Effects of NaCl and silicon on ion distribution in the roots,shoots and leaves of two alfalfa cultivars with different salt tolerance

Abstract

The effects of exogenous NaCl and silicon on ion distribution were investigated in two alfalfa (Medicago sativa. L.) cultivars: the high salt tolerant Zhongmu No. 1 and the low salt tolerant Defor. The cultivars were grown in a hydroponic system with a control (that had neither NaCl nor Si added), a Si treatment (1 mmol L^?1 Si), a NaCl treatment (120 mmol L^?1 NaCl), and a Si and NaCl treatment (120 mmol L^?1 NaCl + 1 mmol L^?1 Si). After 15 days of the NaCl and Si treatments, four plants of the cultivars were removed and divided into root, shoot and leaf parts for Na⁺, K⁺, Ca²⁺, Mg²⁺, Fe³⁺, Mn²⁺, Cu²⁺ and Zn²⁺ content measurements. Compared with the NaCl treatment, the added Si significantly decreased Na⁺ content in the roots, but notably increased K⁺ contents in the shoots and leaves of the high salt tolerant Zhongmu No.1 cultivar. Applying Si to both cultivars under NaCl stress did not significantly affect the Fe³⁺, Mg²⁺ and Zn²⁺ contents in the roots, shoots and leaves of Defor and the roots and shoots of Zhongmu No.1, but increased the Ca²⁺ content in the roots of Zhongmu No.1 and the Mn²⁺ contents in the shoots and leaves of both cultivars, while it decreased the Ca²⁺ and Cu²⁺ contents of the shoots and leaves of both cultivars under salt stress. Salt stress decreased the K⁺, Ca²⁺, Mg²⁺ and Cu²⁺ contents in plants, but significantly increased Zn²⁺ content in the roots, shoots and leaves and Mn²⁺ content in the shoots of both cultivars when Si was not applied. Thus, salt affects not only the macronutrient distribution but also the micronutrient distribution in alfalfa plants, while silicon could alter the distributions of Na⁺ and some trophic ions in the roots, shoots and leaves of plants to improve the salt tolerance.     

Aluminum tolerances of two snapbean cultivars related to organic acid content evaluated by high‐performance liquid chromatography

High‐performance liquid chromatography (HPLC) was used to determine aluminum (Al)‐induced changes in organic acid (OA) concentrations of Al‐tolerant ‘Dade’ and Al‐sensitive ‘Romano’ snapbean cultivars. Two week old ‘Dade’ and ‘Romano’ snapbean were grown in 1/5‐strength Steinberg nutrient solution for 10 days and then subjected to 0, 2, 4, 6, and 8 mg L^‐1 Al treatments at pH 4.5 for an additional 3–15 days. Current studies confirmed earlier findings that the Dade cultivar was significantly more tolerant to Al than the Romano variety. Organic acid analyses were performed on extracts of root and leaf, and on stem exudates. The organic acids were separated on an ion exclusion column using a mobile phase of 0.01 N H₃PO₄. Individual OA were quantified with a variable wavelength detector operating at 210 nm. Aluminum stress tended to reduce the concentrations of citric, malonlc, malic, glycolic, fumaric, and acetic acids in the roots and increased the OA concentrations in stem exudates. In the presence or absence of Al stress, the Al tolerant Dade cultivar contained higher OA concentrations than did the Al‐sensitlve Romano. Aluminum stress reduced total OA levels in root extracts from Al‐sensltive Romano plants to a greater extent than in those of the Al‐tolerant Dade. Malic and citric acid concentrations were decreased more than those of the other organic acids examined. Results indicate that the Al‐tolerant Dade snapbean cultivar has a higher potential for Al‐chelation and detoxification than does the Al‐sensitive Romano. Hence, an Al‐chelation mechansism may be involved in differential Al tolerance within this species.     

