Leaf Emergence of Spring Wheat Receiving Varying Nitrogen Supply at Different Stages of Development

We examined effects of nitrogen (N) supply on leaf emergenceof spring wheat (Triticum aestivum L.) grown in sand with nutrientsolution containing different N concentrations (9NO₃: 1NH₄).In expt 1, the cultivar 'Gamenya' received nutrient solutiontwice weekly containing a constant N supply ranging from 50to 2400 µM N. In expts 2 and 3, cultivars 'Aroona' and'Gamenya' were irrigated hourly with nutrient solution containingeither low (L = 50 µM N) or high (H = 2000 µM N)N supply. In expt 2, the N supply to half of the plants receivingL and H was changed at the double ridge stage of apical development,producing plants receiving LL, LH, HL and HH. In expt 3, N supplywas changed firstly when the main stem apex was vegetative (oneto two leaves) and secondly when the main stem apex was at doubleridge stage (four to five leaves), producing plants receivingLLL, LHL, HLH and HHH. Leaves on the main stem and primary tillerswere counted. Rate of leaf emergence was estimated from regressionof number of leaves against thermal time; the phyllochron wascalculated as 1/ rate of emergence. Severely N-deficient plants (which had at least a 60% reductionin shoot dry weight) had slower rates of leaf emergence (expt1). Fluctuating N supply sometimes, but not always, changedthe rate of leaf emergence (expts 2 and 3). The N supply beforedouble ridge stage had bigger effects on the phyllochron thanthat afterwards (expt 3). The phyllocrons of the main stemswere generally lower than those of tillers, with a greater differencebetween stems in N-deficient plants. Low N supply at the vegetativeapex stage decreased the total number of leaves on the mainstem, while low N supply after double ridge did not.Copyright1994, 1999 Academic Press Nitrogen, stress, spring wheat, Triticum aestivum, leaf emergence, phyllochron, apical development     

Increased Defoliation Frequency Depletes Remobilization of Nitrogen for Leaf Growth in Grasses

Plants ofLolium perenneandFestuca rubrawere grown in sand culturereceiving all nutrients as a complete nutrient solution containing1.5 mMNH₄NO₃, and subjected to one of three defoliation treatments:undefoliated, defoliated on one occasion, or defoliated weekly.¹⁵Nlabelling was used to determine the rate of N uptake, allowingthe amount of N remobilized from storage for the growth of thetwo youngest leaves (subsequently referred to as ‘newleaves’) growing over a 14 d period after defoliationto be calculated. The total plant N uptake by both species wasreduced, compared with undefoliated plants, by both a singleand repeated defoliation, although neither caused complete inhibitionof uptake. Regularly defoliatedL. perennehad a greater reductionin root mass, concomitant with a greater increase in N uptakeper g root than did regularly defoliatedF. rubra. In both species,the amount of N derived from uptake recovered in the new leaveswas unaffected by the frequency of defoliation. BothL. perenneandF.rubramobilized nitrogen to the new leaves after a single defoliation,mobilization being sufficient to supply 50 and 41%, respectively,of the total nitrogen requirement. In regularly defoliated plants,no significant nitrogen was mobilized to the new leaves inL.perenne, and only a small amount was mobilized inF. rubra. Plantsachieved greater leaf regrowth when only defoliated once. Weconclude that increasing the frequency of defoliation of bothL.perenneandF. rubrahad little effect on the uptake of nitrogenby roots which was subsequently supplied to new leaves, butdepleted their capacity for nitrogen remobilization, resultingin a reduction in the rate of growth of new leaves. Lolium perenne; Festuca rubra; defoliation frequency; mobilization; root uptake; nitrogen     

Effects of Constant and Variable Nitrogen Supply on Sunflower (Helianthus annuus L.) Leaf Cell Number and Size

