Photosynthesis,respiration, and carbon allocation of two cool-season perennial grasses in response to surface soil drying

The study was conducted to investigate carbon metabolic responses to surface soil drying for cool-season grasses. Kentucky bluegrass (Poa pratensis L.) and tall fescue (Festuca arundinaceae Schreb.) were grown in a greenhouse in split tubes consisting of two sections. Plants were subjected to three soil moisture regimes: (1) well-watered control; (2) drying of upper 20-cm soil (upper drying); and (3) drying of whole 40-cm soil profile (full drying). Upper drying for 30 d had no dramatic effects on leaf water potential (Ψ_leaf) and canopy photosynthetic rate (P_n) in either grass species compared to the well-watered control, but it reduced canopy respiration rate (R_canopy) and root respiration rate in the top 20 cm of soil (R_top). For both species in the lower 20 cm of wet soil, root respiration rates (R_bottom) were similar to the control levels, and carbon allocation to roots increased with the upper soil drying, particularly for tall fescue. The proportion of roots decreased in the 0-20 cm drying soil, but increased in the lower 20 cm wet soil for both grass species; the increase was greater for tall fescue. The Ψ_leaf, P_n, R_canopy, R_top, R_bottom, and carbon allocation to roots in both soil layers were all significantly higher for upper dried plants than for fully dried plants of both grass species. The reductions in R_canopy and R_top in surface drying soil and increases in root respiration and carbon allocation to roots in lower wet soil could help these grasses cope with surface-soil drought stress. This revised version was published online in June 2006 with corrections to the Cover Date.     

Root Growth and Water Uptake by Maize Plants in Drying Soil

Sharp, R. E and Da vies, W. J. 1985. Root growth and water uptakeby maize plants in drying soil.— J. exp. Bot. 36: 1441–1456. The influence of soil drying on maize (Zea mays L.) root distributionand use of soil water was examined using plants growing in thegreenhouse in soil columns. The roots of plants which were wateredwell throughout the 18 d experimental period penetrated thesoil profile to a depth of 60 cm while the greatest percentageof total root length was between 20–40 cm. High soil waterdepletion rates corresponded with these high root densities.Withholding water greatly restricted root proliferation in theupper part of the profile, but resulted in deeper penetrationand higher soil water depletion rates at depth, compared withthe well watered columns. The deep roots of the unwatered plantsexhibited very high soil water depletion rates per unit rootlength. Key words: Maize, roots, water deficit, soil water depletion     

Root effects on soil water and hydraulic properties

Plants can affect soil moisture and the soil hydraulic properties both directly by root water uptake and indirectly by modifying the soil structure. Furthermore, water in plant roots is mostly neglected when studying soil hydraulic properties. In this contribution, we analyze effects of the moisture content inside roots as compared to bulk soil moisture contents and speculate on implications of non-capillary-bound root water for determination of soil moisture and calibration of soil hydraulic properties. In a field crop of maize (Zea mays) of 75 cm row spacing, we sampled the total soil volumes of 0.7 m × 0.4 m and 0.3 m deep plots at the time of tasseling. For each of the 84 soil cubes of 10 cm edge length, root mass and length as well as moisture content and soil bulk density were determined. Roots were separated in 3 size classes for which a mean root porosity of 0.82 was obtained from the relation between root dry mass density and root bulk density using pycnometers. The spatially distributed fractions of root water contents were compared with those of the water in capillary pores of the soil matrix. Water inside roots was mostly below 2–5% of total soil water content; however, locally near the plant rows it was up to 20%. The results suggest that soil moisture in roots should be separately considered. Upon drying, the relation between the soil and root water may change towards water remaining in roots. Relations depend especially on soil water retention properties, growth stages, and root distributions. Gravimetric soil water content measurement could be misleading and TDR probes providing an integrated signal are difficult to interpret. Root effects should be more intensively studied for improved field soil water balance calculations. Presented at the International Conference on Bioclimatology and Natural Hazards, Pol’ana nad Detvou, Slovakia, 17–20 September 2007.     

