Distribution and redistribution of sulphur taken up from nutrient solution during vegetative growth in barley

Barley plants were grown in a nutrient solution containing 25 μ M sulphate and the roots were pulsed with [³⁵S]sulphate for 48-h periods at 6 different times between the emergence of leaf 5 (L5) and the emergence of leaf 8 (L8). Growth was continued in unlabelled solution until the emergence of L10. Within the shoot system sulphur was directed principally into the leaf undergoing expansion. A large proportion of the ³⁵S-label delivered to young expanding leaves (> 40% of full expansion) did not occur at the time of the pulse, but subsequently during the ensuing chase indicating slow redistribution of sulphur from another site. During the later stages of leaf expansion (40–100%), most of the sulphur entered the leaf during the pulse, suggesting that sulphur was delivered more directly from the nutrient solution. Up to 75% of the sulphur delivered to L3–L6 at the time they approached or attained full expansion (70–100%) was re-exported. At least some of the sulphur exported from fully expanded leaves was redistributed to developing leaves.     

Inhibition of sulphur redistribution into new leaves of vegetative soybean by excision of the maturing leaf

When soybean plants are pulsed with [³⁵S]sulphate, label is subsequently redistributed from the roots to the leaves. This confounds studies to measure the redistribution of label from leaves. Accordingly, soybean plants ( Glycine max [L.] Merr. cv. Stephens) were grown in 20 μ M sulphate and a small portion of the root system (donor root) was pulsed with [³⁵S]sulphate for 24 h. After removing the donor root, the plants were transferred into unlabelled solution, either without sulphate (S20→SO) or with 20 μ M sulphate (S20→20) (intact plants). Also at this time, the expanding leaf (L3) was excised from half of the plants in each treatment (excised plants). Immediately after the pulse, only ca 15% of the label occurred in the roots and ca 40% in the expanding leaf, L3, mostly in the soluble fraction. In intact S20→20 plants, ³⁵S-label was exported from the soluble fraction of L3, mostly as sulphate, whilst L4 and L5 imported label. Similar responses occurred in S20→SO plants except that export of label from L3 was more rapid. Excision of L3 from S20→S20 plants inhibited labelling of leaves L4-L6 but not total sulphur, whereas in S20→SO plants, excision of L3 inhibited the import of both total sulphur and ³⁵S-label in leaves L4, L5 and L6. The data suggest that the soluble fraction of almost fully expanded leaves is an important reserve of sulphur for redistribution to growing leaves. The ³⁵S-label in the root system exhibited fluctuations consistent with its proposed role in the recycling of soluble sulphur from the leaves.     

Effect of nitrogen nutrition on the export of sulphur from leaves in soybean

Soybean plants were grown in complete solution for 33 days and then transferred to medium containing inadequate sulphur (5 t M) and nitrogen at 15, 7.5, 2 or 0.25 mt M. In mature leaves (L1 and L2), and leaves that were 70% expanded at day 33 (L3), the net loss of sulphur over the ensuing 25 days was inversely related to the level of nitrogen nutrition. Leaf 5, which formed during the study period, exhibited complementary characteristics; the increase in the sulphur content was inversely related to the level of nitrogen nutrition even though low nitrogen nutrition supported less growth. L4, which was 31% expanded at day 33, exhibited intermediate characteristics. 35S-Labelled sulphate was supplied to all of the plants for 48 h at day 31 and was distributed principally to L3 at day 33. During early development, L5 became heavily labelled but, at low nitrogen nutrition, the massive import of total sulphur into L5 during the late stages of development was not accompanied by a commensurate increase in 35S-label, indicating that redistribution of soluble sulphur from mature leaves was not involved. The loss of sulphur from mature leaves was parallelled by similar changes in nitrogen at all levels of nitrogen nutrition. Collectively, the data suggest that a common mechanism, presumably proteolysis, is involved in the export of sulphur and nitrogen from mature leaves and that this process is inhibited at high levels of nitrogen nutrition, even under conditions of sulphur deficiency.     