The effects of nitrogen (N) availability on cell number andcell size, and the contribution of these determinants to thefinal area of fully expanded leaves of sunflower (Helianthusannuus L.) were investigated in glasshouse experiments. Plantswere given a high (N =315 ppm) or low (N=21 ppm) N supply andwere transferred between N levels at different developmentalstages (5 to 60% of final size) of target leaves. The dynamicsof cell number in unemerged (< 0.01 m in length) leaves ofplants growing at high and low levels of N supply were alsofollowed. Maximum leaf area (LA_max) was strongly (up to two-fold)and significantly modified by N availability and the timingof transfer between N supplies, through effects on leaf expansionrate. Rate of cell production was significantly (P<0.05)reduced in unemerged target leaves under N stress, but therewas no evidence of a change in primordium size or in the durationof the leaf differentiation–emergence phase. In fullyexpanded leaves, number of cells per leaf (N_cell), leaf areaper cell (LA_cell) and cell area (A_cell) were significantly reducedby N stress. WhileLA_cell and A_cellresponded to changeover treatmentsirrespective of leaf size, significant (P<0.05) changes inN_cellonly occurred when the changeover occurred before the leafreached approx. 10% of LA_max. There were no differential effectsof N on numbers of epidermal vs. mesophyll cells. The resultsshow that the effects of N on leaf size are largely due to effectson cell production in the unemerged leaf and on both cell productionand expansion during the first phase of expansion of the emergedleaf. During the rest of the expansion period N mainly affectsthe expansion of existing cells. Cell area plasticity permitteda response to changes in N supply even at advanced stages ofleaf expansion. Increased cell expansion can compensate forlow N_cellif N stress is relieved early in the expansion of emergedleaves, but in later phases N_cellsets a limit to this response.Copyright 1999 Annals of Botany Company Helianthus annuus, leaf expansion, leaf cell number, leaf cell size, nitrogen, leaf growth, sunflower.     

Density Studies on Lupins. II. Components of Seed Yield

Components of seed yield of cv. Ultra (Lupinus albus L.) andcv. Unicrop (L. angustifolius L.) were measured when grown atthree densities. The low density (10 plants m^–2) Unicropyield (34 g seed per plant) was 1.8 times that of Ultra as ithad more branches, pods and seeds per pod. Ultra seeds (310mg per seed) were heavier than Unicrop seeds (180 mg). The branchingpattern of Ultra was less dependent on plant density, henceat 93 plants m^–2 it gave a higher per plant yield (7.4vs 6.4 g) than Unicrop at lower densities (83 plants m^–2).Density had most influence on pod formation and only small effectson seeds per pod and seed weight. Yield components on the main-steminflorescence were influenced less by density than componentson branch inflorescences. Later formed, higher order generationsof inflorescences were most affected by increased inter- andintra-plant competition. Pod numbers on the main-stem were similarfor both species. Pods formed at higher flower nodes in Unicrop,but the lower flower nodes were less fertile than those in Ultra.Node position of flowers had no influence on seed set in main-stemUnicrop pods, but pods from higher nodes in Ultra formed fewerseeds. Seed weights in Unicrop were similar among main-stemnodes but in Ultra seed weights tended to increase at highernodes. Lupinus spp, lupins, seed yield, planting density     

Effects of elevated CO2 concentrations on three montane grass species: III. Source leaf metabolism and whole plant carbon partitioning

