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When attacked by herbivores, plants produce electrical signals which can activate the synthesis of the defense mediator jasmonate. These wound-induced membrane potential changes can occur in response to elicitors that are released from damaged plant cells. We list plant-derived elicitors of membrane depolarization. These compounds include the amino acid l-glutamate (Glu), a potential ligand for GLUTAMATE RECEPTOR-LIKE (GLR) proteins that play roles in herbivore-activated electrical signaling. How are membrane depolarization elicitors dispersed in wounded plants? In analogy with widespread turgor-driven cell and organ movements, we propose osmoelectric siphon mechanisms for elicitor transport. These mechanisms are based on membrane depolarization leading to cell water shedding into the apoplast followed by membrane repolarization and water uptake. We discuss two related mechanisms likely to occur in response to small wounds and large wounds that trigger leaf-to-leaf electrical signal propagation. To reduce jasmonate pathway activation, a feeding insect must cut through tissues cleanly. If their mandibles become worn, the herbivore is converted into a robust plant defense activator. Our models may therefore help to explain why numerous plants produce abrasives which can blunt herbivore mouthparts. Finally, if verified, the models we propose may be generalizable for cell to cell transport of water and pathogen-derived regulators., (© The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Experimental Biology.)

Chloride (Cl - ) has traditionally been considered a micronutrient largely excluded by plants due to its ubiquity and abundance in nature, its antagonism with nitrate (NO 3 - ), and its toxicity when accumulated at high concentrations. In recent years, there has been a paradigm shift in this regard since Cl - transporters, to being considered a beneficial macronutrient whose transport is finely regulated by plants. As a beneficial macronutrient, Cl 3 - , and better water- and nitrogen-use efficiency. While optimal growth of plants requires the synchronic supply of both Cl - determines increased fresh and dry biomass, greater leaf expansion, increased elongation of leaf and root cells, improved water relations, higher mesophyll diffusion to CO 2 , and better water- and nitrogen-use efficiency. While optimal growth of plants requires the synchronic supply of both Cl - and NO 3 - molecules, the NO 3 - /Cl - plant selectivity varies between species and varieties, and in the same plant it can be modified by environmental cues such as water deficit or salinity. Recently, new genes encoding transporters mediating Cl - influx ( ZmNPF6.4 and ZmNPF6.6 ), Cl - efflux ( AtSLAH3 and AtSLAH1 ), and Cl - compartmentalization ( AtDTX33 , as well as for cell turgor regulation and stress tolerance in plants.AtDTX35 , AtALMT4, and GsCLC2 ) have been identified and characterized. These transporters have proven to be highly relevant for nutrition, long-distance transport and compartmentalization of Cl - , as well as for cell turgor regulation and stress tolerance in plants.

As multicellular organisms, plants acquire characteristic shapes through a complex set of biological processes known as morphogenesis. Biochemical signalling underlies much of development, as it allows cells to acquire specific identities based on their position within tissues and organs. However, as growing physical structures, plants, and their constituent cells, also experience internal and external physical forces that can be perceived and can influence key processes such as growth, polarity, and gene expression. This process, which adds another layer of control to growth and development, has important implications for plant morphogenesis. This review provides an overview of recent research into the role of mechanical signals in plant development and aims to show how mechanical signalling can be used, in concert with biochemical signals, as a cue allowing cells and tissues to coordinate their behaviour and to add robustness to developmental processes., (© The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Abscission is a developmental process with important implications for agricultural practices. Ethylene has long been considered as a key regulator of the abscission process. The existence of an ethylene-independent abscission pathway, controlled by the complex of INFLORESCENCE DEFICIENT IN ABSCISSION (IDA) peptide and the HAESA (HAE) and HAESA-like2 (HSL2) kinases, has been proposed, based mainly on observations that organ abscission in ethylene-insensitive mutants was delayed but not inhibited. A recent review on plant organ abscission signaling highlighted the IDA-HAE-HSL2 components as the regulators of organ abscission, while the role of auxin and ethylene in this process was hardly addressed. After a careful analysis of the relevant abscission literature, we propose that the IDA-HAE-HSL2 pathway is essential for the final stages of organ abscission, while ethylene plays a major role in its initiation and progression. We discuss the view that the IDA-HAE-HSL2 pathway is ethylene independent, and present recent evidence showing that ethylene activates the IDA-HAE-HSL2 complex. We conclude that the ability of an organ to abscise is tightly linked to cell turgidity in the abscission zone, and suggest that lack of cell turgidity might contribute to the failure of floral organ abscission in the ida mutants., (© The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Species' differences in the stringency of stomatal control of plant water potential represent a continuum of isohydric to anisohydric behaviours. However, little is known about how quasi-steady-state stomatal regulation of water potential may relate to dynamic behaviour of stomata and photosynthetic gas exchange in species operating at different positions along this continuum. Here, we evaluated kinetics of light-induced stomatal opening, activation of photosynthesis and features of quasi-steady-state photosynthetic gas exchange in 10 woody species selected to represent different degrees of anisohydry. Based on a previously developed proxy for the degree of anisohydry, species' leaf water potentials at turgor loss, we found consistent trends in photosynthetic gas exchange traits across a spectrum of isohydry to anisohydry. More anisohydric species had faster kinetics of stomatal opening and activation of photosynthesis, and these kinetics were closely coordinated within species. Quasi-steady-state stomatal conductance and measures of photosynthetic capacity and performance were also greater in more anisohydric species. Intrinsic water-use efficiency estimated from leaf gas exchange and stable carbon isotope ratios was lowest in the most anisohydric species. In comparisons between gas exchange traits, species rankings were highly consistent, leading to species-independent scaling relationships over the range of isohydry to anisohydry observed., (© 2017 John Wiley & Sons Ltd.)

