Browsing by Subject "Vapor pressure deficit"

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Constant hydraulic supply and ABA dynamics facilitate the trade-offs in water and carbon
(2023) Abdalla, Mohanned; Schweiger, Andreas H.; Berauer, Bernd J.; McAdam, Scott A. M.; Ahmed, Mutez Ali
Carbon-water trade-offs in plants are adjusted through stomatal regulation. Stomatal opening enables carbon uptake and plant growth, whereas plants circumvent drought by closing stomata. The specific effects of leaf position and age on stomatal behavior remain largely unknown, especially under edaphic and atmospheric drought. Here, we compared stomatal conductance (gs) across the canopy of tomato during soil drying. We measured gas exchange, foliage ABA level and soil-plant hydraulics under increasing vapor pressure deficit (VPD). Our results indicate a strong effect of canopy position on stomatal behavior, especially under hydrated soil conditions and relatively low VPD. In wet soil (soil water potential > -50 kPa), upper canopy leaves had the highest gs (0.727 ± 0.154 mol m-2 s-1) and assimilation rate (A; 23.4 ± 3.9 µmol m-2 s-1) compared to the leaves at a medium height of the canopy (gs: 0.159 ± 0.060 mol m2 s-1; A: 15.9 ± 3.8 µmol m-2 s-1). Under increasing VPD (from 1.8 to 2.6 kPa), gs, A and transpiration were initially impacted by leaf position rather than leaf age. However, under high VPD (2.6 kPa), age effect outweighed position effect. The soil-leaf hydraulic conductance was similar in all leaves. Foliage ABA levels increased with rising VPD in mature leaves at medium height (217.56 ± 85 ng g-1 FW) compared to upper canopy leaves (85.36 ± 34 ng g-1 FW). Under soil drought (< -50 kPa), stomata closed in all leaves resulting in no differences in gs across the canopy. We conclude that constant hydraulic supply and ABA dynamics facilitate preferential stomatal behavior and carbon-water trade-offs across the canopy. These findings are fundamental in understanding variations within the canopy, which helps in engineering future crops, especially in the face of climate change.
Effects of temperature and vapor pressure deficit on genotypic responses to nitrogen nutrition and weed competition in lowland rice
(2021) Vu, Duy Hoang; Asch, Folkard
Since rice is the major food for more than half of the world’s population, rice production and productivity have significant implications for food security. In adaptation to increasing water scarcity, as well as to reduce greenhouse gas emissions, water-saving irrigation measures (e.g., alternate wetting and drying – AWD) have been introduced in many rice growing regions. Previous studies have shown that AWD increases water use efficiency and reduces methane (CH4) emissions, while grain yield remains equal or is slightly increased compared to continuous flooding. However, the absence of a ponded water layer in formerly flooded rice fields creates new challenges, such as altered root zone temperature (RZT), enhanced nitrification leading to higher nitrate (NO3-) concentrations in the soil, or stimulated weed germination leading to changes in weed flora. All these factors may affect nutrient uptake and assimilation of rice plants and thus plant growth. Further, vapor pressure deficit (VPD) drives transpiration and water flux through plants, so nutrient uptake and assimilation by plants may be subject to adjustment under varying VPD conditions. As VPD varies largely between rice growing regions and seasons, and is also predicted to continuously increase under global warming, it was included as a factor in this study. The overall objective of the study was to evaluate the response of different rice varieties to arising challenges under water-saving irrigation. Experiments were conducted in the greenhouse and VPD chambers at the University of Hohenheim, where plants were grown in hydroponics. Both during day and night, nutrient uptake rates of rice increased linearly with RZT in the observed temperature range up to 29°C, implying that the optimum temperature for nutrient uptake of rice must be above 29°C. However, the uptake rates of different nutrient elements responded differently to RZT, with the increase in nitrogen (N) uptake per °C being greater than that of phosphorus (PO43-) and potassium (K+), which can potentially lead to an imbalance in plant nutrition. Therefore, the increase in RZT either due to climate change or water management may call for an adjusted fertilizer management. In general, the increase in nutrient uptake per °C was more pronounced during the day than during the night, while the amino acid concentration in the leaves both during the day and night was positively correlated with N uptake during the day, suggesting that plants may benefit more from increased temperature during the day. When both ammonium (NH4+) and NO3- were supplied, rice plants took up a higher share of NH4+. However, after depletion of NH4+ in the nutrient solution, plants took up NO3- without decreasing the total N uptake. The N form taken up by the rice plant had no effect on leaf gas exchange at low VPD, whereas NO3- uptake and assimilation increased stomatal conductance in some rice varieties at high VPD, resulting in a significantly higher photosynthetic rate. However, the increase in photosynthesis did not always result in an increase in dry matter, probably due to a higher energy requirement for NO3- assimilation than for NH4+. The effect of N form on leaf gas exchange of some rice varieties was only found at high VPD, indicating genotype-specific adaptation strategies to high VPD. However, maintenance of high stomatal conductance at high VPD will only be beneficial at sufficient levels of water supply. Therefore, we hypothesize that with increasing VPD, intensified nitrification under water-saving irrigation may improve leaf gas exchange of rice plants, provided a careful choice of variety and good water management. Furthermore, N form had an effect on the competition between rice and weeds. In mixed culture with rice, a large share of NO3- increased the growth and competitiveness of upland weeds but reduced the growth and competitiveness of lowland weeds. Consequently, enhanced nitrification under AWD may reduce the competitive pressure of lowland weeds, but increase the competition of upland weeds. In contrast to rice, growth of the upland weed was not reduced by high VPD, while its nutrient uptake was correlated with water uptake, suggesting that upland weeds will more successfully compete with rice for nutrients as VPD increases. Selection of rice varieties better adapted to NO3- uptake will improve rice growth and its competitiveness against weeds under AWD. The cumulative effects of RZT and soil nitrification on rice growth should be considered when evaluating the effects of climate change on rice growth.
