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In some forest systems, stomata have also been observed to reopen rapidly on recovery from drought, with delays in gas exchange recovery only observed once embolism-induced declines in hydraulic conductance occur ([29]). (B) When relief from a drought occurs after embolism has formed in the xylem then gas exchange recovery can take many months in species that must construct new xylem and organs to regain pre-drought gas exchange capacity ([3], [1]). [2] report that on rewatering from a drought severe enough to close stomata, the complete recovery of leaf gas exchange took >7 days, yet water potentials recovered within 12 h of rewatering. [Extracted from the article]

Clarifying the mechanisms underlying the recovery of gas exchange following drought is the key to providing insights into plant drought adaptation and habitat distribution. However, the mechanisms are still largely unknown. Targeting processes known to inhibit gas exchange during drought recovery, we measured leaf water potential, the leaf hydraulic conductance, stomatal reopening, abscisic acid (ABA) and the ethylene emission rate (EER) following moderate drought stress in seedlings of the globally pervasive woody tree Fraxinus chinensis. We found strong evidence that the slow stomatal reopening after rehydration is regulated by a slow decrease in EER, rather than changes in leaf hydraulics or foliar ABA levels. This was supported by evidence of rapid gas exchange recovery in plants after treatment with the ethylene antagonist 1-methylcyclopropene. These findings provide evidence to rigorously support ethylene as a key factor constraining stomatal reopening from moderate drought directly, thereby potentially opening new windows for understanding species drought adaptation. [ABSTRACT FROM AUTHOR]

The study of ancient species provides valuable information concerning the evolution of specific adaptations to past and current environmental conditions. Araucaria araucana (Molina) K. Koch belongs to one of the oldest families of conifers in the world, but despite this, there are few studies focused on its physiology and responses to changes in environmental conditions. We used an integrated approach aimed at comprehensively characterizing the ecophysiology of this poorly known species, focusing in its stomatal, mesophyll and biochemical traits, hypothesizing that these traits govern the carbon assimilation of A. araucana under past and present levels of atmospheric CO2. Results indicated that A. araucana presents the typical traits of an ancient species, such as large stomata and low stomatal density, which trigger low stomatal conductance and slow stomatal responsiveness to changing environmental conditions. Interestingly, the quantitative analysis showed that photosynthetic rates were equally limited by both diffusive and biochemical components. The Rubisco catalytic properties proved to have a low Rubisco affinity for CO2 and O2, similar to other ancient species. This affinity for CO2, together with the low carboxylation turnover rate, are responsible for the low Rubisco catalytic efficiency of carboxylation. These traits could be the result of the diverse environmental selective pressures that A. araucana was exposed during its diversification. The increase in measured temperatures induced an increase in stomatal and biochemical limitations, which together with a lower Rubisco affinity for CO2 could explain the low photosynthetic capacity of A. araucana in warmer conditions. [ABSTRACT FROM AUTHOR]

Rehschuh and Ruehr did find lower F SB v sb /F SB M sb in the heatwave and droughted heatwave plants; however, it did not lead to long-term damage, as F SB v sb /F SB M sb slowly recovered post-heatwave and drought. Broader questions for ecosystem response to hot drought Rehschuh and Ruehr provide excellent insight into how coniferous seedlings might respond to a heatwave-drought event; however, it is still unclear how these results might scale seasonally, and with mature trees or other plant functional types. This scientific commentary refers to 'Diverging responses of water and carbon relations during and after heat and hot drought stress in Pinus sylvestris' by Rehschuh and Ruehr (doi: 10.1093/treephys/tpab141). [Extracted from the article]

