硅缓解水稻根系铁毒害

Silicon (Si) can enhance the resistance of plants to many abiotic stresses. To explore whether Si ameliorates Fe2+ toxicity, a hydroponic experiment was performed to investigate whether and how Si detoxifies Fe2+ toxicity in rice (Oryza sativa L.) roots. Results indicated that rice cultivar Tianyou 998 (TY998) showed greater sensitivity to Fe2+ toxicity than rice cultivar Peizataifeng (PZTF). Treatment with 0.1 mmol L-1 Fe2+ inhibited TY998 root elongation and root biomass significantly. Reddish iron plaque was formed on root surface of both cultivars. TY998 had a higher amount of iron plaque than PZTF. Addition of Si to the solution of Fe treatment decreased the amount of iron plaque on root surface by 17.6% to 37.1% and iron uptake in rice roots by 37.0% to 40.3%, and subsequently restored root elongation triggered by Fe2+ toxicity by 13.5% in the TY998. Compared with Fe treatment, the addition of 1 mmol L-1 Si to the solution of Fe treatment increased xylem sap flow by 19.3% to 24.8% and root-shoot Fe transportation by 45.0% to 78.6%. Furthermore, Si addition to the solution of Fe treatment induced root cell wall to thicken. These results suggested that Si could detoxify Fe2+ toxicity and Si-mediated amelioration of Fe2+ toxicity in rice roots was associated with less iron plaque on root surface and more Fe transportation from roots to shoots.     

Silicon Increases Tolerance to Boron Toxicity and Reduces Oxidative Damage in Barley

ABSTRACT

Silicon (Si) protects plants from multiple abiotic and biotic stresses The effect of exogenous Si levels (50, 75, and 100 mg kg^?1) on the growth, boron (B) and Si uptake, lipid peroxidation (MDA), lipoxygenase activity (LOX; EC 1.13.11.12), proline, and H₂O₂ accumulation, non-enzymatic antioxidant activity (AA) and the activities of major antioxidant enzymes (superoxide dismutase, SOD, EC 1.15.1.1; catalase, CAT, EC 1.11.1.6 and ascorbate peroxidase, APX, EC 1.11.1.11) of barley (Hordeum vulgare L.) were investigated under glasshouse conditions. Increasing levels of Si supplied to the soil with 20 mg kg^?1 B counteracted the deleterious effects of B on shoot growth. Application of B significantly increased the B concentration in barley plants. However, Si application decreased B concentrations. Increasing application of Si increased the Si concentration in barley plants. The concentration of H₂O₂ was increased by B toxicity but decreased by Si supply. Boron toxicity decreased proline concentrations and increased lipid peroxidation (MDA content) and LOX activity of barley. Compared with control plants, the activities of AA, SOD, CAT, and APX in B stressed plants grown without Si decreased, and application of Si increased their activities under toxic B conditions. The LOX activity was decreased by Si. Based on the present work, it can be concluded that Si alleviates B toxicity by possibly preventing oxidative membrane damage, both through lowering the uptake of B and by increasing tolerance to excess B within the tissues.     

