Root growth and nitrate uptake by wheat (Triticum aestivum L.) following wetting of dry surface soil

The nitrate uptake capacity of surface roots of spring wheat(Triticum aestivum L. cv. Kulin) was investigated followingwetting of dry surface soil. Plants were grown to stem elongationstage with adequate watering at depth while the surface soilwas allowed to dry. Eight weeks after sowing, water or a ¹⁵N-nitratesolution was added to the surface soil to simulate rainfall.Root growth and nitrate uptake were measured up to 4 d afterwetting on plants with unconfined nodal root growth and on plantswith the majority of nodal roots confined within small vials.Prior to wetting, plants from both nodal treatments had seminalroots with collapsed cortices along the upper 10 cm and manyshort, viable lateral roots. Nodal roots, where present, wereonly a few cm long and unbranched. Only plants with unconfinednodal roots were able to take up nitrate within the 24 h beforeany new root growth. By 2 d after wetting there was significantgrowth of the seminal lateral roots, and rapid growth and branchingof nodal roots. From 2 d after wetting, plants with confinednodal roots also took up nitrate, presumably due to the growthof the seminal lateral roots. Hence it appears as though thenodal roots in the unconfined treatment could immediately takeup nitrate, but the seminal roots required new lateral rootgrowth to become active in nitrate uptake. The plants with confinednodal roots had a lower nitrate uptake than those with unconfinednodal roots 4 d after wetting, indicating that the seminal rootsystem was not able to compensate for lack of nodal roots. Insufficientnitrate was taken up after 4 d, by plants from either nodalroot treatment, to increase the shoot N concentration significantly. Key words: Triticum aestivum, nitrate uptake, drought, seminal roots, nodal roots     

Root-Tiller Interrelationships in Spring Barley (Hordeum distichum (L.) Lam.)

Root-tiller relations were investigated in spring barley grownin soil in deep pots. The total dry wt of the root system reachedits maximum 6 weeks from sowing, when the shoot weight was only50 per cent of its value at maturity. Seminal and nodal rootscomprised 40 and 60 per cent, respectively, of the total rootdry wt at maturity; the majority of the nodal root weight wasassociated with the main shoot. The main shoot had approximatelytwice as many nodal roots as either of the first two primarytillers (T1 and T2), and the primary and secondary tillers appearinglater were very poorly rooted. Some tillers, especially secondarytillers that died prematurely, produced no nodal roots. Theweight of the seminal roots and nodal roots attached to themain shoot continued to increase up to maturity but the drywt of nodal roots on tillers declined with time. This patternof growth was closely related to the pattern of ¹⁴C assimilateddistribution within the root system. A very small proportionof ¹⁴C assimilated by the main shoot and T1 and T2 was exported.The majority of the exported assimilate went to the seminalroot system and to nodal roots attached to the main shoot. Individualnodal and seminal roots seemed to have different roles in supplyingnutrients to the shoot system, with the former mainly providing³²P-phosphate to its tiller of origin and the latter generallysupplying the main shoot and primary tillers. Hordeum distichum. (L.) Lam., barley, root growth, nodal roots, seminal roots, tillering, assimilate distribution, ³²P-distribution     

Abscisic acid produced in dehydrating roots may enable the plant to measure the water status of the soil

Abstract. Maize plants were grown in 1-m-long tubes of John Innes No. 2 potting compost. From the start of the experimental period, half of the plants were unwatered. Stomatal conductance of these plants was restricted 6 d after last watering and continued to decline thereafter. This was despite the fact that as a result of solute accumulation, unwatered plants showed consistently higher leaf turgors than well-watered plants. Leaf water potentials of unwatered plants were not significantly lower than those of plants that were watered well. Main seminal and nodal roots showed solute regulation in drying soil and continued to grow even in the driest soil, and plants growing in drying soil showed consistently higher root dry weights than did well-watered plants, water potentials and turgors of the tips of fine roots in the upper part of the column decreased as the soil dried. Soil drying below a water content of around 0–25 g cm⁻³ (a bulk soil water potential of between -0.2 and -0.3 MPa) resulted in a substantial increase in the ABA content of roots. As soil columns dried progressively from the top, ABA content increased in roots deeper and deeper in the soil. These responses suggest that ABA produced by dehydrating roots and which was subsequently transported to the shoots provided a sensitive indication of the degree of soil drying.     

