钾局部供应对玉米根系生长和钾吸收速率的影响

采用自制培养装置,在玉米种子根的局部根段供应含钾营养液。研究证明钾局部供应不影响地上部和总根系干物质的积累。试验开始后第１０ 天钾局部供应使供钾区的根系总长明显增加,这是由于二次侧根长度和数量的增加,但一次侧根生长增加不明显。试验开始第３ 天起,钾供应区的钾吸收速率明显加快。因此,早期可能主要通过钾吸收速率的加快来补偿由于钾局部供应的不足,二次侧根长出以后,根系生长的增加可能部分补偿供钾的不足。１４ Ｃ示踪试验表明,钾局部供应时,植株中的光合产物运向供钾根区的量多于无钾根区     

低磷胁迫对水稻苗期侧根生长及养分吸收的影响

用蛭石与石英砂作为混合培养介质研究了低磷胁迫对水稻（Oryza sativa L.)苗期侧根发生发育的影响及其与磷吸收的相关关系。结果表明：低磷对水稻的侧根发生发育具有明显的诱导作用及基因型差异。相关性分析表明：单位侧根长度的增加与单位根表面积的增大极显相关,而单位侧根数量的增多与单位根表面积的增大无显的相关性。表明单位根表面积的增加主要来自于单位侧根的伸长。侧根参数与磷含量的相关性分析表明：低磷条件下,侧根总长度和侧根数量都与植株磷含量存在显的正相关,根系总表面积与磷含量存在极显的正相关。表明在低磷条件下,侧根的发生发育对水稻的磷吸收具有重要的作用。根系和地上部的可溶性糖含量分析表明;低磷胁迫改变了同化物在地上部和根系的分配。生物量测定表明：低磷胁迫显增大了植株的根冠比。     

丛枝菌根真菌和磷水平对番茄幼苗侧根形成的影响

为了探讨丛枝菌根真菌(AMF)和磷水平对植物根系构型的影响,在两个磷水平下对番茄幼苗接种AMF菌株Rhizophagus irregularis BGC JX04B,研究AMF和磷水平对番茄幼苗侧根形成的影响.结果表明: AMF对植株生物量的促进效应不明显,但显著降低了植株的根冠比;显著增加了主根长而减少了1级侧根长,并与侵染时期存在互作;显著降低了2～3级侧根数量及2级侧根数与1级侧根数的比值,对1~2级侧根密度无显著影响.高磷(50 mg·kg^-1P)显著促进了植株生长,降低了植株的根冠比;对主根长和1级侧根长无显著影响,显著增加了1~3级侧根数量及2级侧根数与1级侧根数的比值,提高了1~2级侧根密度.表明AMF和磷水平对番茄侧根形成的影响机制不同,高磷的影响可能基于对养分吸收和生长的促进效应,而AMF的影响则更为复杂,且AMF与侵染时期的互作效应预示着碳素分配(糖信号)可能参与了AMF对根系构型的调控.     

缺磷胁迫下的小麦根系形态特征研究

研究了缺磷条件下不同基因型小麦（Triticum aestivum L.)苗期根系形态学适应特征,以明确环境因子对根系不同组分（根轴和侧根）生长发育调控作用的强度和根系形态与磷营养效率关系。在缺P环境中,小麦根轴数量和侧根长度明显减小,同化物向根部的分配比例增加,根轴长度、侧根数量和根系长度等均有显著提高。供试基因型小麦的根轴数量及其长度的差异在每个供磷水平及不同供磷水平之间均呈显著,说明这两种性状的差异是由基因型和环境因素共同决定的;而侧根特征的差异只在不同供磷水平间显著,表明侧根性状主要受环境因素的控制。对6种基因型小麦的研究表明,根轴数量、根轴长度、根生长角度和根系长度根角之间存在着显著的基因型差异。相关分析表明,小麦的相对产量与缺磷条件下的小麦苗期根系形态指标的交互作用之间具有显著的线性关系。这种关系说明根系形态性状可作为早期有效地筛选磷高效小麦品种的指标。     

