[Growth of maize seedling root cells following irradiation with high doses of x-rays. I. Inhibition of cell division, duration and rate of root growth after irradiation].
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Although cessation of growth is the most apparent symptom of boron deficiency, the biochemical function of boron in growth processes is not well understood. We propose that the action of boron in root meristems is associated with ascorbate metabolism. Total inhibition of root growth in squash (Cucurbita pepo L.) plants transferred to boron-free medium coincided with a major decrease (up to 98%) in the ascorbate concentration of root apices. Under low-boron conditions, in which root growth was partially inhibited, ascorbate concentration declined in proportion to growth rate. The decline in ascorbate concentration in boron-deficient root tips was not related to ascorbate oxidation. Ascorbate added to the medium improved root growth in plants supplied with insufficient boron. Increasing concentrations of aluminum in the nutrient medium caused progressive inhibition of root growth and a parallel reduction in ascorbate concentration of root apices. Elevated boron levels improved root growth under toxic aluminum conditions and produced root apices with higher ascorbate concentrations. To our knowledge, this is the first report of a correlation between boron nutrition, ascorbate concentration in root apices, and growth. These findings show that root growth inhibition resulting from either boron deficiency or aluminum toxicity may be a consequence of disrupted ascorbate metabolism.
Root growth promoters, 4-hydroxykigelin (1) and 6-demethylkigelin (2), together with 6-hydroxymellein (3) were isolated from cultures of the fungus Aspergillus terreus and their structures were identified by spectroscopic analysis. The biological activities of the three dihydroisocoumarins, 1, 2, and 3, have been examined using a bioassay method with lettuce seedlings. Furthermore, interactions between the dihydroisocoumarins and indole-3-acetic acid against the root growth have been examined.
The effect of low pH on net H(+) release and root growth of corn (Zea mays L.) and broad bean (Vicia faba L.) seedlings was investigated in short-term experiments at constant pH. Broad bean was more sensitive to low pH than corn: the critical values (pH values below which net H(+) release and root growth ceased) were pH 4.00 (broad bean) and pH 3.50 (corn) at 1 millimolar Ca(2+). Both proton release and root growth were progressively inhibited as the medium pH declined. Additional Ca(2+) in the root medium helped to overcome the limitations of low pH for net H(+) release and root growth. Potassium (for corn) and abscisic acid (for broad bean) increased both net H(+) release and root growth rate at the critical pH value. It is concluded that poor root growth at low pH is caused by a lack of net H(+) release that may decrease cytoplasmic pH values. Inhibited net H(+) release at high external H(+) activity is not due to a shortage of energy supply to the H(+) ATPase. Instead, a displacement of Ca(2+) by H(+) at the external side of the plasmalemma may enhance reentry of H(+) into root cells.
OBJECTIVES: To introduce a method for assessment of root growth on panoramic radiographs exemplified by a case report on an autotransplanted lower third molar. MATERIAL AND METHODS: A lower left third molar (T) with incomplete root formation was transplanted for replacement of the lower left first molar in an 18-year-old woman. T was monitored clinically and, together with its neighboring lower second molar (37) with constant root length, also radiographically by means of two panoramic radiographs (OPGs) produced 12 days and 20 months postoperatively. A method for calculation of the root length as a multiple of the crown length is introduced, using accurately reproducible landmarks defining the coronal and apical endpoints of the examined tooth in all OPGs of the series. This method minimizes error due to different magnifications within the set of radiographs. RESULTS: Using the method introduced, the root length of the constant tooth 37 varied at 2.7% within the set of OPGs, whereas it revealed a 5.6% variation when the evaluation was based on direct measurement. Based on the described method, T revealed a postoperative root growth of approximately one-third of its final length and showed clinically no pathological findings during the observation period. CONCLUSIONS: Our results indicate that with the described method root growth assessment on panoramic radiographs is more accurate than with direct measurement.
When dormant Sitka spruce (Picea sitchensis (Bong.) Carr.) transplants were lifted from the nursery in March and transferred to favorable growing conditions in a controlled environment chamber, new roots emerged and elongated even when the plants were bark-ringed so that the roots could not receive metabolites from the shoot by phloem translocation. Carbohydrate analysis showed that starch reserves in the roots of the bark-ringed plants were depleted, indicating that these reserves provided the energy source for new root growth. The shoot also had a role in new root growth as excised root systems showed greatly reduced root growth. This response is compared to that of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) in which bark-ringing prevented root growth indicating that current photosynthate is needed for new root growth. The findings are discussed in relation to the problems of establishing these species in forest plantations.