干旱区膜下滴灌条件下土壤深层水对棉花根系生长、分布及产量的影响

在土柱栽培条件下研究膜下滴灌土壤深层水对棉花根系生长的影响及与植株地上部生长的关系,设置土壤(60～120 cm)有深层水和无深层水2个处理,每处理设2个生育期间灌溉处理,分别为田间持水量70%和55%.结果表明：棉花总根质量密度、40～120 cm土层根长密度、根系活力等与地上部干质量间均具有显著的相关关系.生育期间耕层70%田间持水量条件下,土壤有深层水处理的总根质量密度与无深层水处理无明显差异,但40～120 cm土层的根长密度增加,根系活力增强,提高了土壤贮备水消耗量,增加了地上部干质量,最终获得较高的经济产量及水分利用效率.土壤有深层水条件下,生育期间耕层55%田间持水量处理的根冠比较大,40～120 cm土层根长密度和80～120 cm土层根系活力相对较高,土壤贮备水消耗量大幅提高,但仍无法弥补生育期间水分亏缺对根系及地上部生物量造成的负面影响,导致经济产量显著低于70%田间持水量处理.综上,充足的土壤深层水配合生育期间耕层65%～75%田间持水量,可促进棉花根系向下生长,有利于实现膜下滴灌棉花节水高产高效生产.     

Root growth and water relations of oak and birch seedlings

Summary First year seedlings of English oak (Quercus Cobur) and silver birch (Betula pendula) were subjected to pressure-volume analysis to investigate the water potential components and cell wall properties of single leaves. It was hoped that this rapid-drying technique would differentiate between reductions in plant solute potential resulting from dehydration and the effects of solute accumulation.Comparison of results from these experiments with those of slow drying treatments (over a number of days) with plants growing in tubes of soil, indicated that some solute accumulation may have occurred in drying oak leaves. High leaf turgor and leaf conductance were maintained for a significant period of the drying cycle. Roots of well-watered oak plants extended deep into the soil profile, and possibly as a result of solute regulation and therefore turgor maintenance, root growth of unwatered plants was greater than that of their well-watered counterparts. This was particularly the case deep in the profile. As a result of deep root penetration, water deep in the soil core was used by oak plants to maintain plant turgor, and quite low soil water potentials were recorded in the lower soil segments.Root growth of well-watered birch seedlings was prolific but roots of both well-watered and unwatered plants were restricted to the upper part of the profile. Root growth of unwatered plants was reduced despite the existence of high soil water potentials deep in the profile. Shallow rooting birch seedlings were unable to use this water.Pressure-volume analysis indicated that significant reductions of water potential, which are required for water uptake from drying soil, would occur in oak with only a small reduction in plant water content compared to the situation in birch. This was a result of the low solute potential in oak leaves combined with a high modulus of elasticity of cell walls. Deep rooting of oak seedlings, combined with these characteristics, which will be particularly important when soil deep in the profile begins to dry, mean that this species may be comparatively successful when growing on dry sites.     

Vertical distribution of fine roots in relation to soil factors in Pinus tabulaeformis Carr. forest of the Loess Plateau of China

Growth and vertical distribution of fine root closely depend on soil resource availability. Better understanding of relationships of root profile with vertical distribution of available soil resource and soil characteristics can allow ecologists to predict the fine root distribution on the scales ranging from individual plants to vegetation communities. The objective of the study was to understand the fine root mass density (FRMD), fine root length density (FRLD), fine root area density (FRAD), mean root diameter and specific root length (SRL), vertical distribution in soil profile and their relation with soil environment factors in semiarid and arid Loess Plateau of China. The vertical fine root distribution and soil bulk density, soil moisture and soil inorganic N in 0-60 cm soil profile (0–15, 15–30, 30–45 and 45–60 cm intervals) were investigated by soil coring methods in three Pinus tabulaeformis Carr. forests chosen at three locations. The fine root density parameters (FRMD, FRLD and FRAD) and SRL peaked in the most upper soil layer (0–15 cm interval) and decreased with increased soil depth. The results provided a strong support that soil water rather than soil inorganic N is a key control on fine root distribution in the Loess Plateau. With increased soil moisture, the root mass, length and SRL increased and the mean root diameter decreased. The effects of soil bulk density on the fine root parameters were consistent with those of the soil water. An unexpected result was obtained about the relationships between soil organic N and the root distributions and occurrences because of no differences among the soil depth intervals in soil inorganic N content. It might be associated with severe soil water deficit limiting soil nitrogen utilization efficiency in arid Loess Plateau.     

