Clarifying the coordination of leaf hydraulic traits with gas exchange across closely-related species adapted to varying rainfall can provide insights into plant habitat distribution and drought adaptation. The leaf hydraulic conductance (K leaf), stomatal conductance (g s), net assimilation (A), vein embolism and abscisic acid (ABA) concentration during dehydration were quantified, as well as pressure-volume curve traits and vein anatomy in 10 Caragana species adapted to a range of mean annual precipitation (MAP) conditions and growing in a common garden. We found a positive correlation between Ψ leaf at 50% loss of K leaf (K leaf P 50) and maximum K leaf (K leaf-max) across species. Species from low-MAP environments exhibited more negative K leaf P 50 and turgor loss point, and higher K leaf-max and leaf-specific capacity at full turgor, along with higher vein density and midrib xylem per leaf area, and a higher ratio of K leaf-max : maximum g s. Tighter stomatal control mediated by higher ABA accumulation during dehydration in these species resulted in an increase in hydraulic safety and intrinsic water use efficiency (WUE i) during drought. Our results suggest that high hydraulic safety and efficiency combined with greater stomatal sensitivity triggered by ABA production and leading to greater WUE i provides drought tolerance in Caragana species adapted to low-MAP environments.

γ-aminobutyric acid (GABA) is a non-protein amino acid involved in various physiological processes; it aids in the protection of plants against abiotic stresses, such as drought, heavy metals, and salinity. GABA tends to have a protective effect against drought stress in plants by increasing osmolytes and leaf turgor and reducing oxidative damage via antioxidant regulation. Guard cell GABA production is essential, as it may provide the benefits of reducing stomatal opening and transpiration and controlling the release of tonoplast-localized anion transporter, thus resulting in increased water-use efficiency and drought tolerance. We summarized a number of scientific reports on the role and mechanism of GABA-induced drought tolerance in plants. We also discussed existing insights regarding GABA’s metabolic and signaling functions used to increase plant tolerance to drought stress.

Members of the SNF1-related protein kinase 2 (SnRK2) family are plant-specific serine or threonine kinases that play a pivotal role in the response of plants to abiotic stresses. Members of this plant-specific kinase family have included a critical regulator (SnRK2) of abscisic acid (ABA) response in plants. Plant organ development is governed substantially by the interaction of the SnRK2 and the phytohormone abscisic acid (ABA). Recent research has revealed a synergistic link between SnRK2 and ABA signaling in a plant’s response to stress such as drought and shoot growth. SnRK2 kinases play a dual role in the control of SnRK1 and the development of a plant. The dual role of SnRK2 kinases promotes plant growth under optimal conditions and in the absence of ABA while inhibiting the growth of plants in response to ABA. In this review, we have uncovered the roles of ABA-activated SnRK2 kinases in plants, as well as their physiological mechanisms.

Drought is a cyclical phenomenon in natural environments. During dehydration, stomatal closure is mainly regulated by abscisic acid (ABA) dynamics that limit transpiration in seed plants, but following rehydration, the mechanism of gas exchange recovery is still not clear. In this study, leaf water potential (ψleaf), stomatal conductance (gs), leaf hydraulic conductance (Kleaf), foliar ABA level, ethylene emission rate in response to dehydration and rehydration were investigated in four Caragana species with isohydric (Caragana spinosa and C. pruinosa) and anisohydric (C. intermedia and C. microphylla) traits. Two isohydric species with ABA‐induced stomatal closure exhibited more sensitive gs and Kleaf to decreasing ψleaf than two anisohydric species which exhibited a switch from ABA to water potential‐driven stomatal closure during dehydration. Following rehydration, the recovery of gas exchange was not associated with a decrease in ABA level but was strongly limited by the degradation of the ethylene emission rate in all species. Furthermore, two anisohydric species with low drought‐induced ethylene production exhibited more rapid recovery in gas exchange upon rehydration. Our results indicated that ethylene is a key factor regulating the drought‐recovery ability in terms of gas exchange, which may shape species adaptation to drought and potential species distribution.

Investigating plant morphological traits can provide insights into plant drought tolerance. To date, many papers have focused on plant hydraulic responses to drought during dehydration, but atmospheric water absorption by trichomes to mitigate drought stress by influencing leaf hydraulics in plant species that inhabit arid environments has been largely ignored. The experiment in this study was designed to assess how dew absorbed by leaf trichomes helps Caragana korshinskii withstand drought.The results showed that under a drought stress and dew (DS & D) treatment, C. korshinskii displayed a strong capacity to absorb dew with trichomes; exhibited slow decreases in leaf water potential (Ψ leaf ), leaf hydraulic conductivity (K leaf ), and gas exchange; experienced 50% K leaf and gas exchange losses at lower relative soil water content levels than plants treated with drought stress and no dew (DS & ND); and experienced 50% K leaf loss (K leaf P 50 ) at similar Ψ leaf levels as DS & ND plants. Its congener C. sinica, which does not have leaf trichomes, displayed little ability to absorb dew under drought stress and did not show any remarkable improvement in the above parameters under the DS & D treatment. Our results indicated that leaf trichomes are important epidermal dew-uptake structures that assist in partially sustaining the leaf hydraulic assimilation system, mitigate the adverse effects of drought stress and contribute to the distribution of C. korshinskii in arid environments.