Studies on Extension Growth in Coleoptile Sections: I. The Influence of Age of Coleoptile upon the Response of Sections of IAA

One of the problems involved in carrying out large-scale coleoptilecylinder straight growth assays is the effect of coleoptileage upon the behaviour of the sections. This effect, as measuredboth by the length of coleoptile and the time from sowing theseeds, has been investigated by an examination of the growthof sections cut from coleoptiles of several length grades onfive occasions 6–10 hours apart. The response of thesesections to a range of concentrations of ß-indolylaceticacid (IAA) was followed during the period of growth to ascertainthe most suitable time for measurement of sections in a routinetest. A number of general trends associated with coleoptile age (whethermeasured by length, or time from planting) were observed inamount of growth, growth-rate, period of growth, and sensitivity.It is suggested that these characteristics are associated withthe amount of the total growth already made by the parent coleoptileat the time of taking the section, and also that the sectionexhibits an ‘intrinsic growth-rate’ related to thegrowth-rate of the coleoptile at the time the section is cut. A period of growth of 17–20 hours seems satisfactory forroutine tests except where very young coleoptiles are used;in this case growth less than that in water is sometimes observedin very low concentrations of IAA.     

Pilot scale exponential growth of Escherichia coli W to high cell concentration with temperature variation

An efficient method to grow Escherichia coli W to high cell concentrations on the pilot scale is described and discussed. The method involves growth linked introduction of glucose; and ammonia to the culture, sparing with oxygen, and maintenance of aerobic conditions by gradually decreasing the temperature in the culture in order to keep the oxygen demand within the limits of the capacity of supply. Under these conditions the linear rate of cell mass production is actually the result of exponential growth with a gradually decreasing growth-rate constant. About 10 kg packed cells were produced in a 50 liter working-volume fermentor in one run of 13 hr. The concentration of the cells at the end of the growth was about 47 g dry cells/liter. The expenditure for nutrients was minimal and the controls were of simple automatic nature. From the determined yield constants for glucose, nitrogen, phosphorus, and oxygen it may be inferred that the cells grown by this method are similar to those grown exponentially at constant temperature.     

The Kinetics of Extracellular Glycollate Production by Chlorella pyrenoidosa

Extracellular glycollate is liberated by Chlorella pyrenoidosaduring growth in medium bubbled with air or 3 per cent carbondioxide in air. With air the rate of release of glycollate percell decreases, with 3 per cent carbon dioxide it increases,with increase in cell number. Glycollate is released duringshort-term experiments when C. pyrenoidasa, grown under lowlight and high carbon dioxide, is transferred suddenly to highlight and low carbon dioxide. No other combination of thesefactors produces a comparable release of glycollate. The quantityof glycollate released in short-term experiments increases exponentiallywith the relative growth-rate of the culture from which thecells are derived. A crucial condition for maximum glycollaterelease is that growth of the culture prior to the experimentshould not be limited by carbon-dixoide concentration. The effectof pH is related to its effect on growth-rate; i.e. C. pyrenoidosahas a lower relative growth-rate at pH 8.3 and produces correspondinglyless glycollate than faster growing cultures at pH 6.4. Duringshort-term experiments under high light and low carbon dioxidethe rate of glycollate release drops after 50–100 minutessuggesting exhaustion of the glycollate precursor.     

Carbon Dioxide Effects on Auxin Responses of Coleoptile Sections

In the wheat cylinder bioassay technique as previously usedhere 5 sections have been enclosed in a 2 x 38 in, assay tubetogether with 0.5 ml. of the test solution. A method developedfor estimating the amount of carbon dioxide which accumulatesin these tubes through the respiration of the enclosed sectionshas shown that the level can rise to 20 per cent. after 24 hrs.at 25°C. In the presence of a 100 p.p.m. IAA(6x10^-4M.) testsolution, growth of 5 enclosed sections is depressed from 8hrs. onwardas and they eventually shrink, releasing their accumulatedIAA back into the solution. The growth of sections under various gas mixtures of carbondioxide in air has also been followed and these experimentsshow that section length is reduced approximately lineraly withrespect to increasing carbon dioxide concentration up to 20per cent. in air, both in the presence and absence of a 100p.p.m. IAA solution. The slope of the fitted regression line,however, is much steeper when the test solution contains IAA—i.e.there is a large interaction. In the presence of IAA, growth-time data show that a reductionin the growth rate, as compared with that in normal air, canbe detected after only 4 hrs, at the highest carbon dioxideconcentration. In the absence of IAA, high concentrations ofcarbon dioxide accelerate growth during the first 8 hrs. ofthe assay but depress it later. The mechanism of action of this interaction is unknown but itis not shown at very high concentrations of IAA, e.g. 1,000p.p.m. (6x10^-3M.).     