Effect of mutual shading on the emergence of nodal roots and the root/shoot ratio of maize

The effect of mutual shading on the root/shoot ratio and on the number of nodal roots of maize was studied. Plants of two varieties (Dea and LG2281) were grown in individual pots of 9 L, at three plant densities: 7.5, 11 and 15 plants m^–2. A control experiment was carried out in order to study if root growth was affected by the small size of the pots. Maize plants (cv Dea) were grown at a low plant density (7.5 plants m^–2) in pots of two different volumes (9 and 25 L respectively). In both experiments plants were watered every two hours with a nutrient solution. Some plants were sampled at five dates in the main experiment and the following data were recorded: foliar stage; root, stem and leaf dry weight; number of root primordia and number of emerged roots per phytomer. The final sampling date occurred at silking.Results of the control experiment showed that the root biomass was lower in small pots but the number of nodal roots per phytomer was not affected.Results of the main experiment showed that the total plant biomass and the root/shoot ratio were lower at high plant density. The number of emerged roots was strongly reduced on the upper phytomer (P₈). This reduction was mainly due to a lower percentage of root primordia which elongated. A proposed interpretation is that the number of roots which emerge on upper phytomers is controlled by carbohydrate availability.     

Plagiogravitropism of maize roots

The direction of root growth can be studied by analyzing the trajectories of roots growing in soil. Both the primary seminal root and nodal roots of maize attain a preferred, or liminal, angle of growth that deviates from the vertical. These roots are said to be plagiogravitropic. Experiments using plants grown in soil-filled boxes revealed that the primary seminal root is truly plagiogravitropic. It shows both positive and negative gravitropism in response to gravity stimuli and tends to maintain its direction even after growing around obstacles. These are experimental results suggesting that plagiogravitropic growth is controlled by internal factors. The orientation of the grain affects the establishment of the liminal angle of the primary seminal root, and both the position of their node of origin and the root diameter are closely related to the plagiogravitropic behaviour of nodal roots. Several external factors are also known to influence plagiogravitropism. Low soil water content causes a decrease in the angle of growth and soil mechanical resistance suppresses the gravitropic curvature. Plagiogravitropic behaviour of both seminal and nodal roots plays a significant role in shaping the root system.     

Performance of seminal and nodal roots of wheat in stagnant solution: K+ and P uptake and effects of increasing O2 partial pressures around the shoot on nodal root elongation

Roots of intact wheat plants were grown for 7-12 d in stagnant nutrient solution, containing 0.1% agar, to mimic the lack of convection in waterlogged soil. Net K+ and P uptakes by seminal and nodal roots were measured separately using a split root system. For seminal roots in stagnant solution, net uptakes as a percentage of aerated roots were between 0% and 16% for P, while K+ ranged between 15% uptake and 54% loss. For the more waterlogging-tolerant nodal roots, net uptakes in stagnant nutrient solution, as a percentage of aerated roots, were 31-73% for P and 69-115% for K+. Elongation rates of nodal roots in stagnant nutrient were about 35-43% of those for roots in aerated solution. This partial inhibition occurred in these nodal roots despite their 15% porosity (v/v). Elevation of O2 partial pressures around the shoots to 40 kPa and then to 80 kPa substantially accelerated nodal root elongation in stagnant solution, demonstrating that most of the inhibition seen with ambient O2 around the shoots was associated with a restricted O2 supply to these nodal roots. Thus, in wheat nodal roots, with a partial pressure of 20 kPa O2 around the shoots, O2 diffusion from the shoots did not completely relieve the restrictions on elongation resulting from stagnancy in the nutrient solution. These results contrast with those in the literature for rice, in which roots function efficiently in stagnant solutions (0.1% agar). So, when wheat roots are aerenchymatous there are still restrictions to O2 diffusion in the gas space continuum between the atmosphere and the functional tissues of the roots. This poor acclimation must have been due to inefficiency of the aerenchymatous axes, which may include persistence of anoxic steles, and/or restricted O2 diffusion in other parts of the gas space continuum, in either the shoots and shoot-root junction or in the root tip.     

