scholarly journals Maize nodal root growth under water deficits

2016 ◽  
Author(s):  
◽  
Kara J. Riggs

The nodal root system is critical for the development of the mature root system in maize (Zea mays L.) and other grasses. Under drought conditions, nodal root axes may need to grow through surface soil that is dry, hard, and hot. These roots are known to have a superior ability to continue elongation at low water potentials relative to other organs of the plant, but the physiology of this response has been little studied. The objective of this study was to develop an experimental system that models the field situation in which upper soil layers dry, to enable studies of nodal root growth regulation under water deficit conditions. A divided-chamber experimental system was developed to allow the growth of maize primary and seminal root systems in well-watered conditions while the nodal root system is exposed to precise conditions of low soil water potential. The divided-chamber system was used to characterize nodal root growth responses to a range of soil water potentials under steady-state and reproducible conditions. Two contrasting genotypes, selected for differences in root growth response to water stress based on a previous study of the primary root, displayed similarly sensitive growth responses to -0.3 MPa soil, but different capacities to maintain high root tip water potential corresponding with different growth responses at lower soil water potentials. Both genotypes maintained relatively high nodal root tip water potentials in -2.0 MPa soil, despite the decreased soil water potential, suggesting a stress-induced response that enhances water transport to the root tip. The difference in high tissue water potential maintenance was seen not only between the contrasting genotypes but also between the first two developmental nodes of roots. The divided-chamber system provides a powerful experimental approach to investigate the physiological mechanisms regulating nodal root growth responses to adverse soil conditions. Future studies may include measurements of hydraulic conductivity, anatomical characterization of vascular elements near the growth zone, aquaporin content and activity, and suberin deposition in response to low soil water potentials.

HortScience ◽  
2005 ◽  
Vol 40 (3) ◽  
pp. 795-798 ◽  
Author(s):  
Dana L. Baumann ◽  
Beth Ann Workmaster ◽  
Kevin R. Kosola

Wisconsin cranberry growers report that fruit production by the cranberry cultivar `Ben Lear' (Vaccinium macrocarpon Ait.) is low in beds with poor drainage, while the cultivar `Stevens' is less sensitive to these conditions. We hypothesized that `Ben Lear' and `Stevens' would differ in their root growth and mortality response to variation in soil water potential. Rooted cuttings of each cultivar were grown in a green-house in sand-filled pots with three different soil water potentials which were regulated by a hanging water column below a fritted ceramic plate. A minirhizotron camera was used to record root growth and mortality weekly for five weeks. Root mortality was negligible (2% to 6%). Whole plant relative growth rates were greatest for both cultivars under the wettest conditions. Rooting depth was shallowest under the wettest conditions. Whole-plant relative growth rates of `Ben Lear' were higher than `Stevens' at all soil water potentials. `Stevens' plants had significantly higher root to shoot ratios and lower leaf area ratios than `Ben Lear' plants, and produced more total root length than `Ben Lear' at all soil water potentials. Shallow rooting, high leaf area ratio, and low allocation to root production by `Ben Lear' plants may lead to greater susceptibility to drought stress than `Stevens' plants in poorly drained cranberry beds.


1994 ◽  
Vol 24 (5) ◽  
pp. 869-877 ◽  
Author(s):  
W.H. Fogal ◽  
S.J. Coleman ◽  
M.S. Wolynetz ◽  
H.O. Schooley ◽  
S.M. Lopushanski ◽  
...  

The numbers of seed strobili and pollen strobilus clusters and the extent of branch terminal growth were determined on 6-year-old containerized jack pine (Pinusbanksiana Lamb.) trees following modification of the soil nitrogen (N) supply (NH4NO3 at 3, 100, or 300 mg N/L; NO3− at 100 mg N/L; or NH4+ at 100 mg N/L in a nutrient solution), soil water supply (soil water potentials above −20 kPa compared with potentials near −70 kPa), and tree crown size (intact trees outside polythene shelters and lightly versus severely topped trees under polythene shelters). These factors were tested with or without biweekly foliar applications of spray solutions containing 400 mg/L of GA4/7. Intact trees outside polythene shelters did not display sexual or growth responses to N or GA4/7 treatments. Seed strobilus production on topped trees under shelters was not influenced by the level of topping or N supply, but it was depressed by low soil moisture potentials and stimulated by GA4/7 with high or low soil water potentials. Pollen strobilus production was depressed by severe topping and by low soil water potential; it was stimulated by GA4/7 on lightly topped trees but not on severely topped trees and by a low (3 mg N/L) N supply. In the year after treatment, terminal growth of a branch from the 2-year-old nodal whorl was not influenced by nitrogen supply or by light topping but it was increased by severe topping; it was increased by GA4/7 treatment if soil water potential was high but not with low water potential; it was depressed by low soil water potential.


