Several studies which reported correlations between root structural traits and plant performance under drought are summarized and presented in Table 1 and Figure 1a,b. Identifying these drought-responsive structural traits in different crops will facilitate plant breeders to utilize these traits for screening drought tolerant genotypes.

Root drought-responsive structural traits are not static but fluctuate readily in conjunction with the environment, management practice, soil microbes, and genotype. Moreover, different root traits interact, sometimes synergistically or antagonistically, affecting drought adaptation. Thus, careful consideration is needed when planning drought-resistant crops based on structural traits only. However, crop-specific drought-responsive structural traits (Table 1) are easy to phenotype and implement for screening genotypes. Therefore, it has importance in terms of ease of applicability and achieving fast results in developing drought-resistant crops.

2. Root Anatomical Responses to Drought

Plants invest photosynthates in establishing root systems for exploring water and nutrients needed for metabolic processes. During drought, the expenditure of photosynthates is high, firstly to invest more in root growth to increase water uptake, and secondly to increase respiration to maintain roots in drying soil, thus, compromising plant productivity [34,35]. Anatomical adaptation during drought reduces metabolic costs and allows plants to distribute resources for further resource acquisition, growth, and essential physiological activities, resulting in improved yield. Chimungu et al. [36] reported cortical tissue with fewer but larger cell sizes, and low cortical cell file numbers in maize reduced metabolic cost by decreasing respiration rates during drought. Large cortical genotypes had increased root growth and water acquisition, deeper roots, better stomatal conductance and leaf CO₂ assimilation, and greater shoot biomass and grain yield. Colombi et al. [34] reported a similar result in wheat, where a genotype with a large root cortical cell diameter significantly reduced root penetration metabolic cost. During drought, root cortical tissue lysed and creates an intercellular vacuum space, cortical aerenchyma [37] (Figure 1c), the formation of which can reduce metabolic costs. This mostly occurs in older roots that no longer take up water efficiently [37], thus having minimal negative impact on water uptake. Instead, it reduces soil exploration metabolic costs [35,38], permits root growth, and improves soil resource acquisition in dry conditions [35]. Under water stress, maize genotypes with high root cortical aerenchyma had 30% more shoot biomass [39].

Water deficit in the soil increases mechanical impedance, thus restricting root penetration into deep soil, which hinders resource capture, consequently reducing crop productivity [40]. Anatomical adaptation facilitates improving root penetration in drying soil. For example, smaller outer cortical cells stabilize the root against ovalization, prevent collapsing, and allow the root to penetrate soil. In contrast, large mesodermis cortical cells and thick axial roots with more aerenchyma reduce the metabolic cost of soil exploration and allow root growth in hard soils [41]. In deep rooting maize genotypes, the roots generated from node three had a reduced cell file number and increased middle cortical area; while the roots generated from node four had increased aerenchyma [38]. Maize and wheat genotypes with multiseriate cortical sclerenchyma had a 22% increase in deep soil penetration and a 49% increase in shoot biomass compared to genotypes that lacked it [33]. These genotypes also had small cells with thick walls in outer cortical tissue, increased root lignin concentration, tensile strength, and root tip bending force.

Roots absorb water and nutrients through the root epidermis, hairs, and avascular mycorrhizal (AM) hyphae. The AM colonize in root cortical cells and extend their hyphae into the soil, sometimes expanding soil volume exploration at least 15 cm beyond the root surface [42]. The AM receives organic C from the root and, in return, delivers nutrients to the root [43]. This mutual relationship increases drought resistance and reduces yield loss [44,45,46,47]. Root anatomical traits play an essential role in microbial symbiosis. In maize, larger root diameters and larger aerenchyma lacunae increase mycorrhizal colonization, whereas increased aerenchyma and decreased living cortical area reduce mycorrhizal colonization [31]. Cortex thickness is also crucial for AM colonization in woody species [48,49]. Dreyer et al. [50] reported that a continuous sclerenchymatic ring in the outer cortex and aerenchyma in the inner cortex decrease AM colonization in three palm species. They suggested that the sclerenchymatic ring acts as a physical barrier preventing penetration of AM fungal, while the empty aerenchyma area reduces the available tissue in the root for AM colonization.

Root anatomical traits have a substantial influence on water uptake. Through concentric layers of root cells, water first enters from the soil to the root stele, then into the xylem, and finally into the shoot [2]. Transportation in the xylem is vertical, as casparian strips limit radial movement, with the size and number of xylem vessels affecting the water transportation rate [51,52]. During root development, two types of xylem vessels are formed, the narrow protoxylem vessels and larger metaxylem vessels, through which the majority of the water is transported [51]. Prince et al. [30] reported soybean genotypes with large xylem vessels, increased xylem diameter, and metaxylem numbers performed well in water-limited environments. Large xylem vessels in olive (Olea eurpaea) increased root conductivity during drought stress, allowing deep rooting and extended water acquisition [53].

Phenotyping root anatomical traits is still low throughout, therefore, less research has focused on drought adaptive root anatomical traits. Further research in this area will improve phenotypic efficiency, accelerate the discovery of additional anatomical traits that assist directly in drought adaptation or indirectly through the facilitation of AM colonization, and ultimately contribute to developing drought-resilient crops.