MITIGATION EFFECTS OF SILICON ON TOMATO PLANTS BEARING FRUIT GROWN AT HIGH BORON LEVELS

Interactive effects of silicon (Si) and high boron (B) on growth and yield of tomato (Lycopercison esculentum cv. ‘191 F1’) plants were studied. Treatments were: 1) control (B1), normal nutrient solution including 0.5 mg L^?1 B (boron), 2) B1 +Si treatment: 0.5 mg L^?1 boron plus 2 mM Si, 3) B2 treatment: 3.5 mg L^?1 B, 4) B2 +Si treatment: 3.5 mg L^?1 B plus 2 mM Si, 5) B3 treatment: 6.5 mg L^?1 B, and 6) B3 +Si: 6.5 mg L^?1 B plus 2 mM Si. High B reduced dry matter, fruit yield and chlorophyll (Chl) in tomato plants compared to the control treatment, but increased the proline accumulation. Supplementary Si overcame the deleterious effects of high B on plant dry matter, fruit yield and chlorophyll concentrations. High B treatments increased the activities of superoxide dismutase (SOD; EC 1.15.1.1), peroxidase (POD; EC. 1.11.1.7) and polyphenol oxidase (PPO; EC 1.10.3.1). However, supplementary Si in the nutrient solution containing high B reduced SOD and PPO activities in leaves, but POD activity remained unchanged. These data suggest that excess B-induced oxidative stress and alterations in the antioxidant enzymes. Boron (B) concentrations increased in leaves and roots in the elevated B treatment as compared to the control treatment. Concentrations of calcium (Ca) and potassium (K) were significantly lower in the leaves of plants grown at high B than those in the control plants. Supplementing the nutrient solution containing high B with 2 mM Si increased both nutrients in the leaves. These results indicate that supplementary Si can mitigate the adverse effects of high B on fruit yield and whole plant biomass in tomato plants.     

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.     

Chemistry of Lowland Rice Soils and Nutrient Availability

Rice is the staple food crop for about 50% of the world's population. It is grown mainly under two ecosystems, known as upland and lowland. Lowland rice contributes about 76% of the global rice production. The anaerobic soil environment created by flood irrigation of lowland rice brings several chemical changes in the rice rhizosphere that may influence growth and development and consequently yield. The main changes that occur in flooded or waterlogged rice soils are decreases in oxidation–reduction or redox potential and increases in iron (Fe²⁺) and manganese (Mn²⁺) concentrations because of the reductions of Fe³⁺ to Fe²⁺ and Mn⁴⁺ to Mn²⁺. The pH of acidic soils increased and alkaline soils decreased because of flooding. Other results are the reduction of nitrate (NO₃ ^?) and nitrogen dioxide (NO₂ ^?) to dinitrogen (N₂) and nitrous oxide (N₂O); reduction of sulfate (SO₄ ^2?) to sulfide (S^2?); reduction of carbon dioxide (CO₂) to methane (CH₄); improvement in the concentration and availability of phosphorus (P), calcium (Ca), magnesium (Mg), Fe, Mn, molybdenum (Mo), and silicon (Si); and decrease in concentration and availability of zinc (Zn), copper (Cu), and sulfur (S). Uptake of nitrogen (N) may increase if properly managed or applied in the reduced soil layer. The chemical changes occur because of physical reactions between the soil and water and also because of biological activities of anaerobic microorganisms. The magnitude of these chemical changes is determined by soil type, soil organic-matter content, soil fertility, cultivars, and microbial activities. The exclusion of oxygen (O₂) from the flooded soils is accompanied by an increase of other gases (CO₂, CH₄, and H₂), produced largely through processes of microbial respiration. The knowledge of the chemistry of lowland rice soils is important for fertility management and maximizing rice yield. This review discusses physical, biological, and chemical changes in flooded or lowland rice soils.     

Relationship between Callus Growth and Mineral Nutrients Uptake in Salt-Stressed Indica Rice Callus

ABSTRACT

One month old rice calli were exposed to 0, 50, and 100 mol m^?3 sodium chloride (NaCl) in the liquid LS basal medium supplemented with 2.5 mg L^?1 2,4-dichlorophenoxy acetic acid (2,4-D) and 0.5 mg L^?1 kinetin. Callus relative growth rate (RGR; fresh) of both cultivars indicated a progressive decrease; however, callus dry weight increased as the NaCl level increased in the culture medium. Salinity stress increased the callus sodium (Na⁺), manganese (Mn²⁺), and magnesium (Mg²⁺) contents while potassium (K⁺), calcium (Ca²⁺), and iron (Fe²⁺) contents decreased. ‘Basmati-385’ showed less reduction in callus RGR, K⁺, and Ca²⁺ contents and a larger increase in callus dry weight, Na⁺, Mn²⁺, and Mg²⁺ contents as compared to ‘Basmati-Karnal’. However, the reverse was true for Fe²⁺ contents. K⁺/Na⁺ and Ca²⁺/Na⁺ ratios generally decreased under salt stress. Overall, reduction in callus relative growth rate was found to be inversely correlated with decrease in K⁺, Ca²⁺, and Fe²⁺ uptake and directly correlated with increased Na⁺ and Mg²⁺ concentration in callus tissue.     