Effects of Temperature on the Growth and Development of Lemna minor, under Conditions of Natural Daylight

The effects of temperature on the growth and development ofLemna minor in the open have been studied in the east of Scotlandby means of four water baths constructed to maintain constantwater temperatures of 12.5, 17.5, 22.5, and 27.5 °C whensubjected to natural insolation. Experiments were conductedat weekly intervals between August and November in 1958 andMay and July in 1959. At the beginning of every experiment,for all temperature treatments, 134 fronds were placed in eachof six containers. From the initial and final samples, the weightsof roots and fronds together with frond (leaf) area were measured,so that weekly values for net assimilation rate, leaf-area ratio,and relative growth-rate could be calculated. Daily solar radiationwas recorded by means of bimetallic radiation recorder. In 1958 linear regressions of a satisfactory fit were obtainedwhen the data for net assimilation rate, leaf-area ratio, andrelative growth-rate were calculated on the logarithms of theradiation for each temperature. Since radiation remained relativelyconstant in 1959 it was not possible to evaluate very reliablythe effects of radiation on the growth parameters but only occasionally,notably for the final leaf-area ratio (12.5 °C) were thelines for 1958 and 1959 significantly different. Single lineswere fitted to the points for both years. In all the regressions,apart from that for final leaf-area ratio (12.5°C) the proportionof the variation accounted for ranged from 87 to 97 per cent. The results showed that the net assimilation rate was positivelylinked with radiation and was optimal at 17.5 °C, thoughthe rise from 12.5 to 17.5 °C was not significant. At thehigher temperatures (22.5 and 27.5 °C) there was a significantnegative effect of temperature on the net assimilation rate.The leaf-area ratio and relative growth-rate were positivelydependent on radiation and reached the highest values at thehighest temperatures. The maximum growth-rate recorded amountedto no less than 0.39 g.g^–1 day^–1. The results are discussed in relation to those for other aquaticand terrestrial plants.     

The Effect of High Concentrations of Auxin on the Extension of Avena Coleoptile Sections

The response of Avena coleoptile sections to high concentrationsof auxin has been determined in the absence of all additivesexcept sucrose. In most experiments the growth-time curves with75 p.p.m. IAA showed two linear phases. In the first phase,which lasted for only 2–4 hours, extension was as rapidwith 75 p.p.m. IAA as with 5 p.p.m. IAA. This rapid initialexpansion phase was then succeeded by a second phase which persistedfor at least 20 hours. During this second linear phase the growth-ratewith 75 p.p.m. IAA was lower than with an auxin concentrationof 5 p.p.m. In some experiments the first phase was absent andonly the second phase was present. The response of sections to high concentrations of auxin wasnot influenced by the presence of buffers or absorbable cations.Omission of sucrose or the presence of moderate amounts of ethanolcaused the resulting growth curves to be non-linear. The rate of uptake of auxin into the tissues was dependent onthe auxin concentration and was constant for at least 24 hours.     

