Partitioning and Utilization of Net Photosynthate in a Nodulated Annual Legume

The economy of carbon in nodulated white lupin (Lupinus albusL.) was studied in terms of consumption of net photosynthatein nitrogen fixation, in maintenance of respiration, and inthe production of dry matter and protein. Net photosynthesisrose to a maximum in early fruiting and then fell abruptly dueto shedding of leaves. Nodulated roots acquired translocateequivalent to 51% of the plant's net photosynthate, 78% of thecarbon of this translocate being respired, 10% entering drymatter, and 12% returning to the shoot attached to productsof nitrogen fixation. Nodules utilized 4?0–6?5 g C infixing 1 g nitrogen. Photosynthate was utilized most effectivelyfor nitrogen fixation in late vegetative growth. Fruits sequestered16% of the plant's net photosynthate, shoot night respiration17%, and dry matter formation in shoot vegetative parts 22%.Averaged over growth, 9?9 g net photosynthate was required toproduce 1 g seed dry matter and 31 g net photosynthate to produce1 g seed protein. Budgets for utilization of the carbon of netphotosynthate were constructed for 10 d intervals of the plant'sgrowth cycle. Feeding of shoots with ¹⁴CO₂ resulted in radiocarbonbecoming partitioned approximately as predicted by these budgets.The dependence of root respiration on recent photosynthate wasassessed by following the time course of release of ¹⁴CO₂ tothe rooting medium of the ¹⁴CO-labelled plants.     

The Quantitative Role of 'Dark' Respiratory Processes in Heterotrophic and Photolithotrophic Plant Growth

The hypothesis that ATP and reductant generated in photosyntheticpartial reactions can be used in vivo for energy-requiring reactionsother than the photosynthetic carbon reduction cycle is supportedby much experimental evidence. When such direct use of photo-producedcofactors occurs, it might be expected that the alternativesource of ATP and reductant, i.e. ‘dark’ respiration,occurs to a smaller extent than in heterotrophic cells. Thispaper uses data from the literature to compute the CO₂/C ratio(CO₂ produced in ‘dark’ respiration processes perC incorporated into cell material) for photolithotrophic andheterotrophic growth of a range of unicellular algae and angiosperms.The minimum CO₂/C value observed for heterotrophic growth issimilar to, but rather higher than, that calculated using thestoichiometry of known respiratory, biosynthetic and transportreactions for the conversion of carbohydrate and the suppliedminerals into a plant of the appropriate composition. However,for unicellular algae the CO₂/C for photolithotrophic growthis much lower than either of these values for the heterotrophicCO₂/C value, and strongly supports the view that the directuse of photo-produced cofactors for processes other than thephotosynthetic carbon reduction cycle is an important aspectof energy metabolism in these organisms. The minimum CO₂/C observedis similar to that predicted when dark respiratory reactionsserve only to produce essential C skeletons. For angiosperms,the evidence is more equivocal, but is consistent with somedirect use of photo-produced cofactors for processes other thanCO₂ fixation. The spatial separation of energy-requiring processesfrom chloroplasts could partly account for this smaller emphasison nonrespiratory energy supply to processes other than CO₂fixation in angiosperms compared with unicellular algae.     

A Comparison of the Rate of Maintenance Respiration in Some Crop Legumes and Tobacco Determined by Three Methods