Iron Toxicity in Lowland Rice

Lowland rice is a staple food for more than 50% world population. Iron toxicity is one of the main nutritional disorders, which limits yield of lowland rice in various parts of the world. The toxicity of iron is associated with reduced soil condition of submerged or flooded soils, which increases concentration and uptake of iron (Fe^{2 +}). Higher concentration of Fe^{2 +} in the rhizosphere also has antagonistic effects on the uptake of many essential nutrients and consequently yields reduction. In addition to reduced condition, increase in concentration of Fe^{2 +} in submerged soils of lowland rice is associated with iron content of parent material, oxidation-reduction potential, soil pH, ionic concentration, fertility level, and lowland rice genotypes. Oxidation-reduction potential of highly reduced soil is in the range of –100 to –300 mV. Iron toxicity has been observed in flooded soils with a pH below 5.8 when aerobic and pH below 6.5 when anaerobic. Visual toxicity symptoms on plants, soil and plant tissue test are major diagnostic techniques for identifying iron toxicity. Appropriate management practices like liming acid soils, improving soil fertility, soil drainage at certain growth stage of crop, use of manganese as antagonistic element in the uptake of Fe^{2 +} and planting Fe^{2 +} resistant rice cultivars can reduce problem of iron toxicity.     

Effect of long-term intensive rice cultivation on the available silica content of sawah soils: Java Island,Indonesia

Abstract

The dramatic increases in rice productivity and cultivation intensity through the implementation of green revolution (GR) technology using high yielding varieties (HYVs) of rice and chemical fertilizers were not long lasting in Indonesia. The stagnancy of rice productivity in recent years without any scientific reasons presents a challenge for agronomists and soil scientists in Indonesia. This study describes the effects of long-term intensive rice cultivation on the change in available silica (Si) in sawah soil. The term sawah refers to a leveled and bounded rice field with an inlet and an outlet for irrigation and drainage. Soil samples collected by Kawaguchi and Kyuma in 1970 and new samples taken in 2003 from the same sites or sites close to the 1970 sites were analyzed and compared. From 1970 to 2003, the average content of available Si decreased from 1,512 ± 634 kg SiO₂ ha^?1 to 1,230 ± 556 kg SiO₂ ha^?1 and from 6,676 ± 3,569 kg SiO₂ ha^?1 to 5,894 ± 3,372 kg SiO₂ ha^?1 in the 0–20 cm and 0–100 cm soil layers, respectively. Cultivation intensity differences between seedfarms planted with rice three times a year and non-seedfarms rotating rice and upland crops appeared to affect the changing rates of available Si within the study period. In the 0–20 cm soil layer, the average content of available Si decreased from 1,646 ± 581 kg SiO₂ ha^?1 to 1,283 ± 533 kg SiO₂ ha^?1 (?22%) and from 1,440 ± 645 kg SiO₂ ha^?1 to 1,202 ± 563 kg SiO₂ ha^?1 (?17%) in seedfarms and non-seedfarms, respectively. Differences in topographical position also influenced the decreasing rate of available Si in this study. Using similar management practices and cultivation intensity, upland sampling sites lost more Si compared with lowland sites. Planted rice under a rain fed system with no Si addition from rain water in an upland position may be a reason for the higher loss of Si, particularly in non-seedfarms. The Si supply from irrigation water might have contributed to the slowdown in the decreasing rate of available Si in Java sawah soils.     

