulation between C₃- and CAM-pathway of photosynthesis in Mesembryanthemum crystallinum.

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Abkürzungen CAM Crassulaceensäurestoffwechsel - FG Frischgewicht - TG Trockengewicht - D Ende Dunkelphase - L Ende Lichtphase Herrn Prof. Dr. Otto Stocker zum 85. Geburtstag gewidmet