Nitrate supply and plant development influence nitrogen uptake and allocation under elevated CO<Subscript>2</Subscript> in durum wheat grown hydroponically

Growth in elevated CO₂ often leads to decreased plant nitrogen contents and down-regulation of photosynthetic capacity. Here, we investigated whether elevated CO₂ limits nitrogen uptake when nutrient movement to roots is unrestricted, and the dependence of this limitation on nitrogen supply and plant development in durum wheat (Triticum durum Desf.). Plants were grown hydroponically at two N supplies and ambient and elevated CO₂ concentrations. Elevated CO₂ decreased nitrate uptake per unit root mass with low N supply at early grain filling, but not at anthesis. This decrease was not associated with higher nitrate or amino acid, or lower non-structural carbohydrate contents in roots. At anthesis, elevated CO₂ decreased the nitrogen content of roots with both levels of N and that of aboveground organs with high N. With low N, elevated CO₂ increased N allocation to aboveground plant organs and nitrogen concentration per unit flag leaf area at anthesis, and per unit aboveground dry mass at both growth stages. The results from the hydroponic experiment suggest that elevated CO₂ restricts nitrate uptake late in development, high N supply overriding this restriction. Increased nitrogen allocation to young leaves at low N supply could alleviate photosynthetic acclimation to elevated CO₂.     

Nitrate Nutrition and Temperature Effects on Wheat: a Synthesis of Plant Growth and Nitrogen Uptake in Relation to Metabolic and Physiological Processes

Lawlor, D. W., Boyle, F. A., Keys, A. J., Kendall, A. C. andYoung, A. T. 1988. Nitrate nutrition and temperature effectson wheat: a synthesis of plant growth and nitrogen uptake inrelation to metabolic and physiological processes.—J.exp. Bot. 39: 329-343. Growth of spring wheat was measured in cool (13°C day/10°Cnight) or warm (23°C/18°C) temperatures, combined withlarge and small amounts of nitrate fertilizer. The rate of growthof dry matter was less at cool temperatures but total growthover the same period of development was slightly greater inthe cool than in the warm. Main-shoot and tiller leaves grewslower and, despite growing for a longer period, were shorterin the cool than in the warm. They had greater fresh and drymass and content of starch and fructosans per unit area. Coolconditions increased root dry mass, root to shoot ratio andnitrogen content in dry matter. Additional nitrate increasedleaf area of main shoots slightly but of tillers greatly; itincreased leaf and tiller dry matter and total plant dry mass.Additional nitrate decreased the proportion of dry matter inroots and in stems and the N content of dry matter in all plantparts. Regulation of growth by temperature, nitrate supply andthe rôle of photosynthesis and nitrogen uptake, is consideredin relation to the mechanisms of incorporation of carbon andnitrogen into biochemical constituents. It is concluded thattemperature regulates the rate of protein synthesis, which determinesplant growth rate. Nitrogen flux into the plant is not directlylinked to protein synthesis so that the content of NO^–₃and of amino acids is related both to growth and to conditionsgoverning NO^–₃ uptake and its reduction. When nitrogensupply is large, growth is limited by temperature, not NO^–₃.Inadequate nitrate supply decreases protein synthesis (and thereforegrowth) more than it decreases carbon assimilation, so thatorgans such as roots and stems increase in dry matter relativeto shoots and all tissues have smaller proportions of nitrogenin dry matter. Cool conditions, although decreasing the rateof protein synthesis, increase its duration and decrease thesize of leaves, so that the content of protein per unit leafarea is greater in cool than in warm grown leaves. Consequencesof changes in the balance of N and C supply and growth ratefor dry matter distribution in plants are discussed. Key words: Wheat, nitrate nutrition, temperature     

Growth pattern and carbon allocation to volatile leaf terpenes under nitrogen-limiting conditions in Heterotheca subaxillaris (Asteraceae)

Summary Rosettes of Heterotheca subaxillaris were grown at four levels of nitrate. Individual leaf volatile mono- and sesquiterpene content, leaf nitrogen content, and root and shoot dry weight were measured on individual leaves every two weeks for 18 weeks. Rosettes with the highest nitrate availability had 2.2-fold greater leaf nitrogen levels compared to plants with the lowest availability. As nitrate availability became increasingly limited, carbon allocation to both volatile leaf terpenes and root growht increased. Leaf mono- and sesquiterpene content was greatest in the young leaves of individuals growing at the lowest nitrate availability conditions. Higher levels of carbon-based herbivore-deterring chemicals in nitrate-limited plants may increase net productivity through retention of nitrogen that would otherwise be lost to herbivory.     