Carbon exchange was measured on whole plants of field bean,lucerne, chick pea, kidney bean, pea and tobacco. The maintenance respiration rate was measured in three ways:(i) by allowing the CO₂ efflux to decay in prolonged darknessto an asymptotic value which was then taken to be the maintenancevalue (the dark decay method); (ii) by plotting the dark CO₂efflux as a function of the net CO₂ uptake over a range of irradiancesand taking maintenance as the dark CO₂ efflux when the net CO₂uptake was zero (the dynamic method); and (iii) by plottingthe total CO₂ uptake as a function of the growth rate and takingmaintenance respiration as the CO₂ efflux when the growth ratewas zero (the zero growth rate method). The range of valuesfor the maintenance coefficient over all species was from 1.6to 2.1 per cent of the dry weight per day, 1.8 to 2.1 per centand 2.7 to 2.9 per cent as determined by these three methodsrespectively. There was a linear relationship, common to allspecies, between the maintenance respiration rate (dark decaymethod) and dry weight, total nitrogen and the organic nitrogencontent. The growth coefficient (0.69±0.01) was the samefor field bean, chick pea and lucerne and was unaffected bythe method of estimation. It was concluded that the dark decay method provided the bestestimate of the minimal maintenance requirements in the plantsstudied. Vicia faba L., Medicago sativa L., Cicer arientinum L., Phaseolus vulgaris L., Pisum sativum L., Nicotiana tobacum L., field bean, lucerne, chick pea, kidney bean, pea, tobacco, respiration, maintenance, growth, nitrogen content     

The Respiration of Mature Field Bean (Vicia faba L.) Leaves During Prolonged Darkness

Dark respiration in attached and detached mature leaves of thefield bean (Vicia faba L.) was studied whilst leaves experiencedup to 60 h of darkness. The results showed: (1) the initialrespiration rate to vary according to the irradiance duringthe previous photoperiod; (2) the dark respiration rate (perunit area) of attached leaves to be essentially constant duringa normal 12 h night although there was a rapid loss in leafd. wt during this time; (3) after 12 h, the respiration rateof attached leaves decayed to an asymptotic value at about 36h; (4) the respiration rate of leaves detached at the end ofthe photoperiod and maintained in the dark on deionised water,decayed only after 36 h of darkness; (5) there was no differencebetween the respiration rate of attached and detached leavesduring the normal 12 h night. It is concluded that the dark respiration of attached fieldbean leaves is intially related to the synthesis and translocationof sucrose in addition to maintenance. After about 36 h, whenthe rate of CO₂ efflux is more or less steady, the CO₂ effluxreflects the intensity of maintenance processes only. The maintenancerespiration rate (determined after 60 h in the dark) rangedfrom 062 to 151 mg CO₂ (g d. wt)^–1 h^–1 but wasrelatively unaffected by several applied treatments. Vicia faba L., field bean, respiration, maintenance, nitrate, non-structural carbohydrate, export     

CO2浓度增加和不同氮肥水平对冬小麦根系呼吸及生物量的影响

 依托FACE(Free-air CO₂ enrichment)研究平台, 利用特制分根集气生长箱, 采用静态箱-GC(Gas chromatography)法, 连续两年研究 了大气CO₂浓度升高和不同氮肥水平对冬小麦拔节期、孕穗抽穗期和灌浆末期的根系呼吸及生物量的影响。两季结果表明, CO₂浓度升高和高氮 肥量均不同程度地增加了3个阶段的地上部和地下部的生物量, 这有利于增加根茬的还田量; CO₂浓度升高对冬小麦不同生长阶段的根系呼吸影 响不同, 在拔节期影响较小;孕穗抽穗期显著增加了根系呼吸, 2004~2005季分别增加33.8%(148.1 mg N&;#8226;kg^-1 干土, HN)和43.9%(88.9 mg N&;#8226;kg^-1 干土, LN), 2005~2006季分别为23.8%(HN)和28.9%(LN); 而灌浆末期显著降低了根系呼吸, 2004~2005季分别降低31.4%(HN)和23.3% (LN), 2005~2006季分别为25.1%(HN)和18.5%(LN); 高施氮量比低施氮量促进了根系呼吸; 随着作物生长根系呼吸与地下生物量呈显著线性负相 关, 高CO₂环境中的R²变小,表明随着作物生长发育高CO₂浓度降低了作物根系呼吸与地下部生物量积累间的相关性.     