The effects of different physical and chemical factors on hairy root growth and flavonoids production were studied in suspension culture of Saussurea medusa hairy root in 1/2 MS medium. The results showed that the following culture conditions, nitrogen concentratiaon (involved NH4+ and NO3-), 30 mmol/L; the ratio of ammonium to nitrate, 5:25; the combination of 2% sucrose and 3% glucose; 0.5 mg/L GA3; 0.5 mg/L IBA; initial pH 5.8; light cycle, 18 h/d (3500lx); temperature, 24 degrees C; shaker revolutions per minute, 100 r/min, were favourable to hairy root growth and flavonoids production. Under the above culture conditions, up to 12.8 g/L (DW) of hairy root and 1922 mg/L of flavonoids were obtained after 21 days of culture. The content of total flavonoids in hairy root was 15%, which was about 25 times as that in the wild plantlet.
Light intensity is crucial for plant growth. In this study, the hypothesis was tested whether a sudden increase in light intensity leads to an immediate increase of root growth. Seedlings of Nicotiana tabacum grown in agar-filled Petri dishes were subjected to light intensities of 60 and 300 micromol m(-2) s(-1), respectively. Seedling biomass, sucrose, glucose and fructose concentration as well as primary root growth increased significantly with light intensity. The dynamics of the increase in root growth were analysed here in more detail. In transition experiments from low to high light intensities, root growth increased by a factor of four within 4 d, reaching the steady-state level measured in plants that were cultivated in high-light conditions. The distribution of relative elemental growth rates along the root growth zone retained a constant shape throughout this transition. During the first three hours after light increase, strong growth fluctuations were repeatedly observed with the velocity of the root tip cycling in a sinusoidal pattern between 120 and 180 microm h(-1). These dynamic patterns are discussed in the context of hydraulic and photosynthetic acclimation to the altered conditions. Experiments with externally applied sucrose and with transgenic plants having reduced capacities for sucrose synthesis indicated clearly that increasing light intensity rapidly enhanced root growth by elevating sucrose export from shoot to root.
OBJECTIVE: To assess and measure the diagnostic and prognostic value of individual aortic root growth in children and adolescents with Marfan syndrome. DESIGN: From 1983 to 1996, 250 children were screened for Marfan syndrome. Serial echocardiographic aortic root measurements of 123 children (57 Marfan, 66 control) were available for evaluation of aortic root growth. Aortic root diameters were correlated with body surface area. Based on individual growth of the aortic root a discrimination formula was derived to distinguish Marfan patients from control subjects. RESULTS: Sensitivity and specificity of this method, which were dependent on the number of measurements, were 84% and 73%, respectively, for three serial measurements. The discrimination score also predicted a five year complication free survival in all patients. CONCLUSIONS: In children and adolescents with Marfan syndrome, aortic root growth differs significantly from subjects in whom Marfan syndrome was definitely ruled out during screening. Measurement of individual aortic root growth may serve to establish diagnosis at an early stage and is of prognostic value for occurrence of aortic complications.
Many bottomland tree species are tolerant of compacted soil and perform well in urban environments; however, the mechanism underlying this tolerance is unknown. Increased soil water content has been shown to alleviate some of the effects of soil compaction on plant growth, presumably because increasing soil water reduces soil strength. We hypothesized that tree species tolerant of very wet soils would have opportunities for root growth in compacted soil when high soil water contents reduced soil strength, whereas species intolerant of bottomland conditions would not. We tested this hypothesis on flowering dogwood (Cornus florida L.), a mesic species intolerant of inundation, and silver maple (Acer saccharinum L.), a bottomland species. Seedlings of both species were grown in pots for 21 and 30 days, respectively, in a growth chamber in native loam soil maintained at various combinations of soil strength and soil water tension. Downward root growth rate decreased in response to increasing soil strength in both species. At low soil strength (0.6 MPa), downward root growth rate of dogwood seedlings slowed when soil was either excessively wet or dry, whereas root growth rate of silver maple seedlings increased linearly with soil water content. In moderately compacted soil (1.5 g cm(-3) bulk density), silver maple seedlings had greater root growth rate, root length per plant, and ratio of root length to root dry weight in wet soil (0.006 MPa soil water tension) than in moist and dry soils (0.026 and 0.06 MPa, respectively), even though mean oxygen diffusion rate (ODR) was only 0.28 &mgr;g cm(-2) (SE = 0.05). No such effect was detected in highly compacted soil (1.7 g cm(-3) bulk density) in either species. Mean ODR showed a weak positive correlation with soil water tension (r = 0.40, P = 0.07), but was unrelated to soil strength. We conclude that silver maple roots can grow in moderately compacted soil when high soil water content decreases soil strength, whereas dogwood is unable to take advantage of this opportunity.
