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     

Nutrient Relations of Groundsel (Senecio vulgaris) Infected by Rust (Puccinia lagenophorae) at a Range of Nutrient Concentrations II. Uptake of N, P and K and Shoot-Root Interactions

Groundsel (Senecio vulgaris), healthy or infected with rust,Puccinia lagenophorae, was grown at a range of nutrient concentrationsin sand culture. Specific absorption rates calculated on thebasis of root dry weight (SAR_W) were greater in rusted thancontrol groundsel for nitrogen, potassium and phosphorus. Whilethe magnitudes of these stimulations varied, they occurred acrossthe whole range of nutrient concentrations. By contrast, specificabsorption rate on the basis of root length (SAR_L) were littlechanged by rust at any external nutrient concentration; SAR_Lfor phosphate and potassium were slightly reduced when nutrientswere freely available. Water flux per unit dry root weight and length was stimulatedby rust because transpiration per unit leaf area was more rapidin infected plants after fungal sporulation. However, water-fluxand the rate of uptake of nutrients were correlated only whenexpressed on the basis of root weight and increased transpirationdid not appear to be the mechanism underlying increased rootactivity. Rather, increased SAR_W for N, P and K could very largelybe attributed to increased shoot demand per unit root, whichresulted from the higher shoot: root (S: R) ratios of infectedindividuals. Changes in S: R accounted for 92, 81 and 57% oftotal variation in SAR_W for K, P and N respectively. Greatervalues for SAR_W were possible because specific root length (SRL)increased, producing more functional root per unit root weight.The lack of stimulation in SAR_L in response to rust could beexplained since the higher SRL of infected plants resulted instable values of shoot weight per unit root length, i.e. shootdemand was not increased by infection on this basis. Senecio vulgaris, Puccinia lagenophorae, rust infection, nutrient uptake, water uptake, shoot: root interactions     

Regulation of Glyoxysomal Enzymes during Germination of Cucumber: 2. Isolation and Immunological Detection of Isocitrate Lyase and Catalase

The glyoxysomal enzymes isocitrate lyase and catalase have been isolated from etiolated cucumber (Cucumis sativus) cotyledons. The enzymes co-purified through polyethyleneimine precipitation and (NH₄)₂SO₄ precipitation, and were resolved by gel filtration on Sepharose 6B followed by chromatography on diethylaminoethyl-cellulose (isocitrate lyase) or hydroxylapatite (catalase). Purity of the isolated enzymes was assessed by sodium dodecyl sulfate-polyacrylamide electrophoresis, isoelectric focusing, and immunoelectrophoresis. Antibodies raised to both enzymes in rabbits and in tumor-bearing mice were shown to be monospecific by immunoelectrophoresis against total homogenate protein. Isocitrate lyase and catalase represent about 0.56% and 0.1%, respectively, of total extractable cotyledonary protein. Both enzymes appear to be present in a single form. Molecular weights of the native enzymes and its subunits are 225,000 and 54,500 for catalase, and 325,000 and 63,500 for isocitrate lyase. The pH optimum for isocitrate lyase is about 6.75 in morpholinopropane sulfonic acid buffer, but varies significantly with buffer used. The K_m for d-isocitrate is 39 micromolar. A double antibody technique (rabbit anti-isocitrate lyase followed by ¹²⁵I-labeled goat anti-rabbit immunoglobulin G) has been used to visualize isocitrate lyase subunit protein on sodium dodecyl sulfate-polyacrylamide with high specificity and sensitivity.     

The action of exogenous gibberellic acid on isocitrate lyase —mRNA in germinating castor bean seeds

Gibberellic acid (GA₃) stimulates isocitrate lyase activity of the endosperm during germination of castor bean seeds. Isocitrate lyase from castor bean was purified and an antibody to it was prepared from rabbit serum. This antibody was used to measure the amounts of isocitrate lyase-mRNA using an in vitro translation system. No specific stimulation of isocitrate lyase-mRNA by application of GA₃ was detected. The stimulation of isocitrate lyase activity by exogenous GA₃ may be accounted for by the action of the growth substance in advancing the overall production of rRNA and mRNA which accelerates the rate of total protein synthesis during germination. The application of Amo 1618 retards the production of isocitrate lyase activity but also retards protein synthesis in general. This suggests that endogenous gibberellins also act non-specifically in the regulation of protein synthesis during castor bean germination.Abbreviations SDS sodium dodecyl sulphate - GA₃ gibberellic acid - PAGE polyacrylamide gel electrophoresis     

Composition, Degradation and Utilization of Endosperm During Germination in the Oil Palm (Elaeis guineensis Jacq.)