Agrostis capillaris L.⁵, Festuca vivipara L. and Poaalpina L.were grown in outdoor open-top chambers at either ambient (340 3µmol mol^–1) or elevated (6804µmol mol^–1)concentrations of atmospheric carbon dioxide (CO₂) for periodsfrom 79–189 d. Photosynthetic capacity of source leaves of plants grown atboth ambient and elevated CO₂ concentrations was measured atsaturating light and 5% CO₂. Dark respiration of leaves wasmeasured using a liquid phase oxygen electrode with the buffersolution in equilibrium with air (21% O₂, 0.034% CO₂). Photo-syntheticcapacity of P. alpina was reduced by growth at 680 µmolmol^–1 CO₂ by 105 d, and that of F. vivipara was reducedat 65 d and 189 d after CO₂ enrichment began, suggesting down-regulationor acclimation. Dark respiration of successive leaf blades ofall three species was unaltered by growth at 680 relative to340 µmol mol^–1 CO₂. In F. vivipara, leaf respirationrate was markedly lower at 189 d than at either 0 d or 65 d,irrespective of growth CO₂ concentration. There was a significantlylower total non-structural carbohydrate (TNC) concentrationin the leaf blades and leaf sheaths of A. capillaris grown at680µmol mol^–1 CO₂. TNC of roots of A. capillariswas unaltered by CO₂ treatment. TNC concentration was increasedin both leaves and sheaths of P. alpina and F. vivipara after105 d and 65 d growth, respectively. A 4-fold increase in thewater-soluble fraction (fructan) in P. alpina and in all carbohydratefractions in F. vivipara accounted for the increased TNC content. In F. vivipara the relationship between leaf photosyn-theticcapacity and leaf carbohydrate concentration was such that therewas a strong positive correlation between photosynthetic capacityand total leaf N concentration (expressed on a per unit structuraldry weight basis), and total nitrogen concentration of successivemature leaves reduced with time. Multiple regression of leafphotosynthetic capacity upon leaf nitrogen and carbohydrateconcentrations further confirmed that leaf photosynthetic capacitywas mainly determined by leaf N concentration. In P. alpina,leaf photosynthetic capacity was mainly determined by leaf CHOconcentration. Thus there is evidence for down-regulation ofphotosynthetic capacity in P. alpina resulting from increasedcarbohydrate accumulation in source leaves. Leaf dark respiration and total N concentration were positivelycorrelated in P. alpina and F. vivipara. Leaf dark respirationand soluble carbohydrate concentration of source leaves werepositively correlated in A. capillaris. Changes in source leafphotosynthetic capacity and carbohydrate concentration of plantsgrown at ambient or elevated CO₂ are discussed in relation toplant growth, nutrient relations and availability of sinks forcarbon. Key words: Elevated CO₂, Climate change, grasses, carbohydrate partitioning, photosynthesis, respiration     

Interaction between Nitrogen Deficit of a Plant and Nitrogen Content in the Old Leaves

We examined changes in nitrogen content of the first leavesin relation to growth and nitrogen status of sunflower (Helianthusannuus L.) plants that were raised hydroponically at two irradiancelevels (high and low light, HL and LL) and at two nitrogen concentrations(high and low nitrogen, HN and LN). Initial increases in totaldry mass and total nitrogen of the whole plant were faster inHL-plants than in LL-plants irrespective of nitrogen supply,but in LN-plants the increase in total nitrogen was soon blunted.When plants grown under the same irradiance were compared, nitrogencontent of the first leaves (leaf N) decreased faster in LN-plantsthan in HN-plants, while for the plants grown at the same nitrogenconcentrations, it decreased faster in HL-plants than in LL-plants.Since these changes in leaf N were not explained solely by thechanges in plant dry mass or plant nitrogen, we introduced anindex, ‘nitrogen deficit (ND^*)’, to quantify nitrogendeficit of the whole plant. ND^* was expressed as ND^*(t)=[N_max–N(t)]xDM(t),where N_max and N(t) were nitrogen contents in the young, expandingleaves that had just unfolded to expand, at the initial stagewith sufficient nitrogen and at time t, respectively, and DM(t),plant dry mass at t. The decrease in leaf N was expressed asa liner function of ND^* irrespective of the growth conditions,which indicates validity of this index. Limitation of the useof ND^*, and mechanisms by which leaves sense nitrogen demandare also discussed. (Received June 17, 1996; Accepted August 30, 1996)     

The Relation Between the Nitrogen Concentration and Photosynthetic Capacity of Potato (Solanum tuberosum L.) Leaves

Measurements of the rate of light-saturated photosynthesis (P_max)were made on terminal leaflets of potato plants growing in cropssupplied with 0, 3, 6, 12, 24 and 36 g N m^–2. Measurementswere made between 100 and 154 d after planting. Two types ofleaf were selected—the fourth leaf on the second-levelbranch (L₄, _B1) and the youngest terminal leaflet that was measurable(L_YM). Later, the total nitrogen concentration of each leaflet(N_L) was measured. A linear regression between P_max and N_L,common to both leaf positions, explained 68.5% of the totalvariation. With L₄, _B1 leaves there was a significant improvementin the proportion of variation explained when regressions withseparate intercepts and a common slope were fitted to individualfertilizer treatments. These results suggest that an increasingproportion of leaf nitrogen was not associated with the performanceof the photosynthetic system with increasing nitrogen supply.This separation between nitrogen treatments was not as clearfor L_YM leaves. Stomatal conductance to transfer of water vapourwas neither influenced by leaf position nor directly by nitrogensupply. Rather conductance declined in parallel with the declinein photosynthetic capacity. Solanum tuberosum, potato, nitrogen, photosynthesis, stomatal conductance, leaf     