Effect of soil water content on the gravitropic behavior of nodal roots in maize

The direction of root growth is an important factor that determines the spatial distribution of roots in the soil. The influence of soil water content on the direction of growth of maize nodal roots was studied both in the field and in the greenhouse. In the field experiment, the one plot was regularly irrigated (I-plot) and the other non-irrigated (N-plot). In the greenhouse experiment, three water treatments were conducted on plants grown in pots: continuously wet (CW), early drying (ED), and late drying (LD). The direction of root growth was quantified by the angle from the vertical, measured at 1 cm intervals for 10 cm from the first five internodes. Nodal roots grew more vertically in the N-plot and ED treatment than those in the I-plot and CW treatment. This was due to the decrease of the initial angle and/or the liminal angle. It is therefore thought that two events regulate the growth direction of nodal roots under dry soil conditions: gravitropic bending at root emergence from the stem and the later establishment of the angle of growth. Nodal roots appearing after rewatering in the ED treatment grew in a similar direction as those in the CW treatment. It follows from this that the water content of the surrounding soil has a direct effect on the direction of growth. Nodal roots that emerged in rapidly drying soil in the LD treatment ceased growing after showing negative gravitropism. The possible mechanisms determining the growth direction of nodal roots in drier soils are discussed.     

The impact of limited soil moisture and waterlogging stress conditions on morphological and anatomical root traits in maize (Zea mays L.) hybrids of different drought tolerance

Effects of soil drought or waterlogging on the morphological traits of the root system and internal root anatomy were studied in maize hybrids of different drought tolerance. The investigations comprised quantitative and qualitative analyses of a developed plant root system through determining the number, length and dry matter of the particular components of the root system and some traits of the anatomical structure of the seminal root. Obtained results have demonstrated a relatively broad variation in the habit of the root system. This mainly refers, to the number, length and dry matter of lateral roots, developed by seminal root, seminal adventitious and nodal roots as well as to some anatomical properties of the stele, cortex and metaxylem elements. Plants grown under waterlogging or drought conditions showed a smaller number and less dry matter of lateral branching than plants grown in control conditions. The harmful effect of waterlogging conditions on the growth of roots was greater when compared with that of plants exposed to drought. In the measurements of the root morphological traits, the effect of soil drought on the internal root anatomical characteristic was weaker than the effect of soil waterlogging. The observed effects of both treatments were more distinct in a drought sensitive hybrid Pioneer D than in drought resistant Pioneer C one. The drought resistant hybrid Pioneer C distinguished by a more extensive rooting and by smaller alterations in the root morphology caused by the stress conditions than drought sensitive hybrid Pioneer D one. Also the differences between the resistant and the sensitive maize hybrids were apparent for examined root anatomical traits. Results confirm that the hybrid Pioneer D of a high drought susceptibility was found to be also more sensitive to periodieal soil water excess. A more efficient water use and a lower shoot to root (S:R) ratio were found to be major reasons for a higher stress resistance of the hybrid Pioneer C. The reasons for a different response of the examined hybrids to the conditions of drought or waterlogging may be a more economical water balance and more favourable relations between the shoot and root dimensions in the drought resistant genotype. The observed modifications of the internal root structure caused by water deficit in plant tissues may partly influence on water conductivity and transport within roots. The results suggest that the morphological and anatomical traits of the maize root system may be used in practice as direct or indirect selection criteria in maize breeding.     

Morphological and architectural development of root systems in sorghum and maize

Root systems determine the capacity of a plant to access soil water and their architecture can influence adaptation to water-limited conditions. It may be possible to associate that architecture with root attributes of young plants as a basis for rapid phenotypic screening. This requires improved understanding of root system development. This study aimed to characterise the morphological and architectural development of sorghum and maize root systems by (i) clarifying the initiation and origin of roots at germination, and (ii) monitoring and quantifying the development of root systems in young plants. Three experiments were conducted with two maize and four sorghum hybrids. Sorghum produced a sole seminal (primary) root and coleoptile nodal roots emerged at the 4th–5th leaf stage, whereas maize produced 3–7 seminal (primary and scutellum) roots and coleoptile nodal roots emerged at the 2nd leaf stage. Genotypic variation in the flush angle and mean diameter of nodal roots was observed and could be considered a suitable target for large scale screening for root architecture in breeding populations. Because of the relatively late appearance of nodal roots in sorghum, such screening would require a small chamber system to grow plants until at least 6 leaves had fully expanded.     

