Responese of Two Cultivars of Winter Wheat Differing In Sensitivity to Aluminum Toxicity

A experiment was carried to evaluate the effects of Al on growth,accumulations of free proline and amino acid in 2 wheat cultivars(Triticum aestivum L.),Yangmai No.5 and Jian 864,differing in Al Sensitivity.Plants grew initially in a nutrient solution without Al for 13 days before the addition of Al and finally in a nutrient solution containing 0.5mmol Al(L^-1)for 19 days,the results showed that there were marked deceases in dry weight,relative growth rate(RGR) and net assimilation rate (NAR)of Al-treated seedlings compared with control plants.The Al effects were more evident in Yangmai No.5 than Jian 864.Leaf area ratio(LAR) was little affected by Al.RGR was highly correlated with NAR rather than LAR.Aluminum increased the concentrations of free proline and total free amino acid in shoots of both the cultivars.The increases were greater in Yangmai No.5 than in Jian 864.The percentage of free proline in total amino acid in shoots was not affected by Al treatment.It was possible that accumulation of proline was merely a symptom of Al injury.The concentrations of total nitrogen in Al-treated plants did not significantly differ from those of control plants.Nitrate reductase activity(NRA),in leaves was severely decreased by Al,and a greater decrease was noted in Yangmai No.5 than in Jian 864,but NRA in roots of both the cultivars was not affected.The decreases in NRA might be and indirect(accumulation of amino acid) rather than a direct result of Al toxicity.     

Assessment of aluminum sensitivity of maize cultivars using roots of intact plants and excised root tips

Maize cultivars (Zea mays L.) were evaluated for their aluminum (Al) sensitivity using intact plants and excised root tips exposed to 25 μM Al in nutrient solution of low ionic strength and pH 4.3. Aluminum supply increased callose formation and Al concentrations in root tips of intact plants as well as in excised root tips. Using intact plants, differences in Al sensitivity among cultivars could be characterized by Al‐induced callose formation, Al‐induced inhibition of root elongation, as well as Al contents in root tips as parameters. Significant correlations between Al‐induced callose formation and Al contents in root tips (r² = 0.64**) and inhibition of root elongation (r² = 0.80***) were found. Excised root tips did not show a significant Al‐induced inhibition of root elongation. While average Al‐induced callose formation was similar for root tips of intact plants and excised root tips, mean Al contents in excised root tips were up to 1.5‐fold higher than in root tips of intact plants after 24 h of Al treatment. Aluminum‐induced callose formation as found in excised root tips did neither correspond to Al‐induced callose formation nor to inhibition of root elongation of intact plants. The addition of 10 mM glucose to the incubation medium led to a significant increase in the elongation of excised root tips and a 2‐3‐fold increase in Al‐induced callose formation. Staining with triphenyl‐tetrazolium‐chloride (TTC) revealed increased viability of these root segments. However, these effects of glucose supply did not improve the characterization of the cultivars for Al resistance. The results presented suggest that Al exclusion mechanisms expressed in root tips of intact plants might be non‐operational in excised root tips. Therefore, the characterization of maize germplasm for Al resistance using excised root tips appears not to be reliable.     

两种冬小麦对铝毒响应的敏感性差异研究

A experiment was carried to evaluate the effects of Al on growth, accumulations of free proline and amino acid in 2 wheat cultivars (Triticum aestivum L.), Yangmai No.5 and Jian 864, differing in Al sensitivity. Plants grew initially in a nutrient solution without Al for 13 days before the addition of Al and finally in a nutrient solution containing 0.5mmol Al (L^-1) for 19 days. The results showed that there were marked decreases in dry weight, relative growth rate (RGR) and net assimilation rate (NAR) of Al-treated seedlings compared with control plants. The Al effects were more evident in Yangmai No.5 than Jian 864. Leaf area ratio(LAR) was little affected by Al. RGR was highly correlated with NAR rather than LAR. Aluminum increased the concentrations of free proline and total free amino acid in shoots of both the cultivars. The increases were greater in Yangmai No.5 than in Jian 864. The percentage of free proline in total amino acid in shoots was not affected by Al treatment. It was possible that accumulation of proline was merely a symptom of Al injury. The concentrations of total nitrogen in Al-treated plants did not significantly differ from those of control plants. Nitrate reductase activity (NRA) in leaves was severely decreased by Al, and a greater decrease was noted in Yangmai No.5 than in Jian 864, but NRA in roots of both the cultivars was not affected. The decreases in NRA might be an indirect (accumulation of amino acid) rather than a direct result of Al toxicity.     