Density Studies on Lupins: I. Flower Development

In an August-sown experiment the pattern of flower developmentwas followed for cv. Ultra (Lupinus albus L.) and cv. Unicrop(L. angustifolius L.) grown at low (10 plants m^–2) andhigh (93 and 83 plants m^–2, Ultra and Unicrop respectively)densities. Dry weight increase of flowers on the main-stem inflorescenceand first lateral below the main-stem were compared at differentfloral stages. Maximum flower weight was reached just priorto the open flower stage and remained constant or declined untila pod formed or abscission occurred. The time period betweenmaximum flower weight and pod formation or abscission was upto 10 days. Emergence of the inflorescence was earlier and thefirst flower of Ultra opened 10 days before Unicrop. Developmentof each terminal raceme (inflorescence) was acropetal, withpods having formed on lower flower nodes when terminal flowerswere still quite immature. Laterals forming the next generationof inflorescences grew from axillary leaf buds below an inflorescencewhile it was in full flower. Sources of competition from connectedreproductive and vegetative metabolic sinks are discussed. Lupinus spp., lupins, flower development, planting density     

The Effect of Lenient Defoliation on the Nitrogen Economy of White Clover: The Contribution of Mineral Nitrogen to Plant Nitrogen Accumulation During Regrowth

Single plants of white clover (Trifolium repens L.) were grownfrom stolon cuttings rooted in sand. All plants were inoculatedwith Rhizobium trifolii, and for 14 weeks received nutrientsolution containing 0.5 mg N each week, as either ammonium ornitrate. Plants were then leniently defoliated or were leftintact and a ¹⁵N-labelled N source was applied at intervalsof 4 d to replace the unlabelled N. Lement defoliation removedfully expanded leaves only; the remaining immature leaves accountedfor 39–44% of the total. At harvests over the following21 d, leaf numbers were counted and dry matter (DM), N contentsand ¹⁵N enrichments of individual plant organs were determined. Rates of leaf emergence and expansion were accelerated in defoliatedplants; numbers of young leaves were similar in defoliated andintact plants. Total DM and N content were less in defoliatedthan intact plants and were not affected by form of N supplied.DM of young leaves, growing points and stolons and N contentof young leaves were, however, greater when ammonium ratherthan nitrate N was supplied. Rates of increase in the contentof plant total N were 8.2 ± 1.36 mg N d^-1 and 10.2±1.82 mg N d^-1 in defoliated and intact plants respectively.The increases were predominantly due to N₂ fixation, since recoveryof ¹⁵N showed that less than 1% of the increment in plant totalN was assimilated mineral N. Nevertheless, the contributionof mineral N to plant total N was 50% more in defoliated thanin intact plants; higher amounts of mineral N were found particularlyin young leaves and growing points. Partitioning of mineralN to nodulated roots increased over time and was greater whenammonium rather than nitrate N was present. White clover, Trifolium repens L. cv. S184, lenient defoliation, N accumulation, N₂ fixation     

Developmental and Biochemical Regulation of 'Constitutive' Nitrate Reductase Activity in Leaves of Nodulating Soybean