Highlight: At macronutrient levels, chloride has positive effects on plant growth, which are distinct from its function in photosynthesis.., (© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Water transport in plants occurs along various paths and is driven by gradients in its free energy. It is generally considered that the mode of transport, being either diffusion or bulk flow, is a passive process, although energy may be required to sustain the forces driving water flow. This review aims at putting water flow at the various organisational levels (cell, organ, plant) in the context of the energy that is required to maintain these flows. In addition, the question is addressed (1) whether water can be transported against a difference in its chemical free energy, 'water potential' (Ψ), through, directly or indirectly, active processes; and (2) whether the energy released when water is flowing down a gradient in its energy, for example during day-time transpiration and cell expansive growth, is significant compared to the energy budget of plant and cell. The overall aim of review is not so much to provide a definite 'Yes' and 'No' to these questions, but rather to stimulate discussion and raise awareness that water transport in plants has its real, associated, energy costs and potential energy gains., (© 2016 John Wiley & Sons Ltd.)

Water-transport pathways through the leaf are complex and include several checkpoints. Some of these checkpoints exhibit dynamic behavior that may be regulated by aquaporins (AQPs). To date, neither the relative weight of the different water pathways nor their molecular mechanisms are well understood. Here, we have collected evidence to support a putative composite model of water pathways in the leaf and the distribution of water across those pathways. We describe how water moves along a single transcellular path through the parenchyma and continues toward the mesophyll and stomata along transcellular, symplastic and apoplastic paths. We present evidence that points to a role for AQPs in regulating the relative weight of each path in the overall leaf water-transport system and the movement of water between these paths as a result of the integration of multiple signals, including transpiration demand, water potential and turgor. We also present a new theory, the hydraulic fuse theory, to explain effects of the leaf turgor-loss-point on water paths alternation and the subsequent reduction in leaf hydraulic conductivity. An improved understating of leaf water-balance management may lead to the development of crops that use water more efficiently, and responds better to environmental changes.

The two alkali cations Na(+) and K(+) have similar relative abundances in the earth crust but display very different distributions in the biosphere. In all living organisms, K(+) is the major inorganic cation in the cytoplasm, where its concentration (ca. 0.1 M) is usually several times higher than that of Na(+). Accumulation of Na(+) at high concentrations in the cytoplasm results in deleterious effects on cell metabolism, e.g., on photosynthetic activity in plants. Thus, Na(+) is compartmentalized outside the cytoplasm. In plants, it can be accumulated at high concentrations in vacuoles, where it is used as osmoticum. Na(+) is not an essential element in most plants, except in some halophytes. On the other hand, it can be a beneficial element, by replacing K(+) as vacuolar osmoticum for instance. In contrast, K(+) is an essential element. It is involved in electrical neutralization of inorganic and organic anions and macromolecules, pH homeostasis, control of membrane electrical potential, and the regulation of cell osmotic pressure. Through the latter function in plants, it plays a role in turgor-driven cell and organ movements. It is also involved in the activation of enzymes, protein synthesis, cell metabolism, and photosynthesis. Thus, plant growth requires large quantities of K(+) ions that are taken up by roots from the soil solution, and then distributed throughout the plant. The availability of K(+) ions in the soil solution, slowly released by soil particles and clays, is often limiting for optimal growth in most natural ecosystems. In contrast, due to natural salinity or irrigation with poor quality water, detrimental Na(+) concentrations, toxic for all crop species, are present in many soils, representing 6 % to 10 % of the earth's land area. Three families of ion channels (Shaker, TPK/KCO, and TPC) and 3 families of transporters (HAK, HKT, and CPA) have been identified so far as contributing to K(+) and Na(+) transport across the plasmalemma and internal membranes, with high or low ionic selectivity. In the model plant Arabidopsis thaliana, these families gather at least 70 members. Coordination of the activities of these systems, at the cell and whole plant levels, ensures plant K(+) nutrition, use of Na(+) as a beneficial element, and adaptation to saline conditions.

The cell wall (CW) is a thin and rigid layer encasing the membrane of all plant and fungal cells. It ensures mechanical integrity by bearing mechanical stresses derived from large cytoplasmic turgor pressure, contacts with growing neighbors or growth within restricted spaces. The CW is made of polysaccharides and proteins, but is dynamic in nature, changing composition and geometry during growth, reproduction or infection. Such continuous and often rapid remodeling entails risks of enhanced stress and consequent damages or fractures, raising the question of how the CW detects and measures surface mechanical stress and how it strengthens to ensure surface integrity? Although early studies in model fungal and plant cells have identified homeostatic pathways required for CW integrity, recent methodologies are now allowing the measurement of pressure and local mechanical properties of CWs in live cells, as well as addressing how forces and stresses can be detected at the CW surface, fostering the emergence of the field of CW mechanobiology. Here, using tip-growing cells of plants and fungi as case study models, we review recent progress on CW mechanosensation and mechanical regulation, and their implications for the control of cell growth, morphogenesis and survival. [ABSTRACT FROM AUTHOR]

Clarifying the mechanisms of leaf and whole plant drought responses is critical to predict the impacts of ongoing climate change. The loss of rehydration capacity has been used for decades as a metric of leaf dehydration tolerance but has not been compared with other aspects of drought tolerance. We refined methods for quantifying the percent loss of rehydration capacity (PLRC), and for 18 Southern California woody species, we determined the relative water content and leaf water potential at PLRC of 10%, 25%, and 50%, and, additionally, the PLRC at important stages of dehydration including stomatal closure and turgor loss. On average, PLRC of 10% occurred below turgor loss point and at similar water status to 80% decline of stomatal conductance. As hypothesized, the sensitivity to loss of leaf rehydration capacity varied across species, leaf habits, and ecosystems and correlated with other drought tolerance traits, including the turgor loss point and structural traits including leaf mass per area. A new database of PLRC for 89 species from the global literature indicated greater leaf rehydration capacity in ecosystems with lower growing season moisture availability, indicating an adaptive role of leaf cell dehydration tolerance within the complex of drought tolerance traits. The capacity for leaves to rehydrate after dehydration has long been used as a metric of tissue desiccation tolerance. We refined a classical method for quantifying the percent loss of rehydration capacity (PLRC) for 18 Southern California woody species, compared this metric with other indices of drought tolerance, and placed the irreversible loss of rehydration capacity in the known sequence of leaf responses to drought. On average, across species, PLRC of 10% occurred below turgor loss point and at a similar water status as 80% stomatal closure. A compilation of PLRC data from the published literature showed strong variation across ecosystems, with ecosystems experiencing greater aridity in the growing season showing greater capacity for leaf rehydration. Our findings highlight leaf tissue desiccation tolerance as an adaptive trait and the importance of research establishing the mechanisms for leaf damage and resilience during and after drought. [ABSTRACT FROM AUTHOR]