Effect of aluminum on callose synthesis in root tips of tea (Camellia sinensis L.) plants

Aluminum (Al) toxicity is a major factor limiting yield production on acid soils (Foy 1983). The initial symptom of Al toxicity in many plants is manifested by the inhibition of root elongation (Ownby and Popham 1990; Llugany et al. 1994; Sasaki et al. 1994; Horst et al. 1997), which occurs during a very short period of time after exposure to Al (Llugany et al. 1994; Staß and Horst 1995). In a large number of recent reports, it was shown that the root apex plays a major role in the Al-sensitivity and response mechanisms (Zhang et al. 1994; Sasaki et al. 1997; Sivaguru and Horst 1998). However, it is interesting to note that stimulatory effects of Al on the growth of plants have also been reported in some studies (Chenery 1955; Konishi et al. 1985; Huang and Bachelard 1993; Osaki et al. 1997). In tea plant (Camellia sinensis L.) a stimulatory effect of Al on the growth was also demonstrated in some experiments, using intact plant (Chenery 1955; Konishi et al. 1985), cultured roots (Tsuji et al. 1994), and pollen tubes (Yokota et al. 1997). The growth of tea roots was typically more stimulated than that of shoots by Al (Konishi et al. 1985). It was assumed that Al effects might be due to the amelioration of phosphorus absorption (Konishi et al. 1985), secretion of malic acid from roots to dissolve aluminum phosphate in the rhizosphere (Jayman and Sivasubramaniam 1975), stimulation of growth of microorganisms on the root surface (Konishi 1990) or replacement of some functions of boron (Konishi 1992; Yokota et al. 1997). However, the stimulatory effects of Al on tea plant growth have not yet been el ucidated.

The formation of callose (1,3-β-glucan) has been reported as a common plant response to a variety of stresses, as well as mechanical, biophysical, chemical, and biological injury (Jaffe and Leopold 1984; Zhang et al. 1994). Increased synthesis of callose has been observed upon exposure to excess amounts of some elements, such as boron (McNairn and Currier 1965), cobalt, nickel, zinc (Peterson and Rauser 1979), and manganese (Wissemeier and Horst} 1987, 1992). Callose synthesis was also induced by Al in the roots of Triticum aestivum (Zhang et al. 1994) and Zea mays (Horst et al. 1997; Sivaguru and Horst 1998), suspension-cultured cells of Glycine max (Staß and Horst 1995), and protoplasts of Avena sativa (Schaeffer and Walton 1990) and Zea mays (Wagatsuma et al. 1995). Induction of callose synthesis in roots seems to be a very rapid physiological indicator of Al-induced injury or genotypical differences in Al sensitivity (Wissemeier and Horst 1992; Zhang et al. 1994; Horst et al. 1997). Nevertheless, Al-induced callose synthesis in tea plant, whose growth is stimulated by suitable Al concentrations, has not been described yet. Therefore, to elucidate the physiological basic effects of Al on tea plant, callose synthesis affected by Al in the root tips of intact plants was analyzed in the present study.     

Sucrose transporter NtSUT1 confers aluminum tolerance on cultured cells of tobacco (Nicotiana tabacum L.)