Effects of Temperature on the Development of Metaxylem in Primary Wheat Roots and Its Hydraulic Consequence

The effects of different temperatures on the development ofmetaxylem were studied in the primary seminal root of winterwheat (Triticum aestivum L.) seedlings. Xylem development wasstudied microscopically at different distances behind the rootapex after safranin staining to reveal lignification. Diameter of the central late metaxylem (LMX) and its proportionto the stele cross-sectional area increased in the acropetaldirection. Diameter of the LMX and stele decreased with an increasein growing temperature. Numbers of early metaxylem (EMX) wereseven, seven and six at 10, 20 and 30 C, respectively. EMXwas lignified much more rapidly than the LMX along the seminalroot axes. Lignification of xylem elements commenced furthertowards the root apex at the higher temperatures. The LMX vesselsof the roots grown at the higher temperature had thicker secondarywalls. The relative conductivity of seminal roots, calculated fromPoiseuille's equation, decreased as growing temperature increased.In a drought-prone environment where wheat plants rely heavilyon stored soil water, a lowered axial conductivity in the rootswould be advantageous. The plants would tend to conserve waterduring vegetative growth for use during the critical periodsof flowering and grain-filling. Breeders selecting wheat plants for altered LMX diameters shouldcontrol temperatures during primary root development, sectionthe roots at the same distance from the tip and be aware thatcross walls may exist in the LMX for up to 30 cm from the tip. Wheat, Triticum aestivum L., roots, xylem development, hydraulic conductivity, temperature     

Morphological plasticity of wheat and barley roots in response to spatial variation in soil strength

Root systems of individual crop plants may encounter large variations in mechanical impedance to root penetration. Split-root experiments were conducted to compare the effects of spatial variation in soil strength on the morphological plasticity of wheat and barley roots, and its relationship to shoot growth. Plants of spring barley (Hordeum vulgare cv Prisma) and spring wheat (Triticum aestivum cv Alexandria) were grown for 12 days with their seminal roots divided between two halves of a cylinder packed with sandy loam soil. Three treatment combinations were imposed: loose soil where both halves of the cylinder were packed to 1.1 g cm^–3 (penetrometer resistance 0.3 MPa), dense soil where both halves were packed to 1.4 g cm^–3 (penetrometer resistance 1 MPa), and a split-root treatment where one half was packed to 1.1 and the other to 1.4 g cm^–3. In barley, uniform high soil strength restricted the extension of main seminal root axes more than laterals. In the split-root treatment, the length of laterals and the dry weight of main axes and laterals were increased in the loose soil half and reduced in the dense soil half compared with their respective loose and dense-soil controls. No such compensatory adjustments between main axis and laterals and between individual seminal roots were found in wheat. Variation in soil strength had no effect on the density of lateral roots (number per unit main axis length) in either barley or wheat. The nature and extent of wheat root plasticity in response to variation in soil strength was very different from that in response to changes in N-supply in previous experiments. In spite of the compensatory adjustments in growth between individual seminal roots of barley, the growth of barley shoots, as in wheat, was reduced when part of the root system was in compacted soil.     

Enhanced N-Transfer from a Soybean to Maize by Vesicular Arbuscular Mycorrhizal (VAM) Fungi

Using a split-root technique, roots of soybean plants were divided between two pots. In one of the two pots, two maize plants were grown and half of those pots were inoculated with the vesicular arbuscular mycorrhizal (VAM) fungus, Glomus fasciculatus. Fifty-two days after planting, ¹⁵N-labeled ammonium sulfate was applied to the pots which contained only soybean roots. Forty-eight hours after application, significantly higher values for atom per cent ¹⁵N excess were found in roots and leaves of VAM-infected maize plants as compared with the non-VAM-infected maize plants. Results indicated that VAM fungi did enhance N transfer from one plant to another.     