Summary: Epiphytes are common in tropical montane cloud forests (TMCFs) and play many important ecological roles, but the degree to which these unique plants will be affected by changes in climate is unknown. We investigated the drought responses of three vascular epiphyte communities bracketing the cloud base during a severe, El Niño‐impacted dry season. Epiphytes were instrumented with sap flow probes in each site. Leaf water potential and pressure–volume curve parameters were also measured before and during the drought. We monitored the canopy microclimate in each site to determine the drivers of sap velocity across the sites. All plants greatly reduced their water use during the drought, but recovery occurred more quickly for plants in the lower and drier sites. Plants in drier sites also exhibited the greatest shifts in the osmotic potential at full saturation and the turgor loss point. Although all individuals survived this intense drought, epiphytes in the cloud forest experienced the slowest recovery, suggesting that plants in the TMCF are particularly sensitive to severe drought. Although vapor pressure deficit was an important driver of sap velocity in the highest elevation site, other factors, such as the volumetric water content of the canopy soil, were more important at lower (and warmer) sites. [ABSTRACT FROM AUTHOR]

Osmotic adjustment (OA), the accumulation of solutes in higher plant cells in response to water deficits, was first reported more than four decades ago. Since then, variation in OA among genotypes/cultivars in response to drought has been reported in many crop plants, but its role in maintaining growth and yield in water-limited environments has been questioned. The role of OA in the physiological and agronomic adaptation to water stress of crops, the methods of reliably measuring the degree of OA among genotypes or species, the range of OA in many studies, and its impact on grain yield in water-limited environments are reviewed. The genetics of OA has received limited study, and the breeding and selection for high OA has only resulted in the release of one commercial cultivar of wheat as far as is known. The reasons for the limited interest in breeding for the OA trait are discussed. [ABSTRACT FROM AUTHOR]

Abstract: Many plant species experience large differences in soil moisture availability within a season, potentially leading to a wide range of leaf water potentials (ΨLEAF). In order to decrease the risk of leaf dehydration, among species, there is a continuum ranging from strict control (isohydry) to little control (anisohydry) of minimum ΨLEAF. In central Texas USA, species are exposed to a range of soil moisture from wet springs to hot, dry summers. There are diverging water management strategies among the four dominant woody species in this system; two of these species are more isohydric (Prosopis glandulosa, Quercus fusiformis) while two others are more anisohydric (Diospyros texana, Juniperus asheii). To maintain leaf turgor and photosynthesis during periods of limited soil moisture, anisohydric species may adjust leaf hydraulic parameters more than isohydric species. To test this hypothesis, we quantified iso/anisohydry from 3 years of ΨLEAF predawn and midday measurements, and we measured the changes in turgor loss points (ΨTLP), osmotic potential at full hydration (Ψπ100), and resistance to leaf hydraulic dysfunction (leaf P50) throughout the spring and summer of 2016. Diospyros and Juniperus experienced more negative ΨLEAF and adjusted ΨTLP and Ψπ100 in response to both drying soils during the summer also in response to rainfall events during September. In contrast, the more isohydric species (Quercus and Prosopis) did not appear to adjust ΨTLP or Ψπ100 in response to soil moisture. The more anisohydric species also adjusted leaf P50 during periods of reduced soil moisture. Our results suggest that species that experience wider ranges of ΨLEAF have a greater ability to alter leaf hydraulic properties. This provides insight on how species with different strategies for water potential regulation may modify properties to mitigate drought effects in the future. A plain language summary is available for this article. [ABSTRACT FROM AUTHOR]

In the Northeastern U.S., drought is expected to increase in frequency over the next century, and therefore, the responses of trees to drought are important to understand. There is recent debate about whether land-use change or moisture availability is the primary driver of changes in forest species composition in this region. Some argue that fire suppression from the early twentieth century to present has resulted in an increase in shade-tolerant and pyrophobic tree species that are drought intolerant, while others suggest precipitation variability as a major driver of species composition. From this debate, an emerging hypothesis is that mesophication and increases in the abundance of mesophytic genera (e.g., Acer, Betula, and Fagus) resulted in forests that are more vulnerable to drought. This review examines the published literature and factors that contribute to drought vulnerability of Northeastern U.S. forests. We assessed two key concepts related to drought vulnerability, including drought tolerance (ability to survive drought) and sensitivity (short-term responses to drought), with a focus on Northeastern U.S. species. We assessed drought-tolerance classifications for species, which revealed both consistencies and inconsistencies, as well as contradictions when compared to actual observations, such as higher mortality for drought-tolerant species. Related to drought sensitivity, recent work has focused on isohydric/anisohydric regulation of leaf water potential. However, based on the review of the literature, we conclude that drought sensitivity should be viewed in terms of multiple variables, including leaf abscission, stomatal sensitivity, turgor pressure, and dynamics of non-structural carbohydrates. Genera considered drought sensitive (e.g., Acer, Betula, and Liriodendron) may actually be less prone to drought-induced mortality and dieback than previously considered because stomatal regulation and leaf abscission in these species are effective at preventing water potential from reaching critical thresholds during extreme drought. Independent of drought-tolerance classification, trees are prone to dieback and mortality when additional stressors are involved such as insect defoliation, calcium and magnesium deficiency, nitrogen saturation, and freeze-thaw events. Overall, our literature review shows that multiple traits associated with drought sensitivity and tolerance are important as species may rely on different mechanisms to prevent hydraulic failure and depleted carbon reserves that may lead to mortality. [ABSTRACT FROM AUTHOR]

