Stomatal and Non-Stomatal Leaf Traits for Enhanced Water Use Efficiency in Rice

1. Introduction

Water scarcity threatens global food security, mainly because over half the world's population depends on water-intensive crops like rice (Oryza sativa L.) [1,2]. There is substantial evidence that climate change is exacerbating water scarcity, and enhancing the water use efficiency (WUE) of rice crops has become a significant issue for sustaining agricultural productivity [3,4]. Consequently, in addition to testing alternative agronomic methods [5,6,7], researchers worldwide are seeking to breed rice varieties with greater WUE [8,9,10,11,12]. Plant leaves play a pivotal role in water exchange, acting as the primary site for carbon dioxide uptake and water vapour loss through transpiration [4]. Historically, efforts to improve WUE have focused predominantly on stomatal traits, such as stomatal density, size, and conductance. There is, however, mounting evidence that non-stomatal leaf traits, including photosynthetic efficiency, leaf anatomy, and biochemical composition, significantly influence WUE in rice. [13,14,15].

We seek to provide a comprehensive overview of how both stomatal and non-stomatal leaf traits determine WUE in rice. We explore intricate interactions among these traits and their combined impact on water conservation and carbon assimilation. We examine the complex interplay of leaf traits to identify novel strategies for breeding rice varieties with superior WUE without compromising yield potential. Included in our consideration are (1) the varying scales of WUE measurement, from leaf-level gas exchange to whole-plant carbon isotope discrimination, (2) recent advances in the understanding of stomatal behaviour, mesophyll conductance, leaf anatomy, and metabolic adaptations to water stress, (3) emerging technologies, such as high-throughput phenotyping and multi-omic approaches. By integrating these factors, we aim to provide a more holistic understanding of breeding programs for WUE in rice, including potential synergies and trade-offs. Finally, we consider how agronomic practices [16,17] and environmental factors interact with leaf traits to influence WUE under field conditions.

Rice cultivation spans a diverse range of agroecosystems, from traditional continuously flooded paddies to water-limited upland and dryland environments. In flooded systems, WUE traits may contribute to optimising water productivity without imposing stress on the crop, whereas in upland systems, these traits are critical for survival, resilience, and yield stability under drought conditions. The physiological and anatomical mechanisms underlying WUE, such as stomatal behaviour, root architecture, and osmotic adjustment, therefore differ in their functional importance depending on the cultivation system. Recognising this spectrum is essential for developing rice varieties adapted to varying water regimes.

WUE can be broadly defined as the ratio of biomass produced or yield obtained to the amount of water used [9,12]. However, the concept of WUE encompasses multiple scales and definitions depending on the context of measurement. At the leaf level, WUE is typically expressed as the ratio of carbon assimilation to water loss through transpiration [10]. This can be quantified as intrinsic water use efficiency (WUEi), defined as the ratio of net CO₂ assimilation rate (An) to stomatal conductance (g_s); or alternatively, computed as instantaneous water use efficiency (WUEinst), calculated by dividing An by the transpiration rate (E) [10,11,18]. These leaf-level measurements provide insights into the physiological basis of WUE and are influenced by stomatal and non-stomatal leaf traits. Measurement techniques for leaf-level WUE in rice include gas exchange analysis using infrared gas analysers, which allow for the simultaneous measurement of photosynthesis and transpiration rates [11,19] and carbon isotope discrimination (Δ¹³C) over the period of leaf development [20,21]. Additionally, chlorophyll fluorescence techniques can provide insights into photosynthetic efficiency, which is closely linked to WUE [22].

At the whole-plant level, WUE can be assessed as the ratio of biomass accumulation to cumulative water use [23,24,25,26]. This approach captures both productive and non-productive water losses. Field-scale measurements often focus on yield-based WUE, calculated as crop yield per unit of water applied or lost through combined evaporation and transpiration [12]. Recent advances in high-throughput phenotyping, including thermal imaging and remote sensing techniques, enable more rapid and precise measurements of WUE-related traits in large populations [27]. These technologies, combined with genomic approaches, are accelerating the identification of genetic determinants of WUE in rice. Understanding the physiological mechanisms underlying WUE variability at the leaf and whole plant level is essential for developing rice varieties with improved drought tolerance and reduced water requirements.

2. Stomatal Leaf Traits and WUE in Rice

Stomatal leaf traits refer to the characteristics and properties of the stomata, including their density, size, distribution, and conductance, which are regulated by controlling gas exchange between leaves and the atmosphere. As highlighted in a recent herbarium study of plant adaptation to climate change [28], there is extensive knowledge of the dozens of genes involved in stomatal development (density, size, distribution).

2.1. Stomatal Density, Size and Arrangement

Recent studies have demonstrated that modifying stomatal density and size through crop engineering offers a promising approach to enhancing WUE and mitigating water scarcity challenges in agricultural crops [4,29]. Rice exhibits unique stomatal structures compared to other plant species, with greater stomatal densities and smaller stomatal sizes. The stomatal complex in rice comprises two dumbbell-shaped guard cells surrounded by subsidiary cells that regulate the stomatal aperture [30,31].

Four distinct models of leaf stomata were described in mutant populations of the purple rice cultivar, Jao Hom Nin, which varied in stomatal density and size [3]. Rice varieties with low stomatal density and smaller stomatal size exhibited improved WUE and biomass production under both field and greenhouse conditions. Similarly, three purple rice mutants were adapted to severe water stress conditions during the reproductive stage of growth, which resulted in low stomatal density and greater WUE under restricted water conditions [32]. Despite these findings, gaps remain regarding the physiological trade-offs of reduced stomatal density, particularly under fluctuating environmental conditions. While smaller, fewer stomata conserve water, they may limit CO₂ uptake under high demand. These dynamics are not yet fully quantified across diverse environments and growth stages.

Genetic manipulation of stomatal traits has shown promise in improving WUE. The high-yielding rice variety IR64 was engineered to reduce stomatal density by enhancing the expression of OsEPF1, a gene involved in rice epidermal patterning [33]. The resulting plants exhibited reduced stomatal conductance and enhanced water conservation. These traits were interpreted as improving drought tolerance while maintaining or improving yields under elevated atmospheric CO₂ and high-temperature conditions. A previous study explored the impact of the arrangement of leaf stomata on the physiological responses of rice to differing water availability [34]. Yet, the implications of this spatial arrangement for canopy-level water and carbon fluxes remain underexplored. They proposed that greater stomatal density in the upper leaves (flag leaf and second leaf) with reduced density but larger stomata in the lower leaves (third and fourth leaf) constituted an adaptive strategy (reduced water loss) for genotypes under limited water availability. The study concluded that this stomatal configuration could enhance water productivity in rice under aerobic conditions without yield reduction.

2.2. Stomatal Conductance and Aperture

Leaf stomatal conductance (g_s) is a critical physiological parameter influenced by a wide range of environmental and plant factors, including light, temperature, humidity, CO₂ concentration, and plant water status [4,35]. The relationship between g_s and WUE involves a trade-off between maximising CO₂ uptake for photosynthesis and minimising water loss through transpiration. Recent studies have focused on understanding genetic and molecular mechanisms that regulate stomatal conductance and aperture in rice. A previous study revealed that precise control of the stomatal aperture is crucial to maintaining an optimal balance between photosynthesis and water conservation [36]. The study identified genes such as EPF2, OSA1, and SLAC1 involved in stomatal regulation, enabling the enhancement of WUE through genetic manipulation. However, the long-term physiological impacts of manipulating these genes under fluctuating climate conditions remain poorly understood. In particular, the extent to which these molecular interventions affect gas exchange efficiency under combined heat and water stress is underexplored. Comparative evidence from model species like Arabidopsis suggests variability in stomatal responsiveness and downstream signaling efficiency, indicating that gene function may be context-dependent across crops [37].