Patterns of carbon allocation above ground in a deciduous (Vaccinium uliginosum) and an evergreen (Vaccinium vitis-idaea) dwarf shrub

The carbon allocation to current-year shoots of the deciduous Vaccinium uliginosum L. and the evergreen V. vitis-idaea L. was studied in a field experiment using ¹⁴C. During the first week after labelling, 0–50% and 30–80% of the initially assimilated ¹⁴C was lost in V. vitis-idaea and V. uliginosum respectively. Later on, the losses were smaller. After leaf fall in V. uliginosum , 30, 10 and 8% of the initially assimilated ¹⁴C was recovered in the abscised leaves, in plants labelled 1 July, 1 August and 1 September, respectively. The amounts found in the old V. vitis-idaea leaves the year after labelling were 33, 20 and 10%. Only traces of past-year assimilates were found in the current-year V. vitis-idaea leaves, while it was estimated that the V. uliginosum leaves contained 10–15% of the past-year label. It is concluded that V. vitis-idaea is mainly dependent on early summer assimilates - produced by leaves that have overwintered – for the current year shoot growth, while past-years' assimilates probably make an important contribution to the leaf expansion in V. uliginosum. When fruits occurred, a large fraction of the ¹⁴C assimilates was allocated to them.     

Sulphur accumulation and redistribution in wheat (Triticum aestivum): a study using stable sulphur isotope ratios as a tracer system

Wheat plants were grown hydroponically and fed with two sulphate sources differing in stable isotope composition, one having a δ ³⁴S of 13·7‰ and the other 4·1‰. Plant sulphur (S) isotope ratios were determined using an on-line continuous flow-isotope ratio mass spectrometer. This method greatly simplified the procedure for the measurement of S isotope ratios, and was found to be precise for samples containing > 1 mg S g^–1 dry weight. The δ ³⁴S values of plant shoots, which had been grown on a single sulphate source, were very close to the source values, suggesting little isotope fractionation during sulphate uptake and transport from roots to shoots. By changing the sulphate sources at different growth stages, it was possible to estimate S accumulation and redistribution within different plant parts. At maturity, wheat grain derived 14, 30, 6 and 50% of its S from the accumulation during the following successive growth stages: between emergence and early stem extension, between stem extension and flag leaf emergence, between flag leaf emergence and anthesis, and after anthesis, respectively. It was estimated that 39, 32 and 52% of the S present in the flag leaves, older leaves and stems, respectively, at anthesis, was exported during the postanthesis period. These results demonstrate considerable cycling of S within wheat plants, and highlight the importance of S uptake after anthesis to the accumulation of S in grain under the experimental conditions employed.     

De novo shoot morphogenesis and plant growth of mustard (Brassica juncea) in vitro in relation to ethylene

Role of ethylene in de novo shoot morphogenesis from explants and plant growth of mustard ( Brassica juncea cv. India Mustard) in vitro was investigated, by culturing explants or plants in the presence of the ethylene inhibitors aminoethoxyvinylglycine (AVG) and AgNO₃. The presence of 20 μ M AgNO₃ or 5 μ M AVG in culture medium containing 5 μ M naphthaleneacetic acid and 10 μ M benzyladenine were equally effective in promoting shoot regeneration from leaf disc and petiole explants. However, AgNO₃ greatly enhanced ethylene production which reached a maximum after 14 days, whereas ethylene levels in the presence of AVG remained low during 3 weeks of culture. The promotive effect of AVG on shoot regeneration was overcome by exogenous application of 25 μ M 2-chloroethylphosphonic acid (CEPA), but AgNO_3-induced regeneration was less affected by CEPA. For whole plant culture, AVG did not affect plant growth, although it decreased ethylene production by 80% and both endogenous levels of 1-aminocyclopropane-1-carboxylate (ACC) synthase and ACC by 70–80%. In contrast, AgNO₃ stimulated all 3 parameters of ethylene synthesis. Both AgNO₃ and CEPA were inhibitory to plant growth, with more severe inhibition occuring in AgNO₃. Leaf discs derived from plants grown with AVG or AgNO₃ were highly regenerative on shoot regeneration medium without ethylene inhibitor, but the presence of AgNO₃ in the medium was inhibitory to regeneration of those derived from plants grown with AgNO₃.     