Grain filling ability is mainly affected by the translocation of carbohydrates generated from temporarily stored stem starch in most field crops including rice (Oryza sativa L.). The partitioning of non-structural stem carbohydrates has been recognized as an important trait for raising the yield ceiling, yet we still do not fully understand how carbohydrate partitioning occurs in the stems. In this study, two rice subspecies that exhibit different patterns of non-structural stem carbohydrates partitioning, a japonica-dominant cultivar, Momiroman, and an indica-dominant cultivar, Hokuriku 193, were used as the model system to study the relationship between turgor pressure and metabolic regulation of non-structural stem carbohydrates, by combining the water status measurement with gene expression analysis and a dynamic prefixed 13C tracer analysis using a mass spectrometer. Here, we report a clear varietal difference in turgor-associated starch phosphorylation occurred at the initiation of non-structural carbohydrate partitioning. The data indicated that starch degradation in Hokuriku 193 stems occurred at full-heading, 5 days earlier than in Momiroman, contributing to greater sink filling. Gene expression analysis revealed that expression pattern of the gene encoding α-glucan, water dikinase (GWD1) was similar between two varieties, and the maximum expression level in Hokuriku 193, reached at full heading (4 DAH), was greater than in Momiroman, leading to an earlier increase in a series of amylase-related gene expression in Hokuriku 193. In both varieties, peaks in turgor pressure preceded the increases in GWD1 expression, and changes in GWD1 expression was correlated with turgor pressure. Additionally, a threshold is likely to exist for GWD1 expression to facilitate starch degradation. Taken together, these results raise the possibility that turgor-associated starch phosphorylation in cells is responsible for the metabolism that leads to starch degradation. Because the two cultivars exhibited remarkable varietal differences in the pattern of non-structural carbohydrate partitioning, our findings propose that the observed difference in grain-filling ability originated from turgor-associated regulation of starch phosphorylation in stem parenchyma cells. Further understanding of the molecular mechanism of turgor-regulation may provide a new selection criterion for breaking the yield barriers in crop production. [ABSTRACT FROM AUTHOR]

Osmotic adjustment (OA) and cellular compatible solute accumulation are widely recognized to have a role in plant adaptation to dehydration mainly through turgor maintenance and the protection of specific cellular functions by defined solutes. At the same time, there has been an ongoing trickle of skepticism in the literature about the role of OA in supporting crop yield under drought stress. Contrarian reviews argued that OA did not sustain turgor or that it served mainly for plant survival rather than productivity. This critical review examined 26 published studies where OA was compared with yield under drought stress in variable genotypes of 12 crops, namely, barley, wheat, maize, sorghum, chickpea, pea, pigeon pea, soybean, canola, mustard, castor bean and sunflower. Over all crops a positive and significant association between OA and yield under drought stress were found in 24 out of 26 cases. Considering that it is generally difficult to find a singular plant trait responsible for yield advantage of numerous crops under different drought stress conditions, this evidence is no less than remarkable as proof that OA sustains crop yield under drought stress. [ABSTRACT FROM AUTHOR]

During desiccation, plant cells are subjected to very low water potentials. Osmoregulation through increase of soluble materials ( e.g. soluble sugars, compatible inorganic ions) is a response to the decreasing turgor pressure in the cells. In bryophytes, sucrose acts as an osmolyte and also stabilizing membranes and proteins through vitrification. We used psychrometric measurements in the aquatic bryophyte Fontinalis antipyretica Hedw. to construct pressure–volume isotherms and determine the water relations parameters under fast and slow dehydration rates. Sucrose was also quantified. The starting hypothesis was that a slow dehydration rate would increase sucrose concentration, thereby decreasing the osmotic potential at turgor loss point, and would also increase cell wall elasticity, postponing turgor loss and allowing time for induction of molecular and structural acclimation mechanisms. In fact, we found that slowly dehydrated samples presented more elastic cell walls, allowing cells to shrink and maintain turgor, helping to better preserve their metabolic functions and therefore to induce desiccation tolerance (DT). On the other hand, in fast dehydrated samples the osmotic potential at turgor loss point decreased, indicating the activity of osmoregulation processes, possibly connected to the increase observed in sucrose content. Upon rehydration, fast dried samples lost 50% of the sucrose through leakage due to cell membrane rupture, while slow dehydrated leaves maintained their sucrose content constant. DT appears to be achieved through slow dehydration, meaning that a high sucrose content alone does not contribute to DT establishment. Moreover, in natural conditions external water can be maintained at very high values due to the life form of F. antipyretica , which grows in long and compact floating stems in streams, allowing a slow dehydration rate required for induction of other DT mechanisms. [ABSTRACT FROM AUTHOR]

Aquatic organisms are often exposed to dramatic changes in salinity in the environment. Despite decades of research, many questions related to molecular and physiological mechanisms mediating sensing and adaptation to salinity stress remain unanswered. Here, responses of V aucheria erythrospora, a turgor-regulating xanthophycean alga from an estuarine habitat, have been investigated. The role of ion uptake in turgor regulation was studied using a single cell pressure probe, microelectrode ion flux estimation ( MIFE) technique and membrane potential ( Em) measurements. Turgor recovery was inhibited by Gd3+, tetraethylammonium chloride (TEA), verapamil and orthovanadate. A Na Cl-induced shock rapidly depolarized the plasma membrane while an isotonic sorbitol treatment hyperpolarized it. Turgor recovery was critically dependent on the presence of Na+ but not K+ and Cl− in the incubation media. Na+ uptake was strongly decreased by amiloride and changes in net Na+ and H+ fluxes were oppositely directed. This suggests active uptake of Na+ in V . erythrospora mediated by an antiport Na+/ H+ system, functioning in the direction opposite to that of the SOS1 exchanger in higher plants. The alga also retains K+ efficiently when exposed to high Na Cl concentrations. Overall, this study provides insights into mechanisms enabling V . erythrospora to regulate turgor via ion movements during hyperosmotic stress. [ABSTRACT FROM AUTHOR]