2.3. Regulation of Transpiration and Carbon Dioxide Uptake

Abscisic acid (ABA) is widely believed to have a central role as a signal for the closure of stomata during water stress [35,38]. Other hormones, such as cytokinins and gibberellins, also contribute to stomatal regulation. Plant circadian rhythms reflect the significance of stomatal conductance, ensuring that stomatal opening and closing are synchronised with environmental light and temperature patterns [38]. This temporal coordination helps optimise WUE and CO₂ uptake and contributes to plant growth and survival under varying environmental conditions. Similarly, ion transport and osmotic adjustments within stomatal guard cells facilitate rapid changes in the stomatal aperture, balancing the need for CO₂ uptake with water conservation. Fine-tuning these processes enhances plant survival in diverse and changing environments [3,38]. The movement of ions such as potassium (K⁺), chloride (Cl⁻), and calcium (Ca²⁺), along with malate (C₄H₄O₄²⁻), causes water to enter guard cells, leading to stomatal opening for CO₂ uptake during photosynthesis. Conversely, water follows when ions efflux from the guard cells, causing the stomata to close thereby reducing water loss (Figure 1A). The fine-tuning of this mechanism is essential for balancing the demand for CO₂ with the need for water conservation, especially under drought stress [39,40]. Despite this mechanistic clarity, limited studies have explored how these responses are modulated across rice genotypes with varying limited water stress or drought resilience. Moreover, cross-species comparisons of hormonal regulation and ion channel dynamics remain scarce, leaving uncertainties about whether similar mechanisms operate with equal efficiency in monocot cereals versus dicot plants.

In addition to stomatal and cuticular transpiration, grasses such as rice also release water through hydathodes: specialised structures located at leaf margins that facilitate guttation under conditions of high soil moisture and low transpiration demand. Hydathodes, unlike stomata, remain open and serve as low-resistance pathways for liquid exudation, playing a role in water release and nutrient exudation [41]. This process complements transpiration and may contribute to maintaining xylem flow when evaporative demand is low. Furthermore, rice leaves contain well-defined vascular bundles composed of xylem and phloem, which are responsible for the transport of water, nutrients, and photosynthates. These vascular structures are closely associated with companion cells and are integral to leaf physiology, supporting both hydraulic conductance and photosynthate distribution [42].

3. Non-Stomatal Leaf Traits and WUE in Rice

Non-stomatal leaf traits in rice encompass the structural and biochemical characteristics of the leaf which influence photosynthetic efficiency and WUE independent of stomatal behaviour.

3.1. The Role of ΦPSII in Photosynthetic Efficiency

In this review, photosynthetic efficiency is categorised as a non-stomatal leaf trait because it primarily reflects the biochemical and physiological processes within the leaf, including the efficiency of the photosynthetic machinery, such as chloroplasts, enzymes, and photosystems like ΦPSII in converting light energy into chemical energy. Photosynthetic efficiency refers to the ability of plants to convert light energy into chemical energy during photosynthesis [43]. Non-stomatal factors, such as the biochemical capacity of the mesophyll cells, chlorophyll content, and the efficiency of the photosynthetic machinery, play a pivotal role in determining photosynthetic efficiency [4,20,44,45]. These factors can enhance the plant's ability to assimilate CO₂ under varying environmental conditions, thereby optimising WUE. By improving photosynthetic efficiency, plants can achieve higher rates of CO₂ assimilation per unit of water transpired. This balance is achieved by optimising stomatal conductance, so that stomata remain partially open to allow CO₂ uptake while reducing excessive water loss. Improved mesophyll conductance, Rubisco efficiency, or enhanced photoprotection mechanisms can also contribute to higher intrinsic WUE under drought stress [46]. This balance between CO₂ uptake and water conservation is essential for plant productivity and resilience, making photosynthetic efficiency a key target for crop improvement strategies [47].

3.2. Leaf Anatomy

Mesophyll structure, vein density, and bulliform cells significantly impact CO₂ diffusion, light distribution, and water management within leaves [48]. Mesophyll conductance (g_m), an important factor influencing CO₂ diffusion, is discussed in more detail in section 3.5. Leaf thickness and cell arrangements influence light distribution and absorption, while chloroplast positioning optimises light harvesting and minimises photodamage. However, these anatomical features often involve trade-offs. For instance, it has been reported that increased vein density in rice was correlated with greater photosynthetic rates but reduced WUE [49], highlighting the complex interplay between structural traits and physiological efficiency.

Aquaporins, a family of integral membrane proteins, play a dual role in regulating both water transport and CO₂ diffusion across leaf tissues, thereby influencing photosynthetic efficiency and WUE in rice. While CO₂ is abundant in the atmosphere, its diffusion into the chloroplasts, where photosynthesis occurs, is limited by mesophyll conductance, which includes movement through intercellular air spaces, cell walls, and membranes. Certain aquaporins, particularly plasma membrane intrinsic proteins (PIPs), facilitate this process by enabling CO₂ to cross cell membranes more efficiently [50]. In parallel, aquaporins influence leaf hydraulic conductance, which refers to the efficiency of water movement from the xylem to the sites of evaporation within the leaf. This conductance affects stomatal behavior and transpiration, thereby indirectly modulating photosynthesis and WUE [48,51]. Environmental factors such as nitrogen availability can regulate aquaporin expression and activity, further linking nutrient status to water and carbon dynamics in leaves [48]. A balanced distribution of aquaporins in mesophyll, bundle sheath, and vascular tissues is considered optimal for improving WUE and enhancing crop resilience under climate stress [52,53].

Studies have emphasised the significance of internal leaf anatomy, including aerenchyma and intercellular air spaces, in regulating CO₂ diffusion to the sites of photosynthesis. CO₂ must first dissolve in the thin water layer lining the mesophyll cell walls before diffusing into the symplast and reaching the chloroplasts. Therefore, a greater intercellular surface area, supported by well-developed aerenchyma, enhances both CO₂ diffusion efficiency and evaporative capacity. This anatomical feature contributes to gₘ and plays a critical role in photosynthetic performance and WUE, particularly under stress conditions (Figure 1B) [54,55,56].

Studies have further demonstrated that the midvein-deficient mutant shows higher vein density and photosynthetic efficiency but significantly lower WUE. Although the study did not include water-stress conditions, the mutants are still recommended as promising rice breeding material due to their enhanced photosynthetic efficiency [49]. In a glasshouse experiment with limited water (60% field capacity), it has been observed that high leaf mass area (LMA) mutants exhibited higher WUE and a more significant total number of veins than low-LMA mutants, which had lower WUE. However, high-LMA mutants also showed lower vein density (veins per centimetre) and fewer bulliform cells than their low-LMA counterparts [14].

Abaxial stomatal dominance, where stomata are mainly located on the leaf’s lower surface, helps reduce water loss by limiting stomatal exposure to direct sunlight and wind. This spatial trait can enhance WUE in rice, especially under drought or high vapor pressure conditions. When combined with other anatomical traits like reduced stomatal density and thicker cuticles (discusses in the next section 3.3), abaxial dominance offers a promising target for breeding rice varieties with improved drought resilience and efficient gas exchange [33,57].