Carbon and Nitrogen Assimilation by Vicia faba L. at Low Temperature: the Importance of Concentration and Form of Applied-N

Low temperature (6 C) growth was examined in two cultivarsof Vicia faba L. supplied with 4 and 20 mol m^–3 N as nitrateor urea. Both cultivars showed similar growth responses to increasedapplied-N concentration regardless of N-form. Total leaf areaincreased, as did root, stem and leaf dry weight, total carboncontent and total nitrogen content. In contrast to findingsat higher growth temperatures, 20 mol m^–3 urea-N gavesubstantially greater growth (all parameters measured) than20 mol m^–3 nitrate-N. The increased carbon content per plant associated with increasedapplied nitrate or urea concentration, or with urea in comparisonto nitrate, was due to a greater leaf area per plant for CO₂uptake and not an increased CO₂, uptake per unit area, carbon,chlorophyll or dry weight, all of which either remained constantor decreased. Nitrate reductase activity was substantial inplants given nitrate but negligible in plants given urea. Neitherfree nitrate nor free urea contributed greatly to nitrogen levelsin plant tissues. It is concluded that there is no evidence for a restrictionin nitrate reduction at 6 C, and it is likely that urea givesgreater growth than nitrate because of greater rates of uptake. Vicia faba, broad bean, low temperature growth, carbon assimilation, nitrogen assimilation     

Growth and carbon economy of a fast-growing and a slow-growing grass species as dependent on nitrate supply

In previous experiments systematic differences have been found in the morphology, carbon economy and chemical composition of seedlings of inherently fast- and slow-growing plant species, grown at a non-limiting nutrient supply. In the present experiment it was investigated whether these differences persist when plants are grown at suboptimal nutrient supply rates. To this end, plants of the inherently fast-growing Holcus lanatus L. and the inherently slow-growing Deschampsia flexuosa (L.) Trin. were grown in sand at two levels of nitrate supply. Growth, photosynthesis, respiration and carbon and nitrogen content were studied over a period of 4 to 7 weeks. At low N-supply, the potentially fast-growing species still grew faster than the potentially slow-growing one. Similarly, differences in leaf area ratio (leaf area:total dry weight), specific leaf area (leaf area:leaf dry weight) and leaf weight ratio (leaf dry weight:total dry weight), as observed at high N-supply persisted at low N-availability. The only growth parameter for which a substantial Species × N-supply interaction was found was the net assimilation rate (increase in dry weight per unit leaf area and time). Rates of photosynthesis, shoot respiration and root respiration, expressed per unit leaf, shoot and root weight, respectively, were lower for the plants at low N-availability and higher for the fast-growing species. Species-specific variation in the daily carbon budget was mainly due to variation in carbon fixation. Lower values at low N were largely determined by both a lower C-gain of the leaves and a higher proportion of the daily gain spent in root respiration. Interspecific variation in C-content and dry weight:fresh weight ratio were similar at low and high N-supply. Total plant organic N decreased with decreasing N-supply, without differences between species. It is concluded that most of the parameters related to growth, C-economy and chemical composition differ between species and/or are affected by N-supply, but that differences between the two species at high N-availability persist at low N-supply.     