Enhanced Mn accumulation by snapbean cultivars under FE stress

Iron deficiency in dicots is accompanied by an increased potential for Fe uptake and translocation. The mechanisms responsible for these changes in metabolism (Fe‐stress response) provide for the adaptation of Fe‐efficient genotypes to conditions which limit the availability of Fe. Previous studies indicated that when Fe‐stress response is initiated, the uptake of Mn, as well as Fe, is enhanced in Fe efficient species such as sunflower. The present study was conducted to determine the relationship between Fe‐stress response and Mn uptake in snapbean (Phaseolus vulgaris L., cvs. Bush Blue Lake 290, Bush Blue Lake 274). The plants were grown in complete nutrient solutions containing 0.02 to 0.52 mg L^‐1 Mn, at acid or alkaline pH. Iron stress was induced with 0.22 mg l‐¹ Fe(EDDHA) (molar ratio 1:1 or 1:2), high P (14.3 mg L‐¹) and excess CaCO_3. Bush Blue Lake 290 ('BBL 290') was more sensitive than Bush Blue Lake 274 ('BBL 274') to Mn toxicity in acid (pH 5.2) nutrient solutions with adequate Fe. Under alkaline conditions, Mn accumulation by ‘BBL 290’ snapbean was increased dramatically with Fe stress, while a moderate Increase was found for ‘BBL 274’. Foliar symptoms of Mn toxicity, observed on Fe stressed ‘BBL 290’, increased in severity at higher Mn (0.06 to 0.26 mg L^‐1 ) concentrations. It was concluded that the magnitude of the enhanced Mn uptake was related to the intensity of Fe stress response as well as the cultivar sensitivity to Mn.     

Evaluating quantitative screening methods for manganese toxicity in cotton genotypes 1

Identification of cotton genotypes more tolerant of toxic concentrations of soil solution manganese (Mn²⁺) would integrate well with soil ameliorations of that problem. Several quantitative and semi‐quantitative methods to determine the amount of Mn toxicity were evaluated on three genotypes of Gossypium hirsutum (LaDSIS 12513, LaDASS 5175, and Coker gl 79–501) and one genotype of Gossypium barbadense (Pitnas S‐5). Specific leaf weight (SLW) and the semi‐quantitative, ‘percentage of leaves that were damaged’ (PLD) correlated the least with other methods of Mn toxicity determination. Neither SLW or PLD provided more separation between genotypes than area/leaf (AL), peroxidase (POD) activity, and indole‐3‐acetic acid oxidase (IAAO) activity. Similar genotype separations occurred for AL, POD, and IAAO at 10 mg/L Mn in solution, but POD and IAAO produced more genotype separations than AL at 5 mg/L of Mn. There were differences in enzyme activity between genotypes at control (0.25 mg/L) Mn solution concentration, making assessment difficult, especially between species. Barring this caveat, the relatively fast POD activity assay was considered to be the best method since it paralleled activity of IAAO, the functional enzyme of Mn toxicity, which had a relatively slow assay method.     

Rice genotype differences in nutrient status under excessive ferric‐iron conditions

To investigate the relationship between rice genotypic variation in tolerance to iron (Fe) toxicity and nutrient element status, 10 rice genotypes with different growing performances under Fe toxicity were grown under normal culture solution and with excessive ferrous (Fe²⁺)‐Fe concentrations of 250 and 500 mg Fe²⁺ L^‐1. A close relationship was obtained between the relative ratio of symptomatic leaf numbers to total leaf numbers (SLN/TLN) and a relative decrease in dry matter under Fe²⁺‐toxicity conditions. The genotypic variations in nitrogen (N), phosphorus (P), potassium (K), and magnesium (Mg) uptake were evaluated by the relative decrease in the N, P, K, and Mg content in the plants. Remarkable genotypic variation in tolerance to excessive Fe²⁺ was observed. The results indicated that excessive Fe²⁺ reduced N, P, K, and Mg uptake. The nutrient element concentrations, however, were still higher above deficient criteria even in severely affected plants, suggesting that the retardation of growth may not be intirely due to the deficiency of these elements in plants at the seedling stage. Significant correlations were found between the genotypic variation and the decrease in N, P, K, and Mg uptake and in their tolerance to Fe²⁺ toxicity, which suggests that the ability to maintain higher nutrient element uptake under a Fe²⁺‐toxic condition contributes the tolerance to Fe²⁺ toxicity.     

