Peroxidase activity and isoenzyme pattern were investigated in buds and tubers of Jerusalem artichokes in relation to induction and breaking of dormancy. Peroxidase activity per unit soluble protein is the highest in the dormant stage. Conditions leading to growth,i.e. release of dormancy by the cold, stimulation of axial growth by gibberellic acid or stimulation of radial growth (tuberization) by kinetin, cause rapid loss of total peroxidase activity together with a decrease of intensity of the most cathodic isoperoxidases. Induction of dormancy by AMO-1618 increases peroxidase activity mainly through the same cathodic isoenzymes. The role of the cathodic isoperoxidases is discussed in relation to auxin catabolism and the genesis of oxygenation products inhibitory to plant growth.

Cauliflower plants in the juvenile phase treated on the leaf surface and at the apex with Morphactin solution (100 mg 1^-1) and this concentration failed to develop a curd and also to come to flowering. Instead of a curd the axis formed a conical or dome-shaped structure bearing 'nodal' rings. The number of rings increased with growth of the axis which either formed or did not form a small curd-like structure, which generally dried without flower formation.

Morphactin-butylester (a flourene-9-carboxylic acid derivative) inhibited seed germination of two strains of lettuce. Morphactin induced inhibition of germination could be partially or wholly reversed by simultaneous addition of gibberellic acid. However, gibberellic acid played very little part in reversing the inhibitory effect of morphactin on seedling growth. It is concluded that gibberellin can not reverse all the growth effects induced by morphactin.

Garex packystylis, native of Israël, has been compared in arid zones of Israël and in France under phytotronie conditions. Especially its drought resistance has been studied. Once root formation has stopped through drought action, the shoot apices situated on the rhizomes which are well protected by layers of dry scales, become active and form leaves above the ground when the plants are once again in favorable growth conditions. There is also reumption of the basal growth of leaves incompletely dessicated from the top.

The effects of temperature treatments on rice seeds in the early imbibitional phase were studied with respect to changes in germination percentage, seedling growth in terms of root and shoot lengths, water uptake, respiration and hydrolytic enzymes,viz. α-amylase, adenosine triphosphatase (ATPase) and phytase. As compared with the control, the treatment for 30 min at 50 °C caused a variable degree of increase in all these characters and a positive correlation existed between seedling vigour and hydrolase activities. The treatment for 30 min at 60 °C, on the other hand, elicited a retarding influence on these characters. As regards the enzyme activities, the damaging effect of 60 °C could, however, be visualized only after 72 h of germination which was preceded by an enhancement during the early hours.

The effect of acute gamma rays (⁶⁰Co; 1 to 10 kR) on the vascular differentiation in stems of seedlings of Capsicum annuum L. long fruited cultivar at 8-loaf stage of development. Prooambium, phloem and xylem of irradiated seedlings showed an early initiation and maturation in terms of distance from the tip. Magnitude of these differences increased with the increasing exposures and time following irradiation. In irradiated seedlings there is a ohange in the developmental sequence of metaphloem and metaxylem when they first appear (in terms of number of leaf primordia). There is also a general increase in the number of procambial cells, sieve elements and vessel elements after irradiation.
The early initiation and maturation of the vascular tissue is correlated with the growth inhibition resulting from cell death and suppression of cell division activity in the shoot apex.

The effects of low doses of two mutagens (UV-light and ethyl methansulphonate) on the growth of algae on a solid minimal (anorganic) medium were studied. It was supposed that low doses of mutagens will be more suitable for the induction of growth mutations.
The UV-light had an inhibitory effect in the whole range of the applied doses on the growth of colonies of algae from the cells inoculated on the solid medium immediately after irradiation.
Ethyl methansulphonate produced growth stimulation if applied in the lowest doses. The growth was inhibited in a further range of doses and then there appeared the range of lethal doses.
The growth responses to the influence of these mutagens were different in all the three algal species used and to the previous cultivation conditions before their exposure to the mutagens. It is certain that most of these growth responses are only modifications.
The influence of ethyl methansulphonate differed according to the method of application. If it affected the algae for a long time (it means if they were inoculated directly on the solid medium containing mutagens), or, if the algae were exposed to its influence immediately before their inoculation on the solid medium, the growth responses of colonies were quite different.
Growth responses with the single studied strains differed quantitatively only.