Sodium displaces Ca(2+) from membranes (GR Cramer, A Läuchli, VS Polito Plant Physiol 1985 79: 207-211) and this can be related to the (Ca(2+))/(Na(+))(2) activity ratio in the external solution (GR Cramer, A Läuchli 1986 J Exp Bot 37: 321-330). Supplemental Ca(2+) is known to mitigate the adverse effects of salinity on plant growth. In this report we investigated the effects of NaCl (0-250 millimolar) and Ca(2+) (0.4 and 10 millimolar) on the ion activities in solution and on root growth of cotton (Gossypium hirsutum L.). Ion activities were analyzed using the computer program, GEOCHEM. Most ion activities in a 0.1 modified Hoagland solution were significantly reduced by both NaCl and supplemental Ca(2+). Ion-pair formation and precipitation were significant for some ions, especially phosphate. Root growth of 6-day-old seedlings was stimulated by low NaCl concentrations (25 millimolar). At higher NaCl concentrations, root growth was inhibited; the concentration at which this occurred depended on the Ca(2+) concentration and the growth index used. Supplemental Ca(2+) mitigated the inhibition of root growth caused by NaCl. There was a curvilinear relationship between root growth and the (Ca(2+))/(Na(+))(2) ratio in the nutrient solution. The mechanisms by which Na(+) and Ca(2+) may affect root growth are discussed.
The effects of different concentrations (10-5 - 10-2 M) of copper sulfate on root growth, cell division and nucleoli in root-tip cells of Helianthus annuus L. were investigated. Cu had an inhibitory effect on the root growth at 10-4 - 10-2 M during the entire treatment. Cu has toxic effects on chromosomal morphology including anaphase bridges and chromosome stickiness and on nucleoli, causing some similar silver-stained particulate material scattered in the nuclei. Once the nucleolus is poisoned, showing some silver-stained particles scattered in the nucleus, the root growth of H. annuus is obviously inhibited. And once more silver-stained particles appear in the nucleus, the root growth is almost or completely stopped. The possible mechanism of the Cu poisoning of root-tip cells of H. annuus is also briefly discussed.
Tomato (Lycopersicon esculentum, Mill.) roots were analyzed during growth on agar plates. Growth of these roots was inhibited by the auxin transport inhibitors naphthylphthalamic acid (NPA) and semicarbazone derivative I (SCB-1). The effect of auxin transport inhibitors on root gravitropism was analyzed by measurement of the angle of gravitropic curvature after the roots were reoriented 90 degrees from the vertical. NPA and SCB-1 abolished both the response of these roots to gravity and the formation of lateral roots, with SCB-1 being the more effective at inhibition. Auxins also inhibited root growth. Both auxins tested has a slight effect on the gravity response, but this effect is probably indirect, since auxins reduced the growth rate. Auxins also stimulated lateral root growth at concentration where primary root growth was inhibited. When roots were treated with both IAA and NPA simultaneously, a cumulative inhibition of root growth was found. When both compounds were applied together, analysis of gravitropism and lateral root formation indicated that the dominant effect was exerted by auxin transport inhibitors. Together, these data suggest a model for the role of auxin transport in controlling both primary and lateral root growth.
A technology to increase root growth would be advantageous for phytoremediation of trace metal polluted soil, because more roots would be available for metal uptake. The objective of this study was to determine if the auxin, indole-3-acetic acid (IAA), would increase root growth in soil with metals from sewage sludge, when the tetrasodium salt of the chelate EDTA (ethylenediamine-tetraacetic acid) was added to solubilize the metals. Sunflower (Helianthus annuus L.) plants grew in large pots containing either soil from a sludge farm or composted sludge. The EDTA salt was added at a rate of 1 g kg(-1) soil 37 days after planting. IAA at the rate of 3 or 6 mg l(-1) was sprayed on the leaves (500 ml) and added to the soil (500 ml) three times: 41, 50, and 74 days after planting. At harvest 98 days after planting, oven-dry weights were measured, and plant organs were analyzed for Cd, Cu, Fe, Mn, Ni, Pb, and Zn. Metal uptake was determined as the product of metal concentration in an organ and weight. IAA increased root growth of plants grown in the soil with sludge when no EDTA was present. With no EDTA, Mn and Ni in leaves of plants grown in the soil were higher at 3 and 6 mg l(-1) IAA compared to 0 mg l(-1) IAA. With and without EDTA, Cd and Pb in leaves of plants grown in the compost were higher with 3 and 6 mg l(-1) IAA compared to 0 mg l(-1) IAA.
