Elemental Composition of Biomass and its Relation to Energy Content, Growth Efficiency, and Growth Yield

Biomass synthesis from primary substrate is a principal featureof growth. A short-cut method for the determination of growthyields and efficiency is presented. Elemental analyses of theproducts (individually or collectively) permit one to calculatedirectly and simply the amount of substrate carbon and electronswhich are conserved, and thus the amount of substrate required,and the respiratory gas exchanges associated with the synthesis.Glucose is taken as a standard substrate with the required amounttermed Glucose Equivalent (GE, mol mol^–1) or Glucose Value(GV, g g^–1). Comparisons of GV with Production Values(PV) calculated from biochemical pathways (Penning de Vries,Brunsting and van Laar, 1974) show that PV = 0.88 ±0.01GV. The glucose requirement also serves as a close predictorof the heat of combustion of the product. Biomass, elemental analysis, energy content, growth efficiency, yield, glucose equivalent     

Comparison of Four Methods Calculating the Seasonal Pattern of Plant Growth Efficiency of a Kiwifruit Berry

Four methods of determining the substrate requirements for synthesisof a kiwifruit [Actinidia deliciosa (A. Chev.) C. F. Liang etA. R. Ferguson var. deliciosa cv. Hayward] berry were comparedusing data derived from common kiwifruit berry samples collectedfrom anthesis to fruit maturity. The four methods were basedon fruit proximal analysis, elemental analysis, heats of combustion,or tissue carbon content. All methods gave similar patternsof seasonal costs and values of final cost to the plant (mean1.21 g glucose g^–1 season^–1) but there was lessagreement for growth respiration (mean 0.147 g glucose g^–1season^–1). This is the first time that a continuous recordof growth cost over the course of development has been presented,and the trends in seasonal cost reflect the uptake into andsynthesis of the different biochemical constituents in the fruit.The differences between the results of each method reflect theunderlying assumptions used in their development. It appearsfrom this work that the method of McDermitt and Loomis (1981),utilizing elemental analyses, is most preferred. Actinidia deliciosa (A. Chev.) C. F. Liang et A. R. Ferguson var deliciosa cv Haywood, kiwifruit, true growth yield, plant growth efficiency, production value, glucose value, bioenergetic cost     

Linear Relations between Carbon Dioxide Concentration and Rate of Development Towards Flowering in Sorghum, Cowpea and Soyabean

Negative linear relations were detected (P < 0·005)between the rate of progress from sowing to panicle initiationand CO₂ concentration (210-720 µmol CO₂ mol^-1 air) fortwo genotypes of sorghum [Sorghum bicolor (L.) Moench]. Relationsbetween CO₂ concentration and the rate of progress from sowingto first flowering were also negative in soyabean [Glycine max(L.) Merrill] (P < 0·025), but positive in cowpea[Vigna unguiculata (L.) Walp.] (P < 0·025), albeitthat in both grain legumes sensitivity was much less than insorghum. Thus CO₂ elevation does not delay flowering in allshort-day species. The considerable effect of CO₂ concentrationon times to panicle initiation resulted in large differencesamong the sorghum plants at this developmental stage; with increasein CO₂ concentration, plants were taller with slightly moreleaves and more pronounced apical extension. At the same timeafter sowing however, sorghum plants were heavier (P < 0·05)at 210 than at 360 µmol CO₂ mol^-1 air. In contrast, relationsbetween the dry masses of the soyabean and cowpea plants andCO₂ concentration were positive and curvilinear (P < 0·05).It is suggested that the impact of global environmental changecould be severe for sorghum production in the semi-arid tropics.Copyright1995, 1999 Academic Press Sorghum bicolor (L.) Moench., sorghum, Glycine max (L.) Merrill, soyabean, Vigna unguiculata (L.) Walp., cowpea, development, flowering, CO₂, dry matter accumulation, environmental change     

Plant Growth in Relation to the Supply and Uptake of NO3-: A Comparison Between Relative Addition Rate and External Concentration as Driving Variables