Manganese in substrate clays—harmful for plants?

Mixtures of peat and substrate clays are commonly used as growth media for horticultural plant production. A quality protocol for substrate clays defines a threshold value of active manganese (Mn_act = sum of exchangeable and easily reducible Mn) in substrate clays of < 500 mg kg^–1 to prevent toxic reactions of plants. This threshold value was tested in experiments with peat‐clay blends under various growth conditions, and nutrient solution experiments were additionally conducted to investigate the effects of silicic acid and dissolved organic matter on the occurrence of Mn toxicity. Common bean (Phaseolus vulgaris L.) and hydrangea (Hydrangea macrophylla) plants were cultivated in different peat‐clay substrates and in peat under different moisture and pH levels. The clays varied in their Mn_act content from 4–2354 mg kg^–1. The results of the substrate experiments reveal that a threshold value for Mn in substrate clays is not justified, as plants grown in all peat‐clay substrates did not develop any Mn toxicity even at high substrate moisture or low pH conditions which are known to increase the Mn availability. The extraction of active Mn did not well reflect the Mn concentrations in plant dry matter and substrate solution. As plants tolerated high Mn concentrations in the substrate solution compared to the nutrient solution without toxicity symptoms, the influence of silicic acid and dissolved organic matter (DOM) on Mn toxicity was characterized in a nutrient‐solution experiment. Manganese toxicity was clearly diminished by silicic acid application, but not by DOM. The former effect probably explains the tolerance of bean plants in peat substrates where high silicon concentrations in the substrate solution were observed. Peat‐clay blends even provided up to five times more silicon to plants than pure peat.     

Vanadium induced manganese toxicity in bush bean plants grown in solution culture

Seedlings of two bush bean cultivars (Phaseolus vulqaris L. cvs. Mn‐sensitive ‘Wonder Crop 2’ and Mn‐tolerant ‘Green Lord') were grown for 14 days in full strength Hoagland No. 2 nutrient solution containing 0.05 ‐ 2 mg L^‐1 of vanadium (V) as ammonium vanadate.

Increasing V concentration in the solution decreased total dry weight of both cultivars. Plant tops were stunted and leaf color became dark green at 1 ‐ 2 mg L^‐1 V, especially in ‘Green Lord’. Veinal necrosis similar to that of Mn toxicity was observed in the primary leaves of ‘Wonder Crop 2’ at 0.2 mg L^‐1 V or above, but not in those of ‘Green Lord’.

The V concentrations in the roots increased exponentially with increasing V concentration in the solution; however, V concentrations in the leaves and stems were not affected. The Mn concentrations in the primary leaves increased under the higher V treatment in ‘Wonder Crop 2'; but not in ‘Green Lord’. In contrast, Fe concentration in the leaves of ‘Wonder Crop 2’ decreased markedly with increasing V concentration in the solution. Enhanced Mn uptake and greater reduction of Fe uptake by ‘Wonder Crop 2’ may explain the incidence of V‐induced Mn toxicity.     