Effects of soil structural discontinuity on root and shoot growth and water use of maize

The role of roots penetrating various undisturbed soil horizons beneath loose layer in water use and shoot growth of maize was evaluated in greenhouse experiment. 18 undisturbed soil columns 20 cm in diameter and 20 cm in height were taken from the depths 30–50 cm and 50–70 cm from a Brown Lowland soil, a Pseudogley and a Brown Andosol (3 columns from each depth and soil). Initial resistance to penetration in undisturbed soil horizons varied from 2.5 to 8.9 MPa while that in the loose layer was 0.01 MPa. The undisturbed horizons had a major effect on vertical arrangement of roots. Root length density in loose layer varied from 96 to 126 km m^-3 while in adjacent stronger top layers of undisturbed horizons from 1.6 to 20.0 km m^-3 with higher values in upper horizons of each soil. For specific root length, the corresponding ranges were 79.4–107.7 m g^-1 (on dry basis) and 38.2–63.7 m g^-1, respectively. Ratios of root dry weight per unit volume of soil between loose and adjacent undisturbed layers were much lower than those of root length density indicating that roots in undisturbed horizons were produced with considerably higher partition of assimilates. Root size in undisturbed horizons relative to total roots was from 1.1 to 38.1% while water use from the horizons was from 54.1 to 74.0%. Total water use and shoot growth were positively correlated with root length in undisturbed soil horizons. There was no correlation between shoot growth and water use from the loose layers.     

Photosynthesis,root respiration,and grain yield of spring wheat in response to surface soil drying

The aims of this research were to test the influence of surface soil drying on photosynthesis, root respiration and grain yield of spring wheat (Triticum aestivum), and to evaluate the relationship between root respiration and grain yield. Wheat plants were grown in PVC tubes 120 cm in length and 10 cm in diameter. Three water regimes were employed: (a) all soil layers were irrigated close to field water capacity (CK); (b) upper soil layers (0–40 cm from top) drying (UD); (c) lower soil layer (80–120 cm from top) wet (LW). The results showed that although upper drying treatment maintained the highest root biomass, root respiration and photosynthesis rates at anthesis, the root respiration of the former was significantly (P < 0.05) lower than the latter at the jointing stage. There were no differences in water use efficiency or harvest index between plants from the upper drying and well-watered treatment. However, the grain weight for plants in the upper drying treatment was significantly (P< 0.05) higher than that of in well-watered control. The results suggest that reduced root respiration rate and the amount of photosynthates utilized by root respiration in early season growth may also have contributed to improve crop production under soil drying. Reduced root activity and root respiration rate, in the early growth stage, not only increased the photosynthate use efficiency (root respiration rate: photosynthesis ratio), but also grain yield. Rooting into a deeper wet soil profile before grain filling was crucial for spring wheat to achieve a successful seedling establishment and high grain yield.     

Drought adaptation of field grown wheat in relation to soil physical conditions

In order to investigate the effects of soil texture on possible non-hydraulic signals under field conditions, spring wheat plants (Triticum aestivum L. cv. Cadensa) grown in sand and loam soils and with a well developed root system were exposed to slow soil drying in the late vegetative stage of growth. Soil water potential and content were measured daily at different depths and plant responses were measured in flag leaves. When the average soil water potential in the top soil layers (0–25 cm depth in sand and 0–45 cm depth in loam) dropped to –60 or –70 kPa and the lower soil layers were still at field capacity, morning xylem [ABA] (0.03–0.04 vs. 0.06–0.08 mmol m-3) and midday leaf ABA concentration increased (250–300 vs. 400–450 ng/g DW) and leaf conductance decreased relatively to well-watered (control) plants (0.75–0.88 vs. 0.64–0.70 mol m-2 s-1). These responses took place before any decrease in leaf water potential occurred as compared with control plants, indicating that they were triggered by root-borne signals due to reduced root water status in the top soil layers. At this stage the soil water content was as low as 6% by volume, the fraction of roots in ‘wet’ soil was 0.12 and relative available soil water was 45% in sand and still high 20%, 0.48 and 70%, respectively, in loam of the whole soil profile indicating that roots were responding to soil water availability and not soil water content at a certain evaporative demand. In addition, similar responses occurred at high and low evaporative demands (3.4–5.2 vs. 0.6–4.0 mm/day of potential evapotranspiration). This revised version was published online in July 2006 with corrections to the Cover Date.     