Two approaches to quantifying relationships between nutrientsupply and plant growth were compared with respect to growth,partitioning, uptake and assimilation of NO₃^– by non-nodulatedpea (Pisum sativum L. cv. Marma). Plants grown in flowing solutionculture were supplied with NO₃^– at relative addition rates(RAR) of 0·03, 0·06, 0·12, and 0·18d^–1, or constant external concentrations ([NO₃^–)of 3, 10, 20, and 100 mmol m^–3 over 19 d. Following acclimation,relative growth rates (RGR)approached the corresponding RARbetween 0·03–0.12 d^-1, although growth was notlimited by N supply at RAR =0.18 d^-1. Growth rates showed littlechange with [NO₃–] between 10–100 mmol m^–3(RGR=0·15 –0·16 d^-1). The absence of growthlimitation over this range was suggested by high unit absorptionrates of NO₃^–, accumulation of NO₃^– in tissues andprogressive increases in shoot: root ratio. Rates of net uptakeof NO₃^– from 1 mol m^–3 solutions were assessed relativeto the growth-related requirement for NO₃^–, showing thatthe relative uptake capacity increased with RGR between 0·03–0·06d^–1 , but decreased thereafter to a theoretical minimumvalue at RGR     

Sorghum Seedling Growth as a Function of Sodium Chloride Salinity and Seed Size

Sodium chloride salinity in the range 0–90 mM inhibitedgrowth of sorghum seedlings. Seedlings derived from small seedswere most sensitive to salinity. Salinity, seed size, seedling growth, sorghum, Sorghum bicolor L. Moench     

Effect of Mechanical Stress on Sunflower (Helianthus annuus L.) Hypocotyl Growth

Etiolated seedlings of Sunflower (Helianthus annuus L.) weresubjected to mechanical stress by longitudinally compressingthe hypocotyl with approx. 0·05 N force (equivalent to0·025 MPa for a 1·6 mm diameter hypocotyl). Thisrelatively low compressive stress effected an increase in relativegrowth rates (RGR) of the hypocotyl for a period of 1-2 h, followingwhich RGR returned to the pretreatment rate. RGR was also increasedby an equivalent compressive stress treatment (0·025MPa) for 4 h in water or in 10^-10 mol l^-1 IAA. These resultsare discussed in the context of a possible role for mechanicallyinduced stress in the initiation and maintenance of nutationalgrowth movements.Copyright 1994, 1999 Academic Press Helianthus annuus, Sunflower, hypocotyl growth, mechanical stress, seedling growth, nutational growth movements, circumnutation     

Relationship between Coleoptile Elongation and Alcoholic Fermentation in Rice Exposed to Anoxia. II. Cultivar Differences

The relationship between coleoptile elongation and survivalvs. alcoholic fermentation of rice under anoxia is examinedusing eight cultivars differing in submergence tolerance. Anoxiawas imposed on either 1 or 4 d aerated seeds either by N₂ flushingsubmerged tissues or by incubating tissues in stagnant deoxygenatedagar at 0·1% w/v; the latter simulated the stagnant conditionsof waterlogged soil. Two cultivars that were most tolerant tosubmergence also had the greatest tolerance to anoxia, whilea submergence intolerant cultivar was also intolerant to anoxia. Coleoptile growth under anoxia was related to rates of ethanolsynthesis (R_E), however differences between growth during anoxiaand survival after anoxia indicated that post-anoxic injurymay also be important in rice seeds exposed to anoxia. The correlationbetween coleoptile growth and R_E measured on a tissue basisusing intact seeds was r² = 0·67 among six varietiesover 0-3 d anoxia. This correlation improved to about r² = 0·85using R_E of (embryos plus coleoptiles) over 0-3 d, or coleoptilesat 3 d after anoxia. Coleoptile growth of individual seeds wasusually poorly correlated to R_E in these cultivars at 2-3 dafter anoxia. When coleoptiles of similar lengths were obtainedfrom different cultivars using 4 d aerated seeds, there weredifferences in R_E and coleoptile growth which were related tocoleoptile growth during 3 or 5 d anoxia, either on a tissue(r² = 0·85) or a fresh weight basis (r² = 0·70-0·97respectively). Results are discussed in relation to factorswhich may limit ethanol synthesis in rice exposed to anoxiaand the importance of growth to the survival of seeds and matureplants during submergence in the natural environment.Copyright1994, 1999 Academic Press Anoxia, ethanol, alcoholic fermentation, Oryza sativa L., rice, submergence     

