锌素营养对作物叶片解剖结构的影响

采用水培方法,调节锌素营养供应,观察芹菜、玉米、小麦幼苗生长及幼苗叶片解剖结构。结果看出,锌素营养不足时植株含匀量降低,生长受到抑制:叶肉细胞收缩,细胞间隙增大,叶肉细胞中叶绿体数量减少。禾本科作物维管柬鞘细胞中叶绿体减少尤为明显,但对叶绿体的体积无影响;辅导组织发育受到抑制,机械组织不发达。锌素营养过剩时细胞结构破坏,叶肉细胞严重收缩,叶绿体明显减少。     

不同土壤水分供应下锌对玉米叶片超微结构的影响

选择 土为供试土壤, 进行盆栽玉米试验, 设定0和5.0 mg·kg^-1两个锌处理, 按土壤饱和持水量的40%~45%和70%~75%在玉米的4叶1心期实施干旱和正常水分处理。生长50 d后, 测定不同土壤水分与锌供应状况下植株生物量和锌含量, 利用透射电子显微镜观察完全伸展新叶的超微结构变化, 以期揭示不同土壤水分供应下, 植物对施锌的响应机理。结果表明: 土壤水分供应充足条件下, 与不施锌相比, 施锌玉米地上部生物量和总干重分别增加78%和52%, 根系和地上部锌含量和锌吸收量增加较多; 而干旱条件下, 施锌对玉米生物量无显著影响。干旱条件下缺锌玉米叶片维管束鞘细胞中叶绿体结构基本保持完好, 淀粉粒和基质片层清晰可见, 但叶肉细胞中叶绿体膜受损, 基质片层结构出现皱缩, 基粒片层减少; 施锌玉米叶片维管束鞘细胞中叶绿体结构保持完好, 叶绿体周围的线粒体数目较多, 叶肉细胞中叶绿体中脂肪颗粒增多, 叶片维管束鞘细胞与叶肉细胞之间可见清晰的胞间连丝。土壤水分充足处理下, 缺锌叶片细胞膜出现皱缩, 维管束鞘细胞叶绿体淀粉粒增多, 片层结构受损, 严重时维管束鞘细胞中内溶物消失, 残存的叶绿体中仅有淀粉粒和少许片层; 叶肉细胞中叶绿体可见淀粉粒, 但片层结构少, 有些出现断裂、收缩。土壤水分充足条件下, 施锌玉米维管束鞘核叶肉细胞结构清晰, 叶绿体结构完整。结论认为: 锌对干旱胁迫下玉米叶片细胞结构的破坏有一定的缓解作用; 但土壤水分正常供应下, 缺锌导致细胞结构受损程度比干旱情况下更严重。     

The influence of phosphorus nutrition on growth,chlorophyll formation and 14CO2 fixation of chlorophyllous carrot callus cultures

Freshly isolated carrot root sec. phloem explants were cultured in nutrient solution plus inositol, IAA and kinetin and a varied supply of inorganic phosphorus. ¹⁴CO₂ fixation experiments with the greened cultures were carried out under steady state conditions at the age of 21 days in light and darkness for four minutes. The results show that photosynthetic CO₂ fixation by the Calvin cycle is greatly reduced in phosphorus deficient cultures whereas CO₂ fixation via PEPC is enhanced. Under phosphorus deficiency the export of primary photosynthetates from the chloroplasts seems to be suppressed while the radioactivity of the labelled insoluble fraction, which represents mainly chloroplastic starch after this short time of ¹⁴CO₂ fixation, was increased. The results are discussed with respect to the influence of phosphorus nutrition on photosynthetic CO₂ fixation and PEP carboxylation in carrot tissue cultures.     