部分根系供磷对黄瓜根系和幼苗生长及根系酸性磷酸酶活性影响

通过分根处理研究了部分根系供磷对黄瓜幼苗生长、植株体内的含磷量及根系酸性磷酸酶活性的影响。结果表明 ,2 0 %根系缺磷 (1条根缺磷 ,4条根供磷 )可以促进根系及植株地上部的生长 ,其根系及地上部的生物量分别是正常生长植株的 1.39倍和 1.2 1倍。2 0 %根系缺磷 ,还可以促进其它供磷根系对磷的吸收。分根处理后 ,2 0 %根系缺磷不影响植物对磷营养的需要 ,但却表现出了R/S比增大的典型缺磷反应 ,说明植物感应缺磷根系起着比地上部更为重要的作用。分根处理后不供磷根系的酸性磷酸酶活性显著高于供磷根系的酸性磷酸酶活性 ,并且根系的酸性磷酸酶活性只与根系的含磷量显著相关 ,与地上部的磷营养状况关系不明显。这说明 ,缺磷条件下 ,黄瓜植株根系分泌酸性磷酸酶活性的增高 ,是黄瓜根系对低磷胁迫的适应性机理 ,而不是地上部改善体内磷营养的调控机理。     

磷空间有效性对拟南芥根形态构型的影响

磷空间有效性显著影响拟南芥主、侧根生长。在均一的磷处理下,极度磷胁迫或过量供磷均会导致拟南芥主根变短和侧根密度降低。在分层的磷处理下,上层高磷下层低磷能明显促进主根伸长生长,提高侧根在高磷区域的密度,说明植物根系在下层低磷区感受到磷胁迫信号后,可促进上层高磷区侧根的形成和发育。     

低磷胁迫下磷高效基因型大麦的根系形态特征

在根袋土培盆栽条件下,以磷高效基因型DH110+、DH147和低效基因型DH49大麦为试验材料,利用根系分析系统分析不同施磷(P₂O₅)水平(极低磷25 mg·kg^-1、低磷50 mg·kg^-1和正常磷75 mg·kg^-1)下,磷高效基因型大麦的根系形态特征及其与植株磷素吸收的关系.结果表明： 低磷胁迫显著降低大麦生物量和磷吸收量,其中磷高效基因型的生物量和磷吸收量在各施磷水平下分别为低效基因型的1.24～1.70和1.18～1.83倍;大麦的总根长、总根表面积、平均根系直径、不定根长及其根表面积、侧根长及其根表面积均随施磷水平的降低而显著降低,其中磷高效基因型大麦在各施磷水平下的总根长、总根表面积、比根长、侧根长及根表面积分别为低效基因型的1.46～2.06、1.12～1.51、1.35～1.72、1.69～2.42和1.40～1.78倍,而平均根系直径为低效基因型的70.6%～90.2%;主成分分析表明,平均根系直径、比根表面积和比根长受基因型差异的影响较为明显,是区分两类磷效率基因型大麦根系形态差异的主要指标;偏最小二乘回归分析表明,各施磷水平下,总根长、总根表面积对大麦植株磷素吸收贡献均较大,随施磷水平降低,不定根长、不定根表面积对大麦植株磷素吸收的贡献明显降低,而平均根系直径、比根长、侧根长及其根表面积的贡献明显增加.磷高效基因型大麦可通过维持侧根的生长、根细度和比根长的增加来适应低磷胁迫.     

低磷供应对拟南芥根系构型的影响

在人工气候箱中,采用Johnson培养基对拟南芥在低磷供应条件下根系构型的变化进行了研究,结果表明：拟南芥在磷饥饿诱导下,主根缩短,侧根密度、根毛的数量和长度显著增加,并且,根尖到第一侧根和第一根毛的距离也大大缩短。这些改变增加了根系比表面积,并且使得根系分布更加靠近土壤表层,有利于提高植物吸收土壤中有机磷的效率。低磷胁迫还导致拟南芥根系分生组织区细胞形状变异,柱细胞数量减少;主根生长和细胞伸长的动力学分析显示,磷饥饿促使拟南芥主根生长变缓,细胞长度随磷饥饿程度的加深迅速缩小。CycB1;1:GUS染色分析结果表明,低磷破坏拟南芥根系分生组织细胞分裂能力,这些结果说明磷胁迫同时抑制了细胞的伸长和分裂,从而引起拟南芥主根的缩短。     