1988 ◽  
Vol 18 (11) ◽  
pp. 1392-1396 ◽  
Author(s):  
G. L. Simmons ◽  
P. E. Pope

A greenhouse study was conducted to determine the influence of soil water potential and endomycorrhizal fungi on root growth of yellow-poplar (Liriodendrontulipifera L.) and sweet gum (Liquidambarstyraciflua L.) seedlings grown at three soil bulk densities. Silt loam soil was compacted in PVC pots to bulk densities of 1.25 (low), 1.40 (medium), or 1.55 (high) Mg • m−3, and equilibrated at −10 kPa soil water potential. Newly germinated seedlings were transplanted into the pots, inoculated with fungal chlamydospores of Glomusmacrocarpum or Glomusfasciculaturn, or distilled water (control), and grown for 3 months at −10 or −300 kPa soil water potential. Total porosity, air-filled porosity, water content, and mechanical resistance of the soil were determined for samples compacted to the same bulk densities and equilibrated at the same soil water potentials as were used in the greenhouse study. Root growth was reduced by the high mechanical resistance caused by bulk densities of 1.40 and 1.55 Mg • m−3 at −300 kPa water potential. At both water potentials, total length of lateral roots and fibrosity of the root system of both tree species decreased significantly when bulk density increased from 1.40 to 1.55 Mg • m−3. Air-filled porosity less than 0.12 m3 • m−3 limited root growth when water potential was −10 kPa, and mechanical resistance greater than 3438 kPa restricted growth at −300 kPa. At −10 kPa, root length and fibrosity were greatest for inoculated sweet gum seedlings at each bulk density. At −300 kPa, sweet gum seedlings inoculated with G. fasciculatum had the greatest root length and fibrosity at the low and medium bulk densities. Mycorrhizal effects on root length of yellow-poplar were variable, and fibrosity was not significantly affected by mycorrhizal treatment.


1988 ◽  
Vol 68 (3) ◽  
pp. 569-576 ◽  
Author(s):  
YADVINDER SINGH ◽  
E. G. BEAUCHAMP

Two laboratory incubation experiments were conducted to determine the effect of initial soil water potential on the transformation of urea in large granules to nitrite and nitrate. In the first experiment two soils varying in initial soil water potentials (− 70 and − 140 kPa) were incubated with 2 g urea granules with and without a nitrification inhibitor (dicyandiamide) at 15 °C for 35 d. Only a trace of [Formula: see text] accumulated in a Brookston clay (pH 6.0) during the transformation of urea in 2 g granules. Accumulation of [Formula: see text] was also small (4–6 μg N g−1) in Conestogo silt loam (pH 7.6). Incorporation of dicyandiamide (DCD) into the urea granule at 50 g kg−1 urea significantly reduced the accumulation of [Formula: see text] in this soil. The relative rate of nitrification in the absence of DCD at −140 kPa water potential was 63.5% of that at −70 kPa (average of two soils). DCD reduced the nitrification of urea in 2 g granules by 85% during the 35-d period. In the second experiment a uniform layer of 2 g urea was placed in the center of 20-cm-long cores of Conestogo silt loam with three initial water potentials (−35, −60 and −120 kPa) and the soil was incubated at 15 °C for 45 d. The rate of urea hydrolysis was lowest at −120 kPa and greatest at −35 kPa. Soil pH in the vicinity of the urea layer increased from 7.6 to 9.1 and [Formula: see text] concentration was greater than 3000 μg g−1 soil. There were no significant differences in pH or [Formula: see text] concentration with the three soil water potential treatments at the 10th day of the incubation period. But, in the latter part of the incubation period, pH and [Formula: see text] concentration decreased with increasing soil water potential due to a higher rate of nitrification. Diffusion of various N species including [Formula: see text] was probably greater with the highest water potential treatment. Only small quantities of [Formula: see text] accumulated during nitrification of urea – N. Nitrification of urea increased with increasing water potential. After 35 d of incubation, 19.3, 15.4 and 8.9% of the applied urea had apparently nitrified at −35, −60 and −120 kPa, respectively. Nitrifier activity was completely inhibited in the 0- to 2-cm zone near the urea layer for 35 days. Nitrifier activity increased from an initial level of 8.5 to 73 μg [Formula: see text] in the 3- to 7-cm zone over the 35-d period. Nitrifier activity also increased with increasing soil water potential. Key words: Urea transformation, nitrification, water potential, large granules, nitrifier activity, [Formula: see text] production


Author(s):  
Stefan J. Kupers ◽  
Bettina M. J. Engelbrecht ◽  
Andrés Hernández ◽  
S. Joseph Wright ◽  
Christian Wirth ◽  
...  