Dissolution of slag fertilizers in a paddy soil and Si uptake by rice plant

Abstract

Maize (Zea mays L.) cv. Ganga 2 was grown in refined sand at three levels of copper: deficient (0.00065 mg L^-1), adequate (0.065 mg L^-1), and excess (6.5 mg L^-1), each at three levels, deficient (0.00065 mg L^-1), adequate (0.065 mg L^-1), and excess (6.5 mg L^-1) of zinc. Excess Cu magnified the zinc deficiency effects in maize by lowering further the biomass, the concentration of leaf Zn, activities of carbonic anhydrase, aldolase, and ribonuclease and intensified the visible foliar symptoms of Zn deficiency. The effects of Cu deficiency, low dry weight, the concentration of leaf Cu and activities of cytochrome oxidase and polyphenol oxidase were enhanced by excess Zn. Synergism was observed between combined deficiency of Cu and Zn and Cu or Zn deficiency, because the depression in the parameters characteristic of Cu or Zn deficiency was more pronounced when both Cu and Zn were deficient than when Cu or Zn was deficient. Antagonism was observed in some parameters between combined excess of Cu and Zn and Cu or Zn excess. Dry weight was decreased further when both Cu and Zn were in excess than when either Cu or Zn was in excess. After the infiltration of Cu and Zn together to the leaf discs from deficient Cu-deficient Zn treatment, the increase in the concentration of leaf Zn and the activities of aldolase, carbonic anhydrase, polyphenol oxidase, and cytochrome oxidase was more pronounced than after the infiltration of Cu or Zn singly. Discontinuance of excess Zn supply from the excess Zn-deficient Cu treatment increased the concentration of leaf Cu and activities of polyphenol oxidase and cytochrome oxidase and lowered the concentration of Zn. Similarly the discontinuance of excess Cu supply from the leaf discs in the “excess Cu-deficient Zn” treatment increased the leaf Zn concentration and the activities of carbonic anhydrase and aldolase.     

Phosphorus‐deficiency effects on response of symbiotic N2 fixation and carbohydrate status in soybean to atmospheric CO2 enrichment

The impact of phosphorus (P) deficiency on response of symbiotic N₂ fixation and carbohydrate accumulation in soybean (Glycine max [L.] Merr.) to atmospheric CO₂ enrichment was examined. Plants inoculated with Bradyrhizobium japonicum MN 110 were grown in growth chambers with controlled atmospheres of 400 and 800 μL CO₂ L^‐1 and supplied either 1.0 mM‐P (P‐sufficient) or 0.05 mM‐P (P‐deficient) nitrogen (N)‐free nutrient solution. When plants were supplied with sufficient P, CO₂ enrichment significantly increased whole plant dry mass (83%), nodule mass (67%), total nitrogenase activity (58%), and N (35%) and P (47%) accumulation at 35 days after transplanting (DAT). Under sufficient P supply, CO₂ enrichment significantly increased starch concentrations in nodules compared to the normal atmospheric CO₂ treatment. Under normal CO₂ levels (400 μL L^‐1) nonstructural carbohydrate concentration (starch plus soluble sugar) was significantly higher in leaves of P‐deficient plants than in leaves of P‐sufficient plants in which nonstructural carbohydrate concentration exhibited a strong diurnal pattern. Under deficient P supply whole plant dry mass, symbiotic N₂‐fixation parameters, and N and P accumulation were not enhanced by atmospheric CO₂ enrichment. Phosphorus deficiency decreased nonstructural carbohydrate accumulation in nodules at the end of a 10‐day period in which functional activity was developing by 86% relative to P‐sufficient controls. While P deficiency elicited significant increases in the nonstructural carbohydrate concentration in leaves, it caused significant decreases in the nonstructural carbohydrate concentration in nodules over the diurnal cycle from 30 to 31 DAT. Collectively, these results indicate that the lack of a symbiotic N₂‐fixation response to atmospheric CO₂ enrichment by P‐deficient plants may be related to the decreased carbohydrate status of nodules.     