The Influence of Water Deficit on the Factors Controlling the Daily Pattern of Growth of Phaseolus Trifoliates

Phaseolus seedlings were grown in liquid culture under controlledtemperature and irradiance and measurements were made of dailyvariation in growth of the first trifoliate leaves. Leaf growthrate was significantly enhanced within a few hours of the startof the light period. Over a similar time, a small decrease inleaf turgor and an increase in cell wall plasticity were recorded.Slowly declining growth rates as the light period progressedmay have been caused by decreases in turgor during this time.When water availability to the leaves was restricted by growingthe plants for several days in nutrient solution maintainedat a low temperature (12°C), the daily pattern of growthof the trifoliates was changed quite markedly. Dark-growth rateswere slightly enhanced, while light-growth rates were significantlyreduced when compared to growth rates of plants well-suppliedwith water (roots at 20°C). Relative ‘plateau’growth rates of plants well-supplied (ww) with water or sufferinga restricted supply (ws) in the light (L) and in the dark (D)were as follows: ww L > ws D > ww D > ws L. In thelight, turgors of the two groups of plants were similar, suggestingthat the reduced growth rate of the cooled plants resulted froma change in cell wall structure and/or properties. Immediatelybefore the lights were switched on, plants grown with a restrictedwater supply showed relatively high turgors in the trifoliatesand these were presumably responsible for the enhanced growthrates at this time. Restriction of water availability may haveslightly increased the plasticity of cell walls and decreasedthe yield threshold for growth. The control of leaf growth inplants developing water deficit is discussed. Key words: Leaf growth turgor, Cell wall plasticity, Water deficit, Light     

Growth and Cellular Differentiation in the Wheat Coleoptile (Triticum vulgare): II. FACTORS INFLUENCING THE GROWTH RESPONSE TO GIBBERELLIC ACID, KINETIN AND INDOLYL-3-ACETIC ACID

The sequential growth response of excised wheat coleoptilesduring growth and cellular differentiation to solutions of gibberellicacid, kinetin, and indolyl-3-acetic acid is further analysedin this paper. Excised yound coleoptiles which possess a low potential growth-rate(controls) respond to gibberellic acid and kinetin, whereasexcised older coleoptiles which have a high potential growth-raterespond to indolyl-3-acetic acid. The difference between theseresults and those reported for pea-stem sections is discussed. To obtain a well-defined separation of the sequential growthresponse to gibberellic acid and kinetin it is necessary togrow the wheat coleoptiles at 22.5°C. At a higher temperature(25°C) the two optimal responses tend to overlap. It issuggested that this difference is due to a delayed onset ofcell division at the lower of the two temperatures. Substances diffusing from the primary leaves contained withinthe excised coleoptile do not interfere with the sequentialgrowth response of the coleoptile. Differential uptake of thegrowth regulators into the older coleoptiles does not explainthe lower growth response stimulated in these coleoptiles bygibberellic acid and kinetin as compared to the high activityof indolyl-3-acetic acid. The possible importance of gibberllic acid in primary cell-wallgrowth is discussed.     

The Influence of <Emphasis Type="Italic">P. fluorescens</Emphasis> Cell Morphology on the Lytic Performance and Production of Phage ϕIBB-PF7A

This study aims at assessing the influence of Pseudomonas fluorescence cell morphology on the effectiveness and production of the lytic bacteriophage ϕIBB-PF7A. P. fluorescens were cultured as rods or as elongated cells by varying the temperature and rotary agitation conditions. Cells presented rod shape when grown at temperatures up to 25°C and also at 30°C under static conditions, and elongated morphology only at 30°C when cultures were grown under agitation. Elongated cells were 0.4 up to 27.9 μm longer than rod cells. Rod-shaped hosts were best infected by phages at 25°C which resulted in an 82% cell density reduction. Phage infection of elongated cells was successful, and the cell density reductions achieved was statistically similar (P > 0.05) to those obtained at the optimum growth temperature of P. fluorescens. Phage burst size varied with the cell growth conditions and was approximately 58 and 153 PFU per infected rod and elongated cells, grown at 160 rpm, at 25°C (the optimal temperature) and 30°C, respectively. Phage adsorption was faster to elongated cells, most likely due to the longer length of the host. The surface composition of rod and elongated cells is similar in terms of outer membrane proteins and lipopolysaccharide profiles. The results of this study suggest that the change of rod cells to an elongated morphology does not prevent cells from being attacked by phages and also does not impair the phage infection.     