Modelling the Components of Plant Respiration: Some Guiding Principles

Respiration is poorly represented in whole plant or ecosystemmodels relative to photosynthesis. This paper reviews the principlesunderlying the development of a more mechanistic approach tomodelling plant respiration and the criteria by which modelbehaviour might be judged. The main conclusions are as follows:(1) Models should separate C substrate from structure so thatdirect or indirect C substrate dependence of the componentsof respiration can be represented. (2) Account should be takenof the fact that some of the energy for leaf respiration isdrawn from the light reactions of photosynthesis. (3) It ispossible to estimate respiration associated with growth, nitratereduction, symbiotic N₂fixation, N-uptake, other ion uptakeand phloem loading, because reasonable estimates are availableof average specific unit respiratory costs and the rates ofthese processes can be quantified. (4) At present, it is lesseasy to estimate respiration associated with protein turnover,maintenance of cell ion concentrations and gradients and allforms of respiration involving the alternative pathway and futilecycles. (5) The growth-maintenance paradigm is valuable but‘maintenance ' is an approximate concept and there isno rigorous division between growth and maintenance energy-requiringprocesses. (6) An alternative ‘process-residual’approach would be to estimate explicitly respiratory fluxesassociated with the six processes listed in (3) above and treatthe remainder as a residual with a phenomenological ‘residual maintenance’ coefficient. (7) Maintenance or‘residual maintenance’ respiration rates are oftenmore closely related to tissue N content than biomass, volumeor surface area. (8) Respiratory fluxes associated with differentprocesses vary independently, seasonally and during plant development,and so should be represented separately if possible. (9) Anunforced outcome of mechanistic models should be a constrained,but non-constant, ratio between whole plant gross photosynthesisand respiration. Copyright 2000 Annals of Botany Company Respiration, photosynthesis, growth, maintenance, substrate, N uptake, nitrate reduction, symbiotic N₂fixation, phloem loading, model.     

Mineral nutrition, of cultured chlorophyllous cells of tobacco VII. Effects of the NH4/NO3 ratio and of Cl in the media on the growth and ionic balance of cells

NG, a strain of cultured tobacco cells of Nicotiana glutinosahad high growth rates and carboxylate contents (C—A) of100 to 130 meq/100 g of dry cells on media containing 42 meqNO₃/liter as the sole N source. (C—A) is the amount ofinorganic cations minus inorganic anions in meq per 100 g ofdry cells. NG, cultured on media containing NH₄ 10+NO₃ 42 in meq/liter,had lower growth rates and lower (C—A) values as comparedwith NG on media containing NO₃ as the sole N source. NG, cultured on media containing NH₄ 30+NO₃ 42 in meq/liter,had high growth rates and (A—C) values of 22 to 53 meq/100gof dry cells. In this case, the (A—C) content may correspondto organic cations, basic organic N compounds such as free asprotein-bound basic amino acids. The easily absorbed Cl mayhave been required maintain good growth conditions such as ionicbalance and a favorable pH in the cells. Thus cultured cells of Nicotiana glutinosa may have physiologicaladaptability against variations in a relatively wide range of|C—A| contents [|C—A| being the absolute valuesof (C—A)]. (Received May 15, 1980; )     