Evaluation of nanosilicon dioxide and chitosan on tissue culture of apple under agar-induced osmotic stress

In vitro, applications of nanosilicon dioxide (SiO₂) and chitosan were investigated for their effects on growth and proliferation of apple (Malus domestica Borkh. ‘Gala’) explants under osmotic stress induced by agar to simulate drought stress and under non-stressed conditions. The experiment included five levels of SiO₂ (0, 25, 50, 100, and 200 mg L^?1), two levels of chitosan (0 and 40 mg L^?1), and two levels of agar (7 g L^?1 and 9 g L^?1) added to Murashige and Skoog medium. Under non-stressed conditions (7 g L^?1 agar), application of SiO₂ at 50 or 100 mg ^?1 increased proliferation of apple explants. Use of 50 or 100 mg L^?1 SiO₂ or 40 mg L^?1 chitosan increased growth of apple explants under osmotic stress (9 g L^?1 agar). This research suggests that use of SiO₂ or chitosan may improve plant growth and tolerance to stress.     

Catalytic effect of various metal ions on the methylation of mercury in the presence of humic substances

Methylation of Hg²⁺ (Hg(NO₃)₂) in the presence of fulvic acid (FA) and various metal ions has been studied. The concentrations of Hg²⁺ and FA ranged from 5 to 20 mg L^?1 and 171 to 285 mg L^?1 DOC, respectively. The pH range was 3 to 6.5. FA was isolated from an acid brown-water lake by XAD-8 polymeric adsorbent. Methylmercury production in the dark during 2 to 4 days incubation at 30 °C increased with increasing concentrations of Hg²⁺ ion and FA as well as with additions of metal ions (5 to 10 × 10^?5 mole L^?1 The observed catalytic activity of metal ions followed the order Fe³⁺ (Fe²⁺) > Cu²⁺ ≈ Mn²⁺, > Al³⁺. The production of methylmercury had a pH-optimum around 4 to 4.5 at the conditions tested.     

Desalination of sea water by akadama soil and akadama soil-inorganic adsorbents mixtures

(pp. 33–39)

The purpose of this study is to investigate utilization of Akadama soil and evaluate its ion removal efficiency for seawater desalination. The chemical composition of the Akadama soil was Al₂₀₃ 0.334 kg kg^?1, SiO₂ 0.470 kg kg^?1, Fe₂₀₃ 0.157 kg kg^?1 by weight. X-ray powder diffraction pattern, electron diffraction pattern and IR spectrum of Akadama soil showed that allophane was the main phase and low crystallinity kaolin was generated from the allophane. The column method was carried out to evaluate seawater desalination efficiency, the best mixture ratio of the Akadama soil (particle size was less than 250 m), aluminum silicate adsorbent, aluminium magnesium adsorbent, and magnesium oxide adsorbent was 3:1:1:1. Removal percentages of Na⁺, Mg²⁺, Ca²⁺, K⁺ and Cl^? from artificial seawater were 87.7, 84.4, 91.1, 97.3 and 90.7%, respectively. In the batch method, where the mixed adsorbent was used for removal of heavy metals from 20 mg L^?1 solution, the removal percentages of Cu²⁺, Ni²⁺, Mn²⁺, Zn²⁺, Cd²⁺ and Pb²⁺ were higher than 98%. The removal percentage of PO₄ from river water was 100%.     