Estimation of the Annual Cost of Kiwifruit Vine Growth and Maintenance

Elemental analysis (for carbon, hydrogen, nitrogen and sulphur)and ash data for kiwifruit [Actinidia deliciosa (A. Chev.) C.F. Liang et A. R. Ferguson var. deliciosa cv. Hayward] stems,leaves and fine roots were used to calculate the specific costs(kg carbohydrate kg^-1 dry matter) of organ synthesis with ammoniacalnitrogen supply. Those costs ranged between 1·19 and1·35 for stems and 1·19 and 1·27 for leaves.The mean annual specific cost for fine roots was 1·17.Seasonal vine growth costs were calculated by multiplying thespecific costs by biomass data for a typical vine. Total costof synthesis was 57·2 kg carbohydrate per vine year^-1,taking fine root turnover as three times per season. Nitratenitrogen supply increased that cost by 6·6% to 61·0kg carbohydrate per vine year^-1. Fruit growth accounted forthe largest proportion of synthetic costs. Vine growth respiration(expressed in terms of carbohydrate equivalents) accounted forapproximately 11·5% of the total cost of synthesis. Maintenancerespiration was estimated to be 5·28, 8·44, 1·90,8·62 and 13·3 kg carbohydrate per organ year^-1for stems, leaves, fruit, above-ground perennial componentsand roots, respectively. Total annual cost of growth and maintenancefor a mature vine was 94·7 and 98·5 kg carbohydrateper vine year^-1 with ammoniacal and nitrate nitrogen supply,respectively. Both values are similar to an estimate of vinephotosynthesis. Maintenance respiration accounted for approximately40% of the total annual cost of vine growth, regardless of theform of nitrogen supplied. Peak carbohydrate demand was duringthe period from 60 to 160 d after budbreak.Copyright 1995, 1999Academic Press Actinidia deliciosa, kiwifruit, carbon economy, growth respiration, maintenance respiration     

Nitrogen Utilization in N-limited Barley During Vegetative and Generative Growth: II. METHOD FOR MONITORING GENERATIVE GROWTH AND DEVELOPMENT IN SOLUTION CULTURE

Growth of barley (Hordeum vulgare L., cvs Golf, Mette, and Laevigatum)under N-limitation was investigated in solution culture, withspecial emphasis on the generative growth stage. Three differentregimes for limiting nitrate-N availability while keeping otherelements in surplus were employed. In the ‘high, decreasingnitrogen’ (HN) treatment, the relative nitrogen additionrate (RA) was maintained at 0.08 d^–1 until the ears startedto develop and was then decreased stepwise to, finally, RA 0·005d^–1. In the ‘low, decreasing nitrogen’ (LN)treatment, plants received 45% of the nitrogen added in HN.In the ‘constant nitrogen’ (CN) treatment, RA washeld constant at 0·0375 d^–1. Cumulative nitrogenadditions at termination of the experiment (day 147 after sowing)were 192, 179 and 87 mg plant^–1 for HN, CN, and LN cultures,respectively. Nitrogen availability limited nitrogen acquisitionin all treatments except in the CN culture at plant ages above110 d. Stepwise decrease of RA largely synchronized transitionsin developmental stages in the different cultivars and nitrogenregimes (HN and LN), and eventually yielded plants that wereclose to completing their life cycle. Normal maturation wasnot obtained in the CN treatment. The HN and LN treatments wereused for formal analysis of post-anthesis growth. A sigmoidfunction was fitted to growth data and from this, organ weightsand nitrogen concentrations at maturity (defined as cessationof growth) were derived. The two modern cultivars, Golf andMette, clearly outperformed the more primitive cv. Laevigatumin terms of allocation of nitrogen to ears, particularly inthe LN culture. The stepwise decrease of RA appears suitablefor studies of post-anthesis growth and nitrogen relations inbarley, with regard to both genotypic variation and variationcaused by differences in cumulative amounts of nitrogen added. Key words: Barley, development, growth, nitrogen concentration, post-anthesis     