Studies in Abscission: I. FACTORS AFFECTING THE INHIBITION OF ABSCISSION BY SYNTHETIC GROWTH-SUBSTANCES

1. The general method is described for experimenting on applepedicelsor petioles from which the terminal organ has beenremoved.
2. Two quantitative techniques for applying growth-substancesaregiven in detail, one employing lanolin emulsion as the carrier,the other agar gel.
3. By these methods certain factors affectingthe inhibition ofabscission by the growth-substances -naphthylaceticacid (NAA)and 2:4-dichloro-phenoxyacetic acid (DPOA} have beeninvestigated. A relation between concentration of the growth-substanceandpersistence of the pedicel was established which was usuallylinear. In an experiment with NAA, for instance, the relationwas represented by— Persistence in days=6·52+0·0127xconcentrationin p.p.m.
4. The acid and the sodium salt of both NAA and DPOAgave similarresults when applied in lanolin emulsion.
5. Onboth young pedicels and young shoot internodes NAA was foundto exert a ‘formative’ influence resulting in increasein diameter which was not exhibited by DPOA to the same extent.
6. At least for concentrations of either growth-substance upto100 p.p.m., these were effective only when applied distallyto the abscission zone. At 1,000 p.p.m. there was an effectof application on the proximal side of the abscission region,but it was small compared with the effect of the same concentrationapplied distally.
7. The length of the path of the growth-substancefrom the pointof application to the abscission zone affectedthe degree ofinhibition inversely, the longer the path theless the effectof a given concentration in delaying abscission.The contrastbetween these findings for pedicels, and thoseof other authorsfor petioles, is briefly discussed.
8. A criticalperiod occurs shortly after removing the leaf-bladefrom itspetiole during which the abscission process is initiated,andto be effective in inhibiting this process growth-substancemust reach the abscission zone within this period. It is notat present established whether the pedicel shows a similar modeof behaviour.
9. A working hypothesis is given to account forthe control ofabscission by natural hormones, and extensionsare describedto embrace the results of experiments with syntheticgrowth-substances.

     

Interrelationships between Light Intensity, Temperature, and the Physiological Effects of 2: 4-Dichlorophenoxyacetic Acid on the Growth of Lemna minor

The effects of light intensity and temperature on the changesin growth and development induced by sodium 2 4-dichlorophenoxyacetatehave been studied in multifactorial experiments. Random samplesfrom a clonal population of Lemna minor were subjected to threeintensities (700, 275, and 180 foot-candles) and three temperatures(30°, 25°, and 20° C.), while varying concentrationsof the growth regulator were added to a phosphate-buffered culturesolution (pH 5:1 There were up to five sampling occasions whenthe dry weights and, for some purposes, the total frond areaswere determined. The replication was at least twofold, and thelargest experiment involved 720 dry-weight determinations. At each combination of light and temperature, sublethal concentrationsof the growth regulator induced cumulative reductions in therelative growth rate and the order of the depression increasedprogressively with concentration-3, 9, 27, and 45 p.p.m. Becauseof the cumulative effects and the great differences in the growthrates of the controls under the nine combinations of light andtemperature, the statistical analysis of the data was involved.Employing two different approaches it was concluded that therelative depression in the growth rate increased with temperaturewhile the growth of plants receiving the highest intensity wasslightly more inhibited. At a concentration (27 p.p.m.) which reduced both the relativegrowth and frond area, over all combinations of light intensityand temperature the net assimilation rate during the periodso–2 and 2–4 days was depressed by 2 and 12 per cent.respectively. There was some indication that the depressionwas larger at the highest temperature in the second period. At greatly increased concentrations the fronds exhibited chioroticsymptoms, and the concentrations required to produce a standarddegree of chiorosis at the end of 3 days were determined undertwelve combinations of light intensity and temperature. It wasfound that varying the intensity during the time of treatmentwas without effect, but that there was a highly significantinfluence of the light level prior to treatment: the lower theintensity the smaller was the concentration subsequently requiredto induce chlorosis. Likewise, with a rise in temperature themagnitude of the equi-effective concentration was reduced. These interactions are discussed in relation to changes in theratio of frond area to frond weight, the mechanism of uptake,and possible physiological effects at cell level.     