The insoluble carbohydrate and lipid fractions, and -D-galactosidase,ß-D-mannosidase and isocitrate lyase activities werestudied in the various tissues of oil palm (Elaeis guineensisJacq.) kernels prior to and during germination. In ungerminatedkernels insoluble carbohydrate and lipid constituted 36 and47% of endosperm dry weight respectively. During germinationthe thick endosperm cell walls became markedly thinner, concurrentwith a significant decrease in the percentage of insoluble carbohydrateand an increase in -galactosidase and ß-mannosidaseactivity in both degraded and residual endosperm. The proportionof lipid in degraded endosperm also increased significantly.The insoluble carbohydrate appears to be a galactomannan locatedin the secondary walls of the endosperm. No galactomannan wasdetected in oil palm embryos or haustoria. Isocitrate lyasewas present in, and confined to, tissues of the haustorium ofgerminating kernels. The enzyme was not active in endospermat any stage of germination, nor was it active in embryos beforeor at the end of imbibition. The results suggest that galactomannan is the second largestcomponent of oil palm endosperm and that it is utilized morerapidly than lipid during the early stages of germination. Thefact that isocitrate lyase activity is confined to the haustoriumsuggests that in Elaeis gluconeogenesis, the conversion of triglycerideto carbohydrate, takes place entirely within the cotyledon ofthe seed. Elaeis guineensis, galactomannan, galactosidase, germination, isocitrate lyase, mannosidase, oil palm     

Growth of Plants in Different Oxygen Concentrations

Dwarf french beans (Phaseolus vulgaris var. Canadian Wonder)were grown in chambers at 25?C with the roots aerated at 20per cent oxygen and tops variously maintained at: T₁ O₂ 0.21;CO₂ 270?10^–6: T₂; O₂ 0.05, CO₂, CO₂ 270?10^–6: T₃;O₂ 0.21; CO₂ 550?10^–6. Experiment 1 (T₁ and T₂) lasted2 weeks: Experiment 2 (T₁ T₂ and T₃) only one week. Hourly estimatesof CO₂ uptake were made by gas analysis and weekly estimatesof fresh weight, dry matter in tops and roots, and leaf area,by sampling. Light intensity was 80 W m^–2 of photosyntheticallyactive radiation. An attempt was made to explain the results in terms of a simplelight absorption model such that where dV/dt is the rate of CO₂ uptake per plant, ßis the photosynthetic efficiency, I₀ is the incident light intensity,f is the fraction of incident light absorbed by unit leaf layerand L is the leaf area index. The analysis showed that ß(T₂)was at least double ß(T₁), whilst f(T₂) was smallerthan f(T₁) at a given leaf area. The results also required thatthroughout the period of the experiment, fL(T₁)=fL(T₂) at anygiven time, i.e. the treatment with the larger leaf area (T₂)has the smaller value of f, and therefore intercepts less lightper unit leaf area. This could be advantageous for plant growth,but requires further experiments. The photosynthetic rates per unit leaf are about 40 per centgreater in T₂ than T₁. Over the relatively short period of the experiment the resultsare adequately described by U=btⁿ, where U is the accumulatedcarbon dioxide uptake, b is related to the photosynthetic efficiency(different for the differing treatments), and n is a constant(similar for all treatments). This relationship with time isbelieved to be a relationship with accumulated radiation, forthe light was constant throughout the experiments. Comparisons of carbon fixed (measured gas uptake) and dry matteraccumulation (sampling) show great scatter with an average valueof 0.43. The first week's results were generally smaller thanthis value and the second week's greater. Energy fixation as a fraction of photosynthetically active radiationon the ground area covered by the plants ranged from 3.5 to10 per cent. The results from treatment T₃ were similar to T₂ suggestingthat increasing CO₂ concentration decreases the growth inhibitionat 21 per cent O₂.     