The role of plasma membrane-localized sucrose transporter (NtSUT1) was investigated using cultured tobacco cell (Nicotiana tabacum L.) line BY-2. The wild type (WT) cells were first transformed with the NtSUT1 gene or its fragments cloned from tobacco cell line SL to form the over-expression (OX) and suppression (RNAi) cell lines, respectively. Using OX and RNAi transgenics, the role of NtSUT1 in growth capacity of actively growing cells and in aluminum (Al)-treated cells was examined. During the logarithmic phase of growth in nutrient medium containing 2,4-dichlorophenoxyacetic acid (2,4-D), both the rate of sucrose uptake measured with radio-tracer and the content of soluble sugars were higher in OX and lower in RNAi cell lines compared to WT. Overall, the content of soluble sugars negatively correlated with the time necessary for doubling mass (fresh weight). When cells were treated without (control) or with Al in a simple medium containing calcium, sucrose and 2-(N-morpholino)ethanesulfonic acid (MES; pH 5.0) for up to 18 h, the expression of NtSUT1 under its native promoter, or under the control of strong constitutive cauliflower mosaic virus (CaMV) 35S promoter, was strongly dependent on the presence of 2,4-D. Thereafter, the cells were preferentially treated in the presence of 2,4-D. During 6 h after a start of the control treatment, sucrose uptake rates were, compared to WT, slightly higher and lower in OX and RNAi lines respectively. The addition of Al reduced the sucrose uptake rates of OX and WT to the level of RNAi line, indicating that Al inhibits sucrose uptake via NtSUT1. During the post-Al culture of control and Al-treated cells in a nutrient medium, sucrose uptake rates were much higher in OX compared to WT and RNAi lines, which closely and positively correlated with the growth capacity of the cells. Judging from the growth capacity of Al-treated cells relative to that of control cells, OX cells were more tolerant to Al than WT and RNAi. In summary, we conclude that over-expression of NtSUT1 confers higher growth capacity in actively growing cells as well as in Al-treated cells.     

Aluminum inhibits apoplastic flow of high–molecular weight solutes in root apices of Zea mays L.

Using an aluminum (Al)‐sensitive maize cultivar, we investigated the influence of Al on the apoplastic solute bypass flow and its relationship with Al‐induced (1 h, 50 μM) callose formation and root growth. We selected the fluorescent probes 8‐hydroxypyrene‐1,3,6‐trisulfonic acid, trisodium salt (MW 524) (HPTS) and dextran‐Texas Red (TR) conjugates (MW 3,000, 10,000, and 40,000) to monitor their apoplastic transport. Confocal laser–scanning microscopy (CLSM) analysis and spectrofluorometric quantification showed Al‐induced callose formation in peripheral root cells within 1 h. Pretreatment of plants with the callose synthesis inhibitor 2‐deoxy‐D‐glucose (DDG) reduced the callose formation by half. Uptake experiments with both HPTS and dextrans showed uniform dye distribution in control root apices. After Al treatment for 1 or 2 h, which inhibited root growth by 32% or 50%, respectively, the dyes accumulated in the epidermal and outer cortical cell layers, especially in the 1–2 mm apical root zone. Al treatment reduced the export of the dyes out of the apical 1 cm treatment zone. This was due to strong sorption of HPTS but not of dextrans by Al‐loaded cell walls. Aluminum treatment reduced loading into the xylem sap particularly of higher–molecular weight dextrans. Pretreatment of roots with DDG and presence of 50 mM mannitol during the Al treatment partially forestalled the inhibitory effect of Al on the dye transport, but only slightly reduced the Al‐induced growth inhibition. Exudation experiments revealed that xylem water flow remained unaffected by the Al treatment of the root tips. The results with dextran suggest that Al binding in cell walls of the root apex inhibits apoplastic bypass flow of higher–molecular weight solutes, which might contribute to Al‐induced inhibition of root growth.     

Aluminium Tolerance of Maize Cultivars as Assessed by Callose Production and Root Elongation

The differences in Al tolerance between 12 maize cultivars were investigated using early stress indicators such as relative root elongation rate, induction of callose formation and Al concentrations in 5 mm root tips. Plants were grown in nutrient solution (pH 4.3) and exposed to 0 (control), 20 or 50 μM Al for 24 h. According to the relative root elongation rates, Regent, C 525 M and Adour 250 were the most Al-tolerant cultivars, while BR 201 F, Teosinte, Alarik, Burras and HS 7777 were Al-sensitive. Cultivars Brummi, HS 1230, Lixis and Aladin showed an intermediate behaviour. A significant inverse correlation between relative root-elongation rates and both Al concentration in root tips and callose concentrations could be established. The usefulness of callose as an early indicator of Al stress and the importance of Al exclusion from root tips as an Al tolerance mechanism are discussed.     