The developmental profile of ‘constitutive’ nitratereductase activity (cNRA) in leaves of soybean (Glycine max(L.) cv. Bragg) plants at different ages is described. The youngestleaves had most cNRA and the activity dropped off as a newerleaf developed above it. Each leaf had its distinct active periodof in vivo cNRA. This pattern was different in urea-grown andsymbiotically-grown plants (inoculated with Bradyrhizobium japonicumstrain USDA 110), where the latter had no detectable in vivocNRA in older leaves. Urea-grown plants maintained considerablein vivo NRA in such older leaves. When symbiotically-grown plantshad their nodules removed, in vivo cNRA reappeared in olderleaves within 1 d of removal, nearly reaching levels of youngleaves at 3 d after nodule excision. Allantoic acid (ALL), oneof the known transport ureides of soybeans, was implicated asa possible signal molecule from nodules to leaves. Allantoicacid (100 µM) inhibited in vitro c₁ NRA significantly,with 400 µM ALL resulting in complete inhibition. In contrast,allantoin (ALN) had no inhibitive effect on NRA. Inhibitionof c₁NRA by ALL was by a competitive process, judging from Lineweaver-Burkeplots against nitrate. Kinetics showed a constant Vmax of around105 nmol NO₂ mg^–1 protein h^–1 and a K_m for nitrateof 15 mM, which increased to 60 mM in the presence of 200 µMallantoic acid. Non-specific (ionic and pH-related) influenceswere eliminated. Allantoic acid also had a slight stimulatingeffect of in vitro NRA (up about 25% at 400 µM). Thesefindings suggest that c1NRA may be involved in ureide metabolism,rather than in vivo nitrate metabolism. Key words: Root-shoot interaction, nitrogen metabolism, nodulation, symbiosis     

The Influence of Nitrogen, Light and Water Stress on CO2 Exchange and Organic Acid Accumulation in the Tropical C3-CAM Tree, Clusia minor

The carbon balance and changes in leaf structure in Clusia minorL., were investigated in controlled conditions with regardto nitrogen supply and responses to low and high photosyntheticallyactive radiation (PAR). Nitrogen deficiency and high PAR ledto the production of smaller leaves with higher specific leafdry weight (SLDW) and higher leaf water content, but with lowerchlorophyll content. Nitrogen and PAR levels at growth alsoaffected CO₂ exchange and leaf area. In – N conditions,total daily net CO₂ uptake and leaf area accumulation were slightlyless for high-PAR-grown plants. In contrast, high-PAR-grownplants supplied with nitrogen showed about a 4-fold higher totaldaily CO₂ uptake and about twice the total leaf area of low-PAR-grownplants. Although total daily net CO₂ uptake of +N plants wasonly slightly higher than –N plants under the low PARlevel, –N plants produced almost three times more leafarea but with lower SLDW. Under well-watered conditions, low-PAR-grownplants showed only CO₂ evolution during the night and malicacid levels decreased. However, there was considerable night-timeaccumulation of titratable protons due to day/night changesin citric acid levels. High-PAR-grown plants showed net CO₂uptake, malate and citrate accumulation during the dark period.However, most of the CO₂ fixed at night probably came from respiratoryCO₂. Positive night-time CO₂ exchange was readily observed forlow-PAR-grown plants when they were transferred to high PARconditions or when they were submitted to water stress. In plantsgrown in high and low PAR, CAM leads to a substantial increasein daily water use efficiency for water-stressed plants, althoughtotal net CO₂ uptake decreased.     

Effect of elevated CO2 and nutrient status on growth, dry matter partitioning and nutrient content of Poa alpina var. vivipara L.

Poa alpina var. vivipara L. was grown in an atmosphere containingeither 340 or 680 µmol CO₂ mol^–1 within controlledenvironment chambers. The available nutrient regime was variedby altering the supply of nitrogen and phosphorus within a completenutrient solution. At a high, but not low, N and P supply regime,elevated CO₂ markedly increased growth. Differences betweennutrient supply, but not atmospheric CO₂ concentration, alteredthe allometric relations between root and shoot. Net photosynthesisof mature leaf blades and leaf N and P concentration were reducedin plants grown at the elevated CO₂ concentration. The question was asked: is it possible to ascribe all of theseeffects to elevated CO₂ or are some due to nutrient deficiencycaused by dilution with excess carbon? Several criteria, includingthe nutrient content of sink tissue, root:shoot allometry andthe use of divalent cations to estimate integrated water flowsare suggested in order to make this distinction. It is concludedthat only at a low supply of N and P₁ and elevated CO₂ concentration,was low leaf N concentration due to induced nutrient deficiency.The data are consistent with a model where the capacity of sinksto use photosynthetically assimilated carbon sets both the rateof import into those sinks (and thus rate of export from sourceleaves) and the rate of photosynthesis of source leaves themselves. Key words: Poa alpina L., growth, photosynthesis, carbohydrate, export, nitrogen, phosphorus     