Influence of spectral quality on the growth response of intact bean plants to brassinosteroid, a growth-promoting steroidal lactone. II. Chlorophyll content and partitioning of assimilate

The chlorophyll content and partitioning of assimilate of bean ( Phaseolus vulgaris L. 'Pinto') plants were determined 6 days after treatment of the second internode (I₂ with 5 μg of brassinosteroid (BR), a growth-promoting steroidal lactone. Plants were grown for 6 days under equal levels (90 μmol s^-1 m^-2) of photosynthetic photon flux density (PPFD) provided by cool white fluorescent (CWF) or incandescent (INC) lamps and equal levels of far-red (28 W m^-2, 700–800 nm) radiation provided by the same INC or far-red (FR) fluorescent lamps. Brassinosteroid treatment had no appreciable effect on total biomass production but caused a decrease of 15–20% dry matter distribution in the upper portion of the shoot, a small (4%) but constant increase in dry matter in l₂ and a large (11–16%) increase in dry matter in the lower portion of the shoot (especially I₁). Treatment with BR increased assimilate accumulation in the primary leaves, especially under INC and FR lamps, and reduced dry matter in the trifoliate leaves. BR also caused a 16–21% reduction in total leaf area and even a greater reduction in area of the trifoliate leaves, but significantly increased specific leaf weight of the primary leaves and the first trifoliate leaf and the amount of dry matter in the lateral shoots under all radiation sources. In comparison to controls, BR treatment increased dry matter accumulation in the treated internode 3.3x under CWF and 1.6x under INC or FR. BR treatment also increased chlorophyll content in the primary leaves under all radiation sources and in the trifoliate leaves under CWF and INC lamps. These findings suggest a possible mobilization role of BR and establish the importance of adequate PPFD (and photosynthate) for maximum swelling and splitting response to brassinosteroid.     

Cessation of assimilate uptake in maturing soybean seeds

In vitro assimilate uptake and metabolism were evaluated in embryos of known age isolated from seeds at mid-podfilling through physiological maturity. The capacity of isolated Wye soybean embryos to take up exogenous [¹⁴C]sucrose dropped nearly 4-fold in less than 1 week at incipient cotyledon yellowing. This drop in rate of sucrose uptake coincided with cessation of seed growth as well as rapid decline in leaf photosynthetic rate that preceded leaf yellowing. Conversely, the rate of [³H]glutamine uptake by cotyledons increased as they yellowed. Yellow cotyledons also rapidly converted exogenous [³H]glutamine to ethanolinsoluble components, but converted little exogenous [¹⁴C]sucrose to ethanol-insoluble components, primarily because of greatly reduced sucrose uptake. Sustained import and metabolism of amino acids remobilized from senescing leaves may prolong seed growth beyond loss of photosynthetic competency and sucrose availability.     

Pea seedling growth and development regulated by cotyledons and modified by irradiance

Growth and development of hydroponically grown pea seedlings ( Pisum sativum L. cv. Alaska) were measured using stem and root length as well as number of leaves and lateral roots. The growth was dependent on the presence of cotyledons and was modulated by the irradiance. All plants were grown in a full nutrient solution. If grown at low irradiance (73 μmol m^-2s^-1) they depended more and for a longer time on the cotyledons than plants grown at high irradiance (220 μmol m^-2s^-1). Low irradiance caused stem elongation but decreased root length and number of lateral roots as compared to plants grown at high irradiance. The dark respiration of the leaves was measured as oxygen uptake. In plants grown at the low irradiance, excision of the cotyledons caused the rate of oxygen uptake to increase by a factor of three, and the increase was sensitive to cyanide. Decotyledonized plants showed a high respiration rate and a diminished leaf growth for their entire life cycle. CO₂ fixation also increased in decotyledonized pea seedlings grown at either irradiance. The mobilization of food reserves from the seeds was positively correlated to seed dry weight, but only if the plants were grown at 73 μmol m^-2s^-1. Increasing dry weight of the seed enhanced top growth, whereas root growth was depressed, so that top and root responds differently with regard to that part of growth which depends on mobilization of reserves from the seed.     

Phosphorus translocation in salt-stressed cotton

The effect of salinity on plants has usually been studied at high inorganic P concentration ([Pi]) in the nutrient solution, and salinity × Pi interactions have been examined at much higher [Pi] than found in soil solutions. Short-term ³²Pi experiments were carried out to study the effect of salinity (150 m M NaCl) on phosphorus translocation in cotton plants ( Gossypium hirsutum L. cv. Acala SJ-2) grown in nutrient solutions containing 10 μ M [Pi]. The effect of additional Ca to a concentration of 10 μ M was also tested. Salinity inhibited ³²P translocation from root to shoot. This inhibition was more evident at higher [Pi] in the root medium. Increasing [Pi] 33-fold in the solution resulted in a 4.3-fold increase in [³²P] in the root under saline conditions, but only in a 1,8-fold increase in the shoot. In older shoot tissues total [P] was elevated in the salinized plants. In the young tissues, however, total P concentration was higher in control plants. Inhibition of ³²P translocation by salinity was greater from root to young leaves than to mature shoot tissues. Salinity also decreased ³²P recirculation from the cotyledons to the young leaf. Inhibition by salinity of both ³²P translocation and recirculation to young leaves was fully reversed by increasing Ca supply from 1 to 10     