3.3. Leaf Cuticle and Epicuticular Wax

Leaf cuticles and epicuticular wax (EW) are critical components in regulating non-stomatal water loss and enhancing WUE in rice. In rice, the β-Ketoacyl-CoA Synthase (KCS) enzyme is essential for the elongation of very long-chain fatty acids, which are major components of cuticular wax [58]. It has been reported that increased expression of the OsCUT1 gene in rice resulted in improved drought tolerance and wax synthesis without reducing yield [59]. On the other hand, the OsGL1-1 gene plays a crucial role in cuticular wax deposition and drought resistance in rice. Mutants with reduced OsGL1-1 expression showed decreased cuticular wax deposition, increased water loss, and enhanced sensitivity to drought compared to wild-type plants [60]. Furthermore, previous research has demonstrated that EW traits contribute to rice resistance against pests, evidenced by EW rice mutants exhibiting reduced resistance to the rice water weevil (Coleoptera: Curculionidae) and the fall armyworm (Lepidoptera: Noctuidae) (Figure 1C) [61].

3.4. Metabolomics Changes in the Leaves

Drought stress triggers complex metabolic responses in plants, regulated by gene activity, which impact vital processes like photosynthesis, respiration, and assimilate translocation [62]. These changes help the plant adjust osmotically, manage reactive oxygen species (ROS), and stabilise cell membranes, crucial for maintaining function during drought.

Drought-tolerant rice cultivars often accumulate greater concentrations of osmoprotectants, including low molecular weight osmolytes such as glycine betaine and proline, as well as organic acids and soluble sugars [62,63]. These compounds help sustain cellular functions and contribute to defence mechanisms under water-limited conditions. Additionally, increased concentrations of antioxidants, phenolic compounds, and flavonoids have been observed in drought-stressed rice leaves, with flavonoids like kaempferol and quercetin playing a significant role in enhancing drought tolerance and modulating WUE [64].

3.5. Mesophyll Conductance (gm) and Intrinsic WUE

g_m is a key physiological parameter that governs the rates of CO₂ assimilation [44,65]. Von Caemmerer and Evans (2010) suggested that increasing photosynthesis without altering stomatal function can improve WUE, and it also implied that enhancing g_s could boost photosynthesis if water is not limited. g_m is measured as the rate of CO₂ diffusion from intercellular spaces to chloroplasts, which substantially affects WUE. Varieties with greater g_m also show improved carbon assimilation per unit of water transpired [15]. Additionally, they mentioned that manipulating g_m could increase CO₂ availability at Rubisco, the key enzyme in photosynthesis that catalyses the fixation of CO₂ into organic molecules in the Calvin cycle, potentially improving photosynthesis and WUE [66]. Furthermore, Flexas et al. (2013) stated that to simultaneously improve photosynthesis and WUE, genetic manipulation of g_m should be done without parallel changes in g_s. It was suggested that the optimal trait for enhancing WUE is an increased ratio of g_m to g_s [67].

For rice, g_m plays a significant role in transpiration efficiency (TE) and could affect WUE. Upland rice and O. glaberrima showed a stronger response of TE to the g_m/g_s ratio under drought conditions, suggesting a link between g_m and WUE. Furthermore, it suggested that increasing rice's g_m/g_s ratio, potentially by modifying leaf anatomy, could enhance both TE and WUE under water-limited conditions [68].

Strategies like genetic manipulation or selective breeding can significantly improve WUE without compromising photosynthetic capacity. The α subunit of a heterotrimeric G protein regulates g_m and drought tolerance in rice, suggesting that modifying G protein signalling could enhance WUE in rice cultivars [69].

3.6. Leaf Canopy Architecture

Rice varieties with higher total leaf area and optimised canopy structure exhibited improved WUE under water-limited conditions [34]. Rice mutants with LMA showed increased WUE, increased photosynthetic capacity, and superior carboxylation efficiency compared to low-LMA mutants under both well-watered and water-limited conditions [14,70].

A glasshouse study conducted on the Azucena (tropical japonica) and IR64 (India) rice varieties revealed a correlation between increased leaf width and lower Δ¹³C. Leaves with higher widths have excellent leaf-boundary layers that resist gaseous diffusion, which would lower the Δ¹³C and increase WUE [71].

Higher crop density creates dense canopies and increases the thickness of the boundary layer, the layer of still air that surrounds each leaf. This reduces evaporative demand and water loss and potentially improves WUE. However, it may also limit CO₂ diffusion, affecting photosynthesis [72,73].

Erect leaves, which form smaller angles with the stem, allow greater light penetration to lower canopy layers, thereby enhancing overall photosynthetic efficiency and reducing excessive transpiration in the upper canopy. This spatial leaf arrangement has been demonstrated in rice genotypes to improve light interception and optimise water use, contributing to higher WUE [74,75]. Furthermore, studies on spatial leaf arrangement and canopy architecture in rice show that coordinated leaf positioning around the stem improves light distribution throughout the canopy, enhances carbon assimilation, and reduces water loss. This trait is particularly beneficial in high-density planting systems, where maximizing light use efficiency and conserving water are critical for sustaining productivity under variable environmental conditions [76,77].

3.7. Leaf Pubescence and Boundary Layer Resistance

Leaf hairiness (pubescence) has been understudied in rice despite its potential to enhance water conservation and photosynthetic efficiency. Rice varieties show differences in leaf hairiness, from smooth to densely hairy surfaces. These hairs form a boundary layer that slows water vapour diffusion, reducing transpiration and enhancing light reflectance, which can protect the leaf from excessive radiation (Figure 1D) [73,78].

It has been reported that the genetic basis, feasibility of transferring this trait between rice varieties and physiological benefits of leaf hairiness on WUE in rice by introducing a gene from chromosome 6 from hairy-leafed Oryza nivara into the less hairy IR24 variety, creating an introgression line with the hairy-leaf trait (IL-hairy). The IL-hairy plants exhibited warmer leaf surfaces under sunlight due to the increased boundary layer resistance conferred by the leaf hairs and lower transpiration rates under moderate and high light intensities, leading to significantly higher photosynthetic WUE [73].

3.8. Carbon Fixation Efficiency

Carbon fixation efficiency is discussed in this review as a non-stomatal trait because it primarily reflects the internal biochemical capacity of the plant to assimilate carbon, beyond the regulation of gas exchange at the stomatal level. While stomatal conductance indeed influences CO₂ availability in the intercellular spaces, the efficiency with which CO₂ is fixed into carbohydrates, governed by enzymes like Rubisco, chloroplast function, and mesophyll conductance, is largely non-stomatal in nature.

Δ¹³C and carbon isotope ratio (δ¹³C) are widely used indicators of WUE in C₃ plants like rice. Δ¹³C reflects the degree of discrimination against ¹³CO₂ during photosynthesis, which is influenced both by stomatal behaviour and the biochemical processes involved in carbon fixation [20,79]. Higher Δ¹³C values indicate greater discrimination against ¹³C, typically associated with higher stomatal conductance and lower WUE [80]. Conversely, δ¹³C, which is derived from plant tissue and reflects the integrated effects of carbon assimilation over time, is negatively correlated with Δ¹³C [81]. A higher δ¹³C value suggests reduced stomatal conductance and improved carbon fixation efficiency per unit water loss, thus serving as a reliable proxy for assessing WUE in rice, especially under water-limited conditions [82].