Leaf photosynthesis relies on CO2 diffusing in while water vapour diffuses out. When stomata close, cuticle waxes on the epidermal tissues increasingly affect this diffusion. Also, changes in turgor can shrink or swell a leaf, varying the cuticle size. In this study, the properties of the cuticle were investigated while turgor varied in intact leaves of hypostomatous grape (Vitis vinifera L.) or amphistomatous sunflower (Helianthus annuus L.). For grape, stomata on the abaxial surface were sealed and high CO2 concentrations outside the leaf were used to maximize diffusion through the adaxial, stoma-free cuticle. For sunflower, stomata were closed in the dark or with abscisic acid to maximize the cuticle contribution to the path. In both species, the internal CO2 concentration was measured directly and continuously while other variables were determined to establish the cuticle properties. The results indicated that stomatal closure diminished the diffusion of both gases in both species, but for CO2 more than for water vapour. Decreasing the turgor diminished the movement of both gases through the cuticle of both species. Because this turgor effect was observed in the adaxial surface of grape, which had no stomata, it could only be attributed to cuticle tightening. Comparing calculated and measured concentrations of CO2 in leaves revealed differences that became large as stomata began to close. These differences in transport, together with turgor effects, suggest calculations of the CO2 concentration inside leaves need to be viewed with caution when stomata begin to close. [ABSTRACT FROM AUTHOR]

This study investigated a possible relationship between the relative change of leaf thickness and the relative degree of turgor pressure in leaf cells. Leaf thickness and turgor pressure were measured simultaneously during forced plant desiccation in bean plants. Although leaf thickness followed closely the steep decline of the total water potential ( Ψ ) during the desiccation process, no conclusive relationship could be observed between leaf thickness and the osmotic water potential ( Ψ s ). Thus, a potential link between the relative change of leaf thickness and the relative degree of turgor pressure could not be verified under the experimental conditions. Earlier findings, that the relative change of leaf thickness is closely related to the relative change of the total water potential of leaf cells, are corroborated. Additional observations were: (i) a potential relationship between the relative change of leaf thickness during desiccation and the totally achieved leaf thickness, and (ii) the apparent decrease of leaf thickness during desiccation in discrete levels rather than a truly continuous decline. [ABSTRACT FROM AUTHOR]

Background Turgor pressure is an essential feature of plants; however, whereas its physiological importance is unequivocally recognized, its relevance to development is often reduced to a role in cell elongation. Scope This review surveys the roles of turgor in development, the molecular mechanisms of turgor regulation and the methods used to measure turgor and related quantities, while also covering the basic concepts associated with water potential and water flow in plants. Three key processes in flower development are then considered more specifically: flower opening, anther dehiscence and pollen tube growth. Conclusions Many molecular determinants of turgor and its regulation have been characterized, while a number of methods are now available to quantify water potential, turgor and hydraulic conductivity. Data on flower opening, anther dehiscence and lateral root emergence suggest that turgor needs to be finely tuned during development, both spatially and temporally. It is anticipated that a combination of biological experiments and physical measurements will reinforce the existing data and reveal unexpected roles of turgor in development. [ABSTRACT FROM AUTHOR]

In plants, the vacuole is a multifunctional organelle with an important role in the maintenance of the intracellular space. Tonoplast membranes are highly permeable to water due to their content in aquaporins TIPs (Tonoplast Intrinsic Proteins) that allow the rapid water influx creating an internal turgor pressure responsible for cell expansion, elongation and shape. The aim of the present study was to evaluate if the grapevine Vitis vinifera TIP2;1 would operate as a possible volume regulator gated by membrane surface tension. For that, the wild type VvTIP2;1 and a non-functional mutated form were heterologous expressed in yeast. Using an experimental strategy in which cells are incubated in external media that induce an increase in internal hydrostatic pressure and consequently membrane surface tension, we were able to compare the osmotic permeability (Pf) and the activation energy for water transport (Ea) of yeast strains expressing the functional and a non-functional TIP2;1. We found Pf and Ea dependence on internal turgor pressure only for the strain harboring the functional aquaporin indicating that TIP2;1 activity is regulated by membrane tension changing from an open to a closed state in an internal pressure dependent manner. This turgor dependent gating of TIP2;1 might be a mechanism to regulate vacuolar size and shape in plants withstanding hostile drought conditions such as grapevine. [ABSTRACT FROM AUTHOR]

The Scholander-Hammel pressure chamber has been used in thousands of papers to measure osmotic pressure, πc, turgor pressure, Pt, and bulk modulus of elasticity, ε, of leaf cells by pressure-volume ( PV) curve analysis. PV analysis has been questioned in the past., In this paper we use micromechanical analysis of leaf cells to examine the impact on PV curve analysis of negative turgor in living cells ( Pt)., Models predict negative Pt (−0.1 to −1.8 MPa) depending on leaf cell size and shape in agreement with experimental values reported by J. J. Oertli. Modeled PV curves have linear regions even when Pt is quite negative, contrary to the arguments of M.T. Tyree. Negative Pt is totally missed by PV curve analysis and results in large errors in derived πc and Pt but smaller errors in ε., A survey of leaf cell sizes vs habitat (arid, temperate, and rainforest), suggests that the majority of published PV curves result in errors of 0.1-1.8 MPa in derived πc and Pt, whereby the error increases with decreasing cell size. We propose that small cell size in leaves is an ecological adaptation that permits plants to endure negative values of water potential with relatively little water loss. [ABSTRACT FROM AUTHOR]