Modelling the Components of Plant Respiration: Representation and Realism

This paper outlines the different ways in which plant respirationis modelled, with reference to the principles set out in Cannelland Thornley (Annals of Botany85: 55–67, 2000), firstin whole-plant ‘toy’ models, then within ecosystemor crop models using the growth-maintenance paradigm, and finallyrepresenting many component processes within the Hurley Pasture(HPM) and Edinburgh Forest Models (EFM), both of which separateC and N substrates from structure. Whole-plant models can beformulated so that either maintenance or growth respirationtake priority for assimilates, or so that growth respirationis the difference between total respiration and maintenanceassociated with the resynthesis of degraded tissues. All threeschemes can be converted to dynamic models which give similar,reasonable predictions of plant growth and respiration, butall have limiting assumptions and scope. Ecosystem and cropmodels which use the growth-maintenance respiration paradigmwithout separating substrates from structure, implicitly assumethat maintenance respiration is a fixed cost, uncoupled to assimilatesupply, and use fixed rate coefficients chosen from a rangeof measured values. Separation of substrates in the HPM andEFM enables estimates to be made of respiration associated withlocal growth, phloem loading, ammonium and nitrate N uptake,nitrate reduction, N₂fixation and other mineral ion uptake,leaving a ‘residual maintenance’ term. The lattercan be explicitly related to C substrate supply. Simulated changesin grassland respiration over a season and forest respirationover a rotation show that the ratio of total respiration togross canopy photosynthesis varies within the expected limitedrange, that residual maintenance accounts for 46–48% oftotal respiration, growth 36–42%, phloem loading 10–12%and the other components for the small remainder, with the ratiosbetween components varying during a season or forest rotation.It is concluded that the growth-maintenance approach to respiration,extended to represent many of the component processes, has considerablemerit. It can be connected to reality at many points, it givesmore information, it can be examined at the level of assumptionsas well as at the level of predictions, and it is open to modificationas more knowledge emerges. However, currently, there are stillparameters that require adjustment so that the predictions ofthe model are acceptable. Copyright 2000 Annals of Botany Company Respiration, photosynthesis, growth, maintenance, substrate, N uptake, mineral uptake, phloem loading, model.     

Physiology of Pinus strobus L. Seedlings Grown under High or Low Soil Moisture Conditions

White pine seedlings (Pinus strobus L.) were grown under highor low soil-moisture levels. The increase in the length andin the fresh weight of seedlings, respiration, photosynthesis,transpiration, translocation of photosynthate from shoots toroots, and bio-electric potentials between the tip and the baseof a stem were measured throughout the growing season from Aprilto October 1964. At both moisture levels the lowest translocation of recent photosynthatefrom shoots to roots occurred during early summer, or at thetime when the rate of root growth was the lowest and that ofthe shoot the highest. The specific activity of ¹⁴CO₂, respiredby the shoots of such plants remained high throughout the 8h of the experiment, indicating a continuous utilization ofrecent photosynthate as a respiratory substrate. On the otherhand, early and late in the growing season, when translocationof recent photosynthate from shoots to roots and the rate ofroot growth were high, the specific activity of ¹⁴CO₂, respiredby the shoots rapidly decreased during the 8 h of the experiment,indicating a drop in the utilization of recent photosynthateas respiratory substrate. The highest positive values for thepotential difference between the top and the base of the mainshoot also occurred in early summer or during the period ofhigh rates of transpiration per needle stomatal surface area.     

Effects of Sulphur Dioxide and Nitrogen Dioxide on Growth and Translocation in Winter Wheat

Gould, R. P. and Mansfield, T. A. 1988. Effects of sulphur dioxideand nitrogen dioxide on growth and translocation in winter wheat.—J. exp. Bot 39: 389–99 Winter wheat (Triticum aestivum L. cv. Avalon) was grown undersimulated autumn conditions for 4 weeks and exposed to a mixtureof SO₂ and NO₂. Biomass was measured after 2, 3 and 4 weeksand the flag leaves of sample plants were labelled with ¹⁴CO₂.Biomass yields revealed an increase in shoot-to-root ratiosunder polluted conditions. The labelling experiments showedthat less assimilate was transported to the roots, whilst morewas allocated to the younger components of the plant. It appearedthat NO₂ and SO₂ also caused labelled photosynthate to be retainedin the labelled leaf. Reducing the photon flux exacerbated theeffects of SO₂ and NO₂ as indicated by changes in biomass andby the distribution of ¹⁴C. Key words: Wheat, SO₂, NO₂, growth, translocation     

Growth and Physiology of One-year old Poplar (Populus) Under Elevated Atmospheric CO2 Levels

