Distinct Influence of Root and Shoot Temperature on Nitrogen Fixation by White Clover

White clover (Trifolium repens L.) was grown in controlled environmentsto determine the distinct effects of root and shoot temperatureon the accumulation of total and fixed (¹⁵ N dilution) nitrogenat two levels of nitrate (10 and 75 mM). Nitrogen fixation(BNF) showed a positive response to higher shoot temperature(23 vs. 13 C day temperature), irrespective of whether or notroot temperature was increased in parallel. Low root temperature(5 C) caused a marked reduction in the accumulation of totalnitrogen at both nitrate levels, and led to a lower proportionof N derived from BNF. The temperature response of BNF was attributedfor the major part to an adaptation to the demand for fixedN. It is therefore concluded that BNF is not primarily responsiblefor the reduced clover growth at low temperatures. White clover, Trifolium repens L., temperature, nitrogen fixation, nitrate, root, shoot     

The Partitioning of Nitrate Assimilation Between Root and Shoot of a Range of Temperate Cereals and Pasture Grasses

Nitrate reductase activity (NRA, in vivo assay) and nitrate(NO^-₃) content of root and shoot and NO^-₃ and reduced nitrogencontent of xylem sap were measured in five temperate cerealssupplied with a range of NO^-₃ concentrations (0·1–20mol m^–3) and three temperate pasture grasses suppliedwith 0·5 or 5 0 mol m^–3 NO^-₃ For one cereal (Hordeumvulgare L ), in vitro NRA was also determined The effect ofexternal NO^-₃ concentration on the partitioning of NO^-₃ assimilationbetween root and shoot was assessed All measurements indicatedthat the root was the major site of NO3 assimilation in Avenasatwa L, Hordeum vulgare L, Secale cereale L, Tnticum aestivumL and x Triticosecale Wittm supplied with 0·1 to 1·0mol m^–3 NO^-₃ and that for all cereals, shoot assimilationincreased in importance as applied NO^-₃ concentration increasedfrom 1.0 to 20 mol m^–3 At 5.0–20 mol m^–3 NO3,the data indicated that the shoot played an important if notmajor role in NO^-₃ assimilation in all cereals studied Measurementson Lolium multiflorum Lam and L perenne L indicated that theroot was the main site of NO^-₃ assimilation at 0.5 mol m^–3NO^-₃ but shoot assimilation was predominant at 5.0 mol m^–3NO^-₃ Both NRA distribution data and xylem sap analysis indicatedthat shoot assimilation was predominant in Dactylis glomerataL supplied with 0.5 or 5.0 mol m^–3 NO^-₃ Avena sativa L., oats, Hordeum vulgare L., barley, Secale cereale L., rye, x Triticosecale Wittm., triticale, Triticum aestivum L., wheat, Dactylis glomerata L., cocksfoot, Lolium multiflorum Lam., Italian ryegrass, Lolium perenne L., perennial ryegrass, nitrate, nitrate assimilation, nitrate reductase activity, xylem sap     

Optimization of Plant Root: Shoot Ratios and Internal Nitrogen Concentration

A general theoretical approach is developed to analyze the morphologicaland physiological responses of plants to nitrogen availability.The optimal leaf-nitrogen concentration and corresponding optimalroot: shoot ratio which maximize relative growth rate are foundquantitatively as a function of root—specific activitywhich is assumed to be a function of soil nitrogen availability.The cost of increasing tissue nitrogen concentration is foundto be primarily related to an increase in allocation to roots.Predictions of the analysis are consistent with previous theoriesand general empirical findings, suggesting that plants respondoptimally to soil nitrogen. Relative growth rate is predictedto be a nearly linear function of whole-plant nitrogen concentrationand shoot fraction is a monotonically increasing function oftissue nitrogen concentration when plants respond optimallyto soil nitrogen availability. Plant growth, root:shoot ratios, biomass allocation, nitrogen productivity, optimization     

The Dependence of Plant Root: Shoot Ratios on Internal Nitrogen Concentration

Modifying a model of G. I. Agren, we show that the shoot fractiondepends approximately linearly on internal nitrogen concentration(n) over a broad range of values of n. The root: shoot ratiodecreases monotonically with n; at low nitrogen concentrationsthis differs from the predictions of G. I. Agren and T. Ingestad. Root: shoot ratios, shoot fraction, nitrogen productivity, relative growth rate, specific growth rate     