New root growth of conifer nursery seedlings is dependent on light, but whether this is necessary only for photosynthesis, or also has some other root growth promoting effect is unknown. This question was investigated using one-year-old Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) seedlings grown at two nurseries from the same seed lot and taken from cold storage in March and April. New root production was examined in two 10-day root growth capacity (RGC) experiments. Seedlings were subjected to one of four treatments: (1) control, (2) exclusion of light, (3) low CO(2) concentration, and (4) girdling to separate the phloem connection between shoot and root. Shoots were enclosed in Plexiglas cuvettes and supplied with scrubbed air to reduce the CO(2) concentration to 11 to 22 microl l(-1) in the light. The closed system used in Experiment 1 was opened to the atmosphere briefly each day to restore O(2) to ambient, but this was unnecessary for the open system used in Experiment 2. In Experiment 1, new root production was affected by treatments in the order: control > low CO(2) concentration > dark > girdling. Greater new root production in the low CO(2) treatment compared with the dark treatment was attributed to brief increases in CO(2) to ambient concentrations when O(2) was restored each day. In Experiment 2, new root production at the low CO(2) concentration in the light was essentially the same as in darkness, but only 17% of the control value. Thus light appeared to play no part in new root production other than permitting photosynthesis. Limited production of new roots occurred in the absence of photosynthesis, which was further reduced by girdling, presumably because, after girdling, only root system reserves could be used.
* The blue light photoreceptor phototropin-1 has been shown to enhance fitness in Arabidosis thaliana under field conditions. Here, we ask whether performance consequences of phototropin-1 reflect its impact on root growth and drought tolerance. * We used a PHOT1-GFP gene construct to test whether phototropin-1 abundance in roots is highest at shallow soil depths where light penetration is greatest. We then compared root growth efficiency and size at maturity between individuals with and without functional phototropin-1. Comparisons were made under wet and dry conditions to assess the impact of phototropin-1 on drought tolerance. * Phototropin-1 was most abundant in upper root regions and its impact on root growth efficiency decreased with soil depth. Roots of plants with functional phototropin-1 made fewer random turns and traveled further for a given length (higher efficiency) than roots of phot1 mutants. In dry (but not wet) soil, enhancement of root growth efficiency by phototropin-1 increased plant size at maturity. * Results indicate that phototropin-1 enhances performance under drought by mediating plastic increases in root growth efficiency near the soil surface.
Root development is highly responsive to microbial interactions, yet the mechanisms by which beneficial fungi promote root growth remain incompletely understood. Here, we identified Penicillium melinii 'isolate 2' through a screen of endophytic fungi isolated from Arabidopsis and characterized it as a promoter of root development in both Arabidopsis and crop species. We combined phenotyping in vitro, rhizotron, greenhouse and field assays with reporter and mutant analyses, transcriptomics, phytohormone profiling and sequencing and annotation of the fungal genome to investigate the basis of this interaction. P. melinii consistently stimulated root growth and modified root architecture across experimental systems and host species. These effects were associated with subtle but reproducible host transcriptional reprogramming, supporting a model in which the fungus fine-tunes endogenous developmental programmes rather than broadly perturbing stress or growth pathways. Genetic and reporter analyses further suggested that this interaction modulates root branching through localized developmental reprogramming. Genomic analysis provided a framework for understanding the fungal traits associated with this beneficial interaction. The conservation of the response across model and crop species supports the relevance of P. melinii as both a useful experimental system to study beneficial plant-fungus interactions and a promising candidate for improving root traits and crop performance.
The effects of varied rooting volumes on root growth and source leaf carbohydrate metabolism were studied in greenhouse-grown cucumber (Cucumis sativus L cv Calypso) plants. Plants were grown for 7 weeks in container volumes that ranged from 0.4 to 5.9 liters. Plants grown in the smaller containers exhibited less leaf expansion, lower root and shoot weight, and fewer lateral stems than plants grown in the 5.9 liter containers. Shoot/root ratio was not altered by the container volume, suggesting coordination of root and shoot growth due to rooting volume. Source leaf carbon exchange rates, assimilate export rates, and starch accumulation rates for plants grown in 0.4 liter containers were approximately one-half or less in comparison to those for plants grown in 5.9 liter containers. Starch concentrations per unit leaf area were maintained at high levels in source leaves of plants grown in 0.4 liter containers over the entire day/night cycle. Lower extractable galactinol synthase activities and higher galactinol concentrations occurred in leaves of plants grown in 0.4 liter container volumes. The reduced sink demand, induced by restricted root growth, may have led to increased starch concentrations and to a reduction in stachyose biosynthesis in cucumber source leaves.