Growth and reproduction of Arabidopsis thaliana in relation to storage of starch and nitrate in the wild-type and in starch-deficient and nitrate-uptake-deficient mutants

We have investigated the interactions between resource assimilation and storage in rosette leaves, and their impact on the growth and reproduction of the annual species Arabidopsis thaliana. The resource balance was experimentally perturbed by changing (i) the external nutrition, by varying the nitrogen supply; (ii) the assimilation and reallocation of resources from rosette leaves to reproductive organs, by cutting or covering rosette leaves at the time of early flower bud formation, and (iii) the internal carbon and nitrogen balance of the plants, by using isogenic mutants either lacking starch formation (PGM mutant) or with reduced nitrate uptake (NU mutant). When plants were grown on high nitrogen, they had higher concentrations of carbohydrates and nitrate in their leaves during the rosette phase than during flowering. However, these storage pools did not significantly contribute to the bulk flow of resources to seeds. The pool size of stored resources in rosette leaves at the onset of seed filling was very low compared to the total amount of carbon and nitrogen needed for seed formation. Instead, the rosette leaves had an important function in the continued assimilation of resources during seed ripening, as shown by the low seed yield of plants whose leaves were covered or cut off. When a key resource became limiting, such as nitrogen in the NU mutants and in plants grown on a low nitrogen supply, stored resources in the rosette leaves (e.g. nitrogen) were remobilized, and made a larger contribution to seed biomass. A change in nutrition resulted in a complete reversal of the plant response: plants shifted from high to low nutrition exhibited a seed yield similar to that of plants grown continuously on a low nitrogen supply, and vice versa. This demonstrates that resource assimilation during the reproductive phase determines seed production. The PGM mutant had a reduced growth rate and a smaller biomass during the rosette phase as a result of changes in respiration caused by a high turnover of soluble sugars ( Caspar et al. 1986 ; W. Schulze et al. 1991 ). During flowering, however, the vegetative growth rate in the PGM mutant increased, and exceeded that of the wild-type. By the end of the flowering stage, the biomass of the PGM mutant did not differ from that of the wild-type. However, in contrast to the wild-type, the PGM mutant maintained a high vegetative growth rate during seed formation, but had a low rate of seed production. These differences in allocation in the PGM mutant result in a significantly lower seed yield in the starchless mutants. This indicates that starch formation is not only an important factor during growth in the rosette phase, but is also important for whole plant allocation during seed formation. The NU mutant resembled the wild-type grown on a low nitrogen supply, except that it unexpectedly showed symptoms of carbohydrate shortage as well as nitrogen deficiency. In all genotypes and treatments, there was a striking correlation between the concentrations of nitrate and organic nitrogen and shoot growth on the one hand, and sucrose concentration and root growth on the other. In addition, nitrate reductase activity (NRA) was correlated with the total carbohydrate concentration: low carbohydrate levels in starchless mutants led to low NRA even at high nitrate supply. Thus the concentrations of stored carbohydrates and nitrate are directly or indirectly involved in regulating allocation.     

The role of root nitrate reduction in the systemic control of biomass partitioning between leaves and roots in accordance to the C/N-status of tobacco plants

The root/shoot-ratio is a simple parameter to describe the systemic response of plants to alterations of their nutritional status, as indicated by the C/N-balance of leaves. The ‘functional equilibrium hypothesis’ holds that leaf growth is limited by the supply of nitrogen from the roots, whereas root growth depends on the carbon supply from leaves. The nature of the systemic control that balances root and shoot growth is not fully understood. Previous experiments have shown that root growth of transformed tobacco plants, which lack functional root nitrate reductase, was severely impeded, when plants were grown on NO ₃ ^? as the sole N-source. In these experiments, the root/shoot-ratio was correlated with the Glutamate/Glutamine-ratio of roots. In the present study we tested the hypothesis that high internal Glu contents (in relation to Gln) inhibit root growth. Wild type and transformed tobacco plants were given access to both NH₄ and NO₃, and were cultivated at ambient and elevated pCO₂ in order to vary carbon availability. The uptake and assimilation of NH ₄ ⁺ by the root was significantly higher in transformed than in wild type tobacco, in particular at elevated pCO₂. Consequently, the Glu/Gln-ratio in the root of transformants was significantly lower than in NO ₃ ^? -grown plants, and was, in the present study, not different from the wild type. However, we failed to observe a correlation between plant architecture and the Glu/Gln-ratio of roots, suggesting that signals arising from the immediate products of nitrate reduction (nitrite) are involved in the systemic control of root growth. Furthermore the synthesis of root-derived signals, which affect N-turnover, starch re-mobilization and the growth of leaves, appears to be associated with root nitrate reduction. This enzymatic step seems to be indispensable for the systemic control of biomass partitioning, and plays a crucial role for the integration of carbon and nitrogen metabolism at the whole plant level.     