Proton toxicity interferes with the screening of common bean (Phaseolus vulgaris L.) genotypes for aluminium resistance in nutrient solution

Common bean (Phaseolus vulgaris L.) proved to be very sensitive of low pH (4.3), with large genotypic differences in proton sensitivity. Therefore, proton toxicity did not allow the screening of common bean genotypes for aluminium (Al) resistance using the established protocol for maize (0.5 mM CaCl₂, 8 μM H₃BO₃, pH 4.3). Increasing the pH to 4.5, the Ca²⁺ concentration to 5 mM, and addition of 0.5 mM KCl fully prevented proton toxicity in 28 tested genotypes and allowed to identify differences in Al resistance using the inhibition of root elongation by 20 μM Al supply for 36 h as parameter of Al injury. As in maize, Al treatment induced callose formation in root apices of common bean. Aluminium‐induced callose formation well reflected the effect of Ca supply on Al sensitivity as revealed by root‐growth inhibition. Aluminum‐induced callose formation in root apices of 28 bean genotypes differing in Al resistance after 36 h Al treatment was positively correlated to Al‐induced inhibition of root elongation and Al contents in the root apices. However, the relationship was less close than previously reported for maize. Also, after 12 h Al treatment, callose formation and Al contents in root apices did not reflect differences in Al resistance between two contrasting genotypes, indicating a different mode of the expression of Al toxicity and regulation of Al resistance in common bean than in maize.     

Soil Solution Aluminum,and Nutrient and Aluminum Uptake in Hibiscus Sabdariffa Under Nitrogen and Phosphorous Fertilizers

The result of intensive agriculture in cities is the decline in crop yields and depletion of the resource base. The aims of this study were to assess effects of nitrogen (N) or phosphorus (P) fertilization on bioavailable aluminum (Al) and their contribution on Al and nutrient uptake in Hibiscus sabdariffa. A pot experiment was led to supply a tropical soil with N and P fertilizers. P amendment decreased Al in soil solution, not N amendment. Fertilizers had effects on Al and nutrient uptake in roots and leaves of Hibiscus sabdariffa. The results also showed that the uptake of Al and nutrients depends on Al in soil solution or N supply or P supply. Only P uptake in roots and leaves was explained by combined effects of a nutrient supply × exchangeable Al. Furthermore, P supply does not limit the translocation of Al in shoots of plants in acid soils.     

Aluminium Induced Magnesium Deficiency in Oats

It was the objective to study the effect of Al on Mg uptake by plants, precluding as far as possible the effect of Al on root growth. Oat plants were grown in a complete standard nutrient solution without any differential treatment, in order to obtain a set of plants which did not differ in the size, the morphology and the physiology of the root system. After the first harvest at the beginning of the stem elongation stage 4 different treatments were introduced: pH 5.5-6.0, pH 5.5-6.0 without Mg, pH 3.8-4.1, pH 3.8-4.1 + 0.3 mmole Al/l. Apart from these variations the composition of the nutrient solution remained unaltered. After another 10 days 2 vessels of each treatment were harvested. The final harvest was 14 days after the beginning of the differential treatments. The growth (in terms of dry matter yield) of neither the shoots nor the roots was adversely affected by the differential treatments, although the plants in the Al and Mg₀ treatments showed distinct symptoms of nutritional disorder. The plants in the low and the high pH treatments differed neither in Mg uptakte nor in Mg concentration in the plants. However, the addition of Al to the nutrient solution reduced Mg uptake in the shoots to about 30% of that in the Al₀ treatments, while there was a net loss of Mg in the roots in spite of the fact that dry matter increased. This means that net uptake of Mg was less than was translocated to the shoot during the period of differential treatments. With no Al in the nutrient solution the Mg concentration in the shoots declined by 3–8% between the first and the final harvest, whereas it increased by 22–35% in the roots. If, however, Al was added to the nutrient solution the Mg concentration dropped by 46% in the shoots and 70% in the roots. With the exception of Ca in the roots, the differential treatments had no effect on the uptake and concentration of Ca, K and P in the plants. In terms of dry matter the differential treatments did not influence root growth and it was concluded that Al had a direct effect on Mg uptake by either inactivating or competing for uptake sites or carriers.     