Variation of tolerance to manganese toxicity in Australian hexaploid wheat

High concentrations of manganese (Mn), iron (Fe), and aluminium (Al) induced in waterlogged acid soils are a potential constraint for growing sensitive wheat cultivars in waterlogged‐prone areas of Western Australian wheat‐belt. Tackling induced ion toxicities by a genetic approach requires a good understanding of the existing variability in ion toxicity tolerance of the current wheat germplasm. A bioassay for tolerance to high concentration of Mn in wheat was developed using Norquay (Mn‐tolerant), Columbus (Mn‐intolerant), and Cascades (moderately tolerant) as control genotypes and a range of MnCl₂ concentrations (2, 250, 500, 750, 1000, 2000, and 3000 μM Mn) at pH 4.8 in a nutrient solution. Increasing solution Mn concentration decreased shoot and root dry weight and intensified the development of toxicity symptoms more in the Mn‐intolerant cv. Columbus than in Norquay and Cascades. The genotypic discrimination based on relative shoot (54% to 79%) and root dry weight (17% to 76%), the development of toxicity symptoms (scores 2 to 4) and the shoot Mn concentration (1428 to 2960 mg kg^–1) was most pronounced at 750 μM Mn. Using this concentration to screen 60 Australian and 6 wheat genotypes from other sources, a wide variation in relative root dry weight (11% to 95%), relative shoot dry weight (31% to 91%), toxicity symptoms (1.5 to 4.5), and shoot Mn concentration (901 to 2695 mg kg^–1) were observed. Evidence suggests that Mn tolerance has been introduced into Australian wheat through CIMMYT germplasm having “LERMO‐ROJO” within their parentage, preserved either through a co‐tolerance to Mn deficiency or a process of passive selection for Mn tolerance. Cultivars Westonia and Krichauff expressed a high level of tolerance to both Mn toxicity and deficiency, whereas Trident and Janz (reputed to be tolerant to Mn deficiency) were intolerant to Mn toxicity, suggesting that tolerance to excess and shortage of Mn are different, but not mutually exclusive traits. The co‐tolerance for Mn and Al in ET8 (an Al‐tolerant near‐isogenic line) and the absence of Mn tolerance in BH1146 (an Al‐tolerant genotype from Brazil) limits the effectiveness of these indicator genotypes to environments where only one constraint is induced. Wide variation of Mn tolerance in Australian wheat cultivars will enable breeding genotypes for the genetic solution to the Mn toxicity problem.     

A quick and efficient screen for resistance to iron toxicity in lowland rice

Iron (Fe) toxicity is a major stress to rice in many lowland environments worldwide. Due to excessive uptake of Fe²⁺ by the roots and its acropetal translocation into the leaves, toxic oxygen radicals may form and damage cell structural components, thus impairing physiological processes. The typical visual symptom is the “bronzing” of the rice leaves, leading to substantial yield losses, particularly when toxicity occurs during early vegetative growth stages. The problem is best addressed through genotype improvement, i.e., tolerant cultivars. However, the time of occurrence and the severity of symptoms and yield responses vary widely among soil types, years, seasons, and genotypes. Cultivars resistant in one system may fail when transferred to another. Better targeting of varietal improvement requires selection tools improving our understanding of the resistance mechanisms and strategies of rice in the presence of excess iron. A phytotron study was conducted to develop a screen for seedling resistance to Fe toxicity based on individual plants subjected to varying levels of Fe (0–3000 mg L^–1 Fe supplied as Fe(II)SO₄), stress duration (1–5 d of exposure), vapor‐pressure deficit (VPD; 1.1 and 1.8 kPa), and seedling age (14 and 28 d). Genotypes were evaluated based on leaf‐bronzing score and tissue Fe concentrations. A clear segregation of the genotypic tolerance spectrum was obtained when scoring 28 d old seedlings after 3 d of exposure to 2000 mg L^–1 Fe in a high‐VPD environment. In most cases, leaf‐bronzing scores were highly correlated with tissue Fe concentration (visual differentiation in includer and excluder types). The combination of these two parameters also identified genotypes tolerating high levels of Fe in the tissue while showing only few leaf symptoms (tolerant includers). The screen allows selecting genotypes with low leaf‐bronzing score as resistant to Fe toxicity, and additional analyses of the tissue Fe concentration of those can identify the general adaptation strategy to be utilized in breeding programs.     