Effects of Nitrogen on the Development and Growth of the Potato Plant. 2. The Partitioning of Dry Matter, Nitrogen and Nitrate

Potatoes (Solanum tuberosum L.) were planted in pots in a temperature-controlledglasshouse The treatments consisted of three levels of nitrogensupply, ie 25, 8 and 16 g N per pot (treatments called N1, N2and N3) The accumulation rates of dry matter and nitrogen showedan upper limit of response to nitrogen supply, N3 plants continuedto accumulate dry matter and N at a constant rate for a longerperiod of time than N2 and N1 plants The uptake of nitrogenslowed earlier in time than the rate of dry matter accumulationin all treatments. The proportion of the dry matter in tubersof mature plants was not affected by nitrogen treatment, butthe start of tuber bulking was delayed in the N3 plants Thefinal proportion of total plant nitrogen in the tubers was similarfor all treatments The concentration of nitrogen in the drymatter of mature plants increased with the level of N supplyMaximum haulm weight increased with the level of N supply Apicallateral branches of the first and second order made up largerproportions of the total haulm dry weight and total leaf areaas more nitrogen was supplied. Yet, the distribution of drymatter over stems and leaves was not different between nitrogentreatments Stems were the most responsive to N treatment interms of N concentrations In each of the component organs (stems, leaves, tubers) theconcentration of nitrogen declined with time Fairly strong associationswere observed between the concentrations of N in component organs.The concentration of nitrate in leaves usually increased initiallywith leaf age, peaked and declined. A substantial part of thedifferences between treatments in the concentrations of N inleaf dry matter were attributable to differences in nitrateconcentration Nitrate in stems and tubers fell virtually belowthe limit of detection at total nitrogen concentrations of lessthan 1%, but increased in proportion to total N above that threshold,especially in stems Potato, Solanum tuberosum L, dry matter production, dry matter distribution, nitrogen nutrition, nitrogen distribution, nitrogen concentration     

N uptake and distribution in crops: an agronomical and ecophysiological perspective

The rate of N uptake of crops is highly variable during crop development and between years and sites. However, under ample soil N availability, crop N accumulation is highly related to crop growth rate and to biomass accumulation. Critical N concentration has been defined as the minimum N concentration which allows maximum growth rate. Critical N concentration declines during crop growth. The relationship between critical N concentration and biomass accumulation over the growth period of a crop is broadly similar within major C(3) and C(4) cultivated species. Therefore, the critical N concentration concept is widely used in agronomy as the basis of the diagnosis of crop N status, and allows discrimination between situations of sub-optimal and supra-optimal N supply. The relationship between N and biomass accumulation in crops, relies on the interregulation of multiple crop physiological processes. Among these processes, N uptake, crop C assimilation and thus growth rate, and C and N allocation between organs and between plants, play a particular role. Under sub-optimal N supply, N uptake of the crop depends on soil mineral N availability and distribution, and on root distribution. Under ample N supply, N uptake largely depends on growth rate via internal plant regulation. Carbon assimilation of the crop is related to crop N through the distribution of N between mature leaves with consequences for leaf and canopy photosynthesis. However, although less commonly emphasized, carbon assimilation of the crop also depends on crop N through leaf area development. Therefore, crop growth rate fundamentally relies on the balance of N allocation between growing and mature leaves. Nitrogen uptake and distribution also depends on C allocation between organs and N composition of these organs. Within shoots, allocation of C to stems generally increases in relation to C allocation to the leaves over the crop growth period. Allocation of C and N between shoots and roots also changes to a large extent in relation to soil N and/or crop N. These alterations in C and N allocation between plant organs have implications, together with soil availability and carbon assimilation, on N uptake and distribution in crops. Therefore, N uptake and distribution in plants and crops involves many aspects of growth and development. Regulation of nitrogen assimilation needs to be considered in the context of these interregulatory processes.     

