Four tree, five shrub, and ten herbaceous species growing naturally in an oak-hornbeam forest were used for simultaneous study of the leaf diffusive resistances in the course of several summer days. Absolute minima of the stomatal resistance in the sun tree, the shrub, and the herbaceous species leaves were 1.7 to 6.2 s cm^-1, 6.1 to 10.8 s cm^-1, and 4.8 to 9.7 (17.3 inConvallaria majalis leaves) s cm^-1, respectively. Minimum daily leaf resistances in the course of a day were noted earlier in the morning in sun leaves of large trees than in shade leaves of other species. Stomata were fully opened later in the morning and they began to close sooner in the afternoon in usual shade leaves of the plants in the interior of the forest canopy than those in sun leaves in active surfaces of the canopy (tops of tree crowns). The relatively large differences in leaf resistances found among investigated species may be explained by differences in leaf anatomy (stomata frequency and size) and in ambient leaf or plant environment caused by leaf (plant) position in different vertical layers.

Gmelina arborea L. seedling growth and diurnal stomatal opening (as measured by stomatal resistance) were studied at soil matric potential 0, -0.1 and -0.72 × 10^-5 Pa. Leaf area, leaf number, plant height and dry weights of the vegetative parts were significantly reduced as soil matric potential decreased from 0 to -0.72 × 10^-5 Pa. The growth responses followed the same trend as net assimilation rate and relative growth rate. The highest moisture stress induced leaf senescence and leaf fall. Leaf water potential decreased from - 2 × 10^-5 Pa to - 20 × 10^-5 Pa with increasing soil moisture stress. Results indicate that the diurnal stomatal opening is controlled by photon flux density when this species is grown at soil matrio potential 0 Pa. However, with decreasing soil matrio potential (- 0.10 and -0.72 × 10^-5 Pa) the internal plant water deficit appears to oontrol the stomatal opening.

Apparent photosynthesis (P_n) and root respiration (R_n) of 8 to 10 d old intact bean plants were studied separately at different temperatures and oxygen concentrations acting on the roots using IRGA technique. P_n is reversibly decreasing during 3 h root cooling (+ 5 °C) in accord with bending down of the primary leaves, and closing of the stomata. Plants adapted to low root temperatures show no effect of increasing the latter on P_n. Even 3 h oxygen deficit in the root medium has no influence on P_n but is increasing R_r in consequence of alteration in ' metabolism from respiration to fermentation. One must distinguish between short time reaction and long time adaptation of the plant on root stress.

The nutational movements performed by the leaves of the "Sensitive plant",Mimosa pudica L., result from periodical turgor variations taking place in the parenchymatous cells of specialized motor organs. The trajectories in the three kinds of leaf motor organs usually show irregular elliptical paths with a period ranging from 10 to 60 min. The morphological analogy of these turgor movements is discussed in relation to nutational movements observed in growing organs.

The area ofPlectranthus fructicosus leaves of different origin and cultivation (seedlings, vegetatively propagated plants from growth chambers with different climates, isolated rooted leaves) fitted in average the equationA=L B k. The coefficientk, however, varies during the ontogenesis of the leaves and the plant according to changes in leaf shape from 0.865 to 0.642.

Kinetin at a concentration from 3.10^-6 M to 1.10^-3 M was applied to the plumule ofChenopodium rubrum plants during photoperiodic induction. Different levels of induction were compared (one and three short days). The higher concentrations of kinetin applied to induced plants inhibited flower formation. The rate of leaf initiation was increased under these treatments. Lower concentrations of kinetin (from 3.10^-6 M to 1.10^-5 M) usually promoted lateral bud formation and flowering. The step-wise application of kinetin revealed that the inhibitory effect on flowering had been restricted to the inductive period.
The effects of kinetin, benzyladenine and trans-zeatin were compared in plants partially induced by two short days. High concentrations always inhibited flowering. Benzyladenine was the most effective in this respect.
Root removal diminished the inhibitory effects of cytokinins on flowering as was stated with benzyladenine.
It is assumed that endogenous cytokinins play a role in the regulation of organogenetic activity of the stem apical meristem. Depending on the photoperiodic conditions, they presumably exert their activity by maintaining the vegetative functions of the apex.