Four-day-old rice ( Oryza sativa L.) seedlings were subjected to varying temperatures of 30/20, 35/25, and 42/37 °C [light/dark (15/9 h); light intensity: 350 μmol m s, RH 65-70 %] in glass Petri dishes for 10 days in the absence (control) or the presence of γ-aminobutyric acid (GABA) 1 mM under the controlled conditions of a growth chamber. With rise in temperature, the length of both shoots and roots was inhibited severely and there was a marked decrease in survival, especially at 42/37 °C. Endogenous GABA content increased more than twofold in moderately stressed (MS) 35/25 °C plants, whereas it decreased sevenfold in severely stressed (SS) 42/37 °C plants compared to MS plants, and this decrease was associated with marked reduction in growth and survival. Exogenous application of GABA to the heat-stressed plants significantly improved growth as well as survival. It was linked to reduction in damage to membranes, improvement in cellular reducing ability, chlorophyll content, and photochemical efficiency in shoots. Relative leaf water content and stomatal conductance were also improved with the application of GABA and their improvement was related to increased accumulation of the osmolytes proline and trehalose. In the presence of GABA, the shoots suffered less oxidative damage in terms of malondialdehyde and hydrogen peroxide contents. The activities of enzymatic antioxidants such as superoxide dismutase, catalase, ascorbate peroxidase, and glutathione reductase were severely inhibited in plants growing at 42/37 °C compared to those growing at 35/25 °C. The nonenzymatic antioxidants like ascorbate and glutathione followed a similar pattern. GABA-treated SS plants showed enhanced levels of enzymatic and nonenzymatic antioxidants compared to untreated controls. Thus, GABA appears to impart partial protection from heat stress to rice plants by elevating leaf turgor due to increased accumulation of osmolytes and reduction of oxidative damage by stimulation of antioxidants. These findings provided evidence about the involvement of GABA in governing heat sensitivity in rice. [ABSTRACT FROM AUTHOR]

Abstract: The growth of hypocotyls and epicotyls has been attributed to the turgor-driven enlargement of cells, a process that is under the control of phytohormones such as auxin. However, the experiments presented here and elsewhere using developing sunflower (Helianthus annuus L.) seedlings raised either in darkness (skotomorphogenesis) or in white light (WL) (photomorphogenesis) indicate that auxin-mediated segment elongation ceases after 1 day, whereas hypocotyl growth continues in the intact system. Based on these results and data from the literature, we propose that hypocotyl growth consists of three inter-related processes: (1) cell division in the apical meristematic regions; (2) turgor-driven cell elongation along the stem; and (3) cell maturation in the basal region of the organ. We document that the closed apical hook (or the corresponding region after opening in WL) is the location where cell division occurs, and suggest that the epidermis and the outer cortex plays an important role in a “pacemaker system” for cell division. Results from the literature support the hypothesis that pectin metabolism in the expansion-limiting epidermal cell wall(s) is involved in wall-loosening and -stiffening. During hypocotyl growth in darkness and WL, turgor pressure is largely maintained, i.e., in H. annuus no hydrostatic pressure-regulated growth occurs. These data do not support the “loss of stability theory” of cell expansion. Finally, we document that turgor maintenance during organ elongation is caused by sucrose catabolism via vacuolar acid invertases, resulting in the generation of hexoses (osmoregulation). Based on these data, we present an integrative model of axial elongation in developing seedlings of dicotyledonous plants and discuss open questions. [Copyright &y& Elsevier]

All Illicium spp. have explosive fruits, which is a unique character among the basal grade of angiosperms. Illicium fruits consist of several ventrally dehiscing follicles developing from conduplicate carpels, with a prominent, slightly postgenitally fused ventral slit. The closure of the ventral slit is also secured by two mirror-symmetrical massive longitudinal sclerenchymatous bands in the mesocarp along the edges and by turgor pressure. The pericarp differentiates into a fleshy (or coriaceous) peripheral zone (exocarp and mesocarp) with numerous ethereal-oil-containing cells and a sclerenchymatous (single-layered, palisade) inner zone (endocarp). Dehydration of the fleshy zone of the pericarp and partial compression of the epidermal sclereids with U-shaped wall thickenings lining the ventral suture are instrumental in explosive fruitlet dehiscence. Generally, the fruit structure of Illicium differs dramatically from those in other early diverging angiosperms. Gynoecium and fruit structure (and a probable early Cretaceous divergence from the Schisandra- Kadsura clade) provide evidence for treatment of Illicium as separate from Schisandraceae s.s. © 2013 The Linnean Society of London [ABSTRACT FROM AUTHOR]

Tissue pressure is of vital importance for the stability and stiffness as well as metabolic functions of herbaceous plants and has been studied for more than a century. Several measurement methods have been established but require either sophisticated equipment at a fixed workplace or being applicable only to flat structures. We were looking for a mobile system that can be used under greenhouse conditions for long-term measurement of parenchymatous tissue pressure. The mobile sensor system used consists of a micro-optic-mechanical system with a silicon sensor at the tip of a glass fiber and a control unit (Samba 202) for data logging. The sensors were inserted and became ingrown in succulent leaves of Delosperma cooperi, petioles of Caladium bicolor, and flower stalks of Cyclamen persicum. With this method, three distinct phases could be distinguished in the restoration of the parenchymatous tissue pressure after embedding the sensors without drought stress. Under drought stress, three additional phases were found during wilting of C. bicolor petioles. All plants showed photoperiodic fluctuations of tissue pressure. The results of the tissue pressure measurements were cross-checked by measurements of individual parenchyma cells from the same tissue region using a cell pressure probe. The new method for measuring plant tissue pressure is promising for monitoring parenchymatous tissue pressure during physiological experiments on herbaceous plants and complements the established methods of turgor determination. [ABSTRACT FROM AUTHOR]