Enhancement of callose production by a combination of aluminum and iron in suspension-cultured tobacco (Nicotiana tabacum) cells

In nutrient medium, aluminum (A1) enhances ferrous ion [Fe(II)] -mediated per oxidation of lipids, which results in the loss of the plasma membrane integrity and the accumulation of A1 in tobacco cells. Under these conditions, the mechanism of callose production and possible involvement of callose in the accumulation of Al were investigated. Callose production was enhanced by both Al and Fe(II), but not by A1 or Fe(II) alone, and the enhancement was inhibited by a lipophilic antioxidant, suggesting that the enhancement of callose production is caused by the A1-enhanced, Fe(II)-mediated peroxidation of lipids. The enhancement of callose production depended on the presence of external Ca²⁺ in the treatment medium. The activity of β-l,3-glucan synthase in the microsomes was increased several times by the addition of Ca²⁺ in the assay medium, although the activity in the microsomes was reduced by the treatment of cells with Al and Fe(II) together. Therefore, it is likely that callose production is enhanced by exogenous Ca²⁺ via the AI-enhanced, Fe(II)-mediated peroxidation of lipids. During the exposure of the cells to Al and Fe(II), callose production started and increased simultaneously with Al accumulation. However, the digestion of callose in the cell wall materials prepared from the A1-treated cells by laminarinase did not release A1, suggesting that callose is not involved in the binding or trapping of A1.     

Tea plant (Camellia sinensis L.) roots secrete oxalic acid and caffeine into medium containing aluminum

We examined the response of the tea plant (Camellia sinensis L.) to aluminum (Al) exposure under sterile conditions, focusing specifically on the secretion of low molecular mass organic compounds from roots. After germination in agar medium, tea seedlings together with medium were placed on agar containing 0.4?mM Al with 0.2% hematoxyline (hematoxylin-Al medium). The purple color of the hematoxylin-Al medium was observed to fade gradually, until none of the color remained 6 days later. The tea seedlings were then treated with simple calcium solution (0.2?mM, at pH 4.2) containing AlCl₃, which ranged in concentration from 0 to 0.8?mM, for 24?hrs. The amount of oxalate secreted into the medium increased as the external Al concentration increased, while the concentrations of malate and citrate in the medium remained unchanged. Oxalate secretion started within 30?min after Al exposure and increased linearly thereafter. The findings demonstrated that oxalate was a key compound in the Al-tolerance mechanism employed by the tea plant, which detoxifies Al³⁺ externally in the rhizosphere. In addition to oxalate, caffeine was also secreted by tea roots in response to Al exposure. It is possible that caffeine excretion from the roots of tea plants may stimulate root growth through the inhibition of callose deposition in root tips.     

Tall fescue aluminum tolerance is affected by neotyphodium coenophialum endophyte

Roots of endophyte‐infected (E+) tall fescue (Festuca arundinacea Schreb.) exude more phenolic‐like reductants than roots of endophyte‐free (E‐) plants when mineral stressed. Phenolic compounds are efficient chelators of aluminum (Al) and may influence Al tolerance in many plant species. The objective of our study was to determine if enhanced release of phenolic compounds by roots of E+ plants contributes to Al tolerance in tall fescue. Two cloned genotypes (DN2 and DN11) of tall fescue infected with their naturally occurring fungal endophyte Neotyphodium coenophialum (Morgan‐Jones and Gams) Glenn, Bacon and Hanlin and their noninfected isolines were grown in nutrient solutions at 0 μM Al (Al‐) and at 640 μM Al (Al+) under controlled environment conditions. Root and shoot dry matter (DM) of endophyte‐infected tall fescue was greater in E+ than E‐ plants by 57% and 40%, respectively, when plants were grown without Al. Endophyte infection did not affect root and shoot DM of tall fescue grown with Al but relative (to Al‐treatment) reduction in root and shoot DM was greater in E+ than E‐ plants. In response to Al stress, more Al (47%) and P (49%) could be desorbed from root surfaces of E+ than E‐ plants. Aluminum concentrations in roots of E+ plants were 35% greater and P concentrations were 10% less than those determined in roots of E‐plants. No differences in mineral concentrations were observed in shoots, regardless of endophyte status, or Al level in nutrient solution. Roots of E+ plants increased pH of both Al‐ and Al+ nutrient solutions to a greater extent than roots of E‐ plants in a 48 h interval. Our results show that more Al can be sequestered on root surfaces and in root tissues of endophyte‐infected tall fescue than in plants devoid of endophyte. Aluminum sequestration was greater on root surfaces and in root tissues of E+ than E‐ plants of a given tall fescue genotype. Our results suggest that increased exudation of phenolic‐like compounds from roots of endophyte‐infected tall fescue may be directly involved in Al tolerance and serves as a mechanism for widespread adaptability and success of endophyte‐tall fescue associations.     