Differential manganese tolerances of cotton genotypes in nutrient solution

Cotton genotypes [Gossypium hirsutum (L.)] C‐310–73,‐307 (307) and C‐Sgl, 70–517 (517), shown previously to differ in tolerance to an acid (pH 5.1), high manganese (Mn) Grenada soil from Arkansas, were grown in nutrient solutions containing variable concentrations of excess Mn to confirm and characterize their postulated differences in Mn tolerance. Based on crinkle leaf symptoms and leaf dry weights, the 307 genotype was significantly more tolerant than 517 to 4, 8, or 16 mg Mn/L at a maintained pH of 4.6 (Experiment 1) and also to 4 or 8 mg Mn/L at an initial pH of 5.0, not subsequently adjusted (Experiment 2). In Experiment 1, the relative leaf dry weight (wt. with no Mn/wt. with 8 mg Mn/L × 100) was 94% for genotype 307 and only 27% for 517. In Experiment 2, the corresponding relative leaf weights were 75% and 26% for 307 and 517, respectively. Plant analytical results indicated that the 307 genotype tolerates a higher concentration of Mn in its leaves than does 517. This failure to correlate Mn tolerance with Mn concentrations in plant shoots agrees with previous findings when these two genotypes were grown in acid Grenada soil. Iron (Fe) concentrations, Fe/Mn ratios, and magnesium (Mg) concentrations were higher in the Mn‐tolerant 307 than in the Mn‐sensitive 517, but concentrations of phosphorus (P), potassium (K), calcium (Ca), copper (Cu), and zinc (Zn) were not related to Mn tolerance. Because differential Mn tolerance in these two genotypes is associated with differential internal tolerance to excess Mn, rather than differential Mn uptake, studies are needed to determine the chemical forms of Mn in tolerant and sensitive plants whose leaves contain comparable concentrations of total Mn. Because both Mn and Fe (closely related elements in the Mn toxicity syndrome) have spin resonances, electron paramagnetic resonance (EPR) offers promise in attacking the problem of differential Mn tolerance in plants.     

Aluminum effects on micronutrient uptake by annual ryegrass

Abstract

Four ryegrass (Lolium multiflorumLam.) cultivars were grown in 1/5 Steinberg nutrient solution supplemented with six Al levels (0, 37, 74, 148, 296, or 592 umol L^‐1) at pH initially adjusted to 4.2. Average net Fe influx was stimulated at low nutrient solution Al levels. This stimulation was larger for more Al‐tolerant cultivars Marshall and Gulf. Decreases in average net Mn and Zn influxes were brought about by increasing Al levels in the nutrient solution. The average net influx of Fe, Mn, and Zn was positively correlated with the root tolerance index (relative root yield of plants grown with and without Al added to the nutrient solution). For more Al‐tolerant cultivars, increased total uptake of Fe and Cu was brought about by increased nutrient solution Al levels up to 74 umol L^‐1. Decreases in total uptake of Mn and Zn were generally noted with increased nutrient solution Al levels. Percentage inhibition of total Fe, Mn, Zn, and Cu uptake was negatively correlated with the mean pH of the Al‐containing nutrient solutions. The higher average net influx and the smaller percentage inhibition of total Fe uptake at nutrient solution Al levels up to 74 umol L^‐1can be used as indicators in ranking ryegrass cultivars as more Al‐tolerant     

Differential tolerance of bush bean cultivars to excess manganese in solution and sand culture

Nineteen bush bean cultivars were screened for tolerance to excess Mn in nutrient solution and sand culture experiments. Seven‐day‐old seedlings were treated with full strength Hoagland No. 2 nutrient solution containing different Mn concentrations for 12 days in the greenhouse.

Cultivars showing the greatest sensitivity to Mn toxicity were ‘Wonder Crop 1’ and ‘Wonder Crop 2'; those showing the greatest tolerance were ‘Green Lord’, ‘Red Kidney’ and ‘Edogawa Black Seeded’.

Leaf Mn concentration of plants grown in sand culture was higher than that for plants grown in solution culture. The lowest leaf Mn concentration at which Mn toxicity symptoms developed, was higher in tolerant than in sensitive cultivars. The Fe/Mn ratio in the leaves at which Mn toxicity symptoms developed, was higher in the sensitive cultivars than in the tolerant ones.