不同磷效率小麦品种对缺磷胁迫反应的比较

在营养液培养条件下,以根据相对产量为指标筛选出的6个不同磷效率的小麦(Triticum aestivum L.)品种为材料,对其苗期在缺磷条件下生长、根冠磷含量及其分配,以及叶片韧皮部汁液中磷浓度等进行了比较研究.结果表明,缺磷抑制植株地上部生长,但刺激根系生长,导致植株根/冠比增加.无论在供磷或缺磷条件下,磷高效品种的根冠生长速率都低于磷低效品种.缺磷导致植株体内的磷含量下降与根系相比,地上部磷含量的下降速率更快.但在缺磷条件下,不同磷效率的小麦品种根冠间的磷分配变化没有差异.研究发现,在正常供磷条件下,磷高效小麦品种的叶片韧皮部汁液中磷浓度较低,而磷低效品种的叶片韧皮部汁液中磷浓度较高.但开始缺磷后,磷高效品种的叶片韧皮部汁液中的磷浓度下降较慢,使其相对磷浓度较高.缺磷后1 0天,磷低效品种叶片韧皮部汁液中的磷浓度为供磷对照的35.9%,而磷高效品种叶片韧皮部汁液中的磷浓度为供磷对照的59%.     

不同磷效率小麦品种对缺磷胁迫反应的比较

在营养液培养条件下,以根据相对产量为指标筛选出的6个不同磷效率的小麦(Triticum aestivum L.)品种为材料,对其苗期在缺磷条件下生长、根冠磷含量及其分配,以及叶片韧皮部汁液中磷浓度等进行了比较研究。结果表明,缺磷抑制植株地上部生长,但刺激根系生长,导致植株根／冠比增加。无论在供磷或缺磷条件下,磷高效品种的根冠生长速率都低于磷低效品种。缺磷导致植株体内的磷含量下降与根系相比,地上部磷含量的下降速率更快。但在缺磷条件下,不同磷效率的小麦品种根冠间的磷分配变化没有差异。研究发现,在正常供磷条件下,磷高效小麦品种的叶片韧皮部汁液中磷浓度较低,而磷低效品种的叶片韧皮部汁液中磷浓度较高。但开始缺磷后,磷高效品种的叶片韧皮部汁液中的磷浓度下降较慢,使其相对磷浓度较高。缺磷后10天,磷低效品种叶片韧皮部汁液中的磷浓度为供磷对照的35．9％,而磷高效品种叶片韧皮部汁液中的磷浓度为供磷对照的59％。     

Nutrient Supply and the Growth of the Seminal Root System in Barley: III. COMPENSATORY INCREASES IN GROWTH OF LATERAL ROOTS, AND IN RATES OF PHOSPHATE UPTAKE, IN RESPONSE TO A LOCALIZED SUPPLY OF PHOSPHATE

Responses to a localized supply of phosphate were studied inbarley grown in continuous flow solution culture. Root systemswere either uniformly supplied with 50 µM phosphate (controls)or the same solution was supplied to only a 4 cm or 2 cm lengthof a seminal root (localized supply), the remainder of the rootsystem receiving a nutrient solution lacking phosphate. Little development of laterals occurred on those parts of theroot system receiving no phosphate from the external solution,while an increase in the number and extension of laterals tookplace in the 4 cm zone enriched with phosphate. Compared withsimilar zones on controls, the total length of laterals wasincreased 15-fold in 21 d plants. In addition, rates of ³²P-phosphateuptake and translocation to shoots per unit root weight werehigher than in controls by a factor of 2?5–5?0. Furtherincreases in the growth of lateral roots, and rates of phosphateuptake, were induced when the segment initially supplied withphosphate was restricted to only 2 cm. These localized modifications to root growth and uptake of phosphatelargely compensated for the deficient supply of phosphate tothe remainder of the root system. After an early period of retardedgrowth and phosphate stress, the relative growth rate of plantsand the concentration of phosphate in shoots were restored tolevels similar to that of the controls. The manner in which the supply of phosphate may control rootdevelopment, and the nature of the co-ordination between rootgrowth, phosphate uptake, and shoot growth, are discussed.     