Shoot and root physiological responses to localized zones of soil moisture in cultivated and wild lettuce (Lactuca spp.)

Cultivated crisphead lettuce (Lactuca sativa L.) has a shallower root system than its wild relative, Lactuca serriola L. The effects of localized soil water, at depth, on plant water relations, gas exchange and root distribution were examined in the two species using soil columns with the soil hydraulic-ally separated into two layers, at (0–20 cm and 20–81) cm, but permitting root growth between the layers. Three treatments were imposed on 7-week-old plants, and maintained for 4 weeks: (i) watering, both layers to field capacity; (ii) drying the upper layer while watering the lower layer to field capacity, and (iii) drying both layers. Drying only 0–20 cm of soil had no effect on leaf water status, net photosynthesis, stomatal conductance or biomass production in L. serriola compared to a well-watered control, but caused a short-term reduction (10 d) in leaf water status and photosynthesis in L. sativa that reduced final shoot production. The different responses may be explained by differences in root distribution. Just before the treatments commenced, L. serriola had 50% of total root length at 20–80 cm compared to 35% in L. sativa. Allocation of total biomass to roots in L. serriola was approximately double that in L. sativa. The wild species could provide germplasm for cultivated lettuces to extract more soil water from depth, which may improve irrigation efficiency.     

Involvement of antioxidants and lipid peroxidation in the adaptation of two cool-season grasses to localized drought stress

In natural environments, drought often occurs in surface soil while water is available for plant uptake deeper in the soil profile. The objective of the study was to examine the involvement of antioxidant metabolism and lipid peroxidation in the responses of two cool-season grasses to surface soil drying. Kentucky bluegrass (Poa pratensis L) and tall fescue (Festuca arundinacea Schreb.) were grown in split tubes, consisting of two sections (each 10 cm in diameter and 20 cm long). Grasses were subjected to three soil moisture regimes: (a) well-watered control: whole soil profile was watered; (b) surface drying: surface 20 cm of soil was dried by withholding irrigation and the lower 20 cm of soil was watered; (c) full drying: whole soil profile was dried. Surface drying had no effects on relative water content (RWC) and chlorophyll content (Chl) for both grasses and only slightly reduced shoot growth for tall fescue. Superoxide dismutase (SOD) activity increased, while catalase (CAT) and peroxidase (POD) activities remained unchanged during most periods of surface drying. Malondialdehyde (MDA) content was unaffected by surface drying for tall fescue, but increased initially and then decreased to the control level for Kentucky bluegrass. Under full drying, RWC, Chl content, and shoot dry weight decreased, but MDA content increased in both grasses; SOD and POD activities initially increased transiently and then decreased; CAT remained unchanged for 25 days and then decreased. These results suggested that both Kentucky bluegrass and tall fescue were capable of surviving surface soil drying. This capability could be related to increases in antioxidant activities, particularly SOD and CAT. However, full drying suppressed antioxidant activities and induced lipid peroxidation.     

Transpiration and visual appearance of warm season turfgrasses during soil drying

Warm-season turfgrasses may be subjected to increasing drought as future urban irrigation regulations become more restrictive. Species differences in water use and transpiration response to drying soil may be exploited in the future to increase survival and maintain green color under drying soil conditions. This study was undertaken to provide background documentation on the sensitivity to soil–water deficit of three warm-season grasses: ‘Argentine’ bahiagrass (Paspalum notatum); ‘Floratam’ St. Augustinegrass (Stenotaphrum secundatum), and ‘Empire’ zoysiagrass (Zoysia japonica). Each of these turfgrasses demonstrated a two-phased linear transpiration response to gradually drying soil as expressed by a normalized ratio between the transpiration rates of drought stressed to well-watered plants (NTR). In this study, well-watered bahiagrass used 30% more water on a daily basis than did well-watered St. Augustinegrass or zoysiagrass. However, under drought, the three grass species transpired the same amount of water during the soil drying period up until NTR to 0.1. Since bahiagrass reached an NTR of 0.1 at 10.3 days versus 12.7 and 13.0 days for St. Augustinegrass and zoysiagrass, respectively, bahiagrass demonstrated a more rapid water loss rate during the drying period. The fraction of transpirable soil water (FTSW) remaining in the soil at the breakpoints for bahiagrass, St. Augustinegrass and zoysiagrass were 0.13, 0.16, and 0.19, respectively, in 2010, but were 0.18, 0.30, and 0.22, respectively, under slightly warmer conditions in 2011. The consistently low FTSW breakpoint for bahiagrass means that compared to the other species, bahiagrass continues to use water at a high rate late into the soil drying cycle before conserving soil water by decreasing stomatal conductance. That is, bahiagrass is likely to be subjected to greater soil–water deficits in lengthy droughts and needs mechanisms to better survive these droughts. The differences in breakpoints by year may be due to a combination of soil factors and temperature differences in the greenhouse.     