Studies performed on winter rape plants(Brassica nnpus var.oleifera, cv. 'Gór-czański') revealed that cold treatment affected the cell membranes and led to the temporary increase in electrolytic leakage from a tissue. This was followed by the marked decrease of the electrolytic leakage in the course of hardening. Changes in membrane properties were accompanied by the promotion of soluble protein accumulation. Inhibition of protein accumulation by the cycloheximide treatment brought about wilting of plants under cold conditions. Possible role of soluble protein in protection of cells against secondary water stress caused by the coldinduced changes in membrane properties is suggested. Cold-induced changes in the electrophoretic pattern of soluble protein are described and discussed.

The biosynthesis of L-tryptophan (L-trp) from anthranilic acid-¹⁴C (AA-¹⁴C) in. undamaged organs of the seedlings of kohlrabi and pea, with high L-trp content and ma ze plants, with low L-trp content was compared. As for maize the experiments were carried oiut with normal and opaque-2 phenotypes, both with the seedlings and with the ripening kernels. AA-¹⁴C is metabolized in the plants to L-trp pool (i.e. free and bound L-trp, and secondary metabolites) and to glycosyl esters of AA (i.e. to simple glucosyl ester in pea and kohlrabi and more complex glycosides in maize). In maize seedlings L-trp-¹⁴C is synthesized relatively less. (40% in the 1st and 2nd leaf and 33% in the 3rd leaf of the total radioactivity of the incorporated AA-¹⁴C is transferred into the L-trp-¹⁴C pool after 24 h) than in kohlrabi (52% in the hypocotyl and 85% in the cotyledons) and in pea (58% in the 1st and the 2nd internode and 85% in the 3rd and the 4th internode). Thede novo formation of L-trp-¹⁴C is stoped earlier in maize (after 5 h) than in kohlrabi (after 15 h). The level of free L-trp-¹⁴C is relatively low ill maize (15% and 13% of the total radioactivity of the incorporated AA-¹⁴C is converted to free L-trp-¹⁴C and remains in this form after 24 h) in comparison with kohlrabi (31% and 60%) and pea (30% and 49%). In spite of this the formation of L-trp-¹⁴C from AA-¹⁴C is sufficient in maize to incorporate L-trp both into the proteins and into a secondary metabolite that is not yet defined. At the period of seedlings the incorporation in maize of L-trp into the proteins (11% and 10% of the activity of the incorporated AA-¹⁴C) is comparable with that in kohlrabi (11% and 17%), and it is maximum in pea (29% and 36%). Maize, at the stage of germination, thus forms proteins rich in L-trp. The formation of free L-trp is approximately ten times lower in ripening kernels and in the leaves adjacent to the ear and it further decreases in the course of the ripening of the kernels. Although the activity of the biosynthesis of the AA-¹⁴C → L-trp-¹⁴C pathway is relatively lower in maize than in kohlrabi and pea, this pathway is most responsible for the differences in the content of L-trp in these plants.
Neither amitrol nor histidine affected the biosynthesis of L-trp in kohlrabi; the interaction of the biosynthetic pathways of L-trp and histidine known in microorganisms is thus not important in a higher plant.

In two branched plants ofImpatiens balsamina with intact apex and leaves floral buds are induced only in the branch which is either exposed to 8-h (inductive) photoperiods or receives GA₃ treatment if maintained under 24-h (non-inductive) photoperiods. GA₃ induces floral buds on the treated branch even if the leaves on that branch are removed, showing that while leaves are essential for photoperception, these are not neoessary for GA₃ to cause induction. The effect of the inductive photoperiods or GA₃ treatments to a branch is not transmitted to the other branch which is treated with water and is maintained under non-inductive photoperiods even when the latter is defoliated but is transmitted if the apioal or both the apical and axillary buds on the branch receiving inductive photoperiods or GA₃ treatment are excised. It, therefore, appears that the existence of strong sinks in the form of axillary and apical buds on the treated branch prevents the transmission of photoperiodic as well as GA₃ effects to the other branch in this plant.