The survival and performance of urban forests are increasingly challenged by urban drought, consequently compromising the sustainability and functionality of urban vegetation. Plant–water relations largely determine species drought tolerance, yet little is known about the hydraulics of urban forest species. Here, we report the leaf hydraulic and carbon traits that govern plant growth and drought resistance, including vulnerability to embolism, hydraulic conductivity and leaf gas exchange characteristics, as well as morphological traits that are potentially linked with these physiological attributes, with the aim of guiding species selection and management in urban forests. Plant materials were collected from mature shrubs and trees on our university campus in Beijing, representing 10 woody species common to urban forests in north China. We found that the leaf embolism resistance, represented by the water potential inducing 50% loss of hydraulic conductivity (P 50), as well as the hydraulic safety margin (HSM) defined by P 50 and the water potential threshold at the inception of embolism (P 12), varied remarkably across species, but was unrelated to growth form. Likewise, stem and leaf-specific hydraulic conductivity (K stem and k l) was also highly species-specific. Leaf P 50 was positively correlated with hydraulic conductivity. However, neither P 50 nor hydraulic conductivity was correlated with leaf gas exchange traits, including maximum photosynthetic rate (A max) and stomatal conductance (g s). Plant morphological and physiological traits were not related, except for specific leaf area, which showed a negative relationship with HSM. Traits influencing plant–water transport were primarily correlated with the mean annual precipitation of species climatic niche. Overall, current common woody species in urban forest environments differed widely in their drought resistance and did not have the capacity to modify these characteristics in response to a changing climate. Species morphology provides limited information regarding physiological drought resistance. Thus, screening urban forest species based on plant physiology is essential to sustain the ecological services of urban forests. [ABSTRACT FROM AUTHOR]

Extreme drought is one of the key climatic drivers of tree mortality on a global scale. However, it remains unclear whether the drought-induced tree mortality will increase under nocturnal climate warming. Here we exposed seedlings of two wide-ranging subtropical tree species, Castanopsis sclerophylla and Schima superba , with contrasting stomatal regulation strategies to prolonged drought under ambient and elevated night-time temperature by 2 °C. We quantified the seedling survival time since drought treatment by measuring multiple leaf traits such as leaf gas exchange, predawn leaf water potential and water-use efficiency. The results showed that all seedlings in the ambient temperature died within 180 days and 167 days of drought for C. sclerophylla and S. superba , respectively. Night warming significantly shortened the survival time of C. sclerophylla , by 31 days, and S. superba by 28 days, under the drought treatment. A survival analysis further showed that seedlings under night warming suffered a 1.6 times greater mortality risk than those under ambient temperature. Further analyses revealed that night warming suppressed net leaf carbon gain in both species by increasing the nocturnal respiratory rate of S. superba across the first 120 days of drought and decreasing the photosynthetic rate of both species generally after 46 days of drought. These effects on net carbon gain were more pronounced in S. superba than C. sclerophylla. After 60 days of drought, night warming decreased the predawn leaf water potential and leaf water-use efficiency of C. sclerophylla but not S. superba. These contrasting responses are partially due to variations in stomatal control between the two species. These findings suggest that stomatal traits can regulate the response of leaf gas exchange and plant water-use to nocturnal warming during drought. This study indicates that nocturnal warming can accelerate tree mortality during drought. Night warming accelerates the mortality of two subtropical seedlings under drought. Night warming differently affects the drought response of leaf gas exchange and plant water-use between the two species due to species-specific stomatal morphological traits. Carbon metabolism changes and hydraulic damage play differential roles in driving night-warming impacts on the drought-induced mortality between the two species. [ABSTRACT FROM AUTHOR]

The objective of this study was to quantify the effect of potassium (K) supply on osmotic adjustment and drought avoidance mechanisms of Eucalyptus seedlings growing under short-term water stress. The effects of K supply on plant growth, nutritional status, leaf gas exchange parameters, leaf water potential (Ψw), leaf area (LA), stomatal density (SD), leaf carbon (C) and nitrogen (N) isotopic compositions (δ13C and δ15N ‰) and leaf C/N ratio under polyethylene glycol (PEG)-induced water deficit were measured. Under both control (non-PEG) and osmotic stress (+PEG) conditions, K supply increased plant growth, boosting dry matter yield with decreased C/N leaf ratio and δ15N ‰ values. The +PEG significantly reduced LA, plant growth, dry matter yield, Ψw, number of stomata per plant and leaf gas exchange, relative to non-PEG condition. Potassium supply alleviated osmotic-induced alterations in Eucalyptus seedlings by better regulating leaf development as well as SD, thus improving the rate of leaf gas exchange parameters, mesophyll conductance to CO2 (lower δ13C ‰ values) and water use efficiency (WUE). Consequently, K-supplied plants under drought better acclimated to osmotic stress than K-deficient plants, which in turn induced lower CO2 assimilation and dry matter yield, as well as higher leaf δ13C ‰ and δ15N ‰ values. In conclusion, management practices should seek to optimize K-nutrition to improve WUE, photosynthesis-related parameters and plant growth under water deficit conditions. [ABSTRACT FROM AUTHOR]