Agrobacterium rhizogenes Mediated Transformation of the Forage Legumes Medicago sativa and Onobrychis viciifolia

Three cultivars of M. sativa and one cultivar of O. viciifoliawere evaluated for their response to inoculation with A. rhizogenesstrain A4T (containing pRiA4b). A cultivar-dependent responsewas observed in M. sativa with 94%, 25%, and 4% of infectedstem explants producing transformed roots in the cultivars Vertus,Regen-S, and Rangelander, respectively. In O. viciifolia cv.Hampshire Giant, an explant-dependent response was observedwith 78% and 50% of seedling cotyledon and hypocotyl explantsresponding, respectively. Leaf explants failed to produce transformedroots. Transformed roots showed plagiotropic and negativelygeotropic growth on hormone-free agar MS medium. Productionof transgenic shoots from O. viciifolia root cultures occurredspontaneously. Recovery of transgenic plants from M. salivacv. Rangelander was achieved by transfer of callus (inducedon UM medium containing 2·0mg dm^–3 2,4-D and 0·25mg dm^–3 kinetin) to MS medium containing 0·5 ingdm^–3 BAP and 0·05 mg dm^–3 NAA. Cultured rootsof both species synthesized opines (agropine and mannopine).Extensive morphological variation was observed in plants ofM. sativa (clone Al) and O. viciifolia (clone A4Tl) establishedin the glasshouse. DNA sequences homologous to TL-DNA and TR-DNAwere present in root clones and regenerated plants. Key words: Agrobacterium rhizogenes, Medicago sativa, Onobrychis viciifolia, transformed roots, transgenic plants     

Estimating the Bioenergetic Cost of a Developing Kiwifruit Berry and its Growth and Maintenance Respiration Components

A response surface was developed by regression analysis to quantifythe seasonal respiratory losses by a kiwifruit [Actinidia deliciosa(A. Chev.) C. F. Liang et A. R. Ferguson var. deliciosa cv.Hayward] berry growing in Fresno, CA. The equation of the surfacewas LNRESP = 1·622 + 0·0697 x TEMP –0·0472x DAY + 0·000165 x DAYSQ, where LNRESP is the naturallogarithm of the respiration rate (nmol CO₂ g d. wt^–1s^–1), TEMP is fruit temperature (°C), DAY is the numberof days after flowering, and DAYSQ is the square of the numberof days after flowering. Respiratory losses for a fruit witha final dry mass of 18·5 g were calculated to be 5·57and 5·92 g glucose per fruit per season in 1985 and 1986,respectively. Maintenance respiration was estimated to be 2·84and 3·19 g glucose per fruit per season for 1985 and1986, respectively. The total calculated bioenergetic cost ofkiwifruit berry growth and respiration was 25·25 and25·60 g glucose per fruit per season for 1985 and 1986,respectively. Respiratory losses, expressed as a proportionof the total carbohydrate required for fruit growth, were significant(mean 22·6%). The cost of fruit growth was estimatedto be very similar for two cooler sites (Davis and Watsonville)but estimates of maintenance respiration based on Fresno fruitrespiration data were unrealistically low for the Watsonvillesite. Actinidia deliciosa (A. Chev.) C. F. Liang et A. R. Ferguson var. deliciosa cv. Hayward, kiwifruit, growth respiration, maintenance respiration, bioenergetic costs, model     