This work is a study on the presence of free and bound (mainly proteins) amino acids at the levels of both the individual plants and the producers of a phryganic ecosystem. Therefore the amount of free and bound amino acids (both quantitatively and qualitatively) is determined during two seasons. As far as the producers (green plants) at the ecosystem level are concerned, the amount of free and bound amino acids was determined for both the above ground (stems, leaves) and the below ground (roots) parts during an annual period. On the basis of the above mentioned measurements it was found that, in a year, 17 and 4 g.m~²of bound and free amino acids are produced, respectively. A percentage of about 50% of this quantity remains in the plants, as their annual growth, and the rest returns to the soil because of the litter and root turnover. The model of their flow in the ecosystem was formed considering also data from plant physiology.

The content and distribution of nitrogen substances in wheat, pumpkin and pea seedlings in complete (NS) or deficient ( - Ca²⁺ or - K⁺) nutrient solutions were studied with the aim of establishing whether impairments in the synthesis of nitrogen substances in vegetative tissues due to the deficiencies may be compensated for by storage nitrogenous substances. Pumpkin and pea seedlings were found to accumulate nitrogen mainly from depots of the seed stores. Both the accumulation and the synthesis of nitrogen substances were inhibited by the cation deficiencies, especially by that of calcium. Concomitant morphological deformations were probably the direct cause of the impairments in the mobilization and hence also in the utilization of the substances. With wheat, on the other hand, no morphological changes resulted from the deficiences and nitrogen was accumulated intensively even from the cultivation solution. Still, the rate of the synthesis of the nitrogenous substances was significantly reduced. Under the conditions of calcium or potassium deficiency in the outer nutrient solution the possibility or utilizing the ions from the storage tissues according to the requirements of the plant appeared to be decisive. The extent of the disproportion of the two factors was the original cause of the early morphological changes which, in their turn, impaired the natural circulation of substancs inside the organism, including the substances containing nitrogen.

The growth of callus tissue cultures and the infectivity of twenty fiveSolanum laciniatum Ait. plants and of sixteenNicotiana tabacum L. cv. Samsun plants were investigated. The plants were obtained from callus tissue cultures derived from stem pieces of the respective plants infected with a mycoplasma-like organism (MLO) evoking potato witches' broom. The tissues were cultivated on synthetic nutrient medium with kinetin and IAA. Allde novo obtainedS. laciniatum plants were healthy. On the contrary twelve of the sixteen reconstituted tobacco plants showed MLO presence.
Summarizing these and previous results, the authors suppose that the most important factor influencing MLO persistence in callus tissues cultivated on the applied nutrient medium may be the callus growth rate and the organogenesis set. Both these conditions are determined by the metabolism of the investigated plant species.

The effect was studied of chloride ions, added in the form of different salts, on nitrate reductase (NR) level in excised pea roots, on anaerobic nitrite production in an assay medium lacking both nitrate and n-propanol, on nitrate content in the roots, and on in vivo NR activity determined in an assay medium containing 5% n-propanol. The presence of Cl in nitrate containing nutrient solutions resulted in lower NR levels, however counterions supplied together with Cl tended to modify slightly this general trend. The negative effect of Cl ions was also apparent, when Cl ions were applied before nitrate ions. Anaerobic nitrite production in the medium lacking both nitrate and n-propanol was not influenced by chloride ions. Nitrate content in the roots was reduced in the presence of chloride both at 3 mM and 15 mM NO₃ in nutrient solutions; however, at 16 mM NO₃, nitrate content in the roots exoeeded even in the presence of 15 mM Cl nitrate content in those root segments which were cultivated in a nutrient solution with 6 mM nitrate, which is the concentration at which NR reaches the level of saturation in excised pea roots. The results obtained suggest that a special induction nitrate pool exists in plant cells besides the storage and metabolic nitrate pools.

The effects of foliar application of morphactin (0, 10, 50 and 100 ppm) onPennisetum typhoides (cv. HB3) have been studied under different soil moisture conditions (0.3, 3 and 9 x 10Pa tension). Morphactin application reduced the plant height, increased the tillering and leaf number of the main shoot and adversely affected the growth characters associated with the grain production. The overall performance of plants was not improved by morphactin treatment under low moisture regime and it did not impart any efficiency of water use for grain production. Findings on the phosphorus and potassium levels of the shoot tissue suggested a possibility of its interference in the nutrient uptake process.