Aluminium‐induced increase of zeatin riboside and dihydrozeatin riboside in Phaseolus vulgaris L. cultivars

Toxic effects of aluminium (Al) on root tips are considered to decrease export of cytokinins to shoots, and deficiency of cytokinins has been made responsible for Al‐induced inhibition of shoot growth. But no experimental data on the influence of Al on endogenous cytokinin levels in higher plants have been reported. In this study, the endogenous levels of zeatin riboside (ZR) and dihydrozeatin riboside (DHZR) of roots, stems, and leaves of two bean cultivars (Phaseolus vulgaris L. cv Contender and cv Strike) exposed to Al in continuously flowing nutrient solution (pH 4.5) was analysed. The supply of a high Al concentration (sum of monomeric Al species, 127 μM) caused severe inhibition of root elongation in both cultivars. The cv Strike was more affected by both Al‐induced mineral nutrient disorders and Al‐induced alteration of leaf water relationships. In both cultivars Al‐supply significantly increased ZR and DHZR. Leaves of Al‐treated plants exhibited a more than three times higher concentration of ribosylated cytokinins than controls. Nevertheless, stomatal resistance was significantly increased by Al in both cultivars. Our results support the hypothesis that Al affects plants not by inducing deficiency of cytokinins but of some other factor necessary for the manifestation of cytokinin action.     

Silicon Effect on Nutrient Acquisition of Peanut (Arachis hypogaea L.) Under Aluminum Stress

Aluminum (Al) toxicity represents one of the main yield-limiting factors for crops in acid soils. Silicon (Si) is known to increase tolerance in higher plants. This study was conducted to determine whether treatment with Si could improve nutrient uptake by peanut under Al stress. Peanut (Arachis hypogaea L. cv Zhonghua 4) was raised with or without Si (1.5 mM) in the growth chamber under 0 and toxic Al (0.3 mM) levels. Aluminum stress significantly decreased the root- and total-dry weight by 52.4% and 32.0%, respectively. The content of nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), and magnesium (Mg) was significantly decreased, but that of Al increased markedly in shoots and roots after Al exposure at seedling, flower-needle, and pod-setting stage. Silicon alleviates Al toxicity in peanut plants in relation to Al distribution and allocation of tissue P, K, Ca, and Mg by favoring the partitioning of dry mass to roots.     

Stickstoffernährung und Al-Toxizität bei Buchenjungpflanzen. II: Mineralstoffgehalte junger Buchen in Abhängigkeit von der Form der Stickstoffernährung und dem Al-Gehalt der Nährlösung

Nitrogen nutrition and Al toxicity with young beech plants. II: Mineral contents of young beech plants in relation to the source of nitrogen and the Al content of the nutrient solution Young beech plants were grown in aerated nutrient solutions with different Al concentrations over a period of 14 weeks. Nitrogen was supplied in either NO₃ or NH₄-form. pH-changes of the solutions were either corrected to the initial pH of 4,0 after two days, or not corrected over a period of two weeks. The cation contents of the roots and shoots were greater if the nitrogen was supplied in NO₃-form. Increasing Al concentrations in the nutrient solutions led to an increase in Al contents and a decrease in Ca- and Mg-contents in roots and shoots.     

Chicory (Cichorium intybus L.) and dandelion (Taraxacum officinale Web.) as phytoindicators of cadmium contamination

Chicory (Cichorium intybus L.) and dandelion (Taraxacum officinale Web.) were demonstrated to be potential indicator plants for heavy metal contaminated sites. Chicory, grown with 0.5–50 μM cadmium (Cd) in nutrient solution, accumulated 10–300 μM Cd g^?1 in shoots and 10–890 μg Cd μg^?1 in roots and rhizomes. With dandelion, 20–410 μg Cd μg^?1 was found in shoots and 20–1360 μg Cd μg^?1 in roots and rhizomes. An inverse correlation existed between chlorophyll and Cd concentrations in shoots of both species. Accumulation of Cd from nutrient solution was similar with the counter-anions SO₄ ^2?, Cl^1? and NO₃ ^? in chicory. In chicory grown in Cd-amended (11.2 kg Cd ha^?1 applied five years previously) soils, Cd concentrations were substantially higher than in controls in all plant parts following the order: leaf > caudex > stem > root and rhizome. The above trend was the opposite of that observed in solution culture, where Cd accumulation was higher in roots and rhizomes than in shoots. Higher cadmium accumulation was found from a Cd-treated sand (Grossarenic Paleudult) than from a loamy sand (Typic Kandiudult) soil type. Chicory and dandelion are proposed indicator plants of cadmium contamination, and both have the potential to be an international standard heavy phytomonitor species of heavy metal contaminantion.     