Ecology Letters (2012) 15: 393-405 Abstract Increasing drought is one of the most critical challenges facing species and ecosystems worldwide, and improved theory and practices are needed for quantification of species tolerances. Leaf water potential at turgor loss, or wilting (πtlp), is classically recognised as a major physiological determinant of plant water stress response. However, the cellular basis of πtlp and its importance for predicting ecological drought tolerance have been controversial. A meta-analysis of 317 species from 72 studies showed that πtlp was strongly correlated with water availability within and across biomes, indicating power for anticipating drought responses. We derived new equations giving both πtlp and relative water content at turgor loss point ( RWCtlp) as explicit functions of osmotic potential at full turgor (πo) and bulk modulus of elasticity (ε). Sensitivity analyses and meta-analyses showed that πo is the major driver of πtlp. In contrast, ε plays no direct role in driving drought tolerance within or across species, but sclerophylly and elastic adjustments act to maintain RWCtlp, preventing cell dehydration, and additionally protect against nutrient, mechanical and herbivory stresses independent of drought tolerance. These findings clarify biogeographic trends and the underlying basis of drought tolerance parameters with applications in comparative assessments of species and ecosystems worldwide. [ABSTRACT FROM AUTHOR]

High water availability and mechanical stress can induce opposite responses in plants. In arid areas of Northern China the occurrence of high wind and high water availability tend to be negatively correlated. Since turgor pressure is a determinant of the mechanical stability of annuals, it is hypothesised that the effects of mechanical perturbation (MP) on annuals may depend on soil water availability. To test this proposal, we conducted an experiment in which a pioneering annual Corispermum mongolicum was subjected to two levels of MP and water supply, and then determined its growth and mechanical traits. Brushing had no effect on plant height and total biomass, but stimulated leaf and branch production. Water supply affected plant height, basal diameter, total biomass and stem rigidity, but not leaf and branch number, root/shoot ratio or flexibility. With high water availability, brushing stimulated the production of stiffer stems (thicker and with a higher Young’s modulus) and more roots relative to shoot mass, but with low water availability MP induced the opposite response. This shows that both the degree and direction of plant responses to MP depend on the presence of other factors. We discuss how the interactive effects of MP and water availability on growth and mechanical properties may help C. mongolicum to establish in windy and arid environments. [ABSTRACT FROM AUTHOR]

An advanced non-invasive, field-suitable and inexpensive leaf patch clamp pressure probe for online-monitoring of the water relations of intact leaves is described. The probe measures the attenuated output patch clamp pressure, Pp, of a clamped leaf in response to an externally applied input pressure, Pclamp. Pclamp is generated magnetically. Pp is sensed by a pressure sensor integrated into the magnetic clamp. The magnitude of Pp depends on the transfer function, Tf, of the leaf cells. Tf consists of a turgor pressure-independent (related to the compression of the cuticle, cell walls and other structural elements) and a turgor pressure-dependent term. Tf is dimensionless and assumes values between 0 and 1. Theory shows that Tf is a power function of cell turgor pressure Pc. Concomitant Pp and Pc measurements on grapevines confirmed the relationship between Tf and Pc. Pp peaked if Pc approached zero and assumed low values if Pc reached maximum values. The novel probe was successfully tested on leaves of irrigated and non-irrigated grapevines under field conditions. Data show that slight changes in the microclimate and/or water supply (by irrigation or rain) are reflected very sensitively in Pp. [ABSTRACT FROM AUTHOR]

Mechanical properties data of Iceberg lettuce leaves are described in relation to the applied agronomic variables and post-harvest treatment. Leaf tissue strength and stiffness were both reduced significantly in plants grown with 120 kg/ha applied nitrogen compared with plants grown with 0 kg/ha applied nitrogen. Leaf tissue strength and stiffness were increased significantly in plants grown with added calcium at 80 kg/ha. Significant reductions in stiffness and increases in failure strain were associated with reduced hydration. These findings show that agronomy changes in mechanical properties are as large as maturity and post harvest induced turgor changes, which has implications for both quality and damage of cut salads. [ABSTRACT FROM AUTHOR]

Studies the differences in growth, water relations, gas exchange and mineral content that occur in white-lead rock-rose and Montpellier rock-rose plants following the application of simulated sea aerosol with an anionic surfactant. Increase in leaf turgor potential in the plants treated with both sea aerosol treatments by osmotic adjustment effect; Lower reduction in plant growth and less leaf damage.

The mechanical and physiological bases for root growth against high mechanical impedance are reviewed. The best estimates of maximum axial root growth pressure (σmax) in completely impeded pea roots appear to be from 0.5 to 0.6 MPa, which results from a turgor pressure of about 0.8 MPa. When roots are incompletely impeded, a range of responses has been reported. Roots do not change elongation rate in a simple mechanical way in response to changes in mechanical impedance. Instead, ethylene might play a key role in mediating an increase in root diameter and a decrease in elongation rate. These changes persist for some hours or days after impedance is removed. Differences between species in their ability to penetrate strong soil layers are not related to differences in σmax, but appear to be due to differences in root diameter. In rice, differences between cultivars in the ability of their roots to penetrate strong wax layers are not related to their elongation rates through uniformly strong media. Differences between species or cultivars in their ability to penetrate strong layers may be due to differences in the tendency of roots to deflect or buckle when they grow from a weak to a strong environment. [ABSTRACT FROM AUTHOR]

Internodal cells of a brackish water charophyte, Lamprothamnium succinctum, regulate turgor pressure in response to changes in external osmotic pressure by modifying vacuolar concentrations of KCl. An increase in cytosolic concentration of free Ca2+ ([Ca2+]c) is necessary for the progress of turgor regulation induced by hypotonic treatment. Initial changes in membrane potential and [Ca2+]c upon hypotonic treatment were measured to examine the temporal relationship between the two parameters. Fura-dextran (potassium salt, Mr 10,000, anionic) that had been injected into the cytosol was used to measure [Ca2+]c. Membrane potential and membrane conductance under a current-clamp condition were also measured. Decrease in external osmotic pressure by 0.16 Osm induced a simultaneous increase in [Ca2+]c with both depolarization of the membrane and increase in the membrane conductance. Decrease in external osmotic pressure by 0.05 Osm induced a simultaneous increase in [Ca2+]c with membrane depolarization but the increase in membrane conductance started later than the other two processes. There was a close temporal relationship between the increase in [Ca2+]c and membrane depolarization on the initial response of turgor regulation induced by hypotonic treatment. [ABSTRACT FROM PUBLISHER]

Ionic homeostasis is a fundamental cellular phenomenon. All living cells maintain an intracellular ionic composition compatible with their constituent molecules and this requires the regulation of multiple membrane transporters and signal transduction pathways. Other biophysical parameters such as turgor and electrical potential are also part of this essential regulation. How ionic homeostasis is achieved, however, is not completely understood. Although most transporters have already been identified, their physiological function is only starting to be demonstrated.