Effect of Root and Shoot Meristem Temperature on Shoot to Root Dry Matter Partitioning and the Internal Concentrations of Nitrogen and Carbohydrates in Maize and Wheat

Maize (Zea mays L.) and spring wheat (Triticum aestivum L.)were grown in nutrient solution at uniformly high air temperature(20 °C), but different root zone temperatures (RZT 20, 16,12 °C). To manipulate the ratio of shoot activity to rootactivity, the plants were grown with their shoot base includingthe apical meristem either above (i.e. at 20 °C) or withinthe nutrient solution (i.e. at 20, 16 or 12 °C). In wheat, the ratio of shoot:root dry matter partitioning decreasedat low RZT, whereas the opposite was true for maize. In bothspecies, dry matter partitioning to the shoot was one-sidedlyincreased when the shoot base temperature, and thus shoot activity,were increased at low RZT. The concentrations of non-structuralcarbohydrates (NSC) in the shoots and roots were higher at lowin comparison to high RZT in both species, irrespective of theshoot base temperature. The concentrations of nitrogen (N) inthe shoot and root fresh matter also increased at low RZT withthe exception of maize grown at 12 °C RZT and 20 °Cshoot base temperature. The ratio of NSC:N was increased inboth species at low RZT. However this ratio was negatively correlatedwith the ratio of shoot:root dry matter partitioning in wheat,but positively correlated in maize. It is suggested that dry matter partitioning between shoot androots at low RZT is not causally related to the internal nitrogenor carbohydrate status of the plants. Furthermore, balancedactivity between shoot and roots is maintained by adaptationsin specific shoot and root activity, rather than by an alteredratio of biomass allocation between shoot and roots.Copyright1994, 1999 Academic Press Wheat, Triticum aestivum, maize, Zea mays, root temperature, shoot meristem temperature, biomass allocation, shoot:root ratio, carbohydrate status, nitrogen status, functional equilibrium     

A Balanced Quantitative Model for Root: Shoot Ratios in Vegetative Plants

The vegetative growth of a two-component plant consisting ofroot and shoot only is considered in terms of the transportand utilization of two required substrates, one providing carbonand the other providing nitrogen. The model provides a quantitativescheme for examining how root: shoot ratios depend upon thespecific activities of root and shoot and hence environment.It has been shown that the total shoot activity is proportionalto the total root activity in a plant undergoing steady-stategrowth.     

Effects of Soil Nutrients and Moisture on Root/Shoot Ratios in Lolium perenne L. and Trifolium repens L

The dry weights of foliage and roots (excluding stembases) werecompared in a 3³x2² factorial experiment with Lolium perenneL. and Trifolium repens L. grown in pots with three nitrogen(0–300 ppm N), phosphorus (0–300 ppm P), and soilmoisture (pF 3.2, pF 2.4, and waterlogged) treatments, eachduplicated. Root/shoot ratios were influenced significantly (P < 0.001)by N, P, and W (soil moisture), but these main effects werequalified by highly significant first-order interactions andsecond-order interactions which included N and P. The lowestR/S ratios occurred where N, P, and W were all non-limiting,and the highest where there was an imbalance of these factors. The explanation suggested is that a decrease in the availabilityof N, P, or W causes an increase in the relative weight of roots,but in the presence of N, P, or W deficiency an increase inany one of these factors causes a further increase in the R/Sratio by increasing the relative efficiency of the foliage.     

Leaf Extension Rate in Temperate Pasture Grasses in Relation to Assimilate Pool in the Extension Zone

In two growth cabinet experiments the leaf extension rate (LER)was studied under a 14 h photoperiod followed by prolonged darkness,in tillers of the perennial temperate pasture grasses Phalaristuberosa L. cv. Sirosa and Dactylis glomerata L. cv. Currie.Levels of soluble non-structural carbohydrates and total     

