Plants are permanently facing challenges imposed by the environment which, in the context of the current scenario of global climate change, implies a constant process of adaptation to survive and even, in the case of crops, at least maintain yield. O₂ deficiency at the rhizosphere level, i.e., root hypoxia, is one of the factors with the greatest impact at whole-plant level. At cellular level, this O₂ deficiency provokes a disturbance in the energy metabolism which has notable consequences on the yield of plant crops. In this sense, although several physiological studies describe processes involved in plant adaptation to root hypoxia in woody fruit trees, with emphasis on the negative impacts on photosynthetic rate, there are very few studies that include -omics strategies for specifically understanding these processes in the roots of such species. Through a de novo assembly approach, a comparative transcriptome study of waterlogged Prunus spp. genotypes contrasting in their tolerance to root hypoxia was revisited in order to gain a deeper insight into the reconfiguration of pivotal pathways involved in energy metabolism. This re-analysis describes the classically altered pathways seen in the roots of woody fruit trees under hypoxia, but also routes that link them to pathways involved with nitrogen assimilation and the maintenance of cytoplasmic pH and glycolytic flow. In addition, the effects of root hypoxia on the transcription of genes related to the mitochondrial oxidative phosphorylation system, responsible for providing adenosine triphosphate (ATP) to the cell, are discussed in terms of their roles in the energy balance, reactive oxygen species (ROS) metabolism and aerenchyma formation. This review compiles key findings that help to explain the trait of tolerance to root hypoxia in woody fruit species, giving special attention to their strategies for managing the energy crisis. Finally, research challenges addressing less-explored topics in recovery and stress memory in woody fruit trees are pointed out.

Severe water stress can lead to hydraulic disfunction, reducing plant conductance or even causing death. Some plants exhibit hydraulic vulnerability segmentation between organs to reduce this risk. However, its role in influencing drought tolerance and resistance in grafted plants, such as grapevine, remains unclear. This study evaluates the physiological responses, drought tolerance, hydraulic vulnerability segmentation, and xylem anatomy of 2-year-old Vitis vinifera cv. Tempranillo scion grafted onto two rootstocks: 110-Richter (110R) and Sélection Oppenheim 4 (SO4). After subjecting the plants to drought conditions until the onset of embolism in the leaf (water potential corresponding to 12% loss of xylem hydraulic conductivity, P12), we analysed the physiological consequences during recovery. Grapevine exhibits hydraulic vulnerability segmentation not only within scion organs but also between the scion and rootstock. Although no differences in scion drought tolerance and embolism resistance were observed between combinations, Tempranillo-110R exhibited higher leaf minimum conductance, leaf P12 values, and root biomass. In contrast, Tempranillo-SO4 displayed larger vessel diameter and higher hydraulic conductance. These differences may explain the slower recovery of Tempranillo-110R compared with Tempranillo-SO4, which showed higher stomatal and root-to-stem hydraulic conductance. These findings indicate that in selecting rootstock, consideration should be given to drought resilience alongside vigour and productivity, especially given the increasing occurrence of severe drought periods due to climate change.

Soil waterlogging adversely impacts most plants. Melilotus siculus is a waterlogging-tolerant annual forage legume, but data were lacking for the effects of root-zone hypoxia on nodulated plants reliant on N2 fixation. The aim was to compare the waterlogging tolerance and physiology of M. siculus reliant on N2 fixation or with access to NO3-. A factorial experiment imposed treatments of water level (drained or waterlogged), rhizobia (nil or inoculated) and mineral N supply (nil or 11 mm NO3-) for 21 d on plants in pots of vermiculite in a glasshouse. Nodulation, shoot and root growth and tissue N were determined. Porosity (gas volume per unit tissue volume) and respiration rates of root tissues and nodules, and O2 microelectrode profiling across nodules, were measured in a second experiment. Plants inoculated with the appropriate rhizobia, Ensifer (syn. Sinorhizobium) medicae, formed nodules. Nodulated plants grew as well as plants fed NO3-, both in drained and waterlogged conditions. The growth and total N content of nodulated plants (without any NO3- supplied) indicated N2 fixation. Respiration rates (mass basis) were highest in nodules and root tips and lowest in basal root tissues. Secondary aerenchyma (phellem) formed along basal root parts and a thin layer of this porous tissue also covered nodules, which together enhanced gas-phase diffusion of O2 to the nodules; O2 was below detection within the infected zone of the nodule interior. Melilotus siculus reliant on N2 fixation grew well both in drained and waterlogged conditions, and had similar tissue N concentrations. In waterlogged conditions the relatively high respiration rates of nodules must rely on O2 movement via the aerenchymatous phellem in hypocotyl, roots and the outer tissue layers of nodules.