Studies on Extension Growth in Coleoptile Sections: II. The Effects of High Concentrations of {beta}-indolylacetic Acid on Section Growth

Using wheat coleoptile sections it has been shown that the treatmentgiven between cutting them from the coleoptile and placing themin the test solution greatly affects the early growth-rates. After growing sections in high concentrations of IAA for somehours it is necessary to give a considerable number of washingsto free them from surplus IAA; if these sections are then grownin water they reach lengths greater than those of comparablesections grown in water all the time, and in some cases greaterthan those attained in ‘optimum’ IAA concentrations. There is no suggestion in the experiments described that highconcentrations of IAA result in initial growth-rates higherthan those observed in ‘optimum’ concentrations,and at very high concentrations reduced early growth-rates areindicated. These results, and those described for lower IAA concentrationsin the first paper of this series, have some bearing on theapplication of the enzyme kinetic theory to auxin-induced growth,and this is considered in the discussion.     

The regulation of nitrogen accumulation in the grain of wheat plants (Triticum aestivum)

Nitrogen accumulation in the ear of wheat plants ( Triticum aestivum L. cv. Klein Chamaco) during ear growth was studied under 4 experimental conditions. Plants were grown in pots with Perlite or soil, and fertilized with nutrient solutions. In one experiment the plants were grown in a greenhouse and supplied with high (16m M ) or low (1.6 m M ) N in the nutrient solutions until anthesis, and then with or without nitrogen supply until ripening. In a second experiment the plants were grown with high N supply until anthesis, and then for half of the plants light intensity was decreased by 50%, and at the same time. N supply was terminated for half of the plants within each light treatment. A third experiment was similar to the previous one, but was carried out in a growth cabinet under 20% of the maximal irradiance in the greenhouse. In a fourth experiment half the ear was excised at anthesis in half of the plants, and these plants were then supplied with or without nitrogen.
In all experiments there was a linear relation between the rate of N accumulation and the rate of ear growth. A wide range of final individual grain weights and N concentration was observed among the experiments. The same maximum N concentration was observed for all grain sizes, although the N concentration could be different between grains of the same size. The grain N concentration correlated with the rate of N accumulation per unit of ear weight increase during ear growth. It is suggested that in wheat plants there is a dependence of nitrogen transport on carbon transport to the ear, and to the ear, and that the final grain N concentration is determined by the N/C ratio exported from the vegetative tissues.     

Cell Growth and the Structure and Mechanical Properties of the Wall in Internodal Cells of Nitella opaca: II. MECHANICAL PROPERTIES OF THE WALLS

The internodal cells of Nitella opaca L. have been used in anattempt to assess the part which mechanical properties of thewall may play in the control of cell growth. It is shown thatthe wall is mechanically anisotropic in both its plastic andelastic properties, and evidence is presented which indicatesthat this arises from its anisotropy of structure. The degreeof anisotropy is greater in cells with a high growth-rate thanin those with a low growth-rate. Evidence is presented thatthis variation in properties with growth-rate is due wholly,or in part, to changes in the orientation of the crystallinecomponent, in the relative proportion of wall constituents,and in the condition of active groups of the wall components.The findings are in harmony with the theory that extension growthof the cell wall is due to ‘creep’, i.e. disturbancesof the molecular forces within the wall leading to a slow plasticyielding to turgor pressure.     

The Effects of CO2 Enrichment and Nutrient Supply on Growth Morphology and Anatomy of Phaseolus vulgaris L. Seedlings

Plants of Phaseolus vulgaris were grown from seed in open-topgrowth chambers at the present (P, 350 µmol mol^–1)atmospheric CO₂ concentration and at an elevated (E, 700 µmolmol^–1) CO₂ concentration, and at low (L, without additionalnutrient solution) and high (H, with additional nutrient solution)nutrient supply for 28 d The effects of CO₂ and nutrient availabilitywere examined on growth, morphological and biochemical characteristics Leaf area and dry mass were significantly increased by CO₂ enrichmentand by high nutrient supply Stomatal density, stomatal indexand epidermal cell density were not affected by elevated CO₂concentration or by nutrient supply Leaf thickness respondedpositively to CO₂ increasing particularly in mesophyll areaas a result of cell enlargement Intercellular air spaces inthe mesophyll decreased slightly in plants grown in elevatedCO₂ Leaf chlorophyll content per unit area or dry mass was significantlylower in elevated CO₂ grown plants and increased significantlywith increasing nutrient availability The content of reducingcarbohydrates of leaves, stem, and roots was not affected byCO₂ but was significantly increased by nutrient addition inall plant parts Starch content in leaves and stem was significantlyincreased by elevated CO₂ concentration and by high nutrientsupply Phaseolus vulgaris, elevated atmospheric CO₂, CO₂-nutrient interaction, stomatal density, leaf anatomy, chlorophyll, carbohydrates, starch     