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.     

On the assessment of root and soil respiration for soils of different textures: interactions with soil moisture contents and soil CO2 concentrations

Estimates of root and soil respiration are becoming increasingly important in agricultural and ecological research, but there is little understanding how soil texture and water content may affect these estimates. We examined the effects of soil texture on (i) estimated rates of root and soil respiration and (ii) soil CO₂ concentrations, during cycles of soil wetting and drying in the citrus rootstock, Volkamer lemon (Citrus volkameriana Tan. and Pasq.). Plants were grown in soil columns filled with three different soil mixtures varying in their sand, silt and clay content. Root and soil respiration rates, soil water content, plant water uptake and soil CO₂ concentrations were measured and dynamic relationships among these variables were developed for each soil texture treatment. We found that although the different soil textures differed in their plant-soil water relations characteristics, plant growth was only slightly affected. Root and soil respiration rates were similar under most soil moisture conditions for soils varying widely in percentages of sand, silt and clay. Only following irrigation did CO₂ efflux from the soil surface vary among soils. That is, efflux of CO₂ from the soil surface was much more restricted after watering (therefore rendering any respiration measurements inaccurate) in finer textured soils than in sandy soils because of reduced porosity in the finer textured soils. Accordingly, CO₂ reached and maintained the highest concentrations in finer textured soils (> 40 mmol CO₂ mol⁻¹). This study revealed that changes in soil moisture can affect interpretations of root and soil measurements based on CO₂ efflux, particularly in fine textured soils. The implications of the present findings for field soil CO₂ flux measurements are discussed. This revised version was published online in June 2006 with corrections to the Cover Date.     

根区交替控制灌溉条件下玉米根系吸水规律

为了阐明根区交替控制灌溉(CRDAI)条件下玉米根系吸水规律,通过田间试验,在沟灌垄植模式下采用根区交替控制灌溉研究玉米根区不同点位(沟位、坡位和垄位)的根长密度(RLD)及根系吸水动态。研究表明,根区土壤水分的干湿交替引起玉米RLD的空间动态变化,在垄位两侧不对称分布,并存在层间差异;土壤水分和RLD是根区交替控制灌溉下根系吸水速率的主要限制因素。在同一土层,根系吸水贡献率以垄位最大,沟位最低;玉米营养生长阶段,10—30 cm土层的根系吸水速率最大;玉米生殖生长阶段,20—70 cm为根系吸水速率最大的土层,根系吸水贡献率为43.21%—55.48%。研究阐明了交替控制灌溉下根系吸水与土壤水分、RLD间相互作用的动态规律,对控制灌溉下水分调控机理研究具有理论意义。     

Influence of root density on the critical soil water potential

Estimation of root water uptake in crops is important for making many other agricultural predictions. This estimation often involves two assumptions: (1) that a critical soil water potential exists which is constant for a given combination of soil and crop and which does not depend on root length density, and (2) that the local root water uptake at given soil water potential is proportional to root length density. Recent results of both mathematical modeling and computer tomography show that these assumptions may not be valid when the soil water potential is averaged over a volume of soil containing roots. We tested these assumptions for plants with distinctly different root systems. Root water uptake rates and the critical soil water potential values were determined in several adjacent soil layers for horse bean (Vicia faba) and oat (Avena sativa) grown in lysimeters, and for field-grown cotton (Gossypium L.), maize (Zea mays) and alfalfa (Medicago sativa L.) crops. Root water uptake was calculated from the water balance of each layer in lysimeters. Water uptake rate was proportional to root length density at high soil water potentials, for both horse bean and oat plants, but root water uptake did not depend on root density for horse bean at potentials lower than −25 kPa. We observed a linear dependency of a critical soil water potential on the logarithm of root length density for all plants studied. Soil texture modified the critical water potential values, but not the linearity of the relationship. B E Clothier Section editor     