1984 ◽  
Vol 102 (2) ◽  
pp. 415-425 ◽  
Author(s):  
M. McGowan ◽  
P. Blanch ◽  
P. J. Gregory ◽  
D. Haycock

SummaryShoot and root growth and associated leaf and soil water potential relations were compared in three consecutive crops of winter wheat grown in the same field. Despite a profuse root system the crop grown in the second drought year (1976) failed to dry the soil as throughly as the crops in 1975 and 1977. Measurements of plant water potential showed that the restricted utilization of soil water reserves by this crop was associated with failure to make any significant osmotic adjustment, leading to premature loss of leaf turgor and stomatal closure. The implications of these results for models to estimate actual crop evaporation from values of potential evaporation are discussed.


1994 ◽  
Vol 21 (1) ◽  
pp. 69 ◽  
Author(s):  
JG Phillips ◽  
SJ Riha

A split-root experiment was conducted using Eucalyptus viminalis seedlings which were exposed to three watering regimes in order to investigate root growth and soil water extraction under conditions of a drying soil profile. Seedlings were grown in columns in which the soil was divided horizontally with a soft wax plate. Watering treatments were composed of (1) both upper and lower sections of the column well watered (W/W), (2) only the lower section well watered (D/W), and (3) water withheld completely from both upper and lower sections (D/D). Daily measurements included soil water potential (Ψs), column water loss and leaf elongation. Increase in above- and below-ground biomass was deter- mined from initial and final harvests after 25 days of treatment. Whole-column water loss and leaf extension were depressed as Ψs in the upper section of D/W and D/D decreased to -0.4 MPa over the first 8-10 days. However, water loss did not decrease significantly in the lower section of treatment D/W relative to the lower section of treatment W/W during this period. This indicated that water extraction by roots remaining in wet soil was not severely inhibited by the decrease in transpiration associated with the soil conditions in the upper profile. Root distribution at the end of the experiment indicated significant growth in the lower section of treatment D/W. There was evidence that hydraulic lifting of water between column sections may have occurred, as periodic increases in soil water potential of the unwatered upper section of D/W were observed.


HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 531e-531
Author(s):  
Erik B. G. Feibert ◽  
Clint C. Shock ◽  
Monty Saunders

Onions were grown with different soil water potentials as irrigation criteria to determine the soil water potential at which optimum onion yield and quality occurs. Furrow irrigation treatments in 1992 and 1993 consisted of six soil water potential thresholds (-12.5 to -100 kPa). Soil water potential in the first foot of soil was measured by granular matrix sensors (Watermark Model 200SS, Irrometer Co., Riverside, CA) that had been previously calibrated to tensiometers on the same silt loam series. Both years, yield and market grade based on bulb size (more jumbo and colossal onions) increased with wetter treatments. In 1993, a relatively cool year, onion grade peaked at -37.5 kPa due to a significant increase in rot during storage following the wetter treatments. These results suggest the importance of using moisture criteria to schedule irrigations for onions.


2021 ◽  
Author(s):  
Ali Mehmandoost Kotlar ◽  
Mathieu Javaux

<p>Root water uptake is a major process controlling water balance and accounts for about 60% of global terrestrial evapotranspiration. The root system employs different strategies to better exploit available soil water, however, the regulation of water uptake under the spatiotemporal heterogeneous and uneven distribution of soil water is still a major question. To tackle this question, we need to understand how plants cope with this heterogeneity by adjustment of above ground responses to partial rhizosphere drying. Therefore, we use R-SWMS simulating soil water flow, flow towards the roots, and radial and the axial flow inside the root system to perform numerical experiments on a 9-cell gridded rhizotrone (50 cm×50 cm). The water potentials in each cell can be varied and fixed for the period of simulation and no water flow is allowed between cells while roots can pass over the boundaries. Then a static mature maize root architecture to different extents invaded in all cells is subjected to the various arrangements of cells' soil water potentials. R-SWMS allows determining possible hydraulic lift in drier areas. With these simulations, the variation of root water and leaf water potential will be determined and the role of root length density in each cell and corresponding average soil-root water potential will be statistically discussed.</p>


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