Alleviation of nickel toxicity by ammonium supply to sunflower plants

Phytotoxicity of nickel (Ni) varies within plant species and cultivars as well as with the concentration of Ni in the rooting medium. Moreover, it is known that several nutrients can modify the plant response to excess Ni. Nitrogen can be absorbed by plants as different N forms and because N metabolism and Ni are closely related, a hydroponic experiment was conducted to study the effect of Ni toxicity on the growth, nutrient status of the different plant parts and leaf chlorophyll concentrations in sunflower plants (Helianthus annuus L.) cv Quipu grown with different forms of N supply. The plants were grown under controlled conditions for 35 days. Depending on the N source supplied, there were significant differences in the sensitivity of sunflower plants to excess Ni. Tolerance was lowest when grown with NO₃ ⁻ alone. A high Ni and NO₃ ⁻ as the only N source resulted in reduced dry weight and significant decreases in nutrient concentration. Plants supplied with a mixture of NO₃ ⁻ and NH₄ ⁺ absorbed in the presence of Ni in solution about three times less Ni than those supplied with NO₃ ⁻ alone. Consequently, there were great differences in Ni concentrations between treatments. With a N nutrition of 100% NO₃ ⁻-N, Ni supply led to severe growth inhibition. Just contrary, simultaneous supply of NO₃ ⁻ and NH₄ ⁺ not only reduced Ni toxicity, but growth was even stimulated by Ni if supplied to plants fed with NO₃ ⁻ and NH₄ ⁺. This indicates the significant role of the N form supplied in the behaviour of Ni toxicity in sunflower plants. This revised version was published online in June 2006 with corrections to the Cover Date.     

Studies on the Growth and Respiration of Roots: I. THE EFFECTS OF STIMULATORY AND INHIBITORY CONCENTRATIONS OF {beta}-INDOLYLACETIC ACID ON ROOT SECTIONS OF PISUM SATIVUM

Simultaneous observations on extension growth and respirationrate (oxygen consumption) of 2-mm. sections excised from theextension zone of roots of pea (Pisum sativum) growing in distilledwater and 0·5 per cent. sucrose have yielded resultsclosely similar to those of Brown and Sutcliffe (1950). Respirationrate is not obviously correlated with growth rate either inwater or in sucrose, but it is strongly correlated with sectionlength. Respiration rate per unit section length (¬per unitfresh weight) shows a marked downward drift during extensionand is affected little by growth conditions. Tentative suggestionsare advanced to account for the small differences between driftsin o·5 per cent. sucrose and those in distilled water. Medium agitation produces an immediate and sustained stimulationof growth but no stimulation of oxygen uptake until the latergrowth stages. Thus respiration per unit section length is unaffectedby agitation at any stage. A typical growth response to ß-indolylacetic acid(IAA) was obtained, with a maximum stimulation (of about 35per cent.) at 1 part in 10¹¹ and inhibitions increasing progressivelywith concentration beyond the threshold of about i part in 10⁹.Both percentage stimulation and percentage inhibition of growthwere independent of the presence of sucrose. Respiratory responses to ß-indolylacetic acid werecomplex. In water no immediate response could be detected witheither a growth-stimulatory (10^–11) or a growth-inhibitory(10^–-8) concentration, while in 0·5 per cent. sucrosethe inhibitory concentration prevented the small immediate respiratoryrise due to the sucrose, probably by impeding sugar entry. Duringthe subsequent period of rapid growth (up to 36 hours) the smallrespiratory responses observed closely followed the small growthresponses to both concentrations of IAA, suggesting that theformer are the direct result of the differences in section lengthinduced by the auxin. When growth ceases (at 48 hours) sectionswhich have grown considerably in sucrose show respiratory ratesstill closely correlated with section length, whereas in waterboth concentrations of auxin induce marked depressions in respirationrate. It is concluded that ß-indolylacetic acid in bothgrowth-stimulatory and growth- inhibitory concentrations hasno direct effect on the activity of the respiratory enzyme systemof growing root cells. The small respiratory responses are bestexplained as resulting from differential changes in sectionsize and correlated changes in the enzyme complements of thegrowing cell.     