Effect of Temperature on Nitrogenase Activity in White Clover

Single, clonal plants of white clover were grown without inorganicnitrogen in four contrasting day/night temperature regimes,with a 12 h photoperiod, in controlled environments. Root andnodule respiration and acetylene reduction activity were measuredin a flow-through system during both day and night for plantsacclimated to day/night regimes of 23/18, 15/10 and 10/5 ?C.Similar measurements were made on plants acclimated to 20/15?C and stepwise at temperatures from 4 to 33 ?C. Peak rate of ethylene production, nitrogenase-linked respirationand basal root + nodule respiration increased approximatelylinearly from 5 to 23 ?C both in temperature-acclimated plantsand in plants exposed to varying measurement temperatures. Themeasured attributes did not vary significantly between day andnight. Temperatures above 23–25 ?C did not further enhancethe rate of ethylene production, which remained essentiallythe same up to the maximum measured temperature of 33 ?C. The measurements of nitrogenase-linked respiration between 5and 23 ?C, during both day and night, demonstrated a constant‘energetic cost’ of acetylene reduction of 2.9 µmolCO₂ µmol C₂H₄^–1,. Over the same temperature range,the approximate activation energy of acetylene reduction was60 kJ mol^–1. The integrated day plus night nitrogenase-linkedrespiration accounted for 13.4–16% of the plant‘snet shoot photosynthesis in a single diurnal period: there wasno significant effect of temperature between 5 and 23 ?C. Key words: Trifolium repens, white clover, temperature, N₂ fixation, respiration     

A Study of the Breakdown of Organic Phosphates by Micro-organisms from the Root Region of Certain Pasture Grasses

A survey of micro-organisms isolated from the root surface, rhizosphere soil and nonrhizosphere soil of pasture grasses (Ryegrass, S23; Timothy, S50; Cocksfoot, S143) was made to determine their ability to attack phenolphthalein diphosphate, sodium glycerophosphate, sodium phytate, lecithin, ribonucleic and deoxyribonucleic acids. The total numbers of organisms capable of decomposing these compounds were higher on the root surface and in the rhizosphere soil of the grasses when compared with the numbers in nonrhizosphere soil. Occasionally, preferential stimulation of organisms hydrolysing some of the compounds was observed in the root regions. The addition of deoxyribonucleic acid to medium inhibited the numbers of colonies developing in dilution plate counts. This inhibition was generally more pronounced on root surface organisms than on those from nonrhizosphere soil.     

Effects of Photoperiod and Temperature on Shoot, Root and Rhizome Growth in ThreeLotus uliginosusSchkuhr Populations

The growth of three populations of greater lotus (Lotus uliginosusSchkuhrsyn.L. pedunculatusCav.) was compared at photoperiods of 10,12 and 14 h at a maximum day/minimum night temperature of 21/16°C and at maximum day/minimum night temperatures of 27/22,21/16, 18/13 and 15/10 °C at a photoperiod of 12 h. Shortdays (10 h) favoured root and rhizome development compared tolong days (14 h). A temperature regime of 15/10 °C restrictedrhizome development compared to the 18/13 and 21/16 °C regimes.Shoot growth was restricted at the highest temperature regime(27/22 °C). The cultivar Sharnae had fewer, but heavier,rhizomes than Grasslands Maku; this may indicate adaptationto the dry summers at its site of origin (Algarve, Portugal).The response of rhizome growth to temperature and photoperiodexplains part of the performance of greater lotus in the fieldat a wide range of latitudes. Grazing management to encouragethe persistence ofL. uliginosusin pasture in temperate environmentsmay include the exclusion of grazing livestock in autumn. Inthe sub-tropics, monitoring of rhizome production in the fieldwould be required before deciding the appropriate time intervalbetween grazing.Copyright 1998 Annals of Botany Company Lotus uliginosus(Schkuhr); greater lotus; temperature; daylength; shoots; roots; rhizomes.     

Characterization of C4 Type Leaf Anatomy in Grasses (Poaceae). Mesophyll: Bundle Sheath Area Ratios