The 0.03-0.06% indole-3-acetic acid (IAA) in lanoline paste smeared on the cut surface of decapitated epicotyl of the pea seedling inhibited the growth of the axillary buds of the cotyledons. 0.03-0.06% solution of (2-Chlorethyl) trimethylammonium chloride (CCC) considerably weakened the inhibitory effect of IAA when applied simultaneously to the roots. In a similar way CCC diminishes even the growth inhibition of intact pea epicotyls caused by 0.06% IAA lanoline paste. 0.03% solution of CCC administered to the roots of the decapitated pea seedlings significantly increased growth of the axillary buds. This effect may play a role in the demonstrated antagonism between the low concentration of CCC and IAA.

Using the phenol extraction method and MAK column chromatography the contents of nucleic acids in styles ofNicotiana alata were estimated before and up to 48 h after compatible pollination. As a result of pollination, high-molecular-weight rRNA and DNA registered a significant increase in their content approximating 30% and 16% respectively. The change in sRNA (4-S tRNA and 5-S rRNA) level was very slight and non-significant. In pollen grains there is an unusually high amount of rRNA with respect to the content of other nucleic acids and the rRNA/tRNA ratio approximates 14 : 1. On the other hand, in non-pollinated styles the content of rRNA is only about 6 times higher than that of tRNA. The changes in nucleic acid level found in styles after pollination are at least in a major part the result of the addition of the nucleic acids present in the amount of pollen used for pollination. The high rRNA level relatively to tRNA being generally associated with rapidly growing cells, its significance in pollen may be related to the rapid growth of pollen tubes.

The apical dominance in dormant tubers ofCircaea intermedia preventing the extension of lateral buds under favourable conditions differs from the apically directed growth inhibition inducing true dormancy in the tubers. This acropetal inhibition affects the tuber tip more strongly than its lateral buds, which develop into long stolon-like shoots after the tuber decapitation. The local supply of ABA shows no tuberizing effect, but enhances the dormancy of the tuber top. MH interrupts the correlation between the tuber laterals tuberizing without previous stolon formation. The uppermost leaf structures participate in the apical dominance, inhibiting their own axillaries on intact tubers. Mature scales disclose this correlative influence only on decapitated or dissected tubers on which IAA or BA release their inhibitory effect, but ABA increases it. Two scale pairs occurring regularly at the top of dormant tubers and seen later at the erect base of the stem are involved in the initiation of foliage leaves for the next-year growth period. BA applied to an axil at the top of the tuber provokes its sylleptic branching.

The biological effect of barley root excretions was studied during a 4 to 10 days cultivation period. The effect of root excretions changes according to the cultivation period of barley. It was ascertained by means of a bioassay that growth was either conclusively stimulated or the root excretions did not affect growth of the roots and of the upper part ofNasturtium. No significant inhibitory effect was observed. The effect of the single amino acids and of their mixtures found in the root excretions of barley was quite different. The following amino acids were determined by paper chromatography in root excretions: alanine, asparagine, phenylalanine, glycine, leucine, lysine, serine, tyrosine, glutamic acid and valine plus methionine. During cultivation their total quantity increased from 5.48. 10^-5 up to 1.13. 10^-3 mg per plant. Most of the 20 amino acids observed, displayed in theNasturtium test at a concentration from 0.1 to 1,000 mg/l an inhibitory effect onNasturtium growth. The effect of amino acid mixtures, corresponding qualitatively and quantitatively to the free amino acids in barley root excretions was dependent on their concentration.
Growth regulators of the auxin type were found in culture solutions by chromatographic separation and with bioassay. As it may be seen from the results obtained, there are besides amino acids and indole derivatives other non-identified compounds involved in the effect of barley root excretions.

Minimal diffusive resistances of both leaf epidermes increased during normal and retarded ageing (moving secondary leaves aside, plant decapitation). The retarded ageing of primary leaves slowed down increase in epidermal resistance (r_ep), and was also reflected in the prolongation of their growth, increase of leaf area, size of epidermal and guard cells and stomatal pores. Decrease of stomata density was to some extent balanced by an increase in the pore size; the later rapid rise in diffusion resistance was induced by the loss of stomata ability to open fully.