The effects of elevated atmospheric CO₂ concentrations on theecophysiological responses (gas exchange, chlorophyll a fluorescence,Rubisco activity, leaf area development) as well as on the growthand biomass production of two poplar clones (i.e. Populus trichocarpax P. deltoides clone Beaupré and P. x euramericana cloneRobusta) were examined under open top chamber conditions. Theelevated CO₂ treatment (ambient + 350 µmol mol^-1) stimulatedabove-ground biomass of clones Robusta and Beaupré afterthe first growing season by 55 and 38%, respectively. This increasedbiomass production under elevated CO₂ was associated with asignificant increase in plant height, the latter being the resultof enhanced internode elongation rather than an increased productionof leaves or internodes. Both an increased leaf area index (LAI)and a stimulated net photosynthesis per unit leaf contributedto a significantly higher stem biomass per unit leaf area, andthus to the increased above-ground biomass production underthe elevated CO₂ concentrations in both clones. The larger LAIwas caused by a larger individual leaf size and leaf growthrate; the number of leaves was not altered by the elevated CO₂treatment. The higher net leaf photosynthesis was the resultof an increase in the photochemical (maximal chlorophyll fluorescenceFm and photochemical efficiency Fv/Fm) as well as in the biochemical(increased Rubisco activity) process capacities. No significantdifferences were found in dark respiration rate, neither betweenclones nor between treatments, but specific leaf area significantlydecreased under elevated CO₂ conditions.Copyright 1995, 1999Academic Press Biomass, chlorophyll a fluorescence, elevated CO₂, growth, Populus, poplar, photosynthesis, respiration, Rubisco     

Long-term Respiratory Cost of Maintenance and Growth of Field-grown Young Hinoki Cypress (Chamaecyparis obtusa)

Respiration rate of the entire above-ground parts of field-grown8-year-old hinoki cypress [Chamaecyparis obtusa(Sieb. et Zucc.)Endl.] was measured at monthly intervals over a 5-year period,to evaluate the trend in proportion of maintenance and growthcomponents of respiration with stand development. Representativesample trees were selected for respiration measurements. Theannual respiration rates of individual sample trees were combinedand partitioned into maintenance and growth components by regressingspecific respiration rate on mean relative growth rate. Maintenanceand growth respiration coefficients generated in this way were5.2 mol CO₂kg^-1year^-1and 39 mol  CO₂kg^-1, which are equivalentto 14.3 mg C kg^-1C h^-1(at mean annual air temperature of 15.1°C) and 0.94 kg C kg^-1C. Considering the maintenance andgrowth respiration coefficients, and phytomass and phytomassincrement of individual trees in the stand, the maintenanceand growth respiration rates of the stand were estimated. Theproportion of the maintenance respiration increased, whereasthat of the growth respiration decreased with stand development,due to decreasing relative growth rate.Copyright 1997 Annalsof Botany Company Chamaecyparis obtusa; growth respiration coefficient; hinoki; maintenance respiration coefficient; stand respiration     

Respiratory Utilization of 13C-Labelled Photosynthate in Nodulated Root Systems of Soybean Plants