Nitrogen Utilization in N-limited Barley During Vegetative and Generative Growth: III. POST-ANTHESIS KINETICS OF NET NITRATE UPTAKE AND THE ROLE OF THE RELATIVE ROOT SIZE IN DETERMINING THE CAPACITY FOR NITRATE ACQUISITION

Barley (Hordeum vulgare L., cvs Golf, Mette, and Laevigatum)was grown under nitrogen limitation in solution culture untilnear maturity. Three different nitrogen addition regimes wereused: in the ‘HN’ culture the relative rate of nitrate-Naddition (RA) was 0·08 d^–1 until day 48 and thendecreased stepwise to, finally, 0·005 d^–1 duringgrain-filling; the ‘LN’ culture received 45% ofthe nitrogen added in HN; the ‘CN’ culture was maintainedat RA 0·0375 d^–1 throughout. Kinetics of net nitrateuptake were measured during ontogeny at 30 to 150 mmol m^–3external nitrate. V_max (which is argued to reflect the maximuminflux rate in these plants) declined with age in both HN andLN cultures. A pronounced transient drop was observed just beforeanthesis, which correlated in time with a peak in root nitrateconcentration. Similar, but less pronounced, trends were observedin CN. The relative V_max (unit nitrogen taken up per unit nitrogenin plants and day) in all three cultures declined from 1·3–2·3d^–1 during vegetative growth to 0·1–0·7d^–1 during generative growth. These values are in HN andLN cultures 15- to more than 100-fold in excess of the demandset by growth rates throughout ontogeny. Predicted balancingnitrate concentrations (defined as the nitrate concentrationrequired to support the observed rate of growth) were below6·0 mmol m^–3 in HN and LN cultures before anthesisand then decreased during ontogeny. In CN cultures the balancingnitrate concentration increased during grain-filling. Apartfrom the transient decline during anthesis, most of the effectof ageing on relative V_max can be explained in terms of reducedcontribution of roots to total biomass (R:T). The loss in uptakeper unit root weight is largely compensated for by the declinewith time in average tissue nitrogen concentrations. The quantitativerelationships between relative V_max and R:T in ageing plantsare similar to those observed for vegetative plants culturedat different RAs. The data support the contention that the capacity for nitrateacquisition in N-limited plants is under general growth control,rather than controlled by specific regulation of the biochemicalpathway of nitrate assimilation. Key words: Barley, nitrogen concentration, root: total plant biomass ratio, V_max     

Salinity Reduces Water Use and Nitrate-N-use Efficiency of Citrus

Five-month-old Cleopatra mandarin (Citrus reticulata Blanco)(CM) and Volkamer lemon (Citrus volkameriana Ten. and Pasq.)(VL) seedlings were grown in a glasshouse in 2·3-1 potsof Candler fine sand. Plants were irrigated with either non-saline(EC_e = 0·23 dS m^-1) or saline (6·13 dS m^-1) waterusing 3:1 NaCl:CaCl₂ solution over a 4-week period. A singleapplication of K¹⁵NO₃ (19·64 atom % excess ¹⁵N) at 212mg N1^-1, was substituted for a normal weekly fertilization after3 weeks and plants were harvested 7 d later. The transpirationrate, uptake of nitrogen, growth and nitrogen-use efficiency(NUE) on a dry weight basis (mg d. wt mg^-1 N) of both specieswas reduced by salinity. Based on growth, water-use and chloride(Cl) accumulation in leaves, VL was more salt-sensitive thanCM, but ¹⁵N uptake was equally reduced by salinity in both species.Salinity reduced ¹⁵N uptake relatively more than shoot growthover the 7-d period, such that the ¹⁵NUE (mg d. wt µg^-115N) of new shoot growth of both species increased. There wasno evidence of Cl antagonism of nitrate (NO₃) uptake but totalplant ¹⁵NO₃ uptake was positively correlated with whole planttranspiration in both species. Thus, it appears that reductionsin NO₃ uptake are more strongly related to reduced water usethan to Cl antagonism from salt stress.Copyright 1993, 1999Academic Press Sodium, chloride, salinity, calcium, nitrate, ¹⁵NO₃ uptake, nitrogen allocation, nitrogen-use efficiency, water use, Citrus reticulata, Citrus volkameriana     