A study was made on certain problems connected with the application of methods of stigmatal and placental pollinationin vitro in the snapdragon.
Germinable pollen without microbial contamination could be obtained only from the flowers which were left, after surface sterilization, on the stem till the dehiscence of anthers. The germination of pollen, and especially the growth of pollen tubes was better in a 0.3 M lactose solution with 10^-3 per cent H₃BO₃ than in usual sucrose media.
The seedsin vitro could be obtained only after normal pollination and the successive artificial cultivation of the entire pistil (the method of stigmatal pollinationin vitro). The seeds did not differ either in their morphology or in their size from those developed under natural conditions, they were viable and without dormancy.
Though the pollinated pistils were cultivated in the medium without growth substances, callus formation from uncovered ovules and placenta was observed in some cases. A dependence was revealed of the proliferation on pollination and on the cultivar employed.
When using the method of placental pollinationin vitro we failed to obtain seeds. The main difficulty in the use of this method seems to consist in the fact that pollen tubes are not capable of growing from the surface of ovules and placenta into the micropyle.

Using paper chromatography and conventional methods of isolation, natural growth inhibitors were isolated from green leaves of different plants (Brassica oleracea, Zea mays, Pisum sativum andSalix rubra). All isolated inhibitors were found to be phenolic compounds and the chemical structure of most of them was determined; only the final structure of theBrassica inhibitor has not yet been ascertained. 500 mg of natural inhibitor ofPisum sativum was isolated from 1500 g of leaves and was identified as quercetin-glucosil-p-coumarate (QGC), described earlier byFuruya, Galston andStowe (1961). The structure of the natural inhibitor ofZea mays (4 mg from 100 g of leaves) was identical with p-coumaric acid and the chemical nature of the plant growth inhibitor fromSalix rubra (700 mg from 1,5 kg of leaves and young bark) was that of 2-chalconaringenin-glucoside or isosalipurposide, described earlier byCharaux andRabaté (1931) andHarborne (1966). All isolated substances had inhibiting properties in the straight growth test of wheat coleoptile sections and decreased the growth of isolated stem sections prepared from plants-donors of inhibitors. Thus, maximum growth inhibition (LG max) was attained, if wheat coleoptile sections were incubated with:Brassica inhibitor in the concentration of 0.5 mg/ml, withPisum inhibitor (QGC) in the concentration of 16 mg/ml, withZea inhibitor (p-coumaric acid)-0.35 mg/ml and with Salix inhibitor (isosalipurposide) in the concentration of 0.5 mg/ml. In small concentrations no mentioned substances were able to enhance the growth as actively as indolic auxins (on 250-300%); only slight growth activation in biotests was sometimes observed for low concentrations. Inhibition in p-coumaric acid was much more active in a free form than in the bound form as an acyl-rest of QGC. As a rule, the wheat coleoptile test was much more sensitive (3-5 times) to the plant growth inhibitors, than tests prepared from tissue and organs of plants-donors. The retardation activity of plant growth inhibitors is not correlated with their molecular weight. Dormin (or±abscissin II) was also tested on wheat coleoptile sections. In neither of the applied concentrations (10-0.05 μg/l range) was dormin able to depress straight growth of wheat coleoptile sections, but even in a 1.7 μg/l concentration it inhibited the IAA-activated growth of sections. However, additional experiments showed that dormin in higher concentrations (40 μg/l and more was able even to depress endogenous straight growth of wheat coleoptise sections. The differences between the properties of natural phenolic growth inhibitors and dormin were discussed.

Free and bound gibberellins were estimated in individual leaves of winter wheat using TLC a lettuce hypocotyl bioaasay. Bound gibberellins were extracted from the hydrolyzate of the water remnant after the removal of free gibberellins.
Each leaf exhibits its own dynamics of free and bound gibberellins during its individual ontogeny, the gradual changes tending to be identical in every leaf. In young developing leaves the level of free gibberellins is high and that of bound is low. Further, inhibitors are sometimes present. The free gibberellin level rises with the activisation of growth and vital activity of a given leaf. Towards the end of the life cycle the content of free gibberellins is reduced to its minimum and inhibitory substances appear. The dynamics of bound gibberellins is opposite to that of free ones during ontogeny.

A. latifolia grown in the Borimalan forest block in Prasad range (24°11'N and 73°42' E) exerts clear positive correlations between CBH (circumference breast height)and number of growth rings of bole and branches, tree height, total biomass and leaf area. The net above-ground biomass is 3.95 × 10⁴ kg ha^-1. The average increment in non-photosynthetic (trunk + branch) biomass shows two peaks, the lower peak at 11-16 growth ring period, and the higher one at 34-36 growth ring period. The ratio of leaf dry weight/leaf area is16.3 to 34.8 mg cm^-2, the ratios between shoot net production: leaf weight and leaf area are1.5 g per g and 212 g m^-2 respectively.