The role of potassium in alleviating detrimental effects of abiotic stresses in plants

Plants exposed to environmental stress factors, such as drought, chilling, high light intensity, heat, and nutrient limitations, suffer from oxidative damage catalyzed by reactive oxygen species (ROS), e.g., superoxide radical (O₂equation/tex2gif-sup-1.gif^–), hydrogen peroxide (H₂O₂) and hydroxyl radical (OHequation/tex2gif-sup-4.gif). Reactive O₂ species are known to be primarily responsible for impairment of cellular function and growth depression under stress conditions. In plants, ROS are predominantly produced during the photosynthetic electron transport and activation of membrane‐bound NAD(P)H oxidases. Increasing evidence suggests that improvement of potassium (K)‐nutritional status of plants can greatly lower the ROS production by reducing activity of NAD(P)H oxidases and maintaining photosynthetic electron transport. Potassium deficiency causes severe reduction in photosynthetic CO₂ fixation and impairment in partitioning and utilization of photosynthates. Such disturbances result in excess of photosynthetically produced electrons and thus stimulation of ROS production by intensified transfer of electrons to O₂. Recently, it was shown that there is an impressive increase in capacity of bean root cells to oxidize NADPH when exposed to K deficiency. An increase in NADPH oxidation was up to 8‐fold higher in plants with low K supply than in K‐sufficient plants. Accordingly, K deficiency also caused an increase in NADPH‐dependent O₂equation/tex2gif-sup-6.gif^– generation in root cells. The results indicate that increases in ROS production during both photosynthetic electron transport and NADPH‐oxidizing enzyme reactions may be involved in membrane damage and chlorophyll degradation in K‐deficient plants. In good agreement with this suggestion, increases in severity of K deficiency were associated with enhanced activity of enzymes involved in detoxification of H₂O₂ (ascorbate peroxidase) and utilization of H₂O₂ in oxidative processes (guaiacol peroxidase). Moreover, K‐deficient plants are highly light‐sensitive and very rapidly become chlorotic and necrotic when exposed to high light intensity. In view of the fact that ROS production by photosynthetic electron transport and NADPH oxidases is especially high when plants are exposed to environmental stress conditions, it seems reasonable to suggest that the improvement of K‐nutritional status of plants might be of great importance for the survival of crop plants under environmental stress conditions, such as drought, chilling, and high light intensity. Several examples are presented here emphasizing the roles of K in alleviating adverse effects of different abiotic stress factors on crop production.     

Potassium deficiency impedes elevated carbon dioxide‐induced biomass enhancement in well watered or drought‐stressed bread wheat

Potassium (K) deficiency reduces photosynthesis and biomass production of crop plants and also renders them vulnerable to drought stress, whereas elevated carbon dioxide (CO₂) has a positive effect on photosynthesis and yield and ameliorates the adverse effects of drought stress. This study aimed to characterize the physiological responses of wheat (Triticum aestivum L.) stressed with K deficiency under elevated CO₂ and drought conditions. Increased biomass production caused by elevated CO₂ as a consequence of increased photosynthesis and water use efficiency was absent in young K‐deficient wheat plants. Shoot K concentration was negatively affected by elevated CO₂ particularly under K‐deficient conditions, whereas K content per plant was greatest in plants supplied with adequate K and adequate water. Specific leaf weight was increased as a consequence of carbohydrate accumulation in the source leaves of K‐deficient plants particularly under elevated CO₂ and drought stress. Potassium deficiency clearly impeded the impact of elevated CO₂ in both well watered as well as drought‐stressed plants. Adequate K fertilization is a prerequisite for efficient harvesting of atmospheric CO₂ through increased photosynthesis, decreased transpiration, and increased biomass production under changing atmospheric CO₂ and soil moisture conditions.     

Increase in NAD(P)H‐dependent generation of active oxygen species and changes in lipid composition of microsomes isolated from roots of zinc‐deficient bean plants