4. Integrating Stomatal and Non-Stomatal Traits for WUE Improvement

Improving WUE in rice requires an integrated approach that considers both stomatal and non-stomatal leaf traits. This will enable the development of more effective strategies for sustainable rice production under water-limited conditions.

4.1. Interactions and Trade-Offs Among Leaf Traits

Reducing stomatal density can enhance water conservation [33], but it may also limit CO₂ uptake, potentially impacting photosynthetic efficiency. Conversely, increasing g_m can improve photosynthetic rates but may lead to greater water loss if not balanced with appropriate stomatal control [45]. Hence, some studies have highlighted the importance of considering multiple traits simultaneously. It has been demonstrated that rice varieties with both optimised stomatal traits and enhanced g_m exhibited superior WUE compared to those improved for single traits alone [83]. Further, it has been found that stomatal traits modulated the relationship between leaf nitrogen content and WUE, emphasizing the need for integrated trait selection in breeding programs [84].

4.2. Breeding Strategies for Optimising WUE Through Leaf Traits

Optimising WUE in rice through breeding involves selecting specific leaf traits that improve water management and photosynthetic performance. This multi-trait approach combines traditional breeding with advanced genetic and genomic tools, focusing on stomatal behaviour, leaf morphology, physiological traits, photosynthetic efficiency, and biochemical pathways to develop more water-efficient, productive rice varieties.

Advances in quantitative trait loci (QTL) mapping have allowed the identification of genetic regions linked to desirable leaf traits, such as leaf area, thickness, and orientation. By correlating genetic variations with these traits, QTL mapping helps breeders efficiently integrate these traits into new plant varieties [85,86,87].

Modern genetic technique, marker-assisted selection (MAS), allows for the rapid integration of WUE-related traits by using molecular markers associated with key traits like stomatal conductance, leaf morphology, and Rubisco efficiency. Genomic selection takes this a step further by utilising genome-wide data to predict and select for high WUE traits, streamlining the breeding process and reducing the time needed to develop new varieties. This approach leverages high-throughput genotyping and phenotyping to build predictive models that can accurately identify the best candidates for breeding programs focused on improving WUE [88,89,90].

Recent studies have highlighted the importance of integrating both stomatal and non-stomatal traits to enhance WUE in rice. Stomatal morphology and physiology operate in a coordinated manner, influencing both transpiration efficiency and carbon assimilation [47]. Environmental drivers shape stomatal traits, which in turn interact with broader leaf structural features to modulate WUE at the ecosystem level [91]. Complementing these findings, another study [13] has shown that rice genotypes with low-frequency, large-size stomata exhibited higher intrinsic WUE and more responsive gas exchange under varying vapour pressure deficits. This study also linked epidermal patterning and the expression of key regulatory genes (e.g., ERECTA, TMM, YODA) to stomatal development, reinforcing the need to integrate leaf surface traits with internal physiological and anatomical features. Collectively, these findings support a holistic breeding approach that considers the interplay of multiple leaf traits to develop rice cultivars resilient to climate variability and water-limited environments.

4.3. Agronomic Practices and Environmental Factors Influencing WUE

Anthropogenic water management is an important factor influencing plant performance. Inefficient irrigation methods lead to low WUE and environmental issues. Several alternative rice production methods, such as aerobic rice, direct-seeded rice (DSR), alternate wetting and drying (AWD), and smart irrigation technologies, can improve WUE, though each has specific challenges like high costs or labour intensity [6,92]. Delayed Permanent Water (DPW) is an alternative water management practice extensively used in Australian rice cultivation to increase water productivity for drill-sown rice. In this method, the rice crop is sown and initially managed like conventional drill-sown rice, but the application of permanent water is delayed until at least 50 days after the first flush irrigation [93].

Further, it has been emphasised that to promote water-saving irrigation technology, countries should develop supportive policies, raise farmers' awareness, and offer training and financial assistance tailoring water-saving technologies to specific regions can reduce irrigation water use and improve rice WUE, helping to address global water scarcity challenges [94]. As a country with a well-managed rice industry, the Australian Government's Climate-Smart Agriculture Program provides funding for innovative irrigation projects [95]. Educational campaigns like Brisbane's "Every Drop Counts" raise awareness among farmers about water-saving practices [96]. Organizations such as Irrigation Australia offer training programs and financial subsidies to help farmers adopt new technologies [97].

Nutrient management such as applying balanced fertilisers, particularly nitrogen, in appropriate amounts can enhance plant growth and photosynthetic efficiency, leading to better WUE [9]. Sowing techniques, such as direct seeding and proper transplanting density, can optimise plant establishment and water utilisation. Direct seeding generally achieves higher WUE than traditional transplanting, though wet seeding by broadcast, a common method, results in lower WUE compared to traditional transplanting [98]. Moreover, uncontrolled weeds compete with rice for water and nutrients. It has been found that while weed control does not affect total water consumption, it influences WUE through its impact on yield [99]. Higher temperatures can raise transpiration rates, but practices like mulching help regulate plant temperature and reduce water loss. Non-flooded plastic film mulching and wheat straw mulching are effective options for improving WUE in rice cultivation [7]. Therefore, optimising WUE in rice production requires multiple approaches, integrating breeding for better leaf traits, effective agronomic practices, and consideration of environmental factors to achieve sustainable rice production in water-limited conditions.

Table 1. Comprehensive list of rice genes involved in (A) stomatal and (B) non-stomatal leaf traits affecting water use efficiency. The table includes genes spanning key functional categories including stomatal development and regulation, cuticular wax biosynthesis, leaf morphology, stress response pathways, and metabolic adaptations. Locus IDs correspond to the Rice Annotation Project and were verified via the SNP-Seek database from the International Rice Research Institute [100]. Directional trends in the WUE Association column indicate: ↑ = positive association with increased WUE (gene overexpression or enhanced function improves water use efficiency); ↓ = negative association with WUE (gene overexpression or enhanced function reduces water use efficiency); ± = variable or context-dependent association (effects depend on environmental conditions, genetic background, or developmental stage).