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 growth and water uptake during water deficit and recovering in wheat

Root growth and soil water content were measured in a field experiment with wheat subjected to two periods of water deficit. The first period was induced early in the season between the early vegetative stage (22 DAS) and late terminal spikelet (50 DAS), the second period at mid-season between terminal spikelet (42 DAS) and anthesis (74 DAS). Total root growth was reduced under water deficit by a reduction in the top 30 cm, while the root system continued to grow in the deeper soil profile between 30 and 60 cm. Shortly after rewatering, the growth pattern reverted to fastest root growth rates in the shallow soil layers. In relative terms, the total root system increased in relation to the above ground dry matter under water shortage. The early-, the mid-season water deficit treatments, and the control treatment had total root length of 27.4, 19.4 and 30.6 km m^-2, respectively, about 2 wk before maturity. Evapotranspiration declined under water deficit, but water uptake in deeper layers increased. Water uptake per unit root length was reduced with water deficit and was still low shortly after rewatering. Remarkable was the increase in water uptake at 2–3 weeks after rewatering, both deficit treatments exceeded the control by almost 100%. This increase in water uptake followed the burst of new root growth in the upper regions of the soil. However, water uptake rates subsequently declined towards maturity, being between 0.15 L km^-1 d^-1 and 0.17 L km^-1 d^-1 for the early and mid-season water deficit treatments, slightly higher than the control, 0.12 L km^-1 d^-1. The results showed that the crop subjected to early water deficit could compensate for some of the reductions in root growth during subsequent rewatering, but the impact of the mid-season water deficit treatment was more severe and permanent.     

Rectifier-like Activities of Roots of Two Desert Succulents

Axial and radial water flows for roots in response to appliedhydrostatic pressure drops, water loss from roots after variousperiods of drying, and development of new roots after rewettingdroughted plants were examined for two sympatric desert succulents.Agave deserti Engelm. and Ferocactus acanthodes (Lemaire) Brittonand Rose. For a 40 kPa hydrostatic pressure drop applied to20 mm long root pieces, radial water flows from the epidermisto the root xylem were 2- to 5-fold greater at the tip thanat midlength and were much less than axial flows along the xylem.Upon drying detached roots in air at 20 °C and a water vapoursaturation deficit of 1.2 kPa (50% relative humidity), radialwater flow decreased more than 10-fold in 3–6 h, and couldrecover to the original level 6 h after rewetting. The rateof water loss from attached roots of plants dried in air at20 °C and a 1.2 kPa saturation deficit decreased about 200-foldin 72 h, which would greatly limit water loss from the plantto a drying soil. At 96 h after rewetting roots of A. desertithat had been exposed to air at 20 °C and a 1.2 kPa saturationdeficit for 120 h, rehydration of existing roots and developmentof new roots contributed about equally to water uptake by thewhole plant. In summary, roots of these desert succulents canreadily take up water from a wet soil but do not lose much waterto a dry soil, thus effectively acting like rectifiers withrespect to plant-soil water movement. Key words: Agave, Cactus, Drought, Root, Water flow, Xylem     

Root distribution and water uptake patterns of corn under surface and subsurface drip irrigation

Information on root distribution and uptake patterns is useful to better understand crop responses to irrigation and fertigation, especially with the limited wetted soil volumes which develop under drip irrigation. Plant water uptake patterns play an important role in the success of drip irrigation system design and management. Here the root systems of corn were characterized by their length density (RLD) and root water uptake (RWU). Comparisons were made between the spatial patterns of corn RWU and RLD under surface and subsurface drip irrigation in a silt loam soil, considering a drip line on a crop row and between crop rows. Water uptake distribution was measured with an array of TDR probes at high spatial and temporal resolution. Root length density was measured by sampling soil cores on a grid centered on crop row. Roots were separated and an estimation of root geometrical attributes was made using two different image analysis programs. Comparisons of these programs yielded nearly identical estimates of RLD. The spatial patterns of RWU and RLD distributions, respectively normalized to the total uptake and root length, were generally similar only for drip line on a crop row, but with some local variations between the two measures. Both RLD and RWU were adequately fitted with parametric models based on semi-lognormal and normal Gaussian bivariate density functions (Coelho and Or, 1996; Soil Sci. Soc. Am. J. 60, 1039–1049).