We concluded that Mn tolerance in certain bush bean cultivars is due to a greater ability to tolerate a high level of Mn accumulation in the leaves.     

Phosphorus and acid phosphatase enzyme activity in leaves of tomato cultivars in relation to zinc supply

Abstract

Tomato cultivars Blizzard and Liberto were grown hydroponically in a controlled temperature (C.T.) room for 35 days. The objective was to investigate the relationship between phosphorus (P) concentration and acid phosphatase enzyme [EC.3.1.3.2.] (APE) activity in leaves in relation to zinc (Zn) concentration in nutrient solution. Zinc was added at concentrations of 0.01,0.5, and 5 mg L^‐1. The 0.01 and 5 mg L^‐1 Zn treatments led to a significant reduction in dry matter and total chlorophyll content compared with 0.5 mg L^‐1 for both cultivars. Zinc concentration was considered inadequate in the leaves of plants subjected to 0.01 mg L^‐1 Zn, while it was at toxic level in those in the 5 mg L^‐1 Zn treatment according to values stated for tomato plants. Optimal results for all criteria tested in this experiment were for plants grown in 0.5 mg L^‐1 Zn treatment. In the leaves of plants grown at 0.01 mg L^‐1 Zn, APE concentrations were significantly the lowest and concentrations of P were at a toxic level. The APE activity was noticeably higher in the P‐deficient plants of both cultivars grown in the solutions with high Zn (5 mg L^‐1).     

Differential tolerances of oat cultivars to aluminum in nutrient solutions and in acid soils of Poland

Aluminum tolerant oat cultivars are needed for use on acid soil sites where neutralization of soil acidity by liming is not economically feasible. Oat germplasm in Poland has not been examined for range of Al tolerance. Eleven Polish oat cultivars were screened for Al tolerance in nutrient solutions containing 0, 5 and 15 mg L^‐1 Al. Three of these cultivars showing high to moderate tolerance to Al in nutrient solutions were also grown in greenhouse pots of soil and in field plots of soil over a pH range of 3.8 to 5.5 as determined in 1 N KC1.

The eleven oat cultivars differed significantly in tolerance to Al in nutrient solutions. Based on relative root yield (15 mg L^‐1 Al/no A1%), the cultivars ‘Solidor’ and ‘Diadem’ were most tolerant and ‘Pegaz’ and ‘B‐20’ were least tolerant. For these three cultivars, the order of tolerance to acid soil agreed with the order of tolerance to Al in nutrient solution ‐ namely, Solidor > Diadem > Leanda. Hence, for these cultivars, the nutrient solution methods used appear adequate for selecting plants that are more tolerant to Al in strongly acid soils. Additional study is needed to assess the value of this method for screening a broad range of germplasm.

Superior tolerance of the Solidor cultivar to acid soil was associated with significantly higher concentrations of N in the grain. Hence, results suggest that selecting for acid soil or Al tolerance may increase N efficiency in oats.     

Catalase and ascorbate peroxidase activities are not directly involveded in the silicon‐mediated alleviation of ferrous iron toxicity in rice