The morphological changes of wheat genotypes as affected by the levels of localized phosphate supply

Effects of localized phosphate supply on the seedling growth of wheat (Triticum aestivum L.) genotypes 81(85)5-3-3-3 (P-efficient) and NC37 (P-inefficient) were studied using a device which allowed only 3 cm length of root segment to be exposed to phosphate treatment. Localized supply of 0 mmol P L^–1 and the rest of root supplied with 0.1 mmol P L^–1 (HLH), increased the shoot height, leaf area, root/shoot ratio for 81(85)5-3-3-3, length of root and root axis for NC37, and root axis length and density of first-laterals for both the genotypes, compared to plants with the whole root system in P-sufficient solution (HHH). This suggested that above- and below-ground morphological parameters of wheat were promoted by a localized P-deficiency, presumably via a P deficiency signal. There was a significant difference in the number of first-order laterals between the two wheat genotypes when most of the roots were grown without P and only 3 cm length of root was supplied with 0.3 mmol P L^–1. The relationship between the number and density of 2nd-order lateral roots and level of local P supply was quadratic. Maximum number and density of 2nd-order lateral roots were obtained with a localized P supply of 0.70 mmol L^–1.     

Nutrient Supply and the Growth of the Seminal Root System in Barley: II. LOCALIZED, COMPENSATORY INCREASES IN LATERAL ROOT GROWTH AND RATES OP NITRATE UPTAKE WHEN NITRATE SUPPLY IS RESTRICTED TO ONLY PART OF THE ROOT SYSTEM

The development of the seminal root system, its ability to absorbnitrate, and effects on shoot growth were studied in barleyplants in nutrient solution. The roots received either a uniformsupply of 1.0 mM nitrate (controls), or a supply of the samesolution restricted to a 4-cm length of only one of the mainseminal roots (axes) on each plant, the remainder of the rootsystem receiving a solution containing a low concentration (0.01mM). Marked increases took place in both the growth of lateralroots and the absorption and transport of ¹⁵N-labelled nitrate(per unit root weight) from the zone locally supplied with 1.0mM nitrate. These effects appear largely to compensate for thedeficient supply of nitrate to the remainder of the root system,since after 14 d the relative growth rate (g g^–1d^–1)of the total plant equals that of the controls. Rates of ¹⁵N-nitrateuptake (per unit root weight) remain relatively uniform throughoutthe 29-d experiment, during which root axes develop from theirinitial unbranched form to a complex system of laterals. Theresults are discussed in relation to possible mechanisms bywhich coordination is maintained between root growth, ion uptake,and shoot growth.     

Nutrient Supply and the Growth of the Seminal Root System in Barley: I. THE EFFECT OF NITRATE CONCENTRATION ON THE GROWTH OF AXES AND LATERALS

A method was devised by which different zones along a singleseminal axis of an intact plant could be exposed for extendedperiods to contrasting concentrations of nitrate (either 0.01or 1.0 mM) in continuous flow, the supply of all other nutrientsbeing favourable throughout. The concentration of nitrate wasfound to exert a direct and strictly localized effect upon thegrowth of lateral roots which, depending upon the supply ofassimilates from the shoot, resulted in marked modificationsto the form of the root system. Zones receiving 1.0 mM nitrateshowed an increase in the number and extension rate of bothfirst- and second-order laterals, associated with a preferentialaccumulation of dry matter, compared with zones in 0.01 mM nitrate.The average number of laterals (both first and second order)per cm of parent root was 4.4 in the presence of 1.0 mM nitrateand 2.2 in 0.01 mM. The average extension rates of first-orderlaterals were 0.61 and 0.26 cm d^–1 and second-order laterals,0.10 and 0.05 cm d^–1 for nitrate concentrations of 1.0and 0.01 mM respectively. The precise numbers and extensionrates of laterals in any one zone were affected, however, bythe rate of growth of laterals in other parts of the root system.In contrast, the extension rates of axes were little affectedby the concentration of nitrate to which their apical meristemswere exposed and approached 2.0 cm d^–1 provided the plantswere not nitrogen-starved. The significance of these resultsto the physiology of root growth and soil-plant relations isdiscussed.     