The role of zinc (Zn) in maintaining the structural and functional integrity of plant membranes was investigated in the present work. The relationship between the activity of NAD(P)H oxidases generating active oxygen species and changes in lipid composition and peroxidation was evaluated in microsomal membrane vesicles isolated from roots of Zn‐defícient bean (Phaseolus vulgaris L., cv. Bobis) plants. Zinc content of bean root microsomal membranes was decreased by about 30% by Zn deficiency. Microsomes isolated from roots of Zn‐deficient plants showed higher rates of NAD(P)H oxidation and NAD(P)H‐dependent O₂ ^‐ generation than Zn‐sufficient roots. Microsomal O₂ ^‐ consumption, measured in the presence of pyridine nucleotides, was also considerably enhanced by Zn deficiency. This latter activity was greatly stimulated by Fe(III)EDTA, while inhibited by Superoxide dismutase (SOD) and catalase, indicating that active oxygen species were produced during the oxygen consuming enzyme reaction. Zinc deficiency caused a decline in microsomal phospholipid (PL) content. In addition, saturated fatty acids were present at a higher proportion than unsaturated fatty acids in microsomes from Zn‐deficient roots. Sterol content of microsomal vesicles was also modified by Zn deficiency, which led to an increase in the planar sterol campesterol and a concomitant decrease in stigmasterol and sitosterol content. NADPH‐dependent lipid peroxidation, directly measured in microsomal vesicles as malondialdehyde (MDA) production, was slightly enhanced by Zn deficiency. These results support the idea that Zn deficiency determines an enhanced generation of harmful oxygen species by membrane‐associated enzymes and show that this activity can be more pronounced in the presence of iron (Fe), which accumulates in Zn‐deficient tissues. The relationship between the occurrence of this phenomenon and the changes in membrane lipid profile is discussed.     

Adequate supply of potassium improves plant water‐use efficiency but not leaf water‐use efficiency of spring wheat

Enhancing crop water‐use efficiency (WUE) is a major research objective in water‐scarce agroecosystems. Potassium (K) enhances WUE and plays a crucial role in mitigating plant stress. Here, effects of K supply and PEG‐induced water deficit on WUE of spring wheat (Triticum aestivum L. var. Sonett), grown in nutrient solution, were studied. Plants were treated with three levels of K supply (0.1, 1, 4 mM K⁺) and two levels of PEG (0, 25%). WUE was determined at leaf level (WUE_L), at whole‐plant level (WUE_P), and via carbon isotope ratio (δ¹³C). Effects of assimilation and stomatal conductance on WUE_L were evaluated and compared with effects of biomass production and whole‐plant transpiration (E_P) on WUE_P. Adequate K supply enhanced WUE_P up to 30% and by additional 20% under PEG stress, but had no effect on WUE_L. E_P was lower with adequate K supply, but this effect may be attributed to canopy microclimate. Shoot δ¹³C responded linearly to time‐integrated WUE_L in adequately supplied plants, but not in K‐deficient plants, indicating negative effects of K deficiency on mesophyll CO₂ diffusion. It is concluded that leaf‐scale evaluations of WUE are not reliable in predicting whole‐plant WUE of crops such as spring wheat suffering K deficiency.     

Magnesium deficiency–induced impairment of photosynthesis in leaves of fruiting Citrus reticulata trees accompanied by up‐regulation of antioxidant metabolism to avoid photo‐oxidative damage

Limited data are available on the physiological responses of leaves from fruiting trees to magnesium (Mg) deficiency. Magnesium deficiency–induced effects on photosystem II (PSII) photochemistry in leaves of fruiting (Citrus reticulate cv. Ponkan) trees were assessed by the chlorophyll a fluorescence (OJIP) transient. Magnesium deficiency decreased leaf CO₂ assimilation and carbohydrates, but had no effect on intercellular CO₂ concentration. Activity of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco) and concentrations of Chlorophyll (Chl) and carotenoids (Car) decreased to a lesser extent than CO₂ assimilation. Chlorophyll a fluorescence transient from Mg‐deficient leaves had increased O step and decreased P step, accompanied by positive ΔL, ΔK, ΔJ, and ΔI bands. Magnesium deficiency decreased maximum quantum yield of primary photochemistry (F_v/F_m), quantum yield of electron transport from Q<$>_A^‐<$> to the photosystem I (PSI) end electron acceptors (φ_R0), maximum amplitude of IP phase and total performance index (PI_{tot, abs}), but increased deactiviation of oxygen‐evolving complex (OEC) and energy dissipation. Magnesium‐deficient leaves had higher or similar activities of antioxidant enzymes except for lower catalase (CAT) activity, higher or similar concentrations of antioxidant metabolites, and a higher ratio of Car : Chl. Magnesium‐deficiency did not affect concentration of malondialdehyde (MDA) and ratios of ascorbate (ASC) to ASC + dehydroascorbate (DHA) and reduced glutathione (GSH) to GSH + oxidized glutathione (GSSG). In conclusion, Mg deficiency–induced impairment of the whole photosynthetic electron transport chain may be the main factor contributing to decreased CO₂ assimilation. Enhanced energy dissipation and antioxidant metabolism provide sufficient protection to Mg‐deficient leaves against photo‐oxidative damage.     