Iron toxicity in rice—conditions and management concepts

Iron toxicity is a syndrome of disorder associated with large concentrations of reduced iron (Fe²⁺) in the soil solution. It only occurs in flooded soils and hence affects primarily the production of lowland rice. The appearance of iron toxicity symptoms in rice involves an excessive uptake of Fe²⁺ by the rice roots and its acropetal translocation into the leaves where an elevated production of toxic oxygen radicals can damage cell structural components and impair physiological processes. The typical visual symptom associated with these processes is the “bronzing” of the rice leaves and substantial associated yield losses. The circumstances of iron toxicity are quite well established. Thus, the geochemistry, soil microbial processes, and the physiological effects of Fe²⁺ within the plant or cell are documented in a number of reviews and book chapters. However, despite our current knowledge of the processes and mechanisms involved, iron toxicity remains an important constraint to rice production, and together with Zn deficiency, it is the most commonly observed micronutrient disorder in wetland rice. Reported yield losses in farmers' fields usually range between 15% and 30%, but can also reach the level of complete crop failure. A range of agronomic management interventions have been advocated to reduce the Fe²⁺ concentration in the soil or to foster the rice plants' ability to cope with excess iron in either soil or the plant. In addition, the available rice germplasm contains numerous accessions and cultivars which are reportedly tolerant to excess Fe²⁺. However, none of those options is universally applicable or efficient under the diverse environmental conditions where Fe toxicity is expressed. Based on the available literature, this paper categorizes iron‐toxic environments, the steps involved in toxicity expression in rice, and the current knowledge of crop adaptation mechanisms in view of establishing a conceptual framework for future constraint analysis, research approaches, and the targeting of technical options.     

CALIBRATION OF SOIL AND PLANT SILICON ANALYSIS FOR RICE PRODUCTION*

Calibration of field crop response to nutrient availability is the bases for making a fertilizer recommendation from soil and tissue analyses. The purpose of this study was to evaluate and summarize results from a series of experiments on silicon (Si) fertilization of rice in the Everglades Agriculture Area. Twenty-eight rice field experiments were conducted from 1992 through 1996. The experiments consisted of 2 to 5 rates of calcium silicate applied to soils (Histosols) of varying Si soil-test values. Soil samples were taken before planting and analyzed for acetic acid (0.5 mol L^?1) extractable Si. Straw samples were collected at harvest and analyzed for total Si. Grain yield was determined. The “critical” levels for Si in the soil (point below which response to Si fertilizer is expected) calculated by the Cate & Nelson procedure was 19 mg Si L^?1 soil. The amount of silicon to correct Si deficiency in the soil and to obtain optimum rice yield was 1500, 1120 and 0 kg ha^?1 for low (<6 mg L^?1), medium (6 to 24 mg L^?1), and high (>24 mg L^?1) level of soil Si, respectively. Silicon in the straw was classified as high when Si concentration was >34 g kg^?1, medium when in between 17 and 34, and low when <17 g kg^?1 (3.4 and 1.7%, respectively).

     

Changes in photosynthesis and antioxidant metabolism of cotton (Gossypium hirsutum L.) plants in response to manganese stress

ABSTRACT

This study aimed to assess the physiological and biochemical responses of cotton plants to manganese (Mn²⁺) nutrition. Four cotton genotypes (G1 – TMG 47; G2 – FM 975 WS; G3 – TMG 11 WS and G4 – IMA 8405 GLT) were grown in nutrient solution under two Mn²⁺ concentrations (2 and 200 µmol L^?1) for 10 days. No visible symptoms of Mn²⁺ toxicity were observed in the genotypes tested. All genotypes showed a marked increase in leaf chlorophylls, pheophytins, carotenoids, sucrose and total sugars concentration in response to high Mn²⁺ in a nutrient solution. However, the net photosynthetic rate, stomatal conductance, internal carbon dioxide concentration and transpiration decreased in genotypes G1 and G2 growing under 200 µmol L^?1. Antioxidant enzymes such as superoxide dismutase (SOD), ascorbate peroxidase (APX) and glutathione reductase (GR) activities increased in genotypes G1, G3 and G4. Cotton genotypes showed an increased leaf antioxidant and sugar metabolism as a possible strategy to mitigate oxidative stress. The decrease in the net photosynthetic rate and stomatal conductance; the increased antioxidant enzymes activities (SOD, APX and GR); and the increase in leaf sucrose and total sugar concentration were the main physiological and biochemical responses in cotton plants to Mn²⁺ stress.     