The Influence of Mineral Nutrition on the Root Development of Trees: I. THE GROWTH OF SITKA SPRUCE WITH DIVIDED ROOT SYSTEMS

Sitka spruce seedlings were grown with their root systems dividedbetween two contrasting nutrient regimes. One half of the rootsystem was supplied with a solution containing N, P, and K ata range of concentrations while the untreated half receivedwater only. High-nutrient treatments induced two flushes ofshoot growth resulting in a large shoot system, whereas plantsin the low-nutrient treatments flushed once only and showedsymptoms of nutrient deficiency. Root growth, assessed in terms of dry weight and diameter ofboth primary and woody tissues, was stimulated in the rootsto which the nutrients were actually applied, whereas in theuntreated roots on treated plants only the primary root diameterwas enhanced. However, internal nutrient concentrations on bothsides of the root system were related to the concentrationsapplied, though to a slightly lesser extent in the untreatedroots. Thus, the nutrients which had been internally translocatedto the untreated roots had little effect on their growth. The localized stimulation of xylem production in the woody rootsextended into the stem along a spiral pathway which was demonstratedby the movement of dye. Possible mechanisms are discussed by which differential rootgrowth is brought about by a localized supply of mineral nutrients.     

Development and replenishment of the P-depletion zone around the primary root of maize during the vegetation period

The dynamics of the development and replenishment of P-depletion zones around the primary root of maize (Zea mays L. cv ‘Garbo’) was studied during a vegetation period (80 days) under greenhouse conditions in a loamy sand of low P-availability. A recently described freeze-cutting technique was used to determine radial diffusion of labelled phosphate to the primary root. The development of the depletion zone was biphasic. In the initial phase after two days of growth of the primary root in a soil layer labelled with³³P a minimum of isotopically exchangeable P (EP) was observed which had decreased to about 30% of its original amount at the root surface. At that time the corresponding P-concentration in the soil solution was calculated to be as low as 5×10⁻⁷ M. The depletion zone had already spread 0.4 mm from the root surface. During the second phase, between the 10th and 20th day of plant growth the concentration of EP at the root surface increased slowly but did not change markedly. However, the depletion zone continued to spread and after the 20th day of growth reached its maximal diameter (1.07 mm from the root surface) but remained completely within the root hair cyclinder; the single root hairs never exceeded 1.14 mm in length. The biphasic growth of the depletion zone was probably caused by proton extrusion of the root tip. Acidification of the soil solution from pH 5.8 to about 3.9 results in an about 3-fold rise of the concentration of desorbed phosphate and might also have activated acidophilic P-translocators of the root during the initial phase. Anion over cation uptake normally prevailing during the later stage of root development might resulted in a rise of the soil pH within the root hair zone. Consequently P-availability, as well as P-uptake capacity declined, but P-uptake by the seminal root still continued until the 20th day. Subsequently, the P-concentration within the depletion zone increased again while simultaneously its extent was reduced until it was almost completely replenished after 60 days indicating a loss of P-uptake capacity of the primary root. Within the root tissue³³P was accumulated to about twice the concentration of that in the undepleted soils. This accumulation corresponded to periods of high uptake due to the development of root laterals. In the root cortex a high P-content was observed during the first 30 days of growth. At the onset of the reproductive stage of the plant the P-content of the shoot and especially in the developing seeds rose considerably at the cost of phosphate stored in the root cortex. The accumulation of³³P in the root tissue indicated that nutrient gain was mainly achieved during the early stages of plant development and that P was temporarily stored to some extent within the root system.     

Effect of silicate on the growth and arsenate uptake by rice (Oryza sativa L.) seedlings in solution culture

A solution culture experiment was conducted to investigate the effect of silicate on the yield and arsenate uptake by rice. Rice seedlings (Oryza sativaL. cv. Weiyou 77) were cultured in modified Hoagland nutrient solution containing three arsenate levels (0, 0.5 and 1.0 mg L ^–1 As) and four silicate levels (0, 14, 28 and 56 mg L ^–1 Si). Addition of Si significantly increased shoot dry weight (P=0.001) but had little effect on root dry weight (P=0.43). Addition of As had no significant effect on shoot dry weight (P=0.43) but significantly increased root dry weight (P=0.01). Silicon concentrations in shoots and roots increased proportionally to increasing amounts of externally supplied Si (P < 0.001). The presence of As in the nutrient solution had little effect on shoot Si concentration (P=0.16) but significantly decreased root Si concentration (P=0.005). Increasing external Si concentration significantly decreased shoot and root As concentrations and total As uptake by rice seedlings (P <0.001). In addition, Si significantly decreased shoot P concentration and shoot P uptake (P <0.001). The data clearly demonstrate a beneficial effect of Si on the growth of rice seedlings. Addition of Si to the growth medium also inhibited the uptake of arsenate and phosphate by the rice seedlings.     