The Kinetics of Isocitrate Lyase Formation in Chlorella: Evidence for the Promotion of Enzyme Synthesis by Photophosphorylation

The addition of acetate to aerobic Chlorella pyrenoidosa indarkness was followed by the formations of isocitrate lyaseactiity. After a lag period of 40 minutes the formation proceededat a constant rate. By use of actylamide gel electrophoresisit was shown that the increase in enzyme activity was accompaniedby the formation of a new protein which, after separation byelectrophoresis, contained isocitrate lyase activity. The formationof isocitrate lyase was repressed by glucose; it was repressedby light in the presence of carbon dioxide, but not when DCMUwas added. In light, plus DCMU, isocitrate lyase was formedanaerobically and the capacity for photo-formation of isocitratelyase was saturated at 500 ergs/cm²/sec. In this respect theprocess resembled the photo-conversion of glucose to polysaccharidebut differed from the photo-assimilation of carbon dioxide whichbecame saturated at a heigher light intensity. Monochromaticlight of 706 mµ wavelength supported both isocitrate layseformation and the conversion of glucose to polysaccharide butnot carbon dioxide fixation. It is concluded that ATP generatedby cyclic photophosphorylatin can provide the energy for isocitratelyase synthesis in Chlorella.     

The disappearance of isocitrate lyase from the green alga Chlorella fusca studied by immunoprecipitation

When acetate-adapted cultures of Chlorella fusca were transferred to nitrogen-free medium containing glucose, isocitrate lyase activity was lost over a period of about 25 h. Using a combination of in vivo isotope labelling and immunoprecipitation with anti-isocitrate lyase IgG it was shown that: 1. The onset of loss of enzyme activity preceeded the complete cessation of enzyme synthesis. 2. Disappearance of isocitrate lyase activity was accompanied by loss of enzyme protein, without accumulation of antigenic protein distinguishable from the normal subunit polypeptide of the enzyme, as judged by SDS gel electrophoresis of immunoprecipitated samples from supernatant cell-free extracts. 3. SDS gel electrophoresis of immunoprecipitated isocitrate lyase revealed the presence of antigenic protein bands of M_r about twice that of the normal subunit polypeptide, but the appearance of these apparent dimer forms did not obviously correlate with enzyme degradation. 4. Isoelectric focusing of immunoprecipitated isocitrate lyase showed that the enzyme became progressively more oxidised during the period of its degradation in vivo. 5. By titrating crude broken cell suspensions with anti-isocitrate lyase antibody, preliminary evidence was obtained for transfer of the enzyme from the soluble fraction to an insoluble form as part of the process of disappearance.     

Isocitrate Lyase from Germinating Soybean Cotyledons: Purification and Characterization

Ruchti, M. and Widmer, F. 1986. Isocitrate lyase from germinatingsoybean cotyledons: purification and characterization.—J.exp. Bot. 37: 1685–1690. Isocitrate lyase (E.C. 4.1.3.1 [EC] ) was purified from the cotyledonsof 7-d-old soybean seedlings. Three molecular forms were detectedwith pi values of 6·46, 6·25 and 6·0. Themain form (pl = 6·46) had an approximate Mr of 130000,a pH optimum of 8·0, a K_m (isocitrate) close to 2·0mol m^–3 and a molecular activity of 615 min ^–1 at25 °C. The purified enzyme is not a glycoprotein and isheat labile. Key words: Isocitrate lyase, soybean     

The Dynamics of Leaf Growth and Photosynthetic Capacity in Capsicum frutescens L.

In Capsicum frutescens L. cv. California Wonder the specificleaf weight (dry weight per unit laminar area) at leaf unfoldingis three times higher in the eighth leaf than in the first leafproduced. Intermediate leaves exhibit a trend between the twoThe change in specific leaf weight during laminar expansionis greatest in leaf 1 and least (sometimes zero) in leaf 8.Large changes in specific leaf weight during laminar expansionare associated with a large degree of palisade cell expansion,while leaves showing smaller rates of change have less palisadecell expansion but cell division is more evident. At leaf unfoldingthe fraction I protein content per unit laminar area is higherin upper than in lower leaves. Ribulose diphosphate carboxylaseactivity per unit laminar area and ¹⁴CO₂ fixation per unit laminararea have a similar pattern of development in all leaves andshow no correlation with the changes in specific leaf weight.The peak of activity in all leaves occurs when the laminar areais 10 cm². These results are compared with previous data onlaminar expansion and are seen as in accord with current ideason leaf growth.     