Effects of Nitrogen on the Development and Growth of the Potato Plant. 1. Leaf Appearance, Expansion Growth, Life Spans of Leaves and Stem Branching

Potatoes (Solanum tuberosum L) were planted in pots in a temperature-controlledglasshouse to collect data on the rate of leaf apearance, leafexpansion, apical lateral branching and active life spans ofleaves The treatments consisted of three rates of nitrogen supply,i e the NI treatment with 2 5 g N per pot and the N2 and N3treatments with 8 and 16 g N per pot, respectively The rate of leaf appearance was 0·53 leaves d^–1(one leaf per 28 °C d) and was negligibly affected by nitrogensupply The rate of leaf expansion was related to leaf numberand nitrogen supply The areas of mature leaves increased withleaf number on the main stem to reach a maximum for leaf numbers12–14, and declined for higher leaf numbers Leaves onapical lateral branches declined in mature area with increasein leaf number The expansion rate of leaves was the dominantfactor that determined the mature leaf area, irrespective ofleaf number and nitrogen treatment The smallest leaves wereobserved at the lowest rate of nitrogen supply Nitrogen promotedapical branching and hence the total number of leaves that appearedon a plant The proportion of total leaf area contributed byleaves on apical branches increased with time and nitrogen supply Active life span, i e the period of time between leaf appearanceand yellowing of the leaf, showed a similar relation to leafnumber as mature leaf area, at least in qualitative terms Leavesof the N3 treatment showed systematically longer life spansthan leaves of the NI and N2 treatment in the order of 3 weeksThe number of main stem leaves was not affected by nitrogensupply Potato, Solanum tuberosum L, leaf development, leaf extension, plant structure, nitrogen nutrition     

Is Partitioning of Dry Weight and Leaf Area Within Dactylis glomerata Affected by N and CO2Enrichment?

We examined changes in dry weight and leaf area within Dactylisglomerata L. plants using allometric analysis to determine whetherobserved patterns were truly affected by [CO₂] and N supplyor merely reflect ontogenetic drift. Plants were grown hydroponicallyat four concentrations of in controlled environment cabinets at ambient (360 µll^–1) or elevated (680 µl l^–1) atmospheric[CO₂]. Both CO₂and N enrichment stimulated net dry matter production.Allometric analyses revealed that [CO₂] did not affect partitioningof dry matter between shoot and root at high N supply. However,at low N supply there was a transient increase in dry matterpartitioning into the shoot at elevated compared to ambient[CO₂] during early stages of growth, which is inconsistent withpredictions based on optimal partitioning theory. In contrast,dry matter partitioning was affected by N supply throughoutontogeny, such that at low N supply dry matter was preferentiallyallocated to roots, which is in agreement with optimal partitioningtheory. Independent of N supply, atmospheric CO₂enrichment resultedin a reduction in leaf area ratio (LAR), solely due to a decreasein specific leaf area (SLA), when plants of the same age werecompared. However, [CO₂] did not affect allometric coefficientsrelating dry weight and leaf area, and effects of elevated [CO₂]on LAR and SLA were the result of an early, transient stimulationof whole plant and leaf dry weight, compared to leaf area production.We conclude that elevated [CO₂], in contrast to N supply, changesallocation patterns only transiently during early stages ofgrowth, if at all. Copyright 2000 Annals of Botany Company Allometric growth, carbon dioxide enrichment, Cocksfoot, Dactylis glomerata L., dry weight partitioning, leaf area ratio, nitrogen supply, shoot:root ratio, specific leaf area     

Growth and Biomass Allocation, with Varying Nitrogen Availability, of Near-isogenic Pea Lines with Differing Foliage Structure