Inoculation with arbuscular mycorrhizal fungi enhances growth of Litchi chinensis Sonn. trees after propagation by air-layering

This study investigated the patterns of root growth and water uptake of maize (Zea mays L.) and cowpea (Vigna unguiculata (L.) Walp) grown in a mixture under greenhouse conditions. The plants were grown in root boxes for 5 weeks under 2 watering regimes; fully irrigated and water stress conditions, followed by a 5-day drying cycle imposed during the 6th week of growth. Water uptake patterns were analysed during the drying cycle. The two-dimensional distribution of the roots of both plants in the boxes was determined immediately at the end of the drying cycle. Under well-irrigated conditions, the roots of the component plants grew profusely into all sections of the root box and intermingled considerably. Water stress resulted in the decline of root growth of maize and cowpea but the root:shoot ratios of maize and cowpea were not affected, suggesting that there was no significant effect of water stress on root:shoot partitioning. However, water stress affected the biomass distribution between fine and coarse roots in cowpea. About 64% by weight of cowpea roots under water stress were coarse whereas as against 48% under well-irrigated conditions. Furthermore, water stress generally restricted the lateral extent of the roots of both maize and cowpea with a tendency of clumping together of the root systems and a reduced degree of intermingling. Thus, the extent of mixing of the root systems was apparently controlled by the availability of soil water. Water uptake from the well-irrigated soil in the root boxes was initially restricted to the sections directly below the base of each plant. Although roots of both plants were present in almost all sections of the root box, all the sections did not contribute simultaneously to water uptake by each plant. Water uptake was delayed from the middle intermingled zones. In effect, uptake patterns did not relate generally to the root distribution. The tendency was for the component plants to initially `avoid' water uptake from zones of intense intermingling or competition.     

Root proliferation and seed yield in response to spatial heterogeneity of below-ground competition

Here, we tested the predictions of a 'tragedy of the commons' model of below-ground plant competition in annual plants that experience spatial heterogeneity in their competitive environment. Under interplant competition, the model predicts that a plant should over-proliferate roots relative to what would maximize the collective yield of the plants. We predict that a plant will tailor its root proliferation to local patch conditions, restraining root production when alone and over-proliferating in the presence of other plants. A series of experiments were conducted using pairs of pea (Pisum sativum) plants occupying two or three pots in which the presence or absence of interplant root competition was varied while nutrient availability per plant was held constant. In two-pot experiments, competing plants produced more root mass and less pod mass per individual than plants grown in isolation. In three-pot experiments, peas modulated this response to conditions at the scale of individual pots. Root proliferation in the shared pot was higher compared with the exclusively occupied pot. Plants appear to display sophisticated nutrient foraging with outcomes that permit insights into interplant competition.     

Respiratory potential of maize (Zea mays L.) roots exposed to hypoxia

When hypoxia is not too severe, root aerobic metabolism can be partly supported by oxygen delivery via aerenchymateous tissues. In terms of supplying energy, this adaptation is of special importance in plants with a high metabolic demand, such as maize (Zea mays L.). The ability of maize to respond to hypoxia by morphological changes is well documented; however, little is known on the potential for oxidative metabolism in different types of maize roots. In our study, we assessed the root respiratory potential in seminal and adventious nodal roots of maize exposed to mild short-term hypoxia. Plants responded to the treatment with an increased portion of nodal roots per total root length, while there were no changes in the biomass of shoots and roots. Thick nodal roots had much higher respiratory potential (Electron Transport System Activity – ETS) than nodal roots of smaller diameter or seminal roots, irrespective of the aeration rate. The only change in ETS under oxygen deficiency was found for seminal roots where oxygen consumption increased by 25%. Increased root porosity was observed in all roots, the increase was higher in nodal roots. On the basis of ETS data and taking into account changes of root morphology, it can be concluded that large changes of root respiratory potential are not involved in the response of maize to hypoxia. Obviously, maize can cover the respiratory needs with shifts in the growth of different root types which inherently differ in their potential aerobic respiration.     

Root-to-shoot signalling when soil moisture is heterogeneous: increasing the proportion of root biomass in drying soil inhibits leaf growth and increases leaf abscisic acid concentration

To determine whether root-to-shoot signalling of soil moisture heterogeneity depended on root distribution, wild-type (WT) and abscisic acid (ABA)-deficient (Az34) barley (Hordeum vulgare) plants were grown in split pots into which different numbers of seminal roots were inserted. After establishment, all plants received the same irrigation volumes, with one pot watered (w) and the other allowed to dry the soil (d), imposing three treatments (1 d: 3 w, 2 d: 2 w, 3 d: 1 w) that differed in the number of seminal roots exposed to drying soil. Root distribution did not affect leaf water relations and had no sustained effect on plant evapotranspiration (ET). In both genotypes, leaf elongation was less and leaf ABA concentrations were higher in plants with more roots in drying soil, with leaf ABA concentrations and water potentials 30% and 0.2 MPa higher, respectively, in WT plants. Whole-pot soil drying increased xylem ABA concentrations, but maximum values obtained when leaf growth had virtually ceased (100 nm in Az34, 330 nm in WT) had minimal effects (<40% leaf growth inhibition) when xylem supplied to detached shoots. Although ABA may not regulate leaf growth in vivo, genetic variation in foliar ABA concentration in the field may indicate different root distributions between upper (drier) and lower (wetter) soil layers.     