Growth, dry matter partitioning, and diurnal activities of RuBP carboxylase in citrus seedlings maintained at two levels of CO2

The long-term response of citrus rootstock seedlings to CO₂ enrichment was examined in Carrizo estrange ( Poncirua trifoliata (L.) Raf. x Citrus sinensis (L.) Osbeck] and Swingle citrumelo ( P. trifoliate x C. parodist Macf.]. Plaotlets 14 weeks old were transferred to outdoor controlled-environment chambers and maintained for 5 months from Feb. 14 to July 21. During this period, new growth (cm) of citrange and citrumelo shoots at 660 μl1⁻¹ was 94 and 69% greater, respectively, than at 330 μ1 1⁻¹. Total dry weight of both rootstock shoots had increased by over 100%. Growth of few species is affected this markedly by elevated CO₂ levels.
More carbon was partitioned to above-ground organs in CO₂-enriched citrus seedlings. Stem dry matter per unit length was also 32 and 44% greater in citrange and citrumelo, respectively. Total leaf area was increased by 124% in citrange and 85% in citrumelo due to greater leaf number and size. Variations in overall relative growth rate appeared to be related to the rapid, sequential, flush-type growth in citrus, in which an entire shoot segment with its associated leaves remains an active sink until fully expanded. RuBP carboxylase (EC 4.1.1.39) activity in leaves of recently-expanded flushes was higher in citrumelo plants grown at 660 vs 330 μ1 1⁻¹ CO₂ and changed diurnally for citrange (but not citrumelo) leaves at both CO₂ levels. The results are consistent with the hypothesis that positive long-term effects of CO² enrichment may be greater in species or during growth periods where sink capacity for carbon utilization is high.     

Stomatal and photosynthetic responses to shade in sorghum, soybean and eastern gamagrass

We studied photosynthetic and stomatal responses of grain sorghum ( Sorghum bicolor [L.] Moench cv. Pioneer 8500), soybean ( Glycine max L. cv. Flyer) and eastern gamagrass ( Tripsacum dactyloides L.) during experimental sun and shade periods simulating summer cloud cover. Leaf gas exchange measurements of field plants showed that short-term (5 min) shading of leaves to 300–400 μmol m⁻² s⁻¹ photosynthetic photon flux density reduced photosynthesis, leaf temperature, stomatal conductance, transpiration and water use efficiency and increased intercellular CO₂ partial pressure. In all species, photosynthetic recovery was delayed when leaves were reilluminated, apparently by stomatal closure. The strongest stomatal response was in soybean. Photosynthetic recovery was studied further with soybeans grown indoors (maximum photosynthetic photon flux density 1 200 μmol m⁻² s⁻¹). Plants grown indoors had responses to shade similar to those of field plants, except for brief nonstomatal limitation immediately after reillumination. These responses indicated the importance of the light environment during leaf development on assimilation responses to variable light, and suggested different limitations on carbon assimilation in different parts of the soybean canopy. Photosynthetic oxygen evolution recovered immediately upon reillumination, indicating that the light reactions did not limit soybean photosynthetic recovery. While shade periods caused stomatal closure and reduced carbon gain and water loss in all species, the consequences for carbon gain/water loss were greatest in soybean. The occurrence of stomatal closure in all three species may arise from their shared phenologies and herbaceous growth forms.     