The single-gene mutation afila in pea (Pisum sativum L.) resultsin the replacement of proximal leaflets with branched tendrils,thereby reducing leaf area. This study investigated whethertheafila line could adjust biomass partitioning when exposedto varying nutrient regimes, to compensate for reduced leafarea, compared with wild-type plants. Wild-type and afila near-isogeniclines were grown in solution culture with nitrate-N added toinitially N-starved seedlings at relative addition rates (R_N)of 0.06, 0.12, 0.15 and 0.50 d^-1. The relative growth rate (R_W)of the whole plants closely matched R_Nat 0.06 and 0.12 d^-1,but higher R_Nresulted in a slightly higher growth rate. At agiven R_N, the wild-type line had lower plant nitrogen statusthan the afila line. R_Wof the roots of the afila line was lessthan R_Wof the roots of the wild-type at the three higher ratesof N supply despite a greater accumulation of N in the rootsof the afila plants. Consequently, plant nitrogen productivity(growth rate per unit nitrogen) was lower for afila. Dry matterallocation was strongly influenced by nitrogen status, but nodifferences in shoot–root dry matter allocation were foundbetween wild-type and afila with the same plant N status. Theseresults imply that decreased leaf area as a result of the single-genemutation afila affects dry matter allocation, but only accordingto its effect on the nitrogen status. Copyright 2000 Annalsof Botany Company Pisum sativum, pea, nitrogen limitation, growth, shoot–root allocation, relative growth rate, nitrogen productivity, isolines     

Oxygen Diffusion in Lupin Nodules: I.VISUALIZATION OF DIFFUSION BARRIER OPERATION

Root nodules of Lupinus albus (L.) cv. Multolupa were subjectedto short- and medium-term stresses by lowering rhizosphere temperaturefrom 25 to 16°C (2 h), detopping plants (3 h), darkeningplants (21 h) or exposing roots to 20 mol m^–3 KNO₃ for4 d. All experimental treatments produced increases in oxygendiffusion resistance, compared with control plants. These correlatedwith structural changes in the nodule cortex, which is describedin detail for the first time. The most noticeable change isthe occlusion of intercellular spaces by a glycoprotein whichwas identified using the monoclonal antibody MAC236. This glycoproteinwas also found surrounding bacteria in intercellular spacesof the cortex of control nodules. Key words: Oxygen diffusion resistance, glycoprotein, nodules, nitrogen fixation, Lupinus albus     

Responses of Noogoora Burr (Xanthium occidentale Bertol.) to Nitrogen Supply and Carbon Dioxide Enrichment

We studied the responses of Xanthium occidentale (Bertol.) (cockleburor Noogoora burr), a noxious weed, to atmospheric CO₂ enrichmentand nitrate-N concentrations in the root zone ranging from 0.5to 25 mM. CO₂ enrichment (1500 cm³ m^–3) increased dry-matterproduction to about the same extent (18 per cent) at all levelsof supplied N: most of the increment in dry matter was distributedequally between leaves and roots so that there was little effecton shoot-to-root dry-weight ratios. Growth was stimulated greatlyby N and plateaued at 12 mM supplied N. Shoot-to-root dry-weightand total N ratios increased with increasing N supply. CO₂ enrichmenthad no effect on the total amount of N accumulated by plants,but increased the N-use efficiency of leaves. Enriched plantshad lower concentrations and quantities of N in their leavesthan controls, and therefore lower shoot-to-root total N ratios.Little free NO₃^– accumulated in organs of control or enrichedplants. NO₃^– was the major form of N in xylem sap fromdetopped plants at low supplied NO₃-N, but amino N was equalin importance at high supplied NO₃-N in control and enrichedplants. Concentrations of NO₃^– were lower in the xylemsap of CO₂ enriched plants. It was concluded that the betterN-use efficiency of CO₂ enriched plants could result in increasedgrowth of X. occidentale in regions of marginal soil fertilityas atmospheric levels of CO₂ increase. CO₂ enrichment, nitrogen, Xanthium, Noogoora burr, cocklebur     

Growth Analysis of Solution Culture-grown Winter Rye, Wheat and Triticale at Different Relative Rates of Nitrogen Supply