Physiological changes in, and phosphate uptake by potato plants during development of, and recovery from phosphate deficiency

The development of phosphate deficiency (P-stress) was observed in rooted sprouts of Solanum tuberosum L. cv. Desiree growing in solutions without phosphate. Shoot growth was inhibited by P-stress within 3 to 5 days of terminating the phosphate supply, while significant effects on root growth were not recorded until 7 to 9 days. Thus, the shoot:root dry weight ratio decreased from 4.3 to 2.6 over a 10-day period. Growth in the absence of an exogenous phosphate supply progressively diluted the phosphorus in the plant. The proportional decrease in concentration was similar in roots and shoots over a 7-day period, even though the former were growing more quickly. The potential for phosphate uptake per unit weight of root increased rapidly during the first 3 days of P-stress. When the plants were provided subsequently with a labelled, 1 mol m^?3 phosphate solution, the absorption rate was 3 to 4-fold greater than that of control plants which had received a continuous phosphate supply. The increased rate of uptake by P-stressed plants was accounted for by an increase (3-fold) in the V_max of system 1 for phosphate transport and by a marked increase in the affinity of the system for phosphate (decrease in K_m). In the early stages of P-stress, before marked changes in growth were measured, the proportion of labelled phosphate translocated to the shoots increased slightly relative to the controls when a phosphate supply was restored. In the later stages of stress a greater proportion was retained in the root system of P-stressed plants than in that of controls. In plants with roots divided between solutions containing or lacking a phosphate supply, the increased absorption rate was determined by the general demand for phosphate in the plant and not by the P-status of the particular root where uptake was measured. By contrast, the poportion translocated was strongly dependent on the P-status of the root. The restoration of a phosphate supply to P-stressed plants was marked by a rapid increase in the P concentration in snoots and roots which returned to levels similar to unstressed controls within 24 h. The enhanced uptake rate persisted for at least 5 days, resulting in supra-normal concentrations of P in both shoots and roots, and in the formation of extensive necrotic areas between the veins of mature leaves. Autoradiographs showed accumulations of ³²P in these lesions and at the points where guttation droplets formed on leaves.     

The Uptake of Phosphate by Plants from Flowing Nutrient Solution: IV. EFFECT OF PHOSPHATE CONCENTRATION ON THE GROWTH OF TRIFOLIUM REPENS L. SUPPLIED WITH NITRATE, OR DEPENDENT UPON SYMBIOTICALLY FIXED NITROGEN

Breeze, V. G. and Hopper, M. J. 1987. The uptake of phosphateby plants from flowing nutrient solution. IV. Effect of phosphateconcentration on the growth of Trifolium repens L. suppliedwith nitrate, or dependent upon symbiotically fixed nitrogen.—J.exp. Bot. 38: 618–630. Nodulated white clover plants were subjected to a range of phosphateconcentrations in flowing solution culture (0.32 to 8.0 mmolm^–3 P) at 41 d from sowing, either supplied with nitrateor dependent on symbiotically-fixed nitrogen. No effect of phosphateconcentration in solution on dry matter production, relativegrowth rate, root/shoot ratio, or water soluble carbohydrateconcentration of the plant tissue was observed after 24 d fromthe start of the experiment, although the plants supplied withnitrate yielded more than the others. Phosphate uptake throughoutthe experimental period was related to the solution concentration,but the source of nitrogen did not affect the phosphorus concentrationsof the shoots. However, the roots of the plants dependent onsymbiotically-fixed nitrogen had higher concentrations of phosphorusthan those supplied with nitrate, but this did not appear tobe due to an increased phosphorus requirement for nitrogen fixation,because the amount fixed was unaffected by the phosphate concentrationin solution. The cation-anion balance showed that plants dependenton nitrogen fixation had no larger requirement for calcium thanplants supplied with nitrate, but a requirement for hydroxylions equivalent to over 130 kg lime per tonne of dry shoot.It is suggested that the enhanced phosphate uptake by plantsdependent on nitrogen fixation is due to this need for a cation-chargebalancing anion. Key words: Phosphate uptake, nitrogen fixation, Trifolium repens L., repens L., cation-anion balance, flowing solution culture