The character of endogenous regulators in walnut buds was followed by means of bioassays in the course of vegetation. It was ascertained that a rise in the level of gibberellin-like substances precedes the sprouting of buds. The origination of new buds in the axil of young leaves is accompanied by a fall in the level of auxins, by a low gibberellin content and by the presence of inhibitors. In this situation the primordia of staminate catkins are diferentiated in the basal buds. The vegetative buds which are formed in the axils of further leaves, stop developing because of the accumulating inhibitors. Towards the close of vegetation the primordia of pistillate flowers originate in terminal buds and their differentiation is accompanied by a substantial rise in the level of auxin-like substances, while some of the inhibitors keep asserting themselves. On the basis of these findings we have tested the possibility of affecting the differentiation of staminate primordia and of vegetative buds by the exogenous application of selected regulators. Spraying young leaves with IAA and MH solutions will increase the number of vegetative buds in the twigs. A later spray of other twigs by TIBA and GA₃ solutions will increase the number of staminate buds.

In the basal growth medium only the ovaries excised 15 days after pollination reached maturity. In a medium containing IAA (5ppm) and kinetin (0.5ppm) ovaries excised even 10 days after polliration produced viable seeds.
Young ovaries formed in the pedicel region a callus, which later differentiated into roots; older ovaries (excised 15 days after pollination) produced callus tissue and roots from the ovary wall.

Coleoptile and root tips ofTriticum aestivum cv. Arnej 624 and those ofAvena sativa cv. Victory (Svalöf) as well as dry excised embryos ofTriticum aestivum cv. Rival (Svalöf) and those ofArachis hypogaea cv. 34 3A. H. were cultivated in media containing various concentrations of sucrose and growth regulators, like ascorbic acid, indole-3-acetic acid and gibberellin. Growth, differentiation and water uptake of the various explants were determined at regular time intervals. Further, the concentration of the endogenous ascorbic acid in mg./g. fresh weight, as well as the amount of this growth regulator utilized as per cent of the total were determined.
Although all the three growth regulators promote growth in the explants, their effect is best felt when sucrose of a higher concentration (1.0 per cent) is added to the medium. In fact, the response to 1.0 per cent sucrose is sometimes as good as a combination of a growth regulator with sucrose, especially in the case of root explants.
The results clearly indicate that the biosynthesis of ascorbic acid in the explants is catalyzed by the addition of indole-3-acetic acid as well as gibberellin. Simultaneously, the utilization of ascorbic acid is also appreciably increased by the presence of these growth regulators.
Addition of 1.0 per cent sucrose to the medium containing the above mentioned growth regulators augments to a considerable extent not only the concentration of ascorbic acid, but also steps up its utilization. Enhancement of ascorbic acid as well as its increased utilization are correlated with rapid imbibition of water, growth and differentiation.
The role of ascorbic acid in growth is discussed; and on the basis of the data presented here it is postulated that: (1) auxin and gibberellin function in the growth process by catalyzing the biosynthesis of ascorbic acid; and (2) that ascorbic acid not only participates in activation of various enzyme systems, but also stimulates the production of adenosine triphosphate by acting as an electron donor in photosynthetic phosphorylation as well as oxidative phosphorylation; (3) that the above action of ascorbic acid creates a favourable redox balance for synthesis of nucleic acids, proteins, enzymeproteins, and cell-wall constituents, thus enabling the processes of cell division and enlargement to proceed at a fast rate; and (4) that the relative rates of cell division and cell enlargement as well as "ageing" will determine the pattern of plant development.

The production of ethylene in the leaves ofSalix viminalis L. increased gradually from May till October. The emanation from the leaves, the main constituent of which was ethylene, inhibited the extension growth and the formation of the dry matter of rye seedlings more or less equally during the whole growing season. This indicates that the effect of ethylene on the growth is not, to any great extent, dependent on its concentration.

Growth measurements on individual polycormones ofScirpus lacustris L. cultivated in hydroponic sand cultures from single rhizome cuttings enabled us to analyse the process of offshoot formation. The time interval in the growth of individual subsequent shoots of one polycormone (plastochron), the final length of the shoot and the number of shoots formed during the growth period are suitable parameters for describing the rhythm of offshoot formation. The interdependence of these parameters and the effect of cutting or shading of individual shoots characterize the translocation of assimilates produced by individual shoots, and their use for the growth of subsequent shoots.