Nitrogen Uptake and Plant Growth II. An Empirical Model of Vegetative Growth and Partitioning

An empirical model of vegetative plant growth is presented.The model is based on experimental data on Polygonum cuspidatum,which showed (1) that the partitioning of dry matter and nitrogenamong organs was linearly related to the nitrogen concentrationof the whole plant and (2) that leaf thickness was negativelycorrelated with leaf nitrogen concentration. The model properlydescribes the behaviour of plants. Steady-state solutions ofthe model give the relative growth rate, specific leaf weight,and partitioning of dry matter and nitrogen among organs withthe net assimilation rate and the specific absorption rate asenvironmental variables. The effect of nitrogen removal on drymatter and nitrogen partitioning was examined as non-steady-statedynamic solutions of the model. The model predicted not onlyreduced leaf growth and enhanced root growth but also a fluxof nitrogen from the leaf to the root, which agreed with theexperimental results. Mathematical model, partitioning of dry matter and nitrogen, plant nitrogen, relative growth rate, shoot: root ratio, specific leaf weight     

Effects of Nitrogen Nutrition on Leaf Expansion and Photosynthesis of Trifolium subterraneum L. 1. Comparison between Different Levels of Nitrogen Supply

Growth analysis showed that reductions in the relative growth-rateof subterranean clover plants (cv. Mt. Barker), even those dueto moderate nitrogen deficiencies, were reflected in reductionsof the leaf-area ratio and particularly of the net assimilationrate. A decline in nitrogen supply in the culture solutions was foundto depress net rates of carbon dioxide uptake per unit leafarea and leaf expansion per plant to about the same extent,even at moderate levels of nitrogen stress. Four days aftertransfer of plants grown with adequate nitrogen to solutionswithout nitrogen, leaf area and net carbon dioxide uptake haddeclined to 84 per cent and 89 per cent of the values for thecontrol plants. After a further 4 days these values had decreasedto 71 per cent and 52 per cent respectively. When net carbon dioxide uptake was expressed per unit weightof chlorophyll, the effect of changes in nitrogen supply onnet photosynthesis largely disappeared, indicating a close relationshipwith the chlorophyll content of the leaves. However, anotherand perhaps more direct effect of nitrogen on photosynthesiswas suggested by the fact that, during the early stages of recoveryfrom a severe nitrogen stress, photosynthesis began to increasebefore the chlorophyll content of the leaves.     

Sink-stimulated photosynthesis and sink-dependent increase in nitrate uptake: nitrogen and carbon relations of the parasitic association Cuscuta reflexa–Ricinus communis

Ricinus communis L. was grown under limiting N supply in quartz sand culture, fed with 0.2, 1 or 5 mol m^?3 NO₃^?, or in liquid culture with 0.022, 0.05 or 0.5 mol m^?3 NO₃^?. Some of the plants were infected with Cuscuta reflexa Roxb. As occurred for the host, dry matter production and growth of C. reflexa were severely depressed with decreasing N supply to the host. When parasitized by C. reflexa, the shoot and root dry weight of Ricinus was diminished at all levels of N nutrition, but the total dry weight of host plus parasite was almost the same as that of uninfected Ricinus. In contrast to the situation in Lupinus albus (Jeschke et al. 1994b), infection by Cuscuta resulted in increased tissue N levels in the host and the N content of the system Ricinus plus C. reflexa was the same or even somewhat larger than that of uninfected plants. This indicated a sink-dependent stimulation of nitrate uptake. As a result of decreased root weights, nitrate uptake g^?1 FW was stimulated by 80, 60 or only 40% at 0.2, 1 or 5 mol m^?3 nitrate supply. Increased nitrate uptake was reflected, particularly at low N supply, in xylem transport; xylem sap nitrate concentrations were substantially elevated, while those of amino acids were decreased in parasitized plants. This indicated an inhibition of nitrate assimilation in roots of parasitized plants under limiting N supply. Besides these effects on N relations, C. reflexa induced a substantial sink-dependent stimulation of net photosynthesis in host leaves and a concomitant increase in stomatal opening and transpiration. This stimulation depended on the relative sink size induced by Cuscuta, on nitrogen nutrition and on leaf age, indicating that delayed senescence of leaves contributes to the overall effects of Cuscuta on its host. The Cuscuta-induced inhibition of nitrate assimilation in the roots and the increase in nitrate uptake suggest that nitrate reduction was shifted towards the leaves in the presence of C. reflexa. The stimulating effects of C. reflexa in the Ricinus-Cuscuta association are compared with the strongly inhibitory effects occurring in the tripartite association L. albus–Rhizobium–Cuscuta reflexa.     