Kouchi, H., Akao, S. and Yoneyama, T. 1986. Respiratory utilizationof ¹³C-labelled photosynthate in nodulated root systems of soybeanplants.—J. exp. Bot. 37: 985–993. An improved method for the measurement of respiratory utilizationof current photosynthate in the nodulated root system of water-culturedsoybean (Glycine max L.) plants was developed using a steady-state¹³CO₂ labelling technique. Well-nodulated plants at the latevegetative stage were allowed to assimilate ¹³CO₂ for 10 h incontinuous light at a constant CO₂ concentration with a constant¹³C abundance. The respiratory evolution of ¹³CO₂ from rootsand nodules was measured continuously throughout the periodof ¹³CO₂ assimilation and during a subsequent 36 h chase periodby using a differential infrared ¹³CO₂ analyser. The plantswere grown with nitrogen-free or (15 mmol dm^–3)-containing culture solution for 3 d before¹³CO₂ assimilation. In plants grown without , nodule respiration averaged 69% of the total respiration of the undergroundparts over the full experimental period and the CO₂ respiredreached an apparent isotopic equilibrium at 80–85% labellingafter initiating ¹³CO₂ assimilation. By contrast, the CO₂ respiredfrom the roots did not reach an isotopic equilibrium and labellingwas only 56% at the end of exposure to ¹³CO₂ These findingsdemonstrated that nodule respiration is strongly dependent onrecently assimilated carbon compared with root respiration. Plants supplied with in the culture solution showed a decreased rate of nodule respirationand a slightly increased rate of root respiration. The extentsand time courses of labelling of respired CO₂ from both theroots and nodules were similar in the presence and absence of except that the maximum level of labelling of CO₂ derived from nodule respiration in plantswith was significantly higher (about 91%) than for plants growing without . Key words: Soybean (Glycine max L.), nodule respiration, ¹³CO₂, assimilation, carbon partitioning     

Defoliation in White Clover: Regrowth, Photosynthesis and N2 Fixation

Single plants of white clover, grown in a controlled environmentand dependent for nitrogen on fixation in their root nodules,were defoliated once by removing approximately half their shoottissue. Their regrowth was compared with the growth of comparableundefoliated plants. Two similar experiments were carried out:in the first, plants were defoliated at 2.5 g, and in the secondat 1.2 g total plant d. wt. Defoliation reduced rate of N₂ fixation by > 70 per cent,rate of photosynthesis by 83–96 per cent, and rate ofplant respiration by 30–40 per cent. Nodule weights initiallydeclined following defoliation as a result of loss of carbohydratesand other unidentified components. No immediate shedding ofnodules was observed but nodules on the most severely defoliatedplants exhibited accelerated senescence. The original rates of N₂ fixation were re-attained after 5–6or 9 d regrowth, with increase in plant size at defoliation.In general, the rate of recovery of N₂ fixation was relatedto the re-establishment and increase of the plant's photosyntheticcapacity. Throughout the growth of both defoliated and undefoliatedplants nodule respiration (metabolism) accounted for at least23 ± 2 per cent of gross photosynthesis. The unit ‘cost’of fixing N₂ in root nodules, in terms of photosynthate, appearedto be unaffected by defoliation, except perhaps for plants veryrecently defoliated. Similarly, the percentage nitrogen contentsof shoot, root and nodules of defoliated plants became adaptedwithin a few days to those characteristic of undefoliated plants. Trifolium repens, white clover, N₂ fixation, defoliation, photosynthesis, respiration     

Partitioning and Utilization of Photosynthate Produced at Different Growth Stages after Anthesis in Soybean (Glycine max L. Merr.): Analysis by Long-term 13C-Labelling Experiments

Yamagata, M., Kouchi, H. and Yoneyama, T. 1987. Partitioningand utilization of photosynthate produced at different growthstages after anthesis in soybean (Glycine max L. Merr.): Analysisby long term ¹³C-labelling experiments.—J. exp. Bot. 38:1247–1259. Soybean (Glycine max L. Merr. var. Akishirome) plants were allowedto assimilate ¹³CO₂ with a constant specific activity for 10h at different growth stages (a total of seven times at aboutone week intervals) after anthesis. The plants were harvestedperiodically until the time of full maturity and the partitioningof ¹³C into individual plant parts was investigated with anemphasis on the contribution of carbon assimilated at differentgrowth stages to the seed formation. Carbon assimilated at the middle to late seed-filling stagecontributed most to the seed production; one day contributionaccounted for 3–4% in total carbon of the seed at fullmaturity. Integrated contribution of carbon assimilated afteranthesis was estimated as 96% of the final seed carbon. An approximationbased on the temporal data of the incorporation of labelledcarbon into the seeds indicates that 77% of the final seed carboncame from direct transfer of current photosynthate from sourceleaves, which occurred within a few days after the photosyntheticfixation, while the rest originated from remobilization of carbonreserved mainly in leaves and stems plus petioles. In comparison with the total carbon accumulation in the seeds,protein carbon in the seeds was relatively more dependent onphotosynthate produced during the early period of reproductivegrowth stage, whereas lipid carbon was more dependent on photosynthateproduced during the later reproductive stage. Key words: Photosynthate partitioning, soybean (Glycine max L. Merr.), ¹³CO₂ assimilation, seed formation     