In a greenhouse pot oulture experiment, a dinitrogen (N2) fixing - acetylene reduction activity profile was examined in detail as affected by plant age. Total [μmol C2H4 root-1 h-1] and speoifio nitrogenase [nmol C2H4 (mg nodule d. wt.)-1 min-1] activities peaked 63 days after sowing, near the end of flowering. The nitrogenase activities, nodule dry matter accumulation, top dry matter accumulation, and total nitrogen yield in the top dry matter were found to be highly correlated.

Glutamine synthetase (GS) level is positively influenced by exogenously supplied sucrose in isolated pea roots (similarly as nitrate reductase - NR), glutamate dehydrogenase (GDH) level negatively. Comparison with previous results shows that GS level decreases more slowly than NR level when sucrose is omitted from the medium; the rate of changes in GS level corresponds rather to that in GDH level. The increase in GDH level in the tips of isolated roots cultivated in the medium lacking sucrose stops after approx. 24 h, but continues for at least 72 h in more mature root parts. GS level decreases during the first 24 h in the tips of isolated roots (compared with roots of intact seedlings) cultivated both with sucrose and without it (without sucrose more), however it again rises in the course of further cultivation with sucrose. The differences in GS and GDH levels caused by omission of sucrose are small in isolated roots from which root tips were removed, the difference in NR level in decapitated roots is similar to that found in isolated roots with root tips left. Decapitated isolated roots cultivated without sucrose contain higher amounts of soluble sugars than corresponding roots with root tips left. These facts are dismissed with regard to sugar consumption, transport, and compartmentalisation, and with respect to production in root tips and other plant parts of unknown compounds involved in GS and GDH regulation. The results obtained suggest that GDH functions in pea roots in the deaminating direction.

The determination of electrolyte leakage from the winter rape hypocotyls subjected to desiccation over C_aCl₂ under vacuum was found to be the proper and useful method for the estimation of the direct, water stress-induced injuries in the plant tissue. The described procedure of desiccation allows a differentiation between the tissue drought tolerance and the tissue ability to avoid water stress.

The successive staining alcian blue/aluminium lake of nuclear fast red was proved a useful tool for studies on plant root tip. A simple and reliable procedure is given resulting in blue cell walls, almost colourless cytoplasm and red nuclei. Attempts were made to apply spectrophotometry and paper chromatography to overcome the confusions in manufacturers' labelling of the dye and to check the lake formation.

The content of bound proline sharply increased in proteins of different organs of young plants of winter rape and winter wheat exposed for 72 h to temperatures from 0 to 2 °C while it decreased only in root tips of wheat plants. Free proline which at 20 °C occurs in all plant organs only in trace amounts, accumulated considerably after 72 h exposure to low temperatures in the above-ground organs and only slightly in the roots. Free proline did not accumulate during the first 24 h at 0 to 2 °C in detached leaves of winter wheat but it was incorporated into newly synthetized proteins in which proline content increased after 6 h incubation to its maximum ( + 11.75% in comparison to control); the content of free glutamate sharply decreased during the first 6 h of incubation and the accumulation of bound glutamate was belated in comparison to that of bound proline. Sucrose infiltrated into detached leaves of winter wheat strongly stimulated proline incorporation into proteins at low temperatures, but it did not influence glutamate incorporation. The results suggest that the main reason for thede novo proline biosynthesis during the first six hours of hardening of the plants is the synthesis of proteins rich in proline; free proline accumulates later predominantly in the above-ground organs as a surplus. The above-ground organs are dehydrated in the course of the hardening process approximately to the same extent both in the light and in the dark, but proline content increases much less in the dark than in tho light.

The investigations carried out to find the role of abscisic acid in the phenomena of abscission of flower buds and bolls of cotton (Gossypium hirsutum L. cv. 'H-14') have shown abscisic acid content to be low in retained bolls as compared to that in the abscising ones of the same age, suggesting that relatively higher endogenous abscisic acid content to be promotive of abscission. Abscisic acid applied exogenously either to intact flower buds/bolls or boll explants promoted their abscission. Naphthalene acetic acid not only reduced abscission but also could erase completely the promotive effect of abscisic acid on abscission. Gibberellic acid promoted abscission in intact buds and boll explants but applied to intact bolls it reduced their shedding even more than naphthalene acetic acid. Gibberellic acid could also counteract the promotive effect of abscisic acid in the case of intact bolls but enhanced that of boll explants. All the cytokinin-furfurylamino-purine treatments given other than at the abscission zone promoted abscission. Furfurylaminopurine applied in combination with abscisic acid showed some antagonistic effect in the case of intact bolls and boll explants abscission zone treatments. Ascorbic acid applied at a relatively lower dose (0.025 mM) reduced shedding but applied at a higher dose it showed promotion. Ascorbic acid could erase the promotive effect of abscisic acid on abscission to a significant extent.