Nitrate Supply and the Biophysics of Leaf Growth in Salix viminalis

The influence of nitrogen on leaf area development and the biophysicsof leaf growth was studied using clonal plants of the shrubwillow, Salix viminalis grown with either optimal (High N) orsub-optimal (Low N) supplies of nitrate. Leaf growth rate andfinal leaf size were reduced in the sub-optimal treatment andthe data suggest that in young rapidly growing leaves, thiswas primarily due to changes in cell wall properties, sincecell wall extensibility (% plasticity) was reduced in the LowN plants. The biophysical regulation of leaf cell expansion also differedwith nitrogen treatment as leaves aged. In the High N leaves,leaf cell turgor pressure (P) increased with age whilst in theLow N leaves P declined with age, again suggesting that foryoung leaves, cell wall plasticity limited expansion in theLow N plants. Measurements of cell wall properties showed thatcell wall elasticity (%E) was not influenced by nitrogen treatmentand remained constant regardless of leaf age. Key words: Salix, cell wall extensibility, nitrogen nutrition, biophysics of leaf growth     

The Effect of Applying a Nutrient in Leaf Sprays on the Absorption of the Same Nutrient by the Roots

Ammonium nitrate solution applied to the leaves of sugar-beetincreased plant dry weight and uptake of nitrogen by the roots.Uptake of phosphorus by the roots of swedes, but not sugar-beet,grown with high phosphorus supply to the roots, was decreasedby applying sodium phosphate solution to the leaves; uptakefrom a lower phosphorus supply to the roots was unaffected.Phosphorus applied to the leaves had no effect on dry weight.Potassium uptake by the roots of sugar-beet plants grown withhigh potassium supply to the roots was unaffected by paintingthe leaves with a potassium chloride solution, that of plantswith an intermediate potassium supply was increased, and plantsgrown with a low supply to the roots absorbed almost all theavailable potassium so painting could not much increase uptakeby the roots. Application of potassium to the leaves increaseddry weight of plants with low or medium potassium supply tothe roots and did not affect that of plants with a high potassiumsupply. The top: root ratio for phosphorus content in mg. per plantwas greater for phosphorus absorbed via leaves than for phosphorusabsorbed via roots. Increasing the phosphorus supply to theroots increased this ratio for phosphorus absorbed either vialeaves or roots. Potassium absorbed by leaves was slightly more efficient inincreasing dry weight than potassium absorbed at the same timeby the root. A similar comparison was not possible for nitrogenor phosphorus. The results of these and previous experiments indicate thatall the nitrogen and potassium and over 80 per cent. of thephosphorus applied to leaves was absorbed. The small amountof phosphorus remaining unabsorbed on the surface of the leafwas unaffected by phosphorus supply to the root.     

Controls of biomass partitioning between roots and shoots: Atmospheric CO2 enrichment and the acquisition and allocation of carbon and nitrogen in wild radish

Summary The effects of CO₂ enrichment on plant growth, carbon and nitrogen acquisition and resource allocation were investigated in order to examine several hypotheses about the mechanisms that govern dry matter partitioning between shoots and roots. Wild radish plants (Raphanus sativus × raphanistrum) were grown for 25 d under three different atmospheric CO₂ concentrations (200 ppm, 330 ppm and 600 ppm) with a stable hydroponic 150 mol 1^–1 nitrate supply. Radish biomass accumulation, photosynthetic rate, water use efficiency, nitrogen per unit leaf area, and starch and soluble sugar levels in leaves increased with increasing atmospheric CO₂ concentration, whereas specific leaf area and nitrogen concentration of leaves significantly decreased. Despite substantial changes in radish growth, resource acquisition and resource partitioning, the rate at which leaves accumulated starch over the course of the light period and the partitioning of biomass between roots and shoots were not affected by CO₂ treatment. This phenomenon was consistent with the hypothesis that root/shoot partitioning is related to the daily rate of starch accumulation by leaves during the photoperiod, but is inconsistent with hypotheses suggesting that root/shoot partitioning is controlled by some aspect of plant C/N balance.     