A. Stomatal leaf Traits
Gene	Locus ID	Role	WUE Association
OsEP3	LOC_Os02g15950	Regulates stomatal guard cell development [101]. ERECT PANICLE3	↑ WUE Optimises stomatal development for better water regulation
OsKAT1	LOC_Os01g55200	Regulates stomatal opening and closing by facilitating potassium ion flux, which directly affects stomatal movement and plant water regulation [102,103] K+ TRANSPORTER 1	↑ WUE improves stomatal control
OsSDD1	LOC_Os03g0143100	Mutations lead to higher stomatal density [13] STOMATAL DENSITY AND DISTRIBUTION	↓ WUE increases water loss via excess stomata
OsTMM	LOC_Os01g02060	Mutations can lead to irregular stomatal spacing, affecting gas exchange efficiency [13]. TOO MANY MOUTHS	↓ WUE disrupts stomatal patterning
OsEPF1	LOC_Os04g0637300	Overexpress reduce stomatal density [36] EPIDERMAL PATTERNING FACTOR1	↑ WUE reduces transpiration
OsSPCH1	LOC_Os06g33450	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to guard mother cell (GMC) identity. Overexpression expression leads to higher stomatal density [33,104] SPEECHLESS1	↓ WUE Overexpression results in increased water loss
OsSPCH2	LOC_Os02g15760	alterations in stomatal size and density in stress conditions. Overexpression increases density [13,105] SPEECHLESS2	↓ WUE Overexpression results in increased water loss
OsMUTE	LOC_Os05g51820	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to GMC identity. Involves in the differentiation of stomatal precursor cells. It plays a critical role in determining stomatal size by regulating the development of guard cells [104]	↑ WUE ensures proper stomatal function
OsFAMA	LOC_Os05g50900	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to GMC identity [104]	↑ WUE Maintains correct stomatal identity for optimal function
OsFLP	LOC_Os07g43420	Regulates the orientation of GMC symmetrical division [104] FOUR LIPS	↑ WUE Regulates stomatal spacing for efficient gas exchange
B. Non-stomatal leaf traits
Gene	Locus ID	Role	WUE Association
OSH43	LOC_Os03g56110 LOC_Os03g57560	Overexpression results in broader leaves, increased tiller number, and more flowers [106]. ORYZA SATIVA HOMEOBOX43	↑ WUE No direct evidence.
OsABCG9	LOC_Os04g44610	Mutations can lead to reduced cuticular wax content, resulting in increased sensitivity to drought and other environmental stresses[107]	↓ WUE Mutation increases drought sensitivity due to water loss
GL1	LOC_Os05g02730	controlling wax synthesis in rice leaves [108] GLOSSY1	↑ WUE Improves cuticle barrier to reduce water loss
OSGL1-1	LOC_Os09g25850 LOC_Os09g25850	Increase leaf cuticular wax deposition and enhance drought tolerance [60] GLOSSY1-1	↑ WUE Enhances drought resistance
OsGL1-2	LOC_Os02g08230	Overexpression increases cuticular wax production and improves drought tolerance [108] GLOSSY1-2	↑ WUE Overexpression reduces water loss
OsWR1	LOC_Os02g10760	Overexpression increases the expression of genes involved in wax synthesis [109] WAX SYNTHESIS REGULATORY GENE1	↑ WUE Overexpression reduces water loss
OsCutA1	LOC_Os10g23204	Overexpression increases cuticular wax production and improves drought tolerance, a promising gene for engineering rice plants with enhanced drought tolerance [59]	↑ WUE Overexpression reduces water loss
YGL1	LOC_Os05g28200	Overexpression results in darker green leaves, increased chlorophyll content, and increased photosynthetic activity. This leads to improved growth and increased yields [110]YELLOW-GREEN LEAF1	↑ WUE Overexpression improves carbon assimilation efficiency
OsHB2	LOC_Os10g33960	Overexpression of the OsHB2 gene results in longer roots, broader leaves, and increased tolerance to drought and salinity stress [111] HOMOEOBOX1	↑ WUE Overexpression improves water capture and leaf area for photosynthesis
RCN1	LOC_Os11g05470	Inhibiting flowering transition and delaying heading under drought. Many rachis branches in the panicle and high yield [112] ROOTS CURL IN NAPHTHYLPHTHALAMIC ACID1	± WUE Delays maturity but may improve yield under drought
OsCKX2	LOC_Os01g10110	Produce larger leaves, more flowers, and higher yields [113] CYTOKININ OXIDASE/DEHYDROGENASE2	↑ WUE Improves resource allocation for higher yield
Gn1a	LOC_Os01g10110	Improves grain yield, resulting in more flowers and larger grains [114] GRAIN NUMBER 1a identical to CKX2	↑ WUE Increases yield potential under stress
NAL3	LOC_Os12g01120	Overexpression results in broader leaves, reduced tiller number, increased lateral root development, and larger grains [115]NARROW LEAF3	↑ WUE Overexpression enhances soil water access and light interception
NRL1	LOC_Os12g37190	Overexpression results in wider leaves, increased plant height, larger vascular bundles, stronger stems, and higher yields [106,116] NARROW AND ROLLED LEAF1	↑ WUE Overexpression improves plant robustness and water transport
NAL1	LOC_Os04g52479	Overexpression results in broader leaves, reduced tiller number, increased lateral root development, and larger grains [117] NARROW LEAF1	↑ WUE Improves growth under water-limited conditions
NAL7	LOC_Os03g06654	Increased expression could have wider leaves, taller plants, and higher yields [106,117]. NARROW LEAF7	↑ WUE Enhances light interception and productivity
OsSPL14	LOC_Os08g39890	Regulates tiller number and panicle branching, which can also lead to increased grain yield [118]. SQUAMOSA PROMOTOR BINDING PROTEIN-LIKE14	↑ WUE Enhances yield per unit water use
OsSPL9	LOC_Os05g33810	Increases grain number per panicle and yield, and regulates drought tolerance, which can improve rice performance in dry environments [119]. SQUAMOSA PROMOTOR BINDING PROTEIN-LIKE9	↑ WUE Enhances productivity under drought stress
WSL1	LOC_Os06g39750	Involved in the biosynthesis of cuticular wax in rice leaves [120] WHITE STRIPED LEAF1	↑ WUE Reinforces leaf cuticle to reduce evaporation
OsMyb6	LOC_Os06g10350	Overexpression in rice improves drought and salinity tolerance [121] MYB-TKF6	↑ WUE Overexpression enhances stress response and water retention
OsPIP1;1	LOC_Os02g44630	facilitate osmotic water transport across membranes [122] PLASMAMEMBRANE INTRINSIC PROTEIN1;1	± WUE Can improve water uptake or increase loss depending on conditions
OsPIP2;1	LOC_Os07g26690	contributes to water transport and is highly expressed in roots and leaves [122] PLASMAMEMBRANE INTRINSIC PROTEIN1;1	± WUE Context-dependent water transport regulation
OsNAC6	LOC_Os01g66120	Regulates stress responses, including drought tolerance, by modulating root architecture and other physiological traits. Overexpressing transgenic plants displayed an accelerated leaf senescence phenotype at the grain-filling stage [123] NAM, ATAF1/2, and CUC2-FAMILY6	± WUE Accelerates senescence; balance needed for net benefit
OsDREB2B	LOC_Os05g27930	Involves in water- and heat-shock stress responses and tolerance [124] DEHYDRATION-RESPONSE ELEMENT-BINDING PROTEIN2	↑ WUE Boosts adaptive response under stress
OsbZIP23	LOC_Os02g52780	Overexpression shows improved tolerance to drought and high-salinity stresses and sensitivity to ABA [125] BASIC-ZIPPER23	↑ WUE Enhances tolerance through ABA sensitivity
CFL1	LOC_Os02g31140	Reduced expression resulted in the reinforcement of cuticle structure [126] CURLY FLAG LEAF1	↑ WUE Reduced expression improves barrier to water loss
OsCHR4	LOC_Os07g31450 LOC_Os07g32430	regulates leaf morphogenesis and cuticle wax formation [127] CHROMATIN REMODELLING FACTOR4	↑ WUE Enhances wax formation for water conservation
OsABA8OX3	LOC_Os09g28390	Control ABA level and drought stress resistance in rice [128] ABA 8´HYDROXYLASE3	↑ WUE Enhances wax formation for water conservation
OsAPX7	LOC_Os04g35520	involved in signalling transduction pathways related to drought stress response [129] ASCORBATE PEROXIDASE7	↑ WUE Activates antioxidant pathways under stress
OsTPS1	LOC_Os01g23530 LOC_Os05g44210 LOC_Os05g44310 LOC_Os05g44300 LOC_Os08g34580	enhance the abiotic stress tolerance by increasing the amount of trehalose and proline [130] TREHALOSE-6-PHOSPHATE SYNTHASE1	↑ WUE Accumulates osmoprotectants for drought resilience

Table 1. Comprehensive list of rice genes involved in (A) stomatal and (B) non-stomatal leaf traits affecting water use efficiency. The table includes genes spanning key functional categories including stomatal development and regulation, cuticular wax biosynthesis, leaf morphology, stress response pathways, and metabolic adaptations. Locus IDs correspond to the Rice Annotation Project and were verified via the SNP-Seek database from the International Rice Research Institute [100]. Directional trends in the WUE Association column indicate: ↑ = positive association with increased WUE (gene overexpression or enhanced function improves water use efficiency); ↓ = negative association with WUE (gene overexpression or enhanced function reduces water use efficiency); ± = variable or context-dependent association (effects depend on environmental conditions, genetic background, or developmental stage).