Silicon (Si) is the second most abundant element in the soil and can alleviate several abiotic stresses in many plant species. However, the mechanisms involved in alleviating ferrous iron (Fe²⁺) toxicity by Si are still largely unknown, and no study has investigated the role of Si on the Fe²⁺‐induced oxidative stress and antioxidant system in rice. Four cultivars of Asian and African rice (Oryza sativa L. and Oryza glaberrima Steud) were grown for 4 weeks under hydroponic conditions with or without Fe²⁺ (250 mg Fe²⁺ L^?1) and with or without Si (250 mg SiO₂ L^?1). The plants that were treated with Fe²⁺ suffered Fe²⁺ toxicity, and Si helped to alleviate the toxicity symptoms. The bronzing index and the Fe concentration in the foliar tissue increased in the presence of Fe²⁺ but decreased significantly with the application of 250 mg SiO₂ L^?1. The concentration of malonyldialdehyde, that is commonly used as an indicator of oxidative stress, increased in the foliar tissue in the presence of 250 mg Fe²⁺ L^?1 in the nutrient solution. The application of 250 mg SiO₂ L^?1 in the plant nutrient solution treated with Fe²⁺ considerably limited the increase of malonyldialdehyde. However, no significant effect of Si application on the activities of antioxidant enzymes (catalase and ascorbate peroxidase) and non‐enzymatic antioxidants (total ascorbate, reduced ascorbate, oxidized ascorbate, and the ratio of the reduced to oxidized forms) was observed in the rice plants that were grown in the presence of Fe²⁺. These results suggest that Si does not act directly on the antioxidant defense system of rice but reduces the plant Fe²⁺ concentration, which reduces the oxidative stress.     

Fertigation rate,leaching fraction,and growth of potted poinsettia

Single‐pinched poinsettia (Euphorbia pulcherrima ’V‐14 Glory') in 15‐cm pots received constant fertigation with 50, 100, 200, and 300 mg.L^‐1 nitrogen (N) from a 20N‐4.4 phosphorus (P)‐16.6 potassium (K) fertilizer with a leaching fraction (LF) of 0, 0.2, or 0.4. Plants received 25 irrigations during the 13‐week study. The shoot fresh and dry masses with 50, 100, and 300 mg.L^‐1 N at the 0.4 LF were 30% larger than at the 0 LF. The 300 mg.L^‐1 N fertigated plants had approximately 15% more leaf area and almost 122% more bract area than the 50 mg.L^‐1 N fertigated plants. The leaf N concentration of plants fertigated with 100, 200, and 300 mg.L^‐1 N was near or in the normal range of 4 to 6%, but was below the critical level of 3.5% with 50 mg.L^‐1 N fertigation. In contrast, the leaf P concentration approached or exceeded the toxic level of 0.9% with 100 to 300 mg.L^‐1 N. The N fertigation of 100 to 200 mg.L^‐1 is adequate for producing a quality poinsettia crop. Quality poinsettias can be grown at a 0 LF if quality irrigation water is available. With 11 mg.L^‐1 P via fertigation, the leaf P concentration was in the acceptable range. The P concentration in the 20N‐4.4P‐16.6K complete fertilizer was excessive for poinsettia and would contribute to unnecessary P leaching.     

Effects of aluminum on the growth and element composition of 20 winter cultivars of Triticum aestivum L. (wheat) grown in solution culture

Seedlings of twenty cultivars of Triticum aestivum L. differing in tolerance to aluminum (Al) were grown with Al (74 uM, 2.0 mg L^‐1 ) and without Al at pH 4.5 to examine the effect of Al on the element composition of leaf and root tissues of juvenile plants. Treatment with Al reduced concentrations of Mg and Mn and increased concentrations of Al, P, Ca, and Fe in roots. Treatment with Al reduced concentrations of P, Ca, Mg, Fe, and Mn in leaves. Concentrations of Mg, Fe, and Mn in leaves were in the range considered to be deficient.

Cultivars differed in the effect of Al on element composition. Concentrations of Ca, Mg, Fe, and Mn in leaves of the 20 cultlvars grown with Al were positively correlated with cultivar tolerance to Al as measured by relative root yield. The variance, however, was relatively high. Leaf P concentrations of seedlings grown with Al were not significantly correlated with tolerance to Al. Differences among cultivars in the effect of Al on element, composition were not likely a primary cause of differential tolerance to Al, but Al‐induced element deficiencies may have a secondary effect on the yield of cultivars grown on sub‐lethal, Al‐toxic substrates.     