Deficiency of manganese is alleviated more by low zinc than low copper in wheat

Abstract

Wheat (Triticum aestivum L.) var. Sonalika was grown in purified sand in complete nutrient solution (normal), deficient manganese (Mn) (0.0055 mg L^‐1), deficient copper (Cu) (0.0065 mg L^‐1), deficient zinc (Zn) (0.0065 mg L^‐1), deficient ?n/deficient Cu, deficient ?n/deficient Zn, deficient Cu/deficient Zn, and deficient ?n/deficient Cu/deficient Zn treatments. The deficiency of Mn decreased the biomass, concentration of Mn, chlorophyll, sugars, Hill reaction activity, acid phosphatase activity, and increased that of peroxidase and polyphenol oxidase. The magnitude of Mn deficiency effects was mitigated to variable extent when Mn was deficient along with deficient Cu and/or deficient Zn. The effects of either Cu or Zn deficiency viz., intensification of foliar symptoms, decrease in biomass, leaf Cu/Zn, seed yield and starch content were increased further in combined deficiency of Cu and Zn. The stimulation in acid phosphatase and decrease in the activity of polyphenol oxidase and carbonic anhydrase in Cu or Zn deficient leaves were further aggravated when both Cu and Zn were deficient together. All these changes reveal a synergism between Cu and Zn in wheat.     

An effective antioxidant defense provides protection against zinc deficiency‐induced oxidative stress in Zn‐efficient maize plants

Maize plants (Zea mays L. cv. Ganga 2 and cv. Jaunpuri satha) were grown in solution culture under glasshouse conditions at deficient (0 µM) and normal (1 µM) levels of Zn supply. Appearance of visible effects characteristic of Zn deficiency, depression in plant growth, and dry matter yield of the plants indicated that Ganga 2 was more susceptible to Zn deficiency than Jaunpuri satha. Higher susceptibility of Ganga 2 to Zn deficiency was also manifested by a greater decrease in plant dry mass and an increased accumulation of TBARS (thiobarbituric acid reactive substance, describing lipid peroxidation). While total SOD activity was decreased in Zn deficient plants of Ganga 2, it was increased marginally in case of Jaunpuri satha. The marginal increase in total SOD activity in the Zn‐deficient Jaunpuri satha plants was a result of a marked increase in non‐CuZn SOD and only a slight decrease in CuZn SOD. Though Zn deficiency increased H₂O₂ concentration and the activities of H₂O₂‐scavenging enzymes in both the cultivars, there was less increase in H₂O₂ concentration and the activities of peroxidase, ascorbate peroxidase and glutathione reductase were more prominently increased in the Zn‐efficient Jaunpuri satha. Plants of the susceptible variety, Ganga 2, accumulated higher concentrations of glutathione disulfide. It is concluded that the significant decreases in the activities of CuZn SOD (CN‐sensitive SOD) and glutathione reductase, and high concentrations of H₂O₂ predisposed Zn‐deficient Ganga 2 plants to more severe oxidative stress than those of Jaunpuri satha and, therefore, contributed to a greater decrease in dry matter production.     