The effects of potassium deficiency (KD) and all-macronutrient deficiency (MD) on elongation of tap and lateral roots were studied on maritime pine seedlings (Pinus pinaster Ait.) in hydroponic culture. Tap root elongation was unaffected by either of the two deficiencies. By marked contrast, lateral root elongation was strongly reduced. The analyses of cell turgor pressure and relative elemental growth rate (RECK) profile in the growing zone allowed us to determine the effects of the nutrient stresses on cell-wall properties. For both deficiency treatments, elongation rate, (REGR) profile (measured only for control and KD) and turgor pressure in the fastest growing cells were unaffected in the tap root, suggesting that KD and MD did not modify cell-wall properties in the growing zone. In lateral roots, KD shortened the growing zone and significantly reduced REGR. However, turgor pressure remained unaffected in this region. The absence of turgor pressure change suggests that KD reduced elongation of lateral roots by tightening cell walls. In mature cells of the two types of roots, turgor and osmotic pressures tended to be reduced by the nutrient deficiencies, indicating that these parameters were better maintained in the growing cells. Cell turgor and osmotic pressures of control plants were 0.1MPa lower at 30 mm (mature cells) than at 2-4 mm (expanding cells) from the meristem. Moreover, these parameters were 0.1 MPa lower in expanding cells of lateral roots than in those of tap the root. Turgor and osmotic pressures were not homogeneous throughout the root system and were affected differently by the nutrient deficiencies depending on the location in the root system. [ABSTRACT FROM AUTHOR]

Two cases studies are presented illustrating how the behaviour of plants using crassulacean acid metabolism (CAM) provides adaptation to salinity. Perennial cacti having constitutive CAM show adaptation at the whole-plant level, engaging regulation of stomata, internal CO[sub2]-recycling and root physiology with salt exclusion. They are stress avoiders. Annual plants such as Mesembryanthemum crystallinum, with inducible CAM, are salt includers. They are stress-tolerant and show reactions at an array of levels: (i) regulation of turgor and gas exchange at the whole-plant level; (ii) metabolic adjustments at the cellular level; (iii) adaptive transport proteins at the membrane levels and also (iv) at the macromolecular level; and (v) inductive changes at the gene expression level of the enzyme complement for metabolism (in particular involving glycolysis and malic-acid synthesis with phosphoenolpyruvate carboxylase (PEPC) as the key enzyme, and gluconeogenesis (with pyruvate phosphate dikinase (PPDK) as a key enzyme) and membrane transport (in particular involving the tonoplast ATPase). [ABSTRACT FROM AUTHOR]

Regulation of the in vivo yielding properties of the cell wall, namely cell wall extensibility φ and effective turgor (Pi-Y of Vigna hypocotyl segments during adaptive recovery of growth after osmotic stress was investigated by successive measurements using the pressure-jump method. In the absence of IAA, cell wall extensibility φ showed no significant changes under osmotic stress but effective turgor (Pi-Y reduced to near zero, resulting in no growth recovery. In the presence of 10 μM IAA, the cell wall extensibility was slightly decreased even when distinct recovery of growth took place in response to osmotic stress caused by 60 mM sorbitol. The effective turgor, however, showed a characteristic increase in contrast to the wall extensibility. It is not wall extensibility but effective turgor that regulates the cell wall yielding during the adaptive recovery of growth. In excised hypocotyl segments, however, reduced turgor would not be expected to recover, as has been observed in hollow cylinders (Nakahori et al. 1990). The results presented here suggest that the IAA-dependent adjustment of the yield threshold plays an indispensable role in wall-yielding for rapid adaptive growth recovery under osmotic stress. [ABSTRACT FROM AUTHOR]

As the symptoms of calcium deficiency develop in plants, there is often a stage in which the (issues are water-soaked and one involving cell breakdown with loss of turgor (as in internal breakdown of apples). Eventually the tissue may become desiccated yielding a dry, more or less extensive area of necrosis. Two mechanisms are proposed. There is evidence that calcium deficiency renders membranes permeable which would account for a loss of turgor and permit cell fluids to invade intercellular spaces. An alternative situation may develop in soft, succulent fruits, the cells of which burst under hypotonic conditions in vitro. It is suggested that exogenous water may enter a fruit from the atmosphere or (in apple) through the phloem. Such exogenous water in the intercellular spaces of the fruit may cause cells to swell. so cracking the fruit or it may result in a hunting of the cells. A plea is made for further light microscope studies of the development of symptoms of calcium deficiency. [ABSTRACT FROM AUTHOR]

Current-voltage (I/V) analysis and pharmacological dissection were applied to membranes of Lamprothamnium at the time of hypotonic stress. At least three types of process were found to be involved in the response to this stress. (1) The first 10 min of exposure to hypotonic medium resulted in a depolarization of about 50mV accompanied by a decrease or no change in conductance. This depolarization occurred with either K+ or Ca2+ (and consequently CI-) channels inactivated. (2) The CI- channels opened mainly in the first 15 min of the hypotonic stress, increasing the membrane conductance by about an order of magnitude. (3) The K+ conductance rose as the CL conductance started to diminish and reached a maximum after about 40 min. Both types of channel were strongly potential-dependent with a conductance peak between -150 and 0 mV. An inactivation of K- or CI- channels resulted in moving the membrane potential away from the conductance maximum toward either EK or ECI , diminishing the ion efflux (and turgor regulation). The time courses of the conductance increases remained the same, suggesting that the conductance changes are not driven by feedback to some preset turgor level, The electrophysiology of the Lamprothamniun transporters is compared to that of salt-sensitive charophytes. [ABSTRACT FROM AUTHOR]