Amelioration of cadmium stress in gladiolus (Gladiolus grandiflora L.) by application of potassium and silicon

Gladiolus corms were grown in media contaminated with cadmium (Cd) (50 mg kg^?1) and supplemented with silicon (Si) and potassium (K). The role of Si and K for mitigation of Cd toxicity was evaluated. Cd-induced stress generated significantly increased level of oxidative stress markers including hydrogen peroxide (H₂O₂), and malondialdehyde (MDA) in gladiolus. The application of K and Si improved the production of protein and proline in the treated plants. Moreover, K and Si supplemented plants exhibited an improvement in the activity of antioxidant enzymes and a reduction in the level of MDA, H₂O₂ and Cd uptake under Cd stress. Application of K and Si also enhanced the uptake of mineral nutrients including calcium (Ca), magnesium (Mg), manganese (Mn), sulfur (S) and K. The plants supplemented with K and Si exhibited a higher amount of total phenolics and flavonoids. The combined effect of Si and K was more pronounced regarding beneficial effects on gladiolus plants compared to individual effect of these elements under Cd stress. The current research reveals that Si and K may improve gladiolus growth by decreasing the oxidative stress and Cd uptake and by increasing the activity of antioxidant defense enzymes, the quantity of secondary metabolites and plant nutrition.     

Arsenic–iron interaction: Effect of additional iron on arsenic-induced chlorosis in barley grown in water culture

Abstract

The effect of additional iron (Fe) on arsenic (As) induced chlorosis in barley (Hordeum vulgare L. cv. Minorimugi) was investigated. The treatments were: (1) 0?μmol?L^?1 As?+?10?μmol?L^?1 Fe³⁺ (control), (2) 33.5?μmol?L^?1 As?+?10?μmol?L^?1 Fe³⁺ (As-treated) and (3) 33.5?μmol?L^?1 As?+?50?μmol?L^?1 Fe³⁺ (additional-Fe³⁺) for 14?days. Arsenic and Fe³⁺ were added as sodium-meta arsenite (NaAsO₂) and ethylenediaminetetraacetic acid-Fe³⁺, respectively. Chlorosis in fully developed young leaves was observed in the As-treated plants. The chlorophyll index and the Fe concentration decreased in shoots of the As-treated plants compared with the control plants. Arsenic reduced the concentration of phosphorus, potassium, calcium, magnesium, manganese, zinc and copper. The additional-Fe³⁺ treatment increased the chlorophyll index in plants compared with the As-treated plants. Among the elements, Fe concentration and accumulation specifically increased in the shoots of additional-Fe³⁺ plants compared with As-treated plants, indicating that As-induced chlorosis was Fe-chlorosis. Arsenic and Fe were mostly concentrated in the roots of the As-treated plants. Despite inducing chlorosis in the As-treated plants, phytosiderophores (PS) accumulation in the roots and release from the roots did not increase, rather PS accumulation decreased, indicating that As toxicity hindered PS production in the roots. The PS accumulation in the roots was further reduced in the additional-Fe³⁺ treatment.     

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.     

Redox condition and nitrate change in a newly flooded rice soil under percolation as influenced by oxidative iron and manganese

Nitrate leaching from intermittently flooded rice fields contributes to nitrate pollution in groundwater. In this study, redox conditions and nitrate change in a newly flooded rice soil under the influence of oxidative iron (Fe) and manganese (Mn) were investigated using flooded soil columns under moderate percolation (4.2?mm?d^?1). The amendments of α-Fe₂O₃ and β-MnO₂ powder (5 and 2.7?mg?g^?1, respectively) delayed the establishment of reducing conditions and lowered the rate of nitrate removal in the soil column, and subsequently increased the percolation of soil indigenous nitrate (8.3?mg nitrogen [N]?kg^?1) from 2.0% to 8.0%, and the percolation of externally amended nitrate (250?mg?N?kg^?1) from 11.0% to 26.0%. The pool of oxidative iron-centered metal oxidants needs to be jointly considered with the availability of organic carbon and hydrological conditions in evaluating redox conditions and nitrate change in intermittently flooded rice soils.     