A. Stomatal leaf Traits
Gene	Locus ID	Role	WUE Association
OsEP3	LOC_Os02g15950	Regulates stomatal guard cell development [101]. ERECT PANICLE3	↑ WUE Optimises stomatal development for better water regulation
OsKAT1	LOC_Os01g55200	Regulates stomatal opening and closing by facilitating potassium ion flux, which directly affects stomatal movement and plant water regulation [102,103] K+ TRANSPORTER 1	↑ WUE improves stomatal control
OsSDD1	LOC_Os03g0143100	Mutations lead to higher stomatal density [13] STOMATAL DENSITY AND DISTRIBUTION	↓ WUE increases water loss via excess stomata
OsTMM	LOC_Os01g02060	Mutations can lead to irregular stomatal spacing, affecting gas exchange efficiency [13]. TOO MANY MOUTHS	↓ WUE disrupts stomatal patterning
OsEPF1	LOC_Os04g0637300	Overexpress reduce stomatal density [36] EPIDERMAL PATTERNING FACTOR1	↑ WUE reduces transpiration
OsSPCH1	LOC_Os06g33450	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to guard mother cell (GMC) identity. Overexpression expression leads to higher stomatal density [33,104] SPEECHLESS1	↓ WUE Overexpression results in increased water loss
OsSPCH2	LOC_Os02g15760	alterations in stomatal size and density in stress conditions. Overexpression increases density [13,105] SPEECHLESS2	↓ WUE Overexpression results in increased water loss
OsMUTE	LOC_Os05g51820	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to GMC identity. Involves in the differentiation of stomatal precursor cells. It plays a critical role in determining stomatal size by regulating the development of guard cells [104]	↑ WUE ensures proper stomatal function
OsFAMA	LOC_Os05g50900	Essential for the initiation of stomatal lineage, termination of meristemoid fate and the transition to GMC identity [104]	↑ WUE Maintains correct stomatal identity for optimal function
OsFLP	LOC_Os07g43420	Regulates the orientation of GMC symmetrical division [104] FOUR LIPS	↑ WUE Regulates stomatal spacing for efficient gas exchange
B. Non-stomatal leaf traits
Gene	Locus ID	Role	WUE Association
OSH43	LOC_Os03g56110 LOC_Os03g57560	Overexpression results in broader leaves, increased tiller number, and more flowers [106]. ORYZA SATIVA HOMEOBOX43	↑ WUE No direct evidence.
OsABCG9	LOC_Os04g44610	Mutations can lead to reduced cuticular wax content, resulting in increased sensitivity to drought and other environmental stresses[107]	↓ WUE Mutation increases drought sensitivity due to water loss
GL1	LOC_Os05g02730	controlling wax synthesis in rice leaves [108] GLOSSY1	↑ WUE Improves cuticle barrier to reduce water loss
OSGL1-1	LOC_Os09g25850 LOC_Os09g25850	Increase leaf cuticular wax deposition and enhance drought tolerance [60] GLOSSY1-1	↑ WUE Enhances drought resistance
OsGL1-2	LOC_Os02g08230	Overexpression increases cuticular wax production and improves drought tolerance [108] GLOSSY1-2	↑ WUE Overexpression reduces water loss
OsWR1	LOC_Os02g10760	Overexpression increases the expression of genes involved in wax synthesis [109] WAX SYNTHESIS REGULATORY GENE1	↑ WUE Overexpression reduces water loss
OsCutA1	LOC_Os10g23204	Overexpression increases cuticular wax production and improves drought tolerance, a promising gene for engineering rice plants with enhanced drought tolerance [59]	↑ WUE Overexpression reduces water loss
YGL1	LOC_Os05g28200	Overexpression results in darker green leaves, increased chlorophyll content, and increased photosynthetic activity. This leads to improved growth and increased yields [110]YELLOW-GREEN LEAF1	↑ WUE Overexpression improves carbon assimilation efficiency
OsHB2	LOC_Os10g33960	Overexpression of the OsHB2 gene results in longer roots, broader leaves, and increased tolerance to drought and salinity stress [111] HOMOEOBOX1	↑ WUE Overexpression improves water capture and leaf area for photosynthesis
RCN1	LOC_Os11g05470	Inhibiting flowering transition and delaying heading under drought. Many rachis branches in the panicle and high yield [112] ROOTS CURL IN NAPHTHYLPHTHALAMIC ACID1	± WUE Delays maturity but may improve yield under drought
OsCKX2	LOC_Os01g10110	Produce larger leaves, more flowers, and higher yields [113] CYTOKININ OXIDASE/DEHYDROGENASE2	↑ WUE Improves resource allocation for higher yield
Gn1a	LOC_Os01g10110	Improves grain yield, resulting in more flowers and larger grains [114] GRAIN NUMBER 1a identical to CKX2	↑ WUE Increases yield potential under stress
NAL3	LOC_Os12g01120	Overexpression results in broader leaves, reduced tiller number, increased lateral root development, and larger grains [115]NARROW LEAF3	↑ WUE Overexpression enhances soil water access and light interception
NRL1	LOC_Os12g37190	Overexpression results in wider leaves, increased plant height, larger vascular bundles, stronger stems, and higher yields [106,116] NARROW AND ROLLED LEAF1	↑ WUE Overexpression improves plant robustness and water transport
NAL1	LOC_Os04g52479	Overexpression results in broader leaves, reduced tiller number, increased lateral root development, and larger grains [117] NARROW LEAF1	↑ WUE Improves growth under water-limited conditions
NAL7	LOC_Os03g06654	Increased expression could have wider leaves, taller plants, and higher yields [106,117]. NARROW LEAF7	↑ WUE Enhances light interception and productivity
OsSPL14	LOC_Os08g39890	Regulates tiller number and panicle branching, which can also lead to increased grain yield [118]. SQUAMOSA PROMOTOR BINDING PROTEIN-LIKE14	↑ WUE Enhances yield per unit water use
OsSPL9	LOC_Os05g33810	Increases grain number per panicle and yield, and regulates drought tolerance, which can improve rice performance in dry environments [119]. SQUAMOSA PROMOTOR BINDING PROTEIN-LIKE9	↑ WUE Enhances productivity under drought stress
WSL1	LOC_Os06g39750	Involved in the biosynthesis of cuticular wax in rice leaves [120] WHITE STRIPED LEAF1	↑ WUE Reinforces leaf cuticle to reduce evaporation
OsMyb6	LOC_Os06g10350	Overexpression in rice improves drought and salinity tolerance [121] MYB-TKF6	↑ WUE Overexpression enhances stress response and water retention
OsPIP1;1	LOC_Os02g44630	facilitate osmotic water transport across membranes [122] PLASMAMEMBRANE INTRINSIC PROTEIN1;1	± WUE Can improve water uptake or increase loss depending on conditions
OsPIP2;1	LOC_Os07g26690	contributes to water transport and is highly expressed in roots and leaves [122] PLASMAMEMBRANE INTRINSIC PROTEIN1;1	± WUE Context-dependent water transport regulation
OsNAC6	LOC_Os01g66120	Regulates stress responses, including drought tolerance, by modulating root architecture and other physiological traits. Overexpressing transgenic plants displayed an accelerated leaf senescence phenotype at the grain-filling stage [123] NAM, ATAF1/2, and CUC2-FAMILY6	± WUE Accelerates senescence; balance needed for net benefit
OsDREB2B	LOC_Os05g27930	Involves in water- and heat-shock stress responses and tolerance [124] DEHYDRATION-RESPONSE ELEMENT-BINDING PROTEIN2	↑ WUE Boosts adaptive response under stress
OsbZIP23	LOC_Os02g52780	Overexpression shows improved tolerance to drought and high-salinity stresses and sensitivity to ABA [125] BASIC-ZIPPER23	↑ WUE Enhances tolerance through ABA sensitivity
CFL1	LOC_Os02g31140	Reduced expression resulted in the reinforcement of cuticle structure [126] CURLY FLAG LEAF1	↑ WUE Reduced expression improves barrier to water loss
OsCHR4	LOC_Os07g31450 LOC_Os07g32430	regulates leaf morphogenesis and cuticle wax formation [127] CHROMATIN REMODELLING FACTOR4	↑ WUE Enhances wax formation for water conservation
OsABA8OX3	LOC_Os09g28390	Control ABA level and drought stress resistance in rice [128] ABA 8´HYDROXYLASE3	↑ WUE Enhances wax formation for water conservation
OsAPX7	LOC_Os04g35520	involved in signalling transduction pathways related to drought stress response [129] ASCORBATE PEROXIDASE7	↑ WUE Activates antioxidant pathways under stress
OsTPS1	LOC_Os01g23530 LOC_Os05g44210 LOC_Os05g44310 LOC_Os05g44300 LOC_Os08g34580	enhance the abiotic stress tolerance by increasing the amount of trehalose and proline [130] TREHALOSE-6-PHOSPHATE SYNTHASE1	↑ WUE Accumulates osmoprotectants for drought resilience