Leaf age-dependent differences in sulphur assimilation and allocation in poplar (Populus tremula x P. alba) leaves

35S-sulphate was flap-fed to poplar leaves of different leaf development stages - young developing, expanding, mature, and old mature poplar leaves. (35)S-sulphate was taken up independent of the leaf development stage. Whereas young development leaves did not export the (35)S taken up, export increased with increasing leaf development stage. Expanding leaves allocated the exported (35)S mainly into apical tree parts (73-87%) and only to a minor extent (13-27%) in basipetal direction. Neither lower trunk sections nor the roots were sinks for the exported (35)S. Expanding and developing leaves, but not the shoot apex, were the main sinks for the (35)S allocated in apical direction. In contrast, mature and old mature leaves exported the (35)S taken up mainly in basipetal direction (65-82%) with the roots constituting the main sinks. The (35)S allocated into apical tree parts was found in expanding and developing leaves, but only to a minor extent in the shoot apex. Apical allocated (35)S was identified as sulphate. Apparently the demand of young developing leaves for reduced sulphur was not fulfilled by mature leaves. Therefore, reduced sulphur for growth and development of young developing leaves must be supplied from other sources. In vitro activity of enzymes involved in assimilatory sulphate reduction was measured to investigate whether demand for reduced sulphur by young leaves is met by their own sulphate reduction. ATP sulphurylase and APS reductase activities were not significantly lower in developing than in mature leaves. Sulphite reductase and serine acetyltransferase activities were highest in developing leaves; O:-acetylserine (thiol) lyase activity was similar in all leaf developing stages. Apparently, young developing poplar leaves are able to produce their own reduced sulphur for growth and development. Whether other sources such as storage tissues and/or roots are involved in reduced sulphur supply to developing leaves remains to be elucidated.     

Responses of apple leaf stomata to environmental factors

Abstract. Stomatal conductances ( g _s) were measured on the leaves of 3–4 year old Golden Delicious trees and of seedlings of two other cultivars. Measurements were made on container grown trees in the field with a diffusion porometer in 1975 and 1976, and in controlled conditions in a leaf chamber in the laboratory in 1976. Stomatal densities in the Golden Delicious leaves were assessed from scanning electron micrographs. Stomatal density on extension shoot leaves was higher than on other leaf types after June.
The response to irradiance shown by both the porometer and the leaf chamber results could be described by a rectangular hyperbola: where g _max is maximum conductance and β indicates the sensitivity of g_s to photon influx density ( Q _p). The values of β were in the range 60–90 μmol m⁻² s⁻¹.
There was no evidence that apple stomata are sensitive to temperature per se, but g _s was reduced by increasing leaf to air vapour pressure deficits ( D ). There was a linear relationship between g _s and D which was not attributable to feed-back to leaf water potential (ψ_L) as the latter did not affect g _s until a threshold of about −2.0 to −2.5 MPa was reached. Conductance generally declined with increasing ambient CO₂ concentration.     

Controlling plant growth via the gibberellin biosynthesis system – I. Growth parameter alterations in apple seedlings

'York Imperial' apple seedlings ( Malus domestica Borkh.) were continuously supplied via the roots with paclobutrazol [(2RS, 3RS)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol)], a triazole GA biosynthesis inhibitor, at 0.68 μ M in a nutrient solution. In comparison to controls, seedlings treated with paclobutrazol for 66 days showed a 91% reduction in shoot length, a 66% reduction in leaf area but only a 17% reduction in leaf number. This effect could be reversed by GA₃ applied to the foliage at 71.4 μ M 0, 19 or 35 days after paclobutrazol was initially supplied and leaf area values for paclobutrazol-treated seedlings given both treatments did not differ significantly from controls. Plots of growth data indicate linearity of shoot longitudinal growth of GA₃-treated seedlings. Leaf area increase was non-linear after GA₃ treatment up to approximately 30 days, when the rate dropped. On a per shoot basis, leaf weight closely followed leaf area but on a per unit area basis, paclobutrazol-treated leaves were heavier than controls; GA₃ applications temporarily reversed this trend.     

Effects of zinc toxicity on sugar beet (Beta vulgaris L.) plants grown in hydroponics