NEW ARGININE-CONTAINING PEPTIDES ISOLATED FROM CHLORELLA CELLS

Seven kinds of arginine-containing peptides were isolated fromthe cells of Chlorella ellipsoidea, and their structures wereinvestigated. Their amino acid make-ups and quantities presentin randomly grown algal cells were found to be as follows (indecreasing order of contentin moles per dry weight of cells): Arg-Arg, Arg-Arg-Glu, Arg-Arg-Arg, Arg-Glu> Arg-(Arg₂, Glu)-Glu>Arg-(Arg₃,Glu), Arg-(Glu, Asp) Using synchronously mass-cultured algal cells, the quantitiesof these peptides as they changed during the algal life cyclewere followed. It was found that, except in the case of Arg-Arg-Arg,the contents (in moles per dry weight of cells) of the peptides(i) markedly increased during the stages from D_n to L₁, (ii)remained almost constant or more or less appreciably increasedduring the stages from L₁ to L₃, and (iii) decreased sharplyduring the transformation of L₃-cells (via L₄) into D_n-cellsin the dark. The content of Arg-Arg-Arg remained almost constantduring the period from D_n to L₃, and on transference of L₃-cellsin the dark it increased temporarily and then decreased duringthe transformation of L₄-cells into D_n-cells. Significance andpossible roles of these peculiar peptides in the life cycleof Chlorella were discussed. (Received May 10, 1965; )     

The Effects of Silicon on Cucumber Plants Grown in Recirculating Nutrient Solution

Cucumber plants (Cucumis sativus) cv. Corona were grown in recirculatingnutrient solution containing either 10 mg l^–1 SiO₂ (lowSi) which was the level present in the water supply or givenan additional 100 mg l^–1 SiO₂ (high Si). Silicate wasdepleted from the solution when cucumbers were grown, but accumulatedwhen tomatoes were grown. Major effects on cucumber leaves ofadded Si were: increased rigidity of the mature leaves whichhad a rougher texture and were held more horizontally; theywere darker green and senescence was delayed. The mature highSi leaves acquired characteristics of leaves grown in a higherlight intensity, i.e. they had shorter petioles and an increasedfresh weight per unit area, dry weight per unit area, chlorophyllcontent, RuBPcarboxylase activity and soluble protein (all expressedper unit area of interveinal laminar tissue). Addition of Sidid not affect the final leaf area of the mature leaves butroot fresh weight and dry weight were increased. A pronouncedeffect of Si addition was the increased resistance to the powderymildew fungus Sphaerotheca fuliginea. Despite regular applicationsof fungicide, outbreaks of the fungal disease occurred on mostof the mature leaves on the low Si plants, while the high Siplants remained almost completely free of symptoms. The additionof Si could be beneficial to cucumbers grown in areas wherethe local water supply is low in this element, especially whengrown in recirculating solution or in a medium low in Si, e.g.peat. Cucumber, silicon, fungal resistance, powdery mildew, senescence, RuBPcarboxylase     

Growth, Development, and Yield of Spring Wheat in Artificial Climates

Spring wheat was grown to maturity in three growth rooms providing:(a) 18 h of light at 20° C and 6 h of darkness at 15°C (hot long days, HL); (b) 18 h of light at 15° C and 6h of darkness at 15° C (cold long days, CL); (c) 14 h lightat 20° C and 10 h of darkness at 15° C (hot short days,HS). Plants were moved between environments at spikelet initiationand anthesis, so dividing the growth period into three. Meanlengths in days of these periods in the different environmentswere: Period 1: HL 16, CL 18, HS 25; Period 2: HL 42, CL andHS 61; Period3: HL 53, CL 83, HS 63. The length of periods 2and 3 also depended on previous treatments. Grain dry weight was affected by environmental differences inall periods and effects in successive periods were additive.Compared with HL, CL or HS in period I before initiation increasedgrain yield by 6 per cent by increasing grain number per ear,HS in period 2 between initiation and anthesis decreased itby 24 per cent by decreasing the number of grains per spikeletand the proportion of spikelets that contained grain; CL inperiod 2 increased it by 21 per cent by increasing the numberof ears; CL in period 3 after anthesis increased it by 16 percent because leaves died later; HS in period 3 decreased itby 14 per cent because there was less radiation and hence lessphotosynthesis. Dry weight of shoot and root at maturity wasincreased by CL or HS in periods 1 or 2, and increased by CLand decreased by HS in period 3. The effects on final yieldof treatment during periods 1 and 2 were the consequence ofsimilar effects already produced at anthesis, and shoot androot dry weight changed little during period 3. The effects of environmental differences on grain dry weightcould not be explained by differences in leaf-area durationafter anthesis (D₃), except that CL in period 3 increased bothyield and D₃ but not proportionately, so that, as with HS inthe same period, grain: leaf ratio was decreased. Environmentaldifferences in periods 1 and 2 appeared to affect grain weightby altering the capacity of the ear to accumulate carbohydrates,determined by the number of grains per ear, rather than by alteringthe supply of carbohydrates, determined by D₃. There were some interactions between environments in differentperiods which were usually small compared with the main effects.     