4.4. WUE Optimization Strategies Between Traditional and Dryland Rice Farming Systems

Rice cultivation spans a diverse range of agroecosystems, from continuously flooded lowland paddies to water-limited upland or dryland fields. These contrasting environments impose distinct physiological constraints and selection pressures on rice plants, resulting in divergent strategies for optimising WUE. Figure 2 compares key physiological, anatomical, and agronomic traits of rice grown in traditional paddy systems versus dryland/upland systems.

In traditional irrigated paddy systems, the presence of standing water creates a saturated microenvironment with high humidity and low evaporative demand. This decouples plant water status from atmospheric vapor pressure deficit (VPD), reducing transpirational losses [131]. Consequently, irrigated rice typically develops shallow root systems and extensive aerenchyma tissue to facilitate internal oxygen transport under anaerobic conditions. Stomatal conductance in these systems tends to be relatively high and less responsive to VPD fluctuations. Additionally, non-stomatal adaptations such as epicuticular wax deposition and leaf rolling are minimal, as the consistently moist conditions reduce the need for such drought-avoidance traits [6,132,133,134].

In contrast, dryland or upland rice is cultivated under aerobic conditions where water availability is often intermittent and limiting. These environments favor more conservative water use strategies. Upland rice varieties typically exhibit deeper and more highly branched root systems to access subsoil moisture. They also demonstrate tighter stomatal regulation, with greater sensitivity to both soil water potential and atmospheric VPD. Non-stomatal adaptations are more pronounced, including increased epicuticular wax accumulation, enhanced leaf rolling during drought stress, and the production of osmoprotectants such as proline and soluble sugars that help maintain cellular integrity under dehydration [6].

Management practices to enhance WUE also differ significantly between the two systems. In irrigated paddy fields, techniques like AWD have been adopted to reduce water inputs while maintaining yield stability. This method intermittently drains fields to encourage deeper rooting and reduce methane emissions. In dryland systems, practices such as mulching, deficit irrigation, and optimised planting densities are employed to reduce surface evaporation, improve soil moisture retention, and enhance root-soil contact [135,136]. These contrasting strategies underscore the importance of context-specific breeding and agronomic interventions. While some core physiological principles of WUE, such as efficient stomatal control and root system architecture, are relevant across systems, their functional significance and genetic regulation vary with environmental and management conditions.

5. Future Perspectives and Research Directions

The exploration of WUE in rice is entering an exciting new era, driven by technological advances and interdisciplinary approaches. This last section examines emerging technologies that are revolutionising our ability to study leaf traits and WUE, from high-resolution imaging techniques to multi-omics approaches (Table 2). It also addresses the key challenges facing researchers and breeders in developing water-efficient rice cultivars and discusses the broader implications of this work for sustainable agriculture and climate resilience. By highlighting these future directions, we aim to provide a roadmap for researchers and emphasise the critical importance of continued innovation in this field.

5.1. Emerging Technologies and Approaches for Studying Leaf Traits and WUE

Recent technological advancements have revolutionised our ability to study leaf traits and WUE in rice at unprecedented levels of detail and scale. These innovations span a wide range of disciplines, from advanced imaging techniques to molecular biology approaches, offering researchers powerful new tools to unravel the complexities of plant-water interactions. Confocal microscopy offers high-resolution, 3D images of leaf tissues, focusing on cellular structures and stomatal dynamics [137]. Its advantage lies in cellular-level visualisation, but it is limited to small sample sizes and controlled environments. Thermal imaging with infrared thermography measures canopy temperature, indicating plant water status and transpiration rates. This method is rapid and non-invasive, yet sensitive to environmental fluctuations such as wind and ambient temperature [138,139]. X-ray micro-computed tomography (Micro-CT) and magnetic resonance imaging (MRI) provide non-destructive 3D imaging of leaf anatomy and water distribution. These offer exceptional anatomical insights but require costly equipment and may not be feasible for field-scale studies [140,141]. Chlorophyll fluorescence imaging, such as pulse amplitude modulation (PAM) fluorometry, assesses photosynthetic efficiency. While informative, its interpretation requires specialised knowledge, and results can vary depending on leaf age and environmental stress [142,143]. Field-based platforms use sensors and imaging systems on tractors [144], while greenhouses and growth chambers utilise automated systems to monitor conditions [145]. Unmanned aerial vehicles (UAVs) equipped with multispectral, hyperspectral, and thermal cameras capture data on plant health and water status from above [146]. UAVs enable rapid coverage of large areas but depend on weather and require data processing expertise [147]. Hyperspectral imaging captures detailed spectral information to assess physiological and biochemical traits [148]. Light detection and ranging (LIDAR) creates high-resolution 3D maps of plant structures, helping to evaluate leaf area, canopy architecture, and how these factors influence light interception, transpiration, and overall water use [149]. Both tools provide deep insights into spatial traits, though data complexity and processing time remain significant challenges.