Fe2+对水稻生长及土壤微生物活性的影响

通过盆栽试验,模拟冷浸田土壤亚铁毒害,研究了土壤-水稻-亚铁-微生物相互作用的体系中,外加Fe2+ 不同处理水平 (0、 100、 200、 400、 800和1600 mg/kg) 对水稻苗期和分蘖期相关生理指标、 土壤微生物活性及其生态特征的影响。结果表明, 在含一定亚铁本底（207.77 mg/kg）的正常稻田土壤中,外源性Fe2+的加入将逐步抑制水稻生长、 降低土壤微生物活性。外源Fe2+浓度达100 mg/kg后,水稻的株高、 干物质积累量显著降低; 水稻叶片生理指标叶绿素含量（SPAD值）、 脯氨酸含量、 抗氧化酶系统活性则显著增加,表明外源Fe2+浓度100 mg/kg 是本研究条件下外源Fe2+ 对水稻生长产生显著毒害影响的临界点; 同时随外源Fe2+浓度的增加, 土壤微生物活性指标土壤微生物量碳、 微生物三大基础菌系总量（细菌、 真菌、 放线菌）、 功能菌系总量（氨化细菌、 固氮菌、 纤维分解菌）、 铁还原菌总量总体是先快速下降,后逐渐平稳降低。 半效应浓度EC50分析表明,外源Fe2+浓度100 mg/kg 为多数土壤微生物活性指标（微生物基础菌系总量、 功能菌系总量、 铁还原菌）EC50变化的临界值; 体系中土壤微生物活性指标和水稻生长指标的变化存在显著的相关性, 表明供试土壤亚铁对水稻生长的影响是亚铁对土壤-植物-土壤微生物系统同步影响的结果。综上结果可知,外源Fe2+浓度100 mg/kg为导致供试土壤中水稻生长及土壤微生物活性受到显著负效应的临界值,进而推知,本研究所用土壤对水稻生长和微生物活性的亚铁毒胁迫临界浓度约为300 mg/kg（含本底）, Fe2+含量超出该浓度时,需采取合理的农艺措施控制其负效应。     

Silicon-mediated genotoxic alterations in Brassica juncea under arsenic stress: A comparative study of biochemical and molecular markers

Arsenic (As), one of the most harmful toxicant at the global level, severely affects plant metabolism when taken up. Interestingly, the presence of silicon (Si) as a fertilizer in As-contaminated soil is an effective strategy to decrease As accumulation in plants. Brassica juncea (var. Varuna) were grown hydroponically to investigate the role of Si at biochemical and molecular levels under arsenite (As³⁺) stress. Seedlings of B. juncea were exposed to As³⁺, Si, and a combination of both elements. Our data demonstrated that seedlings exposed to As³⁺ showed an inhibition in shoot length, chlorophyll, carotenoid, and protein, while co-application of Si improved these growth parameters. Silicon supplementation reduced As accumulation in shoot. Increase/decrease was observed in stress-related parameters (cysteine and proline), antioxidant enzymes (superoxide dismutase, ascorbate peroxidase, and catalase), and oxidative stress markers (malondialdehyde and H₂O₂), which were improved upon co-application of Si as compared to As³⁺ alone treatment. Random amplified polymorphic DNA (RAPD) is a suitable biomarker assay for plants for assessing the genotoxicity. Seven RAPD primers produced a total of 39 and 48 bands in the leaves of the untreated and treated seedlings, respectively. The RAPD band-profiles and genomic template stability were consistent with other growth and physiological parameters. In conclusion, the genotoxic alterations along with the biochemical parameters indicate that the exposure to Si mitigates As³⁺-induced oxidative stress by improving the stress-related parameters and antioxidant system in B. juncea.