Effects of Nitrogen Deficiency on Leaf Chlorophyll Fluorescence Parameters in Two Olive Tree Cultivars ‘Meski’ and ‘Koroneiki’

Effects of nitrogen (N) deficiency on photosynthetic carbon dioxide (CO₂) assimilation, photosystem II (PSII) photochemistry and photoinhibition were investigated in young trees of two olive cultivars ‘Meski’ and ‘Koroneiki’ grown in a greenhouse under controlled conditions. The trees were subjected to four different levels of N supply. N deficient trees had a significantly smaller CO₂ assimilatory capacity, but showed little changes in maximum quantum efficiency of PSII photochemistry. However, modifications in PSII photochemistry induced by N deficiency were observed. This was reflected in decreases in quantum yield of PSII electron transport (Φ_PSII) and efficiency of excitation energy capture by open PSII reaction centres (F_v’/F_m’) and in an increase in non-photochemical quenching (NPQ). These results suggest that modifications in PSII photochemistry might be a mechanism to down-regulate photosynthetic electron transport so that production of adenosine triphosphate (ATP) and nicotinamide adenine dinucleotide phosphate (NADPH). would be in equilibrium with the decreased demand in the Calvin cycle in the N deficient trees. Therefore, both CO₂ assimilation rate and total electron flow (J_t) with its compound electron flows devoted to either carboxylation (J_c) or oxygenation (J_o) can be considered as useful tools to assess the N nutrition status of the trees. Clear relationships were found between A_max and the nitrogen nutrition index (NNI) on the one hand, and between J_t and NNI on the other hand. The results demonstrate that ‘Meski’ is more efficient than ‘Koroneiki’ when subjected to N deficiency.     

Zinc uptake kinetics in the low and high‐affinity systems of two contrasting rice genotypes

Rice (Oryza sativa L.) cultivars differ widely in their susceptibility to zinc (Zn) deficiency. The physiological basis of Zn efficiency (ZE) is not clearly understood. In this study, the effects of Zn‐sufficient and Zn‐deficient pretreatments on the time and concentration‐dependent uptake kinetics of Zn were examined at low (0–160 nM) and high Zn supply levels (0–80 μM) in two contrasting rice genotypes (Zn‐efficient IR36 and Zn‐inefficient IR26). The results show that ⁶⁵Zn²⁺ influx rate was over 10 times greater for the Zn‐deficient pretreatment plants than for the Zn‐sufficient pretreatment plants. At low Zn supply, significant higher ⁶⁵Zn²⁺ influx rates were found for the Zn‐efficient genotype than for the inefficient genotype, with a greater difference (over three‐fold) at Zn supply > 80 nM in the Zn‐deficient pretreatments. At high Zn supply levels, however, a difference (2.5‐fold) in ⁶⁵Zn²⁺ influx rate between the two genotypes was only noted in the Zn‐deficient pretreatments. Similarly, the ⁶⁵Zn²⁺ accumulation in the roots and shoots of Zn‐efficient IR36 pretreated with Zn‐deficiency were sharply increased with time and higher than that in the Zn‐inefficient IR26 with an over four‐fold difference at 2 h absorption time. However, with Zn‐deficient pretreatments, the Zn‐efficient genotype showed a higher shoot : root ⁶⁵Zn ratio at higher Zn supply. Remarkable differences in root and shoot ⁶⁵Zn²⁺ accumulation were noted between the two genotypes in the Zn‐deficiency pretreatment, especially at low Zn level (0.05 μM), with 2–3 times higher values for IR36 than for IR26 at an uptake time of 120 min. There appear to be two separate Zn transport systems mediating the low and high‐affinity Zn influx in the efficient genotype. The low‐affinity system showed apparent Michaelis–Menten rate constant (K_m) values ranging from 10 to 20 nM, while the high‐affinity uptake system showed apparent K_m values ranging from 6 to 20 μM. The V_max value was significantly elevated in IR36 and was 3–4‐fold greater for IR36 than for IR26 at low Zn levels, indicating that the number of root plasma membrane transporters in low‐affinity uptake systems play an important role for the Zn efficiency of rice.     