Analysis of the Nitrogen Response of Leaf Extension in Lolium temulentum Seedlings

Lolium temulentum seedlings were grown on a nutrient mediumcontaining NH₄NO₂ at 0, 0·1, 0·5, 1·0 and4·3 mmoll^–1 as the sole N source. Relative andabsolute extension rates, maximal leaf size, duration of extensiongrowth, rate of leaf appearance and plastochron index were determinedfrom the parameters of Richards functions fitted to lengthsof laminae measured at intervals after sowing. The final lengthof leaf I was relatively insensitive to N whereas mean relativeextension rate was increased and duration of growth decreasedwith increasing NH₄NO₂ concentration. Leaves 2 and 3 enlargedprogressively with N at concentrations up to 1·0 mmoll^–1but were unresponsive thereafter. There was no significant correlationbetween final length and mean relative extension rate for leaves1 to 3. Leaves 4 to 6 continued to show increasing length beyond1·0 mmoll^–1 N and final length was significantlycorrelated with mean relative extension rate. Increasing N increasedthe rate of leaf appearance by decreasing the duration of leafextension and plastochron. These results are discussed in relationto the control of leaf and N turnover. Lolium temulentum, rye grass, leaf extension, nitrogen, Richards function, growth analysis     

Studies in the Growth of Young of Pinus sylvestris L.: I. The Annual Cycle of Assimilation and Growth

The annual cycle of growth in plants of P. sylvestris L. varyingin age from 2 to 5 years was studied mainly by following theirweight changes through periodic sampling. Immediately followingbud-break there was a period of about 1 month in which, althoughmeristematic and extension growth were rapid in both shoot androot, there was no gain in weight by the plant. There was evidencethat the needles remaining from previous years contained a considerableamount of storage material which was utilized at this time.During May and June the main increase in weight was in the newshoots, but in August and September assimilates were more evenlydivided between the new shoots on the one hand, and the oldstem and the root on the other. The average relative growth-ratesfor the months May to September were between 1·0 and0·4 per cent, per day in plants growing in favourableconditions, the lower rates being found in older plants. Duringthe months October to March slow increase in weight occurredin needles, stem, and root, and the R.G.R.s in two experimentswere 0·21 and 0·15 per cent, per day. The netassimilation rate fell with increasing age and in the summerof the fifth year was 0·06g./g./week or 0·10g./dm.²/week.This low value of N.A.R. is discussed in relation to the knownhigh rate of production of P. sylvestris stands and their evergreenhabit.     

Endothelia of Schlemm's canal and trabecular meshwork: distinct molecular, functional, and anatomic features

The purpose of this study was to compare human endothelial cells from Schlemm's canal (SCEs) and the trabecular meshwork (TMEs) in terms of ZO-1 isoform expression, hydraulic conductivity (HC) properties, and "giant" vacuole (GV) formation. The principal study methods were Western blot, RT-PCR, immunofluorescence, and perfusion chambers. Blot signals for ⁺-and ^--isoforms were similar in SCEs but less intense for the ⁺-relative to the ^--signal in TMEs. With the anti-⁺ antibody used at 1/50 dilution, binding occurred at cell borders of both cell types, but only to SCEs when used at a =" BORDER="0">1/200 dilution in vitro and in vivo. SCEs were more resistive than TMEs (HC = 0.66 vs. 1.32 µl·min^-1·mmHg^-1·cm^-2; P < 0.001) when perfused from apex to base. When perfused in the other direction, SCEs were again more resistive (5.23 vs. 9.04 µl·min^-1·mmHg^-1·cm^-2; P < 0.01). GV formation occurred only in SCEs as a function of flow direction, perfusion pressure, and time. We conclude that SCEs and TMEs have distinctive phenotypic properties involving their content of ZO-1 isoforms, barrier function, and GV formation. tight junctions; ZO-1; giant vacuoles; conductivity     