Short‐term relationships between membrane permeability and growth parameters in three tomato cultivars grown at low and high zinc

Abstract

An experiment was carried out in a controlled temperature (CT) room for five weeks with tomato cvs., Moneymaker, Liberto, and Calypso, to investigate possible relationships between zinc (Zn) deficiency or toxicity and electrolyte leakage in plant leaves. The concentrations of Zn in nutrient solution were 0.01, 0.5, and 5.0 mg L^?1, respectively. There were significant reductions in the dry matter and chlorophyll content of all three cultivars grown both at 0.01 (low) and 5 mg L^?1 (high) Zn compared to 0.5 mg L^?1. The concentration of Zn at 0.01 mg L^?1 was not sufficient to provide for optimal plant growth, while 5 mg L^?1 in nutrient solution was detrimental to plant growth for all three cultivars. Dry matter production was generally lowest in the plants grown at low (0.01 mg L^?1) Zn except for Moneymaker where the lowest biomass was in the high Zn treatment. Zinc concentration was increased in the leaves and roots with increasing Zn concentration in nutrient solution. Phosphorus concentration was toxic in the leaves of the plants grown at low (0.01 mg L^?1) and was deficienct at high Zn (5 mg L^?1). The electrolyte leakage (%) gradually increased in the plants grown at low and high Zn concentrations and these increases were greatest in the leaves of plants grown at low Zn (except for Moneymaker grown at high Zn where reduction in dry matter was less). The best results for all growth parameters tested were for the plants grown at 0.5 mg L^?1 Zn. The results of this short‐term experiment show that electrolyte leakage which is relatively simple and easy to measure may be a good indicator of cultivar tolerance to Zn deficiency and toxicity.     

Silicon modulates the metabolism and utilization of phenolic compounds in cucumber (Cucumis sativus L.) grown at excess manganese

Cucumber plants (Cucumis sativus L. cv. Chinese long) were grown in nutrient solution with increasing manganese (Mn) concentrations (0.5, 50, and 100 µM) with (+Si) or without silicon (–Si) supplied as silicic acid at 1.5 mM. High external Mn supply induced both growth inhibition of the whole plant and the appearance of Mn‐toxicity symptoms in the leaves. The application of Si alleviated Mn toxicity by increasing the biomass production. Although the total Mn concentration in the leaves did not differ significantly between +Si and –Si plants, symptoms of Mn toxicity were not observed in Si‐treated plants. The concentrations of phenolic compounds, particularly in the leaf extracts of cucumber plants grown at high external Mn concentrations, differed from those of plants grown without Si. The increased tissue concentrations of phenols (e.g., coniferyl alcohol, coumaric and ferulic acids) were in agreement with enhanced enzymes activities, i.e., peroxidases (PODs) and polyphenol oxidases (PPO) in the tissues of –Si plants. The activities of both enzymes were kept at a lower level in the tissue extracts of +Si plants grown at high external Mn concentrations. These results suggest that Si nutrition modulates the metabolism and utilization of phenolic compounds mainly at the leaf level, most probably as a consequence of the formation of Si‐polyphenol complexes.     

Effects of water deficit and manganese toxicity on two cultivars of soybeans (Glycine max (L.) Merr.: Possible applications in remote sensing

The effects of water deficit and excess Mn on leaf temperatures of two soybean cultivars were tested in greenhouse experiments on Mn toxic Loring soil. Cultivars used were Mn sensitive Forrest and Mn tolerant Lee. Water stress was created by withholding known amounts of water for a period of 12–24 hours. The untreated Loring soil produced Mn toxicity in Forrest but not in Lee. Hence, Mn was added as MnSO₄‐H₂O to induce toxicity in both cultivars; Mn treatments were 0 and 200 ug g‐1 for Forrest and 0 and 600 ug g‐1 for Lee. Both Mn and water stress increased leaf temperature. The interaction of water stress and Mn stress on leaf temperature could not be distinguished because both increased leaf temperature. Hence, under field conditions the detection of Mn induced leaf temperature change requires that water stress effects be eliminated. However, the effects of water stress on leaf temperature alone would be useful in assessing drought damage to crops. Since leaf temperature differences can be detected by remote sensing techniques, the results of this experiment will assist in the interpretation of remote sensing data.