The effects of high Zn concentration were investigated in sugar beet ( Beta vulgaris L.) plants grown in a controlled environment in hydroponics. High concentrations of Zn sulphate in the nutrient solution (50, 100 and 300 μ m ) decreased root and shoot fresh and dry mass, and increased root/shoot ratios, when compared to control conditions (1.2 μ m Zn). Plants grown with excess Zn had inward-rolled leaf edges and a damaged and brownish root system, with short lateral roots. High Zn decreased N, Mg, K and Mn concentrations in all plant parts, whereas P and Ca concentrations increased, but only in shoots. Leaves of plants treated with 50 and 100 μ m Zn developed symptoms of Fe deficiency, including decreases in Fe, chlorophyll and carotenoid concentrations, increases in carotenoid/chlorophyll and chlorophyll a / b ratios and de-epoxidation of violaxanthin cycle pigments. Plants grown with 300 μ m Zn had decreased photosystem II efficiency and further growth decreases but did not have leaf Fe deficiency symptoms. Leaf Zn concentrations of plants grown with excess Zn were high but fairly constant (230–260 μg·g⁻¹ dry weight), whereas total Zn uptake per plant decreased markedly with high Zn supply. These data indicate that sugar beet could be a good model to investigate Zn homeostasis mechanisms in plants, but is not an efficient species for Zn phytoremediation.     

On Donor–Acceptor Relations and Growth Correlation in Shoot Development of the Pedunculate Oak Germling

We studied the first cycle of shoot growth of the Quercus robur L. germlings in which the donor–acceptor relations were changed by removing a part of cotyledons, growing in darkness, or removing growing leaf blades. In all cases, the greatest changes in growth and growth correlations were observed in the shoot upper metameres carrying leaf blades and the least, in lower metameres preformed in the acorn embryo. The removal of growing leaves changed the rhythm of shoot growth.     

Effect of irradiance and plant age on the dimensions of the growing shoot of poplar

Populus euramericana (Dode) Guinier cv. Robusta plants were cultivated at irradiances of 7.5, 15 and 30 W m⁻² (32.5, 65 and 130 μmol m² s⁻¹), 400–700 nm at 22°C and a relative humidity between 40 and 60% on a gravel culture subirrigated with Hoagland's nutrient solution. The basal diameter of the growing shoot, a measure of the number of apical cells participating in growth, increased proportionally to irradiance and was correlated with mature leaf length. The development of the length of the growing shoot (L_gs) depended also on the nutritional status of the (young) shoot. L_gs was strongly correlated with the rate of height growth.     

Effects of exogenously applied growth regulators on shoot growth of inbred lines of Plantago major differing in relative growth rate: differential response to gibberellic acid and (2-chloroethyl)-trimethyl-ammonium chloride

The possibility of modulating shoot growth charaeteristics of seedlings of two inbred lines of Plantago major L., differing in relative growth rate (RGR), by exogenously applied 6-benzylaminopurine (BA), α-naphthalene acetic acid (NAA), (gibberellic acid (GA₃) and (2-chloroethyl)-trimethyl-ammonium chloride (CCC) was investigated. BA completely inhibited growth of the shoot at a concentration of 1 m M , while lower concentrations had no effect. NAA reduced growth of the shoot at 10 ü M , while 1 m M completely inhibited growth. Addition of 10 μ M GA₃ or higher stimulated shoot fresh weight up to 20% and leaf area up to 30% for the slow growing inbred line (W9), but less for the fast growing line (A4). Application of 1 m M CCC, an inhibitor of gibberellin metabolism, reduced growth of both inbred lines, but to a larger extent in the fast growing seedlings.
The lower shoot growth of W9 was associated with a lower specific leaf area (SLA) and a higher dry matter percentage of the shoot, as compared with A4. NAA reduced growth by reducing SLA and increasing leaf thickness, but the percentage dry matter of the leaves was unaffected. Stimulation of the shoot growth by GA₃ application was associated with higher SLA and lower dry matter percentage. Application of CCC had opposite effects on SLA and dry matter percentage as compared with GA₃. GA seems to be involved in the regulation of at least part of the genetic difference in RGR in Plantago major .     

A developmental study of Glycine max cell and protoplast isolation in relation to leaf age and photosynthetic competence

Leaf mesophyll cells were isolated from developing first trifoliate leaves of Glycine max (L.) Merr cv. Fiskeby V using a mechanical isolation procedure combined with low speed centrifugation. Cell yields of 17 ± 1.7% were routinely obtained with 55–75% intactness, as assessed by staining techniques, fluorescence transients and the ability of cells to convert to protoplasts after enzyme treatment. Rates of leaf photosynthesis were maximal in 27-day-old plants [280 μmol O₂ evolved (mg chlorophyll)^-1h^-1], from which isolated cells and protoplasts gave rates of up to 140 μmol O₂ evolved (mg chlorophyll)^-1 h^-1. Results are discussed in relation to leaf development and cell status during the attainment of photosynthetic competence.