Nitrate Effects on Pre-emergence Growth and Emergence Percentage of Wheat (Triticum aestivum L.) from Different Sowing Depths

The effects of a range of applied nitrate (NO₃^–) concentrations(0–20 mol m3) on germination and emergence percentageof Triticum aestivum L. cv. Otane were examined at 30, 60, 90and 120 mm sowing depths. Germination percentage was not affectedby either sowing depth or applied NO₃^– concentration whereasemergence percentage decreased with increased sowing depth regardlessof applied NO₃^– concentration. Nitrate did not affectemergence percentage at 30 mm sowing depth, but at 60 to 120mm depth, emergence percentage decreased sharply with an increasedapplied NO₃^– concentration of 0 to 1·0 mol m^–3then decreased only slightly with further increases in appliedNO₃^– of about 5·0 mol m^–3. Root and shoot growth, NO₃^– accumulation and nitrate reductaseactivity (NRA) of plants supplied with 0, 1·0 and 1·0mol m^–3 NO₃^– at a sowing depth of 60 mm were measuredprior to emergence. The coleoptile of all seedlings opened withinthe substrate. Prior to emergence from the substrate, shootextension growth was unaffected by additional NO₃^– butshoot fr. wt. and dry wt. were both greater at 1·0 and1·0 mol m^–3 NO₃^– than with zero NO₃^–.Root dry wt. was unaffected by NO₃^–. Nitrate concentrationand NRA in root and shoot were always low without NO₃^–.At 1·0 and 10 mol m3 NO₃^–, NO₃^– accumulatedin the root and shoot to concentrations substantially greaterthan that applied and caused the induction of NRA. Regardlessof the applied NO₃^– concentration, seedlings which failedto emerge still had substantial seed reserves one month afterplanting. Coleoptile length was substantially less for seedlingswhich did not emerge than for seedlings which emerged, but wasnot affected by NO₃^–. It is proposed that (a) decreasedemergence percentage with increased sowing depth was due tothe emergence of leaf I from the coleoptile within the substrateand (b) decreased emergence percentage with additional NO₃^–was due to the increased expansion of leaf 1 within the substrateresulting in greater folding and damage of the leaf. Key words: Triticum aestivwn L., nitrate, sowing depth, seedling growth, seedling emergence     

Analysis of Shoot Apical Growth of Picea sitchensis Seedlings

During the first 100 days after sowing (March-June) the followingchanges took place at the terminal shoot apices of Picea sitchensisseedlings: plastochrones (T) decreased from over 24 h to 4 h;apical domes enlarged from less than 0·20 mm to 0·45mm diameter (D); the ‘projected’ area of tissuesproduced by the apical domes (i.e. viewed from above) increasedin amount from less than 0·012 to 0·024 mm² day^-1;about 15 per cent of this tissue was re-invested in the apicaldomes, the rest was used to produce primordia; and the volume-doublingtimes of the apical dome tissues decreased from over 150 h to50 h. After 100 days there was no further re-investment in theapical domes, but the domes did not decrease abruptly in size.Less tissue was produced per day, but the primordia were smallerso that the rate of primordia formation did not fall precipitously.Plastochrone ratios were inversely related to D, but the relationshipbetween T and D depended on whether T was decreasing or increasing.Progenies which were known to be fast growing tended to build-uptheir apical domes rapidly (i.e. have large ‘re-investmentratios’) and to be capable of producing small primordia.These attributes can evidently be evaluated on seedlings andcould help to lessen the cost of tree breeding progeny-testprogrammes. meristem, Picea sitchensis, Sitka spruce, growth, shoot apex     

Photoperiodically Induced Changes in Seed Growth Rate of Soybean as Related to Endogenous Concentrations of ABA and Sucrose in Seed Tissues