Interspecific differences in root architecture among maize and triticale genotypes grown under drought,waterlogging and soil compaction

Environmental stresses (soil compaction, drought, waterlogging) cause changes in plants’ root system structure, also affecting the growth of above-ground parts. The aim of this study was to estimate phenotypic variation among maize and triticale genotypes in root penetration ability through petrolatum-wax-layer (RPA). Also, the effect of shortage or excess of soil water on dry matter of shoots and roots and morphological changes in root system structure in sensitive and resistant maize and triticale genotypes grown in low or high soil compaction level was evaluated. To estimate RPA index, the petrolatum-wax-layer method (PWL) was used. The strength of three petrolatum-wax concentrations 60, 50 and 40 % was 0.52, 1.07 and 1.58 MPa, respectively. High coefficients of variation (CV) were observed in 0.52 and 1.07 MPa and for maize were 19.2 and 21.7 %, and for triticale, 12.5 and 18.3 %, respectively. The data indicate that the use of PWL technique is an effective screening method, and makes it possible to divide the genotypes into resistant and sensitive groups. The second part of this study investigated a multistress effect of soil compaction combined with drought or waterlogging on root and shoot growth and morphological changes in root system structure of maize and triticale genotypes differing in susceptibility to environmental stresses. Seedlings were grown for 4 weeks in root-boxes under conditions of low (LSC 1.1 g cm^?3) or severe (SSC 1.6 g cm^?3) soil compaction. Drought or waterlogging stresses were applied for 2 weeks from 14th to 28th day. In comparison to LSC treatment, in SSC treatment the decrease in dry matter of shoots and roots was greater for sensitive genotypes of maize and triticale (Ancora, CHD-147). Soil drought or waterlogging caused greater decrease of dry matter of shoots and roots in seedlings grown in SSC in comparison to LSC. The root penetration index (RPI) was estimated as a ratio of root dry matter in 15–40 cm root-box layer to total root dry matter. On the basis of RPI it was possible to group the genotypes according to their ability to distribute roots in soil profile. In comparison to LSC, SSC exerted a strong influence on the length of seminal and seminal adventitious roots, as well as the number and length of L- and S-type lateral roots developed on seminal and nodal roots. In both species the restriction effect of soil compaction on number and length of roots was more severe in sensitive (Ankora, CHD-147) than in resistant (Tina, CHD-247) genotypes. The restriction in roots propagation was greater in triticale than in maize. Exposure to drought or waterlogging in the case of genotypes grown in LSC and SSC treatments caused a decrease in number and length of particular components of root system structure. In both species the decrease of root number and length in plants grown under waterlogging was greater than under drought. The observed changes in root system were greater in sensitive (Ankora, CHD147) than in resistant (Tina, CHD-247) genotypes. Statistically significant correlations were found between RPA and RPI and also between these indexes and soil compaction, drought and waterlogging susceptibility indexes. This indicates that genotypes resistant to soil compaction were resistant to drought or waterlogging and also that genotypes resistant to drought were resistant to waterlogging.     

QTL mapping and phenotypic variation for root architectural traits in maize (Zea mays L.)

Key message

QTL were identified for root architectural traits in maize.