At low nitrogen (N) supply, it is well known that rye has ahigher biomass production than wheat. This study investigateswhether these species differences can be explained by differencesin dry matter and nitrogen partitioning, specific leaf area,specific root length and net assimilation rate, which determineboth N acquisition and carbon assimilation during vegetativegrowth. Winter rye (Secale cereale L.), wheat (Triticum aestivumL.) and triticale (X Triticosecale) were grown in solution cultureat relative addition rates (R_N) of nitrate-N supply rangingfrom 0.03–0.18 d^-1and at non-limiting N supply under controlledconditions. The relative growth rate (R_W) was closely equalto R_Nin the range 0.03–0.15 d^-1. The maximalR_W at non-limitingnitrate nutrition was approx. 0.18 d^-1. The biomass allocationto the roots showed a considerable plasticity but did not differbetween species. There were no interspecific differences ineither net assimilation rate or specific leaf area. Higher accumulationof N in the plant, despite the same relative growth rate atnon-limiting N supplies, suggests that rye has a greater abilityto accumulate reserves of nitrogen. Rye had a higher specificroot length over a wide range of sub-optimal N rates than wheat,especially at extreme N deficiency (R_N=0.03–0.06 d^-1).Triticale had a similar specific root length as that of wheatbut had the ability to accumulate N to the same amount as ryeunder conditions of free N access. It is concluded that thebetter adaptation of rye to low N availability compared to wheatis related to higher specific root length in rye. Additionally,the greater ability to accumulate nitrogen under conditionsof free N access for rye and triticale compared to wheat maybe useful for subsequent N utilization during plant growth.In general, species differences are explained by growth componentsresponsible for nitrogen acquisition rather than carbon assimilation.Copyright 1999 Annals of Botany Company Growth analysis, nitrogen, nitrogen productivity, partitioning, specific root length, Secale cereale L.,Triticum aestivum L., X Triticosecale, winter rye, winter wheat, winter triticale.     

Nitrogen Supply Affects the Remobilization of Nitrogen for the Regrowth of Defoliated Lolium perenne L.

Nitrogen remobilization from roots and pseudostems during regrowthof Lolium perenne L. was studied in miniswards grown with contrastinglevels of (NH₄)₂SO₄ in solution culture. Growth with a highN supply (5.0 mol m^–3) increased theweight of leaf laminae recovered at each of five weekly clippings,and decreased the proportion of photosynthate used for rootgrowth. Clipped plants growing in a steady-state were suppliedwith ¹⁵N for 48 h and the recovery of labelled N in laminaemeasured after five weekly cuts. Recovery of labelled N in thelaminae from the second clipping onwards was derived only fromremobilization of N from roots and pseudostem. Miniswards grownwith low N (0.5 mol m^–3) relied moreupon remobilization of N for lamina growth than did high N plants.Thus after 14 d 20% of lamina N was labelled in low N plantsbut only 3% was labelled in the high N treatment. Thereafter,N remobilization declined until at the final clipping after35 d, labelled N represented only 4% and 1 % of the lamina Nin the low and high N plants. When plants were not clipped beforethe labelling period, they took up more ¹⁵N if grown with highN than cut plants. Thereafter, the remobilization of N followeda similar pattern as in the cut plants. Exponential models were used to calculate the rate of N transferfrom roots and pseudostem to laminae. When grown with low N,the half-life of remobilization was 1.56 weeks. High N miniswardshad an initial rapid remobilization with a half-life of 0.66weeks, and a slower phase with a half-life of 2.98 weeks. Key words: Lolium perenne L., nitrogen supply, regrowth, remobilization, internal cycling     

The Distribution of Nine Elements in Shoots of Lupinus albus L. and Lupinus angustifolius L. Compared with that of Silicon as a Measure of Passive Transport

The Ca, Mg, K, Na, P, Fe, Mn, Zn, Cu and opaline-Si contentsof leaves, stems and inflorescences from each order of shootaxis was determined in Lupinus albus L. and Lupinus angustifoliusL. The distribution of Si was used as a base for passive transportin the transpiration stream. All of the elements investigatedwere redistributed among the leaves, stems and inflorescencesof either L. albus or L. angustifolius. Most of the elementsinvestigated were enriched in the inflorescences and depletedin either the leaves or the stems. Sodium was enriched in thestems whereas Ca and Mn were redistributed only in L. albus.The pattern of element redistribution was similar in each ofthe lateral shoot axes except for the youngest. For the elementsenriched in the inflorescences, more than half was suppliedby redistribution. Calcium redistribution was similar to thatfor K, which is regarded as phloem mobile, but a mechanism forCa redistribution is uncertain. Lupinus albus L., Lupinus angustifolius L., mineral transport, leaves, inflorescences, transpiration, silicon, calcium