Use of routine soil tests in predicting corn leaf zinc

Abstract

Zinc of index corn leaves samples from 91 Minnesota sites on numerous soil types was correlated with soil Zn extracted by four routine procedures. The EDTA?(NH₄)₂CO₃ ‐ extractable soil Zn was more closely correlated with leaf Zn than soil zinc extracted by 0.1N HCl, EDTA‐NH₄OAc, or by NH₄OAc ‐ dithizone. Soil pH, CaCO₃ equivalent, extractable P, and organic matter of both acid and calcareous soils were negatively correlated with leaf Zn. When EDTA ? (NH₄)₂CO₃ ‐ extractable Zn was included with routine soil tests, a prediction equation for corn leaf Zn was formulated and compared with analytical values. However, the use of 1.4 ppm EDTA ? (NH₃)₂CO₃, ‐ extractable soil Zn alone as a critical value was equally effective in predicting leaf Zn.     

Distribution of magnesium between chlorophyll and other photosynthetic functions in magnesium deficient “sun”; and “shade”; leaves of poplar

Photosynthesis of attached sun and shade grown leaves of poplar (Populus euramericana (Dode) Guinier cv. ‘Robusta') has been measured at 0.03 and 0.5% CO₂ at light limitation and light saturation. Photosynthetic rates were compared for plants grown at normal and low Mg‐supply and related to leaf Mg content.

Photosynthetic rates at high CO₂ level were affected at Mg concentration lower than about 50 μmoles/g dry leaf tissue at both photosynthetic irradiations. This was paralleled by a decrease in chlorophyll concentration. At a low CO₂ level photosynthesis was affected at the same Mg concentration but the degree of the inhibition was higher. This indicates that synthesis of chlorophyll as well as CO₂ fixation are affected at the same “critical”; Mg concentration.

Shade leaves contain more chlorophyll per unit leaf weight than sun leaves but the percentual‐ decrease of chlorophyll in Mg deficient leaves Is similar for sun and shade leaves at the same Mg leaf concentration. As a consequence, in Mg deficient shade leaves extraordinary high portions of leaf Mg are bound to chlorophyll (up to 57%; in contrast: up to 37% in sun leaves).     

Responses of earlirose rice to iron,zinc, and BPDS when grown on calcareous soil

Abstract

The Earlirose cultivar of rice (Oryza sativa L.) grown in calcareous Hacienda loam soil was extremely Fe deficient. The Fe deficiency was corrected by premixing 40 ppm Fe (as FeSO₄) into the soil before transplanting plants. The Fe deficiency appeared to be induced by high plant levels of Cu and Mn. Addition of Zn (40 ppm as ZnSO₄) intensified the Fe deficiency. The Fe addition did not overcome the effect of the Zn. BPDS (bathophenanthroline disulfonate), a chelator of Fe⁺⁺, had little effect on the results.     

Selecting Rice Genotypes Tolerant to Zinc Deficiency and Sodicity: Differences in Concentration of Major Cations and Sodium/Potassium Ratio in Leaves

Zinc (Zn) deficiency is a major nutritional problem for rice under sodic conditions. Seedlings (35-d old) of 30 rice genotypes were transplanted in pots at pH₂ 9.8 [diethylene triamine penta acetic acid (DTPA) Zn 1.8 ppm] to identify genotypes tolerant to both sodicity and Zn deficiency. Ten genotypes (group A) showed potential to tolerate both the stresses. Sixteen genotypes (group B) were sensitive to Zn deficiency. However, some of the seedlings of group B genotypes were normal (without Zn deficiency symptoms). Four genotypes (group C) were sensitive to sodicity. Leaves and their leaf sheaths were analyzed at 33 d after transplanting for Ca, Mg, K, and Na. Group A genotypes (CSR-88IR15, CSR-89IR14, IR4630-22-2-5-1-2, and Trichi) had significantly less Na concentrations in their leaves and the leaf sheaths compared to group B genotypes (CSR10, CSR23, CSR-88IR1, 89H1-931098, and IR47538-3B-9-3B-1). The concentration of Na was invariably higher in the leaf sheath than its leaf in both the groups, but reverse was true for Ca, Mg, and K. Zinc deficient plants had relatively higher concentrations of Ca and Mg in their leaves and the leaf sheaths than group A. Concentration of K was somewhat better in group A than group B genotypes. Higher Na/K ratio in group B genotypes compared to group A may be attributed to increased concentrations of Na rather than decreases in K concentrations. Further studies are needed to understand the processes associated with differential uptake of Na and K by Zn deficient plants of group B genotypes resulting in higher Na/K ratio compared to group A genotypes.     