Flag Leaf Anatomy of Triticum and Aegilops Species in Relation to Photosynthetic Rate

Quantitative anatomical and other measurements were made onfully expanded flag leaves of a series of diploid, tetraploidand hexaploid Triticum and Aegilops species, and photosyntheticrates per unit leaf area were measured at light saturation (P_max). Diploids had the highest P_max, hexaploids the lowest with tetraploidsbeing intermediate. The anatomical features of tetraploids andhexaploids were generally similar, but different from the diploids.The diploids had thinner leaves with less dry matter and chlorophyllper unit area. The surface area of the mesophyll cells per unitvolume of mesophyll tissue was similar for all ploidy levels,as was the ratio mesophyil cell surface area per unit leaf area.It is argued that while these anatomical features are unlikelyto account for the observed variation in Pmax, it is possiblethat other structural factors with which they are correlatedmay causally influence P_max. One such feature is the averagediffusion path length from the plasmalemma at the cell surfaceto the sites of carboxylation. Anatomy, photosynthesis, mesophyll, cell size, Triticum, Aegilops, polyploidy     

An Analysis of Growth of Oil Palms under Nursery Conditions: I. Establishment and Growth in the Wet Season

Growth of oil palm seedlings over the period 2–31 weeksafter planting in the nursery was studied using growth-analysistechniques. Curves of the Gompertz type were fitted to the basicdata of plant dry weight and leaf area, and from the equationsof the fitted curves, net assimilation rate (E_A), relative growth-rate(Rw), and relative leaf growth-rate (R_A) were calculated. The low values of E_A (0.16-0–31 g/dm²/week) and Rw (1.4–2.2per cent./per day) confirm earlier work on oil palm seedlings.The time trend of increasing E_A and R_W over the period studiedis associated with steadily increasing solar radiation overthe second half of the period. Leaf-area ratio is markedly affected by transplanting, and asthis unbalance of leaf area/total dry weight has been shownto be associated with low rates of EA in seedlings, it is suggestedthat the low values of E_A and R_W in the first half of the experimentalperiod are due to the effect of transplanting. These findings are discussed in relation to current nurserypractice.     

Importance of glucose-6-phosphate dehydrogenase activity in cell death

The intracellular redox potential plays an important role incell survival. The principal intracellular reductant NADPH is mainlyproduced by the pentose phosphate pathway by glucose-6-phosphate dehydrogenase (G6PDH), the rate-limiting enzyme, and by6-phosphogluconate dehydrogenase. Considering the importance of NADPH,we hypothesized that G6PDH plays a critical role in cell death. Ourresults show that 1) G6PDHinhibitors potentiatedH₂O₂-inducedcell death; 2) overexpression ofG6PDH increased resistance toH₂O₂-induced cell death; 3) serum deprivation, astimulator of cell death, was associated with decreased G6PDH activityand resulted in elevated reactive oxygen species (ROS);4) additions of substrates for G6PDHto serum-deprived cells almost completely abrogated the serumdeprivation-induced rise in ROS; 5)consequences of G6PDH inhibition included a significant increase inapoptosis, loss of protein thiols, and degradation of G6PDH; and6) G6PDH inhibition caused changesin mitogen-activated protein kinase phosphorylation that were similarto the changes seen withH₂O₂.We conclude that G6PDH plays a critical role in cell death by affectingthe redox potential.     

Relationship between Plant Weight and Growing Period for Vegetable Crops in the United Kingdom

A generalized equation is derived that relates total dry matterproduction to time from emergence for crops grown in the fieldwith adequate water and nutrients. It is: w+K₁lnw+W₀=K₂t where w is the plant dry weight in t ha^–1, t is time indays after emergence, K₂ and K₁ are constants and W₀ equals–(w₀+K₁lnw₀) where w₀ is the value of w at the start ofthe growing period. The increases in the dry matter of 18 different types of vegetablecrop were measured at intervals during growth in the field.In every case the data fitted the equation very satisfactorilywith K₁ set equal to 1 t ha^–1. The fitted values of K₂were similar for many crops; those of W₀ varied considerablybut were always similar to the values calculated from the individualseed weight and the plant population. Good fits were also obtainedwhen time in days was replaced with cumulative evaporation froman open water surface. It is concluded that the growth-time curves of many differentvegetable crops can be described by the same simple equationand that the variation between curves can be largely attributedto differences in seed weight and plant population.     