Short-day photoperiods can increase the partitioning of assimilatesto filling seeds of soybean (Glycine max L. Merr.), resultingin higher seed growth rates. The plant growth substance ABAhas been implicated in the regulation of assimilate transferwithin filling soybean seeds. Thus, we hypothesized that anincreased concentration of endogenous ABA in seeds may enhancesucrose accumulation and seed growth rate of soybeans exposedto short-day photoperiods. Plants of cv. Hood 75 were grownin a greenhouse under an 8-h short-day photoperiod (SD) until11 d after anthesis (DAA) of the first flower, when half ofthe plants were transferred to a night-interruption (NI) treatment(3 h of low-intensity light inserted into the middle of thedark period). Plants remaining in SD throughout seed developmenthad seed growth rates 43% higher than that of plants shiftedto NI (7·6 mg seed^–1 d^–1 vs. 5·3 mgseed^–1 d^–1). On a tissue-water basis, the concentrationof ABA in SD seeds increased rapidly from 7.6 µmol l^–1at 11 DAA to 65·2 µmol l^–1 at 18 DAA, butthen declined to 6·6 µmol l^–1 by 39 DAA.In contrast, the concentration of ABA increased more slowlyin NI seeds, reaching only 47·4 µmol l^–1by 18 DAA, peaking at 57·0 µmol l^–1 on 25DAA, and declining to 10·2 µmol l^–1 by 39DAA. The concentration of sucrose in SD embryos peaked at 73·5mmol l^–1 on 25 DAA and remained relatively constant forthe remainder of the seed-filling period. In NI, the concentrationof sucrose reached only 38·3 mmol 1^–1 by 25 DAA,and peaked at 61·5 µmol l^–1 on 32 DAA. Thusin both SD and NI, sucrose accumulated in embryos only afterthe peak in ABA concentration, suggesting that ABA may havestimulated sucrose movement to the seeds. The earlier accumulationof ABA and sucrose in SD suggests that ABA may have increasedassimilate availability during the critical cell-division period,thus regulating cotyledon cell number and subsequent seed growthrate for the remainder of the seed-filling period. Glycine max L. Merr. cv. Hood 75, soybean, assimilate partitioning, abscisic acid, photoperiod, source-sink     

Structure and Function of an Age Series of Poplar Plantations in Central Himalaya. II Nutrient Dynamics

This paper elucidates nutrient dynamics in 5- to 8-year-oldpoplar (Populus deltoides) clone D₁₂₁ plantations previouslyinvestigated for dry matter dynamics. The nutrient concentrationin different layers of the vegetation were in the order: tree> shrub > herb, whereas the standing state of nutrientswere in the order: tree > herb > shrub. Soil, litter andvegetation, respectively, accounted for 80-89, 2-3 and 9-16%of the total nutrients in the system. Considerable reductions(trees 42-54, shrubs 31-37 and herbs 15-23%) in concentrationof nutrients in leaves occurred during senescence. The uptakeof nutrients by the vegetation and also by the different components,with and without adjustment for internal recycling, has beencalculated separately. Annual transfer of litter nutrient tothe soil by vegetation was 113·7-137·6 N, 11·6-14·6P and 80·1-83·2 K kg ha^-1 year^-1. Turnover rateand time for different nutrients ranged between 0·72-0·89year^-1 and 1·12-1·39 years, respectively. Thehigh turnover rate of litter on the forest floor indicates thegreater productivity of the stands, which was due to the higherdry matter dynamics and nutrient release for the growing vegetation.The nutrient use efficiency in poplar plantations ranged from159-175 for N, 1405-1569 for P and 295-332 for K. Compared withEucalyptus, there was a higher proportion of nutrient retranslocationin poplars largely because of higher tissue nutrient concentrations;this indicates lower nutrient use efficiency as compared tothe eucalypt plantation. Compartment models for nutrient dynamicshave been developed to represent the distribution of nutrientpools and net annual fluxes within the system.Copyright 1995,1999 Academic Press Populus deltoides plantations (Clone D₁₂₁), nutrient retranslocation, net nutrient uptake, nutrient use efficiency, nutrient cycling, nutrient pool, nutrient fluxes