超累积植物油茶中Al的吸收和累积

Oiltea camellia (Camellia oleifera Abel.), an aluminium (Al) hyperaccumulator, grows well on acid soils in tropical or subtropical areas. In this study, the growth of oiltea camellia in response to Al application and the characteristics of Al uptake and accumulation were investigated using laboratory and field experiments. The growth of oiltea camellia seedlings in the nutrient solution tended to be stimulated by addition of Al. Results of the field experiment showed that oiltea camellia accumulated 11000 mg kg-1 Al in leaves within 10 months, and the average rate of Al accumulation in new leaves was about 1100 mg kg-1 month?1; however, the monthly rate varied and was highest in spring and autumn. The results of the laboratory experiment on Al uptake by oiltea camellia seedlings in CaCl2 solutions with various forms of Al showed that large amounts of Al supplied as Al3+ and Al complexes Al-malate (1:1) and Al-F (1:1) were influxed into oiltea camellia roots, whereas Al supplied as Al-citrate (1:1), Al-F (1:6), Al-oxalate (1:3), and Al-oxalate (1:1) complexes exhibited low affnity to oiltea camellia roots. The kinetics of Al3+ cumulative uptake in excised roots and intact plants showed a biphasic pattern, with an initial rapid phase followed by a slow phase. The Al cumulative uptake was una?ected by low temperature, which indicated that Al uptake in oiltea camellia was a passive process. The effcient influx of Al into the roots and the high transport rate in specific seasons were presumed to account for the plentiful Al accumulation in leaves of oiltea camellia.     

Responses to aluminium of suspension-cultured tobacco cells in a simple calcium solution

In a simple solution containing 3 mM CaCl₂ and 3% sucrose (pH 4.5), tobacco cells (Nicotiana tabacum L.) at the logarithmic phase of growth remained viable at least for 24 h. In this medium, the toxic effect of aluminium (Al) on the plasma membrane was investigated for up to 24 h. After the addition of Al to the cell suspension, Al started to accumulate immediately in the cells, and a maximum value was observed at 9 h. Al induced callose deposition, but did not enhance significantly the uptake of Evans blue (a nonpermeating dye), the per oxidation of lipids and the leakage of potassium (K) ions. Furthermore, the AI-treated cells were stained with fluorescein diacetate (FDA) as much as untreated control cells. These results suggest that the accumulation of Al does not damage the membrane. The addition of Fe(II) to the cells which had been exposed to Al for 12 h resulted in immediate lipid peroxidation and Evans blue uptake several hours later. A combination of Al and Fe(II) caused the K leakage, and enhanced the deposition of callose more than Al alone. These results suggest that the accumulation of Al sensitizes the membrane to the Fe(II)-mediated peroxidation of lipids, and that the Al-enhanced per oxidation of lipids is a direct cause of the loss of integrity of the plasma membrane (or cell death) in the Ca medium.     

Time course study of aluminum-induced callose formation in barley roots as observed by digital microscopy and low-vacuum scanning electron microscopy

To clarify the mechanism(s) involved in the short-term inhibition of root elongation by AI, we monitored the morphological changes of barley roots by digital microscopy. Within 30 min after exposure to 37 µM AI, the surface of the root epidermis in the region of a distance of 1.5 mm from the root tip became rough and began to show signs of damage. After 38 min, callose was rapidly excreted from the junction between the root cap and the root epidermis, and formed a spherical lump approximately 60 µm in diameter. The fine structure of the callose deposits on the root surface was analyzed by low-vacuum scanning electron microscopy. After 50 min, there was a significant increase in the callose contents in the distal 0.6 mm part. At the same time, root elongation stopped completely. Fluorescence staining indicated that callose was localized on the surface of the cell elongation area (the elongation zone of primary roots and root hairs), but not on the surface of the meristem. The root growth reduction associated with AI treatment may be due to the use of sugar substrates for callose formation instead of cellulose formation.