Relative growth rate of leaf biomass and leaf nitrogen content in several mediterranean woody species

In many plant species, herbivory is a major determinant of leaf mortality and it can cause a strong reduction in productive potential. Most predation occurs on young, expanding leaves. Thus, a rapid growth of the leaves can reduce the impact of predation. Furthermore, in cold Mediterranean climates the length of the growing season is constrained to a short period in spring and early summer owing both to low winter temperatures and drought stress in early summer. Therefore, a rapid deployment of leaf area and a high photosynthetic capacity during the spring and early summer might have important positive effects on the final carbon balance of the leaf population. Relative growth rates (RGR) of leaf biomass were measured in 19 woody species typical of Central Western Spain with deciduous and evergreen habits. Highly significant differences were detected in the leaf growth rate of the different species. The differences between species, however, did not correlate either with the mean leaf life-span of each of the species or with other leaf traits such as photosynthetic capacity, specific leaf area or nitrogen content. Leaf growth rate was positively correlated with time elapsed between leaf initiation and fruit maturation, so that species with fruit dispersal in spring and early summer in general had lower leaf growth rates than species with autumn fruit shedding. This relationship shows the effects of the concurrence between vegetative and reproductive organs for nutrients and other resources. Nitrogen concentration in the leaves was very high at the time of bud break, and declined during leaf expansion owing to the dilution associated with the increase in structural components. The rate of nitrogen dilution was, thus, positively related to the leaf growth rate. Relative growth rates calculated for nitrogen mass in leaves were very low compared to the growth in total mass. This suggests that most leaf nitrogen is translocated from the plant stores to the leaf biomass before the start of leaf expansion and that the contribution of root uptake during leaf expansion is comparatively low.     

Effects of rhizospheric bicarbonate on net nitrate uptake and partitioning between the main nitrate utilising processes in Populus canescens and Sambucus nigra

Increased levels of rhizospheric dissolved inorganic carbon have repeatedly been demonstrated to enhance plant growth by up to 80%, although carbon from dark fixation accounts for only 1–3% of total plant carbon gain. This study, therefore, aimed at investigating the effects of bicarbonate on nitrate uptake, assimilation and translocation to shoots. Clonal saplings of poplar (Populus canescens(Ait.) Sm.) and elder (Sambucus nigraL.) were grown hydroponically for 35 days in a nutrient solution containing 0, 0.5 and 1 mM bicarbonate and 2 mM nitrate as the sole nitrogen source at pH 7.0. Net nitrate uptake, root nitrate accumulation and reduction, and export of nitrogenous solutes to shoots were measured after incubating plants with ¹⁵N-labelled nitrate for 24 h. Net nitrate uptake increased non-significantly in plant species (19–61% compared to control plants) in response to 1 mM bicarbonate. Root nitrate reduction and nitrogen export to shoots increased by 80 and 95% and 15 and 44% in poplar and elder, respectively. With enhanced root zone bicarbonate, both species also exhibited a marked shift between the main nitrate utilising processes. Poplar plants increasingly utilised nitrate via nitrate reduction (73–88% of net nitrate uptake), whereas the proportions of export (20–9%) and storage in roots (7–3%) declined as plants were exposed to 1 mM external bicarbonate. On the other hand, elder plants exhibited a significant increase of root nitrate reduction (44–66%) and root nitrate accumulation (6–25%). Nitrate translocation to elder shoots decreased from 50 to 8% of net nitrate uptake. The improved supply of nitrogen to shoots did not translate into a significant stimulation of growth, relative growth rates increased by only 16% in poplar saplings and by 7% in elder plants. This revised version was published online in June 2006 with corrections to the Cover Date.     

