The role of root systems in drought tolerance is a subject of very limited information compared with above-ground responses. Adjustments to the ability of roots to supply water relative to shoot transpiration demand is proposed as a major means for woody perennial plants to tolerate drought, and is often expressed as changes in the ratios of leaf to root area (A_L:A_R). Seasonal root proliferation in a directed manner could increase the water supply function of roots independent of total root area (A_R) and represents a mechanism whereby water supply to demand could be increased. To address this issue, seasonal root proliferation, stomatal conductance (g_s) and whole root system hydraulic conductance (k_r) were investigated for a drought-tolerant grape root system (Vitis berlandieri×V. rupestris cv. 1103P) and a non-drought-tolerant root system (Vitis riparia×V. rupestris cv. 101-14Mgt), upon which had been grafted the same drought-sensitive clone of Vitis vinifera cv. Merlot. Leaf water potentials (ψ_L) for Merlot grafted onto the 1103P root system (–0.91±0.02 MPa) were +0.15 MPa higher than Merlot on 101-14Mgt (–1.06±0.03 MPa) during spring, but dropped by approximately –0.4 MPa from spring to autumn, and were significantly lower by –0.15 MPa (–1.43±0.02 MPa) than for Merlot on 101-14Mgt (at –1.28±0.02 MPa). Surprisingly, g_s of Merlot on the drought-tolerant root system (1103P) was less down-regulated and canopies maintained evaporative fluxes ranging from 35–20 mmol vine⁻¹ s⁻¹ during the diurnal peak from spring to autumn, respectively, three times greater than those measured for Merlot on the drought-sensitive rootstock 101-14Mgt. The drought-tolerant root system grew more roots at depth during the warm summer dry period, and the whole root system conductance (k_r) increased from 0.004 to 0.009 kg MPa⁻¹ s⁻¹ during that same time period. The changes in k_r could not be explained by xylem anatomy or conductivity changes of individual root segments. Thus, the manner in which drought tolerance was conveyed to the drought-sensitive clone appeared to arise from deep root proliferation during the hottest and driest part of the season, rather than through changes in xylem structure, xylem density or stomatal regulation. This information can be useful to growers on a site-specific basis in selecting rootstocks for grape clonal material (scions) grafted to them.

Viticulture is facing emerging challenges not only because of the effect of climate change on yield and composition of grapes, but also of a social demand for environmental‐friendly agricultural management. Adaptation to these challenges is essential to guarantee the sustainability of viticulture. The aim of this review is to present adaptation possibilities from the soil‐hidden, and often disregarded, part of the grapevine, the roots. The complexity of soil–root interactions makes necessary a comprehensive approach taking into account physiology, pathology and genetics, in order to outline strategies to improve viticulture adaptation to current and future threats. Rootstocks are the link between soil and scion in grafted crops, and they have played an essential role in viticulture since the introduction of phylloxera into Europe at the end of the 19th century. This review outlines current and future challenges that are threatening the sustainability of the wine sector and the relevant role that rootstocks can play to face these threats. We describe how rootstocks along with soil management can be exploited as an essential tool to deal with the effects of climate change and of emerging soil‐borne pests and pathogens. Moreover, we discuss the possibilities and limitations of diverse genetic strategies for rootstock breeding.

Climate change, and specifically global temperature increase, is expected to alter plant phenology. Temperate deciduous fruit trees have cultivar-specific chill and heat requirements to break dormancy and bloom. In this study, we aimed to estimate chill and heat requirements (in chill portions, CP, and growing degree hours, GDH, respectively) of 25 almond (30–36 years) and 12 apple (14–26 years) cultivars grown under a Mediterranean climate. The set included early and late blooming genotypes. Long-term phenological and temperature records were analyzed by means of partial least squares (PLS) regression. The main difference between early and late genotypes was chill requirement, ranging from 8.40 CP of early genotypes to 55.41 CP of extra-late genotypes. However, as chill requirements are quite easily attained by all almond cultivars in this study, year-to-year variations in actual blooming dates for each genotype are governed by variability of mean forcing temperatures. In contrast, different chill and heat combinations resulted in similar mean blooming dates for the studied apple cultivars. Mean temperature in both chilling and forcing phases determined their blooming time in the location studied. Overlaps and gaps between both phases were obtained. Despite some limitations, the PLS analysis has proven to be a useful tool to define both chilling and forcing phases. Nevertheless, since the delineation of these phases determine the total amount of CP and GDH, further efforts are needed to investigate the transition of these phases.