Response to Temperature in a Stand of Pearl Millet: 10. PARTITION OF ASSIMILATE

Effects of temperature on partition of assimilate between leaves,stems and panicles of pearl millet are analysed in terms ofa duration (t_w) over which a structure increased in weight,and a partition factor (p)—the fraction of new dry matterallocated to the structure during t_w. The value of tw was, forall structures, inversely proportional to temperature abovea base of 10 °C and below an optimum of 28 to 30 °C.For stems and panicles, the value of p was, with one exception,little affected by temperature. The dry weight of these structureswas, therefore, proportional to t_w, and decreased with risein temperature. (The exception was panicles at the lowest temperature,19 °C, for which p was reduced by 40% because few grainswere set.) For leaves, however, p increased with rise in temperature,counteracting the effect on t_w, such that dry weight changedlittle with temperature. The optimum temperature for reproductiveyield was 22 °C, but the proportion of the total dry matterallocated to reproductive structures changed little between22 °C and 31 °C. Key words: Pearl millet, temperature, thermal time, partitioning     

Seed Production in Leafless and Conventional Phenotypes of Pisum sativum L. in Relation to Water Availability Within a Controlled Environment

Water requirements in relation to seed production was studiedin near-isogenic lines of leafless (afafstst) and conventional(++++) pea plants (Pisum sativum). The plants were grown toseed maturity in pots in a controlled environment under conditionsof high, medium and low irrigation levels. When each genotypewas irrigated independently and on demand and the soil moisturecontent maintained at 65–80 per cent of full capacitythere was no significant phenotypic difference in water useefficiency (WUE), defined as g d. wt seed per kg H₂O utilized.There existed genotypically-controlled upper and lower limitsto yield between which the total dry weight of seed per plantcan be determined by water availability. There was no significantdifferential effect of genotype or of irrigation treatment onthe number of pods, number of seed, unit seed dry weight andbiological yield per plant. There was significant interactionon stem length, and leaf area at specified nodes. When the wateractually required in relation to the water available was takeninto account, the leafless phenotype consistently utilized 33–38per cent less water and produced a correspondingly lower totaldry weight of seed than the conventional counterpart. Independentlyof regime the total dry weight seed per phenotype remained anear constant proportion of the above-ground biomass. Pisum sativum L., garden pea, leafless peas, seed production, water availability     

Calcification in the Green Alga Halimeda: II. THE EXCHANGE OF CA2+ AND THE OCCURRENCE OF AGE GRADIENTS IN CALCIFICATION AND PHOTOSYNTHESIS

In Halimeda cylindracea and H. tuna segments, the concentrationof CaCO₃, MgCO₃, protein, and chlorophyll, as well as segmentvolume and wet and dry weight, increase with ‘age’i.e. from the apex of a branch downwards. Photosynthetic andcalcification rates decrease with age as does the degree oflight stimulation of calcification. Studies of the exchange of ⁴⁵Ca between the Halimeda thallusand the sea water under various conditions showed that mostof the Ca exchange is between the cell walls, the aragonitecrystals, and the intercellular space. The cell wall has twodistinguishable phases with half-times (t_0?5) of 200 and 35min while the CaCO₃ has a rapidly exchanging phase with a t_0?5of approximately 6 min. The t_0?5 of the exchange of Ca betweenthe intercellular space and the external medium is estimatedat about 6 min, on the basis of uptake studies. If the integrityof the barrier between the intercellular space and the externalsea water, created by the adpressed peripheral utricles is destroyedthe t_0?5 is smaller (<<3 min). These kinetic studies as well as comparative measurements ofcalcification rates by both isotopic and chemical methods showthat the ⁴⁵Ca method for measuring calcification rates overestimatesthe calcification rate, due to binding of ⁴⁵Ca in the cell wallsand retention of ⁴⁵Ca in the intercellular space. The ¹⁴C methodgives more accurate results and has the further advantage ofallowing simultaneous measurement of the photosynthetic andcalcification rate on the same segment.