Carbon and nitrogen economy of 24 wild species differing in relative growth rate

The relation between interspecific variation in relative growth rate and carbon and nitrogen economy was investigated. Twentyfour wild species were grown in a growth chamber with a nonlimiting nutrient supply and growth, whole plant photosynthesis, shoot respiration, and root respiration were determined. No correlation was found between the relative growth rate of these species and their rate of photosynthesis expressed on a leaf area basis. There was a positive correlation, however, with the rate of photosynthesis expressed per unit leaf dry weight. Also the rates of shoot and root respiration per unit dry weight correlated positively with relative growth rate. Due to a higher ratio between leaf area and plant weight (leaf area ratio) fast growing species were able to fix relatively more carbon per unit plant weight and used proportionally less of the total amount of assimilates in respiration. Fast growing species had a higher total organic nitrogen concentration per unit plant weight, allocated more nitrogen to the leaves and had a higher photosynthetic nitrogen-use efficiency, i.e. a higher rate of photosynthesis per unit organic nitrogen in the leaves. Consequently, their nitrogen productivity, the growth rate per unit organic nitrogen in the plant and per day, was higher compared with that of slow growing species.     

Effect of multiple factor source-sink manipulation on nitrogen and carbon assimilation by soybean

The objectives of this study were to determine the effect of light enhancement and hastened reproductive development on nitrogen and dry matter accumulation by field-grown soybean (Glycine max [L.] Merr.). The impacts of photosynthate supply and reproductive development on change in the season-long profiles of in vivo leaf nitrate reductase (NR) activity and root nodule acetylene reduction (AR) activity were evaluated.

Light enhancement resulted in significant increases in dry matter accumulation, root nodule fresh weight and AR activity. Seed yield was increased in both light enhanced treatments in 1978 and in one in 1979.

Hastened flowering and seed development was accomplished through photoperiod manipulation within a single genotype. Seasonal decline in leaf NR activity was most rapid in plants entering reproductive development early. An early increase in root nodule fresh weight and AR activity was also observed in response to this treatment and was followed similarly by early decline.

The addition of high levels of soil-applied nitrogen increased leaf NR activity and delayed late season decline in NR activity for both control and early reproductive plants. Nitrate supply was therefore implicated as limiting to leaf NR activity during the decline associated with flowering and early seed development. A limited additional increase in leaf NR activity was observed in response to light enhancement plus soil-applied nitrogen. As no significant increase in leaf NR activity was observed in response to light enhancement alone, leaf nitrate supply was further implicated as more limiting to leaf NR activity than was photosynthate supply during flowering and early seed development.

     

Nitrate regulation of nitrate uptake and nitrate reductase expression in barley grown at different nitrate:ammonium ratios at constant relative nitrogen addition rate

Barley (Hordeum vulgare L. cv. Golf) was cultured using the relative addition rate technique, where nitrogen is added in a fixed relation to the nitrogen already bound in biomass. The relative rate of total nitrogen addition was 0.09 day^?1 (growth limiting by 35%), while the nitrate addition was varied by means of different nitrate: ammonium ratios. In 3- to 4-week-old plants, these ratios of nitrate to ammonium supported nitrate fluxes ranging from 0 to 22 μmol g^?1 root dry weight h^?1, whereas the total N flux was 21.8 ± 0.25 μmol g^?1 root dry weight h^?1 for all treatments. The external nitrate concentrations varied between 0.18 and 1.5 μM. The relative growth rate, root to total biomass dry weight ratios, as well as Kjeldahl nitrogen in roots and shoots were unaffected by the nitrate:ammonium ratio. Tissue nitrate concentration in roots were comparable in all treatments. Shoot nitrate concentration increased with increasing nitrate supply, indicating increased translocation of nitrate to the shoot. The apparent V_max for net nitrate uptake increased with increased nitrate fluxes. Uptake activity was recorded also after growth at zero nitrate addition. This activity may have been induced by the small, but detectable, nitrate concentration in the medium under these conditions. In contrast, nitrate reductase (NR) activity in roots was unaffected by different nitrate fluxes, whereas NR activity in the shoot increased with increased nitrate supply. NR-mRNA was detected in roots from all cultures and showed no significant response to the nitrate flux, corroborating the data for NR activity. The data show that an extremely low amount of nitrate is required to elicit expression of NR and uptake activity. However, the uptake system and root NR respond differentially to increased nitrate flux at constant total N nutrition. It appears that root NR expression under these conditions is additionally controlled by factors related to the total N flux or the internal N status of the root and/or plant. The method used in this study may facilitate separation of nitrate-specific responses from the nutritional effect of nitrate.