In addition to the stable carbon isotopes in Δ¹³C, oxygen and hydrogen isotopes (δ18O) and δ2H) offer insights into water sources and usage dynamics [150]. Near-infrared spectroscopy (NIRS) can also analyse the chemical composition of plant tissues, which correlates with water content and WUE [151]. Raman spectroscopy analyses molecular compositions and structures to study biochemical changes in leaves [152]. These spectroscopic methods are fast and non-destructive but may require calibration against destructive sampling methods [153].

Genomic approaches like CRISPR-Cas9 and gene editing, along with transcriptomics, proteomics, and metabolomics, are powerful tools for studying WUE. CRISPR-Cas9 enables precise gene modifications to improve WUE, while transcriptomics and proteomics analyse gene expression and protein profiles to identify key WUE regulators [154]. Metabolomics examines the complete set of plant metabolites to understand metabolic pathways related to water use and stress responses [155]. These molecular approaches allow for targeted breeding and trait discovery, though they are resource-intensive and require validation under field conditions.

Big data and machine learning are transforming the study of WUE by using predictive modelling to combine environmental, genomic, and phenotypic data for optimising breeding strategies. Machine learning algorithms analyse large datasets to identify patterns affecting WUE, such as soil moisture and climate conditions [156]. Satellite imagery and geographic information systems (GIS) provide large-scale vegetation, soil, and climate data to monitor and manage WUE across regions. Smart irrigation systems utilise soil moisture sensors and weather forecasts to optimise water use and reduce waste [157]. While these digital tools offer scalability and precision, their effectiveness depends on data quality, infrastructure, and model accuracy.

Compared to traditional methods, such as manual trait measurements, gas exchange analysis using portable photosynthesis systems, or basic soil moisture probes, these emerging technologies offer greater speed, scale, precision, and data integration. However, they also demand higher technical expertise, infrastructure, and investment. A balanced application that combines traditional and emerging methods may provide the most comprehensive insight into rice physiology and WUE improvement [158].

5.2. Challenges in Developing Water-Efficient Rice Cultivars

Despite significant advances in our understanding of WUE in rice, the development of water-efficient cultivars faces several complex challenges. These obstacles span genetic, physiological, and agronomic domains, necessitating a multidisciplinary approach to breeding and crop improvement. Key challenges include the trade-off between improving WUE and potential reductions in biomass or yield. Genetic complexity is another challenge, as WUE is influenced by many genes and their interactions with the environment [71,168]. Additionally, the diversity of rice-growing ecosystems, from flooded paddies to rainfed fields, necessitates a multifaceted approach to breeding [169]. Therefore, variations in soil type, fertility, and water-holding capacity further complicate efforts to develop effective cultivars.

High-throughput phenotyping for WUE can be challenging due to the technical difficulty and cost of advanced technologies, which may not be accessible to all breeding programs, especially in developing countries. Additionally, traditional rice farming practices and the historical significance of rice cultivation may lead to resistance among traditional farmers to adopt new cultivars due to concerns about their performance or preference for established methods.

Implications for sustainable agriculture and climate resilience. The development of water-efficient rice cultivars has far-reaching implications that extend beyond immediate agricultural productivity, touching on global issues of food security, environmental sustainability, and climate change adaptation. By addressing these critical challenges, advances in rice WUE have the potential to transform agricultural practices and contribute significantly to sustainable development goals. Developing and using water-efficient rice cultivars can reduce irrigation needs, conserving water resources and supporting agriculture in water-scarce areas. This approach lowers energy requirements for water distribution, promotes sustainable farming, and ensures stable yields despite variable water availability, enhancing food security and farmer incomes, especially in drought-prone regions. By improving crop resilience to water stress, these cultivars help farmers adapt to climate change, minimize crop failure risks, and reduce economic losses. Additionally, efficient water use can decrease methane emissions from flooded fields and benefit local ecosystems by lessening the depletion of natural water bodies [1,170,171].

A comprehensive understanding of the interplay between stomatal and non-stomatal traits is vital for enhancing WUE in rice under climate variability. Stomatal traits directly influence transpiration and gas exchange, while non-stomatal traits; such as leaf morphology, cuticular wax load, and root architecture; contribute to water retention and drought adaptation. Together, these traits modulate the plant’s physiological response to biotic and abiotic stresses, offering complementary pathways to improve WUE without compromising yield potential. Integrating both trait types in breeding strategies supports the development of cultivars that are better adapted to diverse and water-limited environments, aligning with the broader goals of sustainable agriculture and climate resilience [13,91].

5.3. Interaction with Root Traits

Another important consideration that is often overlooked is that WUE in rice involves a complex interaction between leaf and root traits. Deeper rooting in rice genotypes increases WUE under drought conditions by reducing the internal concentration of CO₂ (Ci) within the leaf, highlighting variability in root traits and gas exchange parameters among genotypes. Extensive root systems help plants access more water, but efficient stomatal control is vital to prevent excessive water loss. Roots signal leaves to adjust stomatal conductance based on soil water availability. Efficient WUE enhances root growth by providing more photosynthates, further improving water acquisition [11]. It was found that gs and transpiration rates decrease during soil drying before leaf water potential declines, indicating the importance of root signaling [172]. Hence, the interaction of leaf and root traits in enhancing WUE is also an underexplored area of study that warrants further investigation.

6. Towards Enhanced WUE in Rice

The concept map in Figure 3 encapsulates the complex nature of WUE in rice, highlighting the intricate relationships between stomatal and non-stomatal traits. This visual representation underscores the complexity of WUE as a trait and the need for integrated approaches in future research and breeding efforts. Stomatal traits such as density, size, and conductance interact closely with non-stomatal factors like leaf anatomy, photosynthetic efficiency, and metabolic adaptations. The integration and optimisation branch of the map emphasises the importance of considering trade-offs between these traits and leveraging emerging technologies for crop improvement. This holistic view guides future research directions, suggesting that advancements in WUE will likely come from a synergistic approach that combines traditional breeding with cutting-edge technologies like CRISPR gene editing and high-throughput phenotyping. The map also highlights the critical role of environmental interactions, reminding researchers of the need to develop rice varieties that maintain high WUE across diverse and changing climatic conditions.

Moving forward, the challenge lies in translating this complex understanding into practical breeding strategies and agronomic practices. Interdisciplinary collaboration will be key, bringing together expertise in plant physiology, genetics, agronomy, and data science. By addressing the interconnected aspects of WUE illustrated in this concept map, researchers can develop more resilient and water-efficient rice varieties, contributing significantly to sustainable agriculture in the face of global water scarcity and climate change.

7. Conclusion

There is an intricate relationship between stomatal and non-stomatal leaf traits and both collectively have an impact on WUE in rice. Understanding the complex interactions among these traits is essential for developing rice varieties with improved WUE, as well as for implementing agronomic practices that optimise water management in rice cultivation. Further investigation will reveal specific beneficial varieties for special agronomic practices. By focusing on both stomatal and non-stomatal leaf traits, researchers can develop climate-resilient rice varieties that ensure food security for future generations. Insights from this review can guide breeding programs to develop new crop varieties with enhanced WUE, ensuring sustainable production in water-scarce regions. Precision agriculture practices can be optimised based on specific leaf traits linked to efficient water use. The review offers a foundation for future research aimed at elucidating the mechanisms of WUE, facilitating the discovery of novel genetic targets and pathways.