The cross-sectional area of ‘primary carbon assimilation’(PCA) (or mesophyll) tissue and of ‘photosynthetic carbonreduction’ (PCR) (or parenchymatous bundle sheath, PBS)tissue associated with each vein has been measured in transversesections of leaf blades of 124 grass species (Poaceae). Thespecies sample is representative of all major grass taxa, andof all photosynthetic types found in this family, viz. C₃, C₃/C₄intermediate, C₄ NADP-malic enzyme type (NADP-ME), C₄ NAD-malicenzyme type (NAD-ME) and PEP carboxykinase type (PCK). MeanPCA (or mesophyll) area per vein varies between photosynthetictypes in the order C₃ > NAD-ME > PCK = NADP-ME, mean PCR(or PBS) area per vein in the order NAD-ME > PCK = C₃ >NADP-ME, and mean PCA/PCR (or mesophyll/PBS) area ratio in theorder C₃ > NADP-ME > NAD-ME > PCK. Since grass leaveshave parallel venation, tissue areas and area ratios are directlyproportional to tissue volumes and volume ratios. Regressionanalyses of plots of PCA (or mesophyll) area per vein againstPCR (or PBS) area per vein yield characteristic slopes for photosynthetictypes. Differences between types in all these parameters arenearly always statistically significant, even within high leveltaxonomic groups (Eupanicoids and Chloridoids). However, differencesbetween major taxa (Eupanicoids, Andropogonoids, Chloridoids),within a photosynthetic type, are frequently not significant.This histometric characterization of photosynthetic types isdiscussed in relation to the co-operation of PCA and PCR tissuesin C₄ photosynthesis, to possible differences between C₄ typesin PCR spatial requirements and to the developmental originof PCR tissue. Grasses, Poaceae, C₄ photosynthesis, C₄ leaf blade anatomy, ‘Kranz’, NADP-malic enzyme, NAD-malic enzyme, PEP carboxykinase, PCA tissue, PCR tissue, taxonomy     

Regrowth by Swards of Subterranean Clover after Defoliation. 2. Carbon Exchange in Shoot, Root and Nodule

The carbon economy of subterranean clover swards subjected tothree defoliation treatments (removal of 30, 70 and 80% of shootdry weight) was compared with that of uncut swards. Carbon dioxideexchange in shoots and roots was measured independently 0, 4,8 and 12 d after defoliation. The respiration linked to nitrogenaseactivity was estimated by comparing root respiration measuredin an atmosphere containing 3% oxygen with the respiration in21% oxygen. Net photosynthesis fell by up to 100% immediately after defoliation.There was a decline of over 60percnt; in root respiration bythe end of the first light period, composed of a rapid declineof 70% in nitrogenase-linked respiration in all treatments anda slower decline of nearly 40% in root plus nodule growth andmaintenance respiration in the more severe treatments. Recoveryof net photosynthesis to rates achieved by uncut swards occurredover 4 d in the 30% cut treatment and at least 12 d in moresevere treatments. Whilst recovery of photosynthesis was theprinciple determinant of recovery of net positive carbon balance,the early reduction in respiration facilitated this outcome.After the immediate decline in nitrogenase-linked respiration,recovery in this component of respiration appeared to be linkedwith the recovery in net photosynthesis (approximately 10% ofnet photosynthesis). Carbon budgets revealed priorities in allocation towards leafin the first 5 d and later also towards root growth in severelydefoliated swards. Root respiration comprised a large respiratorycost (up to 75% of net photosynthesis) during early regrowth. Carbon budget, defoliation, N₂ fixation, photosynthesis, regrowth, respiration, subterranean clover, Trifolium subterraneum L     

Effects of Nematicides and Plant Resistance on White Clover Performance and Seasonal Populations of Nematodes Parasitizing White Clover in Grazed Pasture

Root-infecting nematodes are a major cause of white clover, Trifolium repens, not reaching its potential in New Zealand pastures. Resistance and/or tolerance are the preferred control options. Greenhouse-based, recurrent selection programs have developed resistance to Meloidogyne trifoliophila and Heterodera trifolii, and a field-based program has developed tolerance. Lines from these programs were compared with commercial cultivars as controls in a series of field trials at four sites over 4 years. Resistant lines from the CCN program performed better than susceptible lines and as well as most cultivars, reflecting the high level of resistance developed in this greenhouse-based program. In stained root from Cambridge, numbers of CCN were lower in resistant lines than in cultivars; numbers in susceptible lines were intermediate. CCN resistance was also reflected to a lesser extent in the number of cysts counted in soil under resistant lines in Palmerston North. The root-knot nematode-resistant material performed better than the susceptible and as well as most cultivars. In one trial of CRKN-resistant lines, resistant and susceptible lines had similar numbers of CRKN which were both lower than the numbers in the cultivars; in the second trial, there were fewer CRKN in resistant than in susceptible lines or cultivars. The tolerant selections, developed under field conditions, performed as well as or better than the cultivars. The selections from the breeding programmes have exhibited strong agronomic potential across locations and years, and the best material has been crossed; progeny are being assessed in current field trials.     