The Effect of Drugs on the Growth of Lemna minor C.

Lemna minor fronds were grown for periods of between 90 and190 days in nutrient solutions to which non-lethal doses ofone of the following drugs were added: sodium nitrite, sodiumazide, brilliant green, proflavine, propamidine isethionate,and dinitrobutyl phenol. Over these periods there was no signof any increase in the growth-rate with time, such as mightbe expected if Lemna showed adaptation to drugs similar to thatfound in micro-organisms. ‘Changeover’ experimentsshowed that the growth-rate of fronds in a drug solution wasgenerally less if they had been previously exposed to that drugthan if they had not. The sensitivity of the fronds, inducedby growth in solutions containing sodium nitrite, persistedover five to six generations of growth in nitrite-free solutions.     

Vertical and horizontal development of the root system of carrots following green manure

Cover crops grown as green manure or for other purposes will affect nitrogen (N) distribution in the soil, and may thereby alter root growth of a succeeding crop. During two years, experiments were performed to study effects of nitrogen supply by green manure on root development of carrots (Daucus carota L). Total root intensity (roots cm⁻² on minirhizotrons) was significantly affected by the green manures, and was highest in the control plots where no green manure had been grown. Spread of the root system into the interrow soil was also affected by green manure treatments, as the spread was reduced where spring topsoil N_min was high. Although N supply and distribution in the soil profile differed strongly among the treatments, no effect was observed on the rooting depth of the carrot crops. Across all treatments the rooting front penetrated at a rate of 0.82 and 0.68 mm day⁻¹ °C⁻¹ beneath the crop rows and in the interrow soil, respectively. The minirhizotrons only allowed measurements down to 1 m, and the roots reached this depth before harvest. Extrapolating the linear relationship between temperature sum and rooting depth until harvest would lead to rooting depths of 1.59 and 1.18 m under the crop rows and in the interrow soil respectively. Soil analysis showed that the carrot crop was able to reduce N_min to very low levels even in the 0.75 to 1.0 m soil layer, which is in accordance with the root measurements. Still, where well supplied, the carrots left up 90 kg N ha⁻¹ in the soil at harvest. This seemed to be related to a limited N uptake capacity of the carrots rather than to insufficient root growth in the top metre of the soil. This revised version was published online in June 2006 with corrections to the Cover Date.     

Regulation of poly(β-hydroxybutyrate) synthesis in Methylobacterium rhodesianum MB 126 growing on methanol or fructose

The intracellular concentration of CoA metabolites and nucleotides was determined in batch cultures of Methylobacterium rhodesianum grown on methanol and shifted to growth on fructose. The intracellular concentration of CoA decreased from a high value of 0.6 nmol/mg poly(β-hydroxybutyrate)-free bacterial dry mass during growth on methanol to a low value of 0.03 nmol/mg poly(β-hydroxybutyrate)-free bacterial dry mass after a shift to fructose as a carbon source. The levels of NADH, NADPH, and acetyl-CoA were also lower. Under these conditions, acetyl-CoA was metabolized by both citrate synthase and β-ketothiolase, and poly(β-hydroxybutyrate) synthesis and growth occurred simultaneously during growth on fructose. Moreover, the level of ATP was approximately 50% lower during growth on fructose, supporting the hypothesis of a bottleneck in the energy supply during the growth of M. rhodesianum with fructose. Received: 15 July 1997 / Accepted: 10 November 1997