Zinc‐efficient wild grasses enhance release of phytosiderophores under zinc deficiency

The effect of the zinc (Zn) nutritional status on the rate of phyto‐siderophore release was studied in three wild grass species (Hordeum murinum, Agropyron orientale, and Secale cereale) grown in nutrient solution under co‐trolled environmental conditions. These wild grasses are highly “Zn‐efficient”; and grow well on severely Zn‐deficient calcareous soils in Turkey (DTPA‐extractable Zn was 0.12 mg/kg soil and CaCO₃ was 37%). In all wild grasses studied, Zn deficiency reduced shoot growth but had no effect on root growth. Low amounts of phytosiderophores were released from roots of all wild grasses adequately supplied with Zn. In plants grown without Zn, release of phytosiderophores progressively increased with the onset of visual Zn deficiency symptoms, such as inhibition of shoot elongation and appearance of chlorotic and necrotic patches on leaves. Compared to Zn‐sufficient plants, phytosiderophore release increased 18–20‐fold in deficient plants. HPLC analysis of root exudates showed that the dominating phytosiderophore in Zn‐deficient Agropyron and Hordeum was 3‐epi‐hydro‐xymugineic acid (epi‐HMA) and was 3‐hydroxy‐mugineic acid (HMA) in Secale. Besides HMA, epi‐HMA and mugineic acid (MA) were also detected in exudates of Zn‐deficient Secale. The results indicate the importance of phytosiderophores in adaptation of wild grasses to Zn‐deficient calcareous soils. Phytosiderophores might enhance mobilization of Zn from sparingly soluble Zn pools and from adsorption sites, both in the rhizosphere and within the plants.     

Influence of Gyttja on Shoot Growth and Shoot Concentrations of Zinc and Boron of Wheat Cultivars Grown on Zinc‐Deficient and Boron‐Toxic Soil

Abstract

Greenhouse experiments were carried out to study the influence of gyttja, a sedimentary peat, on the shoot dry weight and shoot concentrations of zinc (Zn) and boron (B) in one bread wheat (Triticum aestivum L., cv. Bezostaja) and one durum wheat (Triticum durum L., cv. Kiziltan) cultivar. Plants were grown in a Zn‐deficient (DTPA‐Zn: 0.09 mg kg^?1 soil) and B‐toxic soil (CaCl₂/mannitol‐extractable B: 10.5 mg kg^?1 soil) with (+Zn = 5 mg Zn kg^?1 soil) and without (?Zn = 0) Zn supply for 55 days. Gyttja containing 545 g kg^?1 organic matter was applied to the soil at the rates of 0, 1, 2.5, 5, and 10% (w/w). When Zn and gyttja were not added, plants showed leaf symptoms of Zn deficiency and B toxicity, and had a reduced growth. With increased rates of gyttja application, shoot growth of both cultivars was significantly enhanced under Zn deficiency, but not at sufficient supply of Zn. The adverse effects of Zn deficiency and B toxicity on shoot dry matter production became very minimal at the highest rate of gyttja application. Increases in gyttja application significantly enhanced shoot concentrations of Zn in plants grown without addition of inorganic Zn. In Zn‐sufficient plants, the gyttja application up to 5% (w/w) did not affect Zn concentration in shoots, but at the highest rate of gyttja application there was a clear decrease in shoot Zn concentration. Irrespective of Zn supply, the gyttja application strongly decreased shoot concentration of B in plants, particularly in durum wheat. For example, in Zn‐deficient Kiziltan shoot concentration of B was reduced from 385 mg kg^?1 to 214 mg kg^?1 with an increased gyttja application. The results obtained indicate that gyttja is a useful organic material improving Zn nutrition of plants in Zn‐deficient soils and alleviating adverse effects of B toxicity on plant growth. The beneficial effects of gyttja on plant growth in the Zn‐deficient and B‐toxic soil were discussed in terms of increases in plant available concentration of Zn in soil and reduction of B uptake due to formation of tightly bound complexes of B with gyttja.