According to plant age at induction and rate of initial growth ABA leads either to stimulation or inhibition of growth and flowering in youngChenopodium rubrum plants. This differential effect is linked with the morphogenetic potential of the plants at the time of ABA application. Different modes of germination and cultivation of the plants prior to floral induction affect growth and photoperiodic sensitivity of the plants which may also explain differences in the effect of ABA.

Trypsin and chymotrypsin inhibiting activities were detected in a "crude inhibitor" fraction of a lipid free cashew nut (Anacardium occidentale L.) meal. Both activities were shown to be heat resistant and not affected by pepsin at pH 3.0. Molecular weight distribution of tho trypsin inhibiting activity is similar to the known range of molecular weights for trypsin inhibitors of plant origin.
A "crude extract" of the cashew nut meal was shown to contain strong L-leucine-p-nitro-anilide and moderately strong α-N-benzoyl-DL-arginine-p-nitroanilide hydrolyzing activities. This last activity was strongly inhibited by the "crude inhibitor" fraction shown to contain trypsin and chymotrypsin inhibiting activities. The presence of this endogenous inhibitor-endo-peptidase system seems to indicate that the protein proteinase inhibitors of plant origin could be involved in the control of protein mobilization in the seed.

Uridine incorporation into the shoot apex of the short-day plantChenopodium rubrum was investigated during a 16 h period of darkness and the following transfer to light. Uridine incorporation during this single inductive cycle was compared to incorporation under non-inductive conditions of continuous light. After transfer of the plants from light to darkness RNA synthesis was reduced to about half after the first two hours. This occurred not only when the plants were precultivated in continuous light but also after an interruption of the dark period by light for 31/2 h. The low level of uridine incorporation was maintained for the whole duration of the dark period. Incorporation regained its initial level after exposure of the plants to light irrespective of the duration of the preceding dark period. After this immediate rise of uridine incorporation in plants transferred from darkness to light a slight temporary decrease was observed in light. In darkness the decrease of incorporation into the nucleoli was still more marked than the reduction of overall incorporation. After the termination of the dark period incorporation into the nucleolus rose slowly and extranucleolar incorporation was relatively enhanced during the first 10 h of light in induced plants. The fluctuations of RNA synthesis observed in the shoot apex during photoperiodic treatment may be regarded as a necessary condition for the transition from the vegetative to the reproductive state.

The influence of gibberellic acid (GA³) and kinetin (6-furfurylaminopurine) on the regeneration ability of the basal and apical thallus fragments ofFucus vesiculosus L. was examined. The naturally occurring gibberellin and kinetin-like substances in these thallus fragments were also studied. It was found that exogenously applied GA³ markedly increased the number of adventitious branches formed on the cut surface of the thallus fragments taken from the apical parts of plants. The concentration of 0.001 mg GA³ I-1 proved to be the most effective. The growth promoting effect of GA³ was increased by simultaneous action with kinetin. In experiments in which the fragments of the basal parts of the thallus were treated with GA³, as a rule a slight growth inhibition was observed. The growth responses of the investigated plant tissues to gibberellin and kinetin varied according to season. Usually their susceptibility to the applied plant hormones was greater in spring than is summer. The shifts in growth reaction were related to the seasonal changes in the content of endogenous gibberellin and kinetin-like substances in the investigated parts of the thallus. It is suggested that growth regulators of the gibberellin and cytokinin type are involved in the regeneration processes inFucus.

Lunulario aoid was isolated from fresh thalli ofTargionia hypophylla L. This acid was found to enhanoe the destruction of IAA by auxin-oxidase from lentil roots. Such action can explain, at least partially, its inhibitory effect on IAA-induced plant growth.

The inhibitor-A, isolated from the leaves of a saline soil tolerant plantSuaeda fructicosaFoRsk., is phenolic in nature, inhibits the IAA-induced growth, and is resistant towards higher temperature.