The In Vitro Flowering of Kalanchoe blossfeldiana Poellniz: I. ROLE OF CULTURE CONDITIONS AND NUTRIENTS

Dickens, C. W. S. and Van Staden, J. 1988. The in vitro floweringof Kalanchoe blossfeldiana Poellniz. 1. Role of culture conditions.—J.exp. Bot. 39: 461—471. Nodal explants of Kalanchöe blossfeldiana Poellniz. werecultured in vitro on a low nutrient hormone-free medium. Floweringwas achieved in response to short-day inductive cycles. Thissystem was used to test the influence, on the flowering response,of a variety of culture conditions and media. Reduced vesseland medium volume both inhibited flowering, as did renderingthe vessel impervious to gasses. Nitrogen in the form of NH₄NO₃and KNO₃ promoted flowering and vegetative growth in differentways. Increasing sucrose content in the medium caused some increasein the flowering response and in leaf anthocyanin production,but inhibited most aspects of vegetative growth. All of theseaspects are discussed in relation to the induction and evocationof flowering. Key words: Kalanche, flowering, in vitro     

Reproductive Allometry in Soybean, Maize and Sunflower

We compared the relationship between grain yield per plant (Y_P)and shoot biomass per plant (S_P) in three annual crops withcontrasting reproductive strategies: sunflower, a determinatespecies with a single inflorescence; maize, a determinate specieswith a limited capacity to adjust the number of ears in responseto resource availability; and indeterminate soybean, a specieswith a large capacity to adjust the number of inflorescences.Our working hypotheses were: H₁—the relationship betweenY_PandS_P is linear; H₂—the intercept of the model is zero,i.e. there is not a threshold plant mass for reproduction. Awide range of Y_Pand S_Pwas generated by manipulation of plantdensity;S_Pvaried between 0.3 and 196 g per plant in soybean,between 6 and 873 g per plant in sunflower and between 23 and697 g per plant in maize. Within these broad ranges of plantsize, both hypotheses were rejected in five out of six experiments,i.e. the relationship between Y_Pand S_Pdeparted from linearityand there was a threshold for S_Pbelow which no grain set occurred.TheS_P threshold for grain set varied widely among species; itwas close to 2 g per plant for soybean, 27 g per plant for sunflowerand 43–71 g per plant for maize. Because of this sizethreshold and non-linearity, harvest index (HI = Y_PS_P^-1) wasstable for mid-size plants, diminished slightly for large plants,and diminished sharply for smaller plants in all three crops.Harvest index stability was highest in soybean, intermediatein sunflower and lowest in maize. Differential stability ofreproductive partitioning partially derived from contrastingpatterns of meristem allocation. Copyright 2000 Annals of BotanyCompany Helianthus annuus L., Zea mays L., Glycine max(L.) Merrill, grain yield, harvest index, plant density, reproductive allocation, meristem allocation, plasticity     

Comparison of carbon-specific growth rates and rates of cellular increase of phytoplankton in large limnetic enclosures