The Effect of Temperature on Photosynthesis of Ryegrass and White Clover Leaves

The rate of photosynthesis of leaves of perennial ryegrass (Loliumperenne L.) and white clover (Trifollum pratense L.) grown atdifferent temperatures was measured at a range of temperatures.There was a small effect of the temperature at which a leafhad grown on its photosynthetic rate, but a large effect ofmeasurement temperature, especially in bright light, where photosyntheticrates at 15°C were about twice those at 5°C. It appearsthat temperature could affect sward photosynthesis in the field.Ryegrass and clover had similar photosynthetic rates which respondedsimilarly to temperature. Lolium perenne L., ryegrass, Trifolium pratense L., white clover, photosynthesis, temperature, irradiance     

Effect of Root Zone Temperature and Shoot Demand on Uptake and Xylem Transport of Macronutrients in Maize (Zea mays L.)

The effect of shoot demand for nutrients on nutrient uptakeand translocation in the xylem exudate was studied in maizegrowing in nutrient solution at uniform shoot zone (24/2C,day/night), but different root zone temperatures (RZT: 12C,18C, 24C). The shoot base (apical shoot meristem and zoneof leaf extension) was either kept within or lifted above thecooling zone. In plants with their shoot base above the coolingzone (RZT: 12C and 18C) shoot growth was significantly increasedbut not root growth. Therefore, at suboptimal RZT shoot freshweight increment d^–1 g^–1 root fresh weight, whichwas taken as a parameter for the shoot demand for nutrientsper unit root, varied strongly depending on the temperatureof the shoot base (shoot base temperature, SBT). In short-term studies (2 h and 1 d after onset of temperaturetreatment) rates of nutrient (nitrogen, N; potassium, K; phosphorus,P; calcium, Ca) uptake or translocation in the xylem exudatewere markedly decreased at suboptimal RZT (12C, 18C), irrespectiveof the SBT. In long-term studies (3, 5, and 10 d after onsetof temperature treatment) uptake and translocation of K, N,and Ca, but not P, increased in plants at suboptimal RZT whenthe shoot demand was high (shoot base above the cooling zone)but decreased when the shoot demand was low (shoot base withinthe cooling zone). These results suggest, that the increase of translocation ratesof N, K, and Ca after long-term exposure to suboptimal RZT wasa consequence of a higher shoot demand per unit root fresh weightand not due to a direct temperature effect on the nutrient uptakesystem. Key words: Xylem exudate, nutrient translocation, root zone temperature, shoot demand, nutrient circulation     

The Effect of Shade During Leaf Expansion on Photosynthesis by White Clover Leaves

In three experiments measurements of photosynthesis were madeon single leaves of white clover (Trifolium repens L.) on threecultivars grown in a controlled environment. Plants which had grown under an irradiance of 30 J m^–2s^–1, or in shade within a simulated mixed sward, producedleaves with photosynthetic capacities some 30 per cent lowerthan did plants grown at 120 J m^–2 s^–1 without shade.There were no differences between treatments either in photosynthesismeasured at 30 J m^–2 s^–1, or in respiration ratesper unit leaf dry weight. Respiration per unit leaf area washigher in the plants grown at 120 J m^–2 s^–1, reflectingthe lower specific leaf area of these leaves. There were nodifferences between the three cultivars examined. Leaves which were removed from the shade of a simulated swardshortly after becoming half expanded achieved photosyntheticcapacities as high as those which were in full light throughouttheir development. It is suggested that it is this characteristicwhich enables clover plants growing in an increasingly densemixed sward to produce a succession of leaves of high photosyntheticcapacity, even though each lamina only reaches the top of thesward at a relatively late stage in its development. Trifolium repens L., white clover, photosynthesis, leaf expansion, shade, specific leaf area, stomatal conductance     

Adverse Effect of Shoot Growth on Root Growth in Rooted Cuttings of Aspen

In experiments with rooted cuttings of aspen (Populus tremula L). with a small leaf area, it was found that the roots grew well as long as there was no shoot growth. The onset of shoot growth was followed by a period of decreased root growth. When the leaf area had increased sufficiently, root growth recovered. Decreasing the shoot growth by removal of growth points in the shoot or by short day treatment increased the fraction of photosynthesis products used for root growth, leading to increased root/shoot ratios. Competition between growing shoots and roots for carbohydrates formed in photosynthesis is considered to cause the effects noted and to be of importance for maintaining the balance between the root and shoot systems.