Abstract

Root architectural traits, including the number, length, orientation, and branching of the principal root classes, influence plant function by determining the spatial and temporal domains of soil exploration. To characterize phenotypic patterns and their genetic control, three recombinant inbred populations of maize were grown for 28 days in solid media in a greenhouse and evaluated for 21 root architectural traits, including length, number, diameter, and branching of seminal, primary and nodal roots, dry weight of embryonic and nodal systems, and diameter of the nodal root system. Significant phenotypic variation was observed for all traits. Strong correlations were observed among traits in the same root class, particularly for the length of the main root axis and the length of lateral roots. In a principal component analysis, relationships among traits differed slightly for the three families, though vectors grouped together for traits within a given root class, indicating opportunities for more efficient phenotyping. Allometric analysis showed that trajectories of growth for specific traits differ in the three populations. In total, 15 quantitative trait loci (QTL) were identified. QTL are reported for length in multiple root classes, diameter and number of seminal roots, and dry weight of the embryonic and nodal root systems. Phenotypic variation explained by individual QTL ranged from 0.44 % (number of seminal roots, NyH population) to 13.5 % (shoot dry weight, OhW population). Identification of QTL for root architectural traits may be useful for developing genotypes that are better suited to specific soil environments.     

Importance of internal hydraulic redistribution for prolonging the lifespan of roots in dry soil

Redistribution of water within plants could mitigate drought stress of roots in zones of low soil moisture. Plant internal redistribution of water from regions of high soil moisture to roots in dry soil occurs during periods of low evaporative demand. Using minirhizotrons, we observed similar lifespans of roots in wet and dry soil for the grapevine 'Merlot' (Vitis vinifera) on the rootstock 101-14 Millardet de Gramanet (Vitis riparia x Vitis rupestris) in a Napa County, California vineyard. We hypothesized that hydraulic redistribution would prevent an appreciable reduction in root water potential and would contribute to prolonged root survivorship in dry soil zones. In a greenhouse study that tested this hypothesis, grapevine root systems were divided using split pots and were grown for 6 months. With thermocouple psychrometers, we measured water potentials of roots of the same plant in both wet and dry soil under three treatments: control (C), 24 h light + supplemental water (LW) and 24 h light only (L). Similar to the field results, roots in the dry side of split pots had similar survivorship as roots in the wet side of the split pots (P = 0.136) in the C treatment. In contrast, reduced root survivorship was directly associated with plants in which hydraulic redistribution was experimentally reduced by 24 h light. Dry-side roots of plants in the LW treatment lived half as long as the roots in the wet soil despite being provided with supplemental water (P < 0.0004). Additionally, pre-dawn water potentials of roots in dry soil under 24 h of illumination (L and LW) exhibited values nearly twice as negative as those of C plants (P = 0.034). Estimates of root membrane integrity using electrolyte leakage were consistent with patterns of root survivorship. Plants in which nocturnal hydraulic redistribution was reduced exhibited more than twice the amount of electrolyte leakage in dry roots compared to those in wet soil of the same plant. Our study demonstrates that besides a number of ecological advantages to protecting tissues against desiccation, internal hydraulic redistribution of water is a mechanism consistent with extended root survivorship in dry soils.     

Heterogeneity in spatial P-distribution and foraging capability by Zea mays: effects of patch size and barriers to restrict root proliferation within a patch

• Background and Aims Localized proliferation of rootsin nutrient-enriched patches seems to be an adaptive responsein many plants, but its function is still debatable. To understandthe efficiency and limitation of foraging behaviour, the impactof patch size and the presence or absence of a barrier to rootproliferation within phosphorus (P)-enriched patches was examined. • Methods In pots filled with P-poor soil, six treatmentsof heterogeneous P supply were prepared: three patch sizes withor without a root barrier between patches. In addition, a homogeneousP supply treatment was also prepared. Irrespective of thesetreatments, each pot received the same total amount of P. Maize(Zea mays) was grown in each pot for 45 d in a greenhouse. • Key Results P content and biomass were greatest in plantsgrown in the largest patch due to successful root proliferation,and were higher in the presence of a root barrier. Interestingly,plants preferentially developed adventitious nodal roots projectingfrom the stem into the P-enriched soil, particularly in thelargest patch with a root barrier. Removal of the barrier reducedthe P-uptake capacity per unit root surface area or volume inP-enriched patches, revealing that the P-uptake capacity perroot can be suppressed even in P-rich soil if other portionson the root axis encounter P-poor conditions. • Conclusions The results suggest that the efficiency ofroot morphological plasticity is largely determined by the sizeof the P-enriched patch. Furthermore, the results imply a novelaspect of P-uptake physiology that roots in heterogeneous Pcannot demonstrate their potential capacity, as would be observedin roots encountering P continuously; this effect is probablymediated by an internal root factor.