Physiological and growth responses of Jatropha curca L. to water, nitrogen and salt stresses
(2012) Rajaona, Arisoa Mampionona; Asch, Folkard
This thesis provides necessary and complementary information for an improved understanding of jatropha growth to guide further research to evaluate the response of jatropha to abiotic stressors and for designing plantations adapted to the plants? requirements. Given the fact that jatropha is claimed to grow on marginal lands, we studied effects of water supply, salt stress, nitrogen and air humidity as major abiotic stressors on gas exchange parameters and biomass production followed by management options for pruning the trees to positively influence biomass productivity and to contribute to optimize resource use. The effects of water availability (rainfed versus irrigated) on growth and gas exchange parameters were investigated for 4-year old jatropha grown in a semi-arid environment at a plantation site in Madagascar in 2010. The results confirmed that 1250 mm water in addition to a 500 mm rainfall did not affect biomass production and instantaneous gas exchange. Nevertheless, leaf light responses of irrigated plants were higher than that of rainfed plants. The study showed to what extent salt stress affected water use, canopy water vapour conductance, leaf growth and Na and K concentrations of leaves of 3-year old and young jatropha plants. 3-year old plants were exposed to seven salt levels (0-300 mmol NaCl L-1) during 20 days and young plants to five salt levels (0-200 mmol NaCl L-1) during 6 days. In both experiments, plants responded rapidly to salt stress by reducing water loss. The threshold value of responses was between 0 and 5 dS m-1. Leaf area increment of young jatropha had a threshold value of 5 dS m-1 implying that jatropha is sensitive to external salt application in terms of canopy development, conductance and CO2 assimilation rate. Transpiration of plants in both experiments was reduced to 55% at EC values between 11 and 12 dS m-1 as compared to non-stressed plants. These findings indicate that jatropha responds sensitive to salt stress in terms of leaf elongation rate and consequently canopy development, and to immediate physiological responses. Leaf gas exchange characteristics of jatropha as affected by nitrogen supply and leaf age were intensively studied, as carbon assimilation is one of the central processes of plant growth and consequently a key process embedded in modelling approaches of plant productivity. This study showed that N supply effects on leaf gas exchange of jatropha leaves were small with only the treatment without nitrogen resulting in lower rates of CO2 assimilation rate and light saturated CO2 assimilation rate, nevertheless, effects of N supply on biomass formation were pronounced. Instantaneous rates of leaf gas exchange of different leaves subject to variable air humidity (atmospheric vapour pressure deficit (VPD)) were investigated. This study showed that CO2 assimilation rate (A) and stomatal conductance (gs) were correlated in a hyperbolic fashion, and that gs declined with increasing VPD. Maximal stomatal conductance of jatropha was in the range of 382 mmol m-2 s-1 and gs is predicted to be close to zero at 6 kPa. Effects of VPD, via stomatal conductance, by preventing high transpiration rates, have been demonstrated to be decisive on water use efficiency. Our findings are in this regard relevant for the estimation of water use efficiency of jatropha. The outcome further indicates favourable conditions at which stomatal opening is high and thereby allowing for biomass formation. This information should be considered in approaches which aim at quantifying leaf activity of field-grown bushes which are characterized by spatially highly diverse conditions in terms of microclimatic parameters. Microclimatic parameters can be modified by the tree structure. The reported field experiment on 4-year old jatropha indicated that the biomass production and canopy size depended mainly on primary branch length. A comparison of plants of different pruning types with regard to trunk height (43 versus 29 cm) and total length of primary branches (171 versus 310 cm), suggest that higher biomass production and greater leaf area projection was realized by trees with short trunks and long primary branches. Growth of twigs and leaves was positively correlated with total length of branches. Relative dry mass allocation to branches, twigs and leaves, length of twigs per cm of branches and specific leaf area were not affected by pruning and water supply. Trees with shorter branches had a higher leaf area density. As opposed to an allometric relationship between the average diameter of primary branches and total above ground biomass, our data suggest that these traits were not constantly correlated. Our data indicate that the length of newly formed twigs, where the leaves are attached to, can be related to the total length of already established branches. Leaf area density and relative dry mass allocation to leaves were not affected by the two pruning techniques, indicating that pruning differences in leaf area size were proportionally converted to corresponding pruning differences in the canopy volume exploited by plants. The results reported in this study are relevant for understanding jatropha growth. It helps farmers first for a better plantation management and researchers as well as contribution to future modelling purpose concerning jatropha growth under variable climatic conditions. Additionally, it should complement information for a better set of priorities in research, contribute indirectly to breeding programs and adjust agricultural policies in terms of encountering global change.