Potential carbon-specific growth rates of phytoplankton wereestimated from a series of measurements of photosynthetic radio-carbonuptake over 4- and 24-h exposure periods in the light fieldsof three large limnetic enclosures (‘Lund Tubes’),each providing different limnological and trophic conditions.Photosynthetic behaviour and short-term, chlorophyll-specificcarbon-fixation rates conformed to well-established criteriabut, over 24 h, the net retention represented 23–82% ofthe carbon fixed during the daylight hours. Potential mean growthrates (k'_p, of the photo-autotrophic community were calculatedas the net exponential rates of daily carbon-accumulation relativeto derived, instantaneous estimates of the cell carbon-content.Apparent actual community growth rates (k'_D were calculatedas the sum of the exponential rates of change of each of themajor species present, corrected for probable rates of in situgrazing and sinking, and expressed relative to the fractionof total biomass for which they accounted. The correspondingvalues were only occasionally similar, k'_p generally exceedingK'_D by a factor of between 1 and 30 or 1 and 14, depending uponthe carbon:chlorophyll ratio used. The ratio, K'_p/K'_D was foundto vary inversely both to k'_D and to k_n, the net rate of changein phytoplankton biomass, suggesting that measured carbon fixationrates merely represent a capacity for cellular increase which,owing to other likely limitations upon growth, is seldom realized.Apparent rates of loss of whole cells do not account for theloss of carbon; that the ‘unaccounted’ loss rates(K'_p–K'_D varied in direct proportion to K'_p (i.e., losseswere least when chlorophyll-specific photosynthetic productivitywas itself limited) is best explained by physiological voidingof excess carbon (for instance, by respiration, photorespiration,excretion) prior to the formation of new cells.     

Biosynthesis of Anthraquinone by Cells of Galium mollugo L. Grown in a Chemostat with Limiting Sucrose or Phosphate

Growth and anthraquinone biosynthesis by Galium cells were examinedin steady-state substrate-limited conditions using a chemostatcontinuous culture technique. Steady-state growth was obtainedin both sucrose- and phosphate-limiting conditions for periodsup to 60 d. In sucrose-limiting conditions three growth rateswere investigated with doubling times (t_d) of 25 h, 35 h and40 h, and phosphate-limited growth was obtained at t_d= 35 h.The kinetics of the growth response to a change in limitingsubstrate concentration in sucrose-limiting conditions was examinedand found to follow closely that predicted by the applicationof Monod's (1950) model obtained for micro-organisms. The anthraquinone content of cells grown in phosphate and sucroselimitation was uniformly similar and at a relatively low level(0.68 mg g^–1 dry wt.). When the substrate limitation wasrelieved by the addition of the limiting substrate, either phosphate,or sucrose, anthraquinone synthesis was markedly stimulated.The addition of the anthraquinone precursor, orthosuccinyl benzoicacid (OSB) greatly enhanced anthraquinone synthesis in phosphate-limitingconditions but not in sucrose-limited cells. The results show that growth limitation by phosphate and bysucrose causes a suppression of the rate of synthesis of thesecondary metabolite anthraquinone in Galium cells and suggeststhat the metabolic point of suppression is different in eachcase. Key words: Anthraquinone biosynthesis, Galium, Continuous culture, recursor feeding     

Plankton gross production and respiration in the shallow water hydrothermal systems of Milos, Aegean Sea

Plankton gross production, net community production and darkcommunity respiration were measured at coastal sites aroundthe island of Milos, Aegean Sea, during June and September 1996and June 1997. Sampling sites were chosen to include those withand without visible signs of hydrothermal activity. Planktongross production ranged from undetectable (<0.3 mmol O₂ m-³day-¹) to 3 mmol O₂ m-³ day-¹; respiration rates ranged from1 to 6 mmol O₂ m-³ day-¹. No significant difference was foundbetween gross production or respiration rates measured at hydrothermallyactive areas and gross production or respiration rates measuredat non-venting areas. The dissolved inorganic carbon concentrationvaried by ~200 mmol C m-³ between venting and non-venting sites.Temperature had a pronounced stimulatory effect on the rateof plankton dark community respiration. The T_opt for planktondark community respiration always lay above the highest incubationtemperature of 30°C (i.e. >6°C above in situ temperature).Temperature had less of a stimulatory effect on the rate ofgross production.