Nitrate reductase (NO₃R) activity, nitrite reductase (NO₂R) activity and NADH₂ dependent glutamate dehydrogenase (GDH) activity were followed in extracts from excised pea roots incubated under aseptic conditions for 9 and 24 h in nitrate containing nutrient medium to which IAA was added in concentrations promoting lateral root formation (1 × 10^-5; 3 × 10^-5; 5 × 10^-5 M) and kinetin in concentrations which reduce lateral root formation (0.1; 1; 5 mg 1^-1, that is 4.65 × 10^-7;4.65 × 10^-6 and 2.3 × 10^-5 M). NO₃R activity was not influenced by IAA, NO₂R activity was slightly depressed by IAA after 24 h incubation and GDH activity was slightly increased after 24 h incubation in the presence of IAA. Kinetin decreased NO₃R activity significantly both after 9 h and 24 h incubation, slightly increased NO₂R activity after 9 h incubation but slightly decreased it after 24 h incubation, and did not affect GDH activity after 24 h incubation. However, when applied together with IAA, kinetin abolished the promoting effect of IAA on GDH activity. IAA neither reversed nor accentuated the effect of kinetin on NO₂R activity. Nevertheless the depressing effect of kinetin on NO₃R activity was emphasized by the presence of IAA after 9 h incubation. The results obtained indicate that reduced nitrate assimilation due to the depression of nitrate reductase activity caused by kinetin probably contributes to the negative growth effect of kinetin in pea root segments grown in nitrate medium.

1. Kinetin at a supra-optimal dose of 1.0 mg/l reduces the growth inhibitory effect of CCC at 5 × 10^-2 M on tobacco callus and increases it on tobacco crown-gall.
2. CCC increases the content of total, acid soluble, protein anti nucleic acid nitrogm in both tissues. Kinetin partially reduces the effects of CCC on nitrogem metabolism in callus tissue, and increases it in crown-gall.
3. It is suggested that (1) CCC affects the synthesis of RNA directing the synthesis of protein, and (2) interaction of kinetin with CCC realizes via the genetic apparatus of the cell.

The first information concerning the cytogenetic efficiency of thermal neutrons in lentil are presented in this paper. The range of cytologically effective dosages of thermal neutrons in lentil was determined. This determination enables us to compare the efficiency with the mutagenic effect of thermal neutrons and with their effect on the growth and development of plants of M₁ generation. These effects were already evaluated in previous communications.
Thermal neutron irradiation significantly affected all the characters studied. A linear dependence of the effect on the dose of the neutron radiation was found for most of the analyzed characters. From a sample of scored cells, whose nuclei were in the anaphase or early telophase, 9.0 to 72.0% of them had chromosomal bridges and fragments after irradiation with dosages from 3.3×10¹¹ n cm^-2 to 4.5×10¹² n cm^-2. The highest number of rearrangements per one cell reached 2.16 after irradiation with 4.25×10¹² n cm^-2 while the lowest dosage used, 3.3×10¹¹ n cm^-2, induced 0.17 of chromosomal rearrangements per one cell. Irradiation with thermal neutrons is capable of inducing a large number of very complicated chromosome rearragements.

In barley embryos, treated with N-methyl (¹⁴C)-N-nitrosourea, the alkylation of nucleic acids was much higher than that of proteins and lipids. At a concentration inhibiting the growth of M₁ seedlings to 50%, 0.27% of DNA-guanine was methylated to N-7-methylguanine. In barley DNA, alkylatedin vitro, the presence of 3-methyladenine and 0-6-methylguanine was chromatographically detected.

The interaction of GA and IAA in apical dominance was investigated in an experiment in which first of all an IAA paste was applied to the cut areas formed by the decapitation of epicotyl apices of pea seedlings, followed after one week by the application of a 0.25 % GA paste. The latter treatment was able to overcome the growth inhibition of cotylary buds induced by a 0.03 % IAA paste, but not that caused by 0.06 and 0.12 % IAA pastes.
The correlative function of a root in the renewal of the apical dominance can, to some extent, be directly simulated by exogenous gibberellin, as has been demonstrated in the experiment with decapitated pea seedlings deprived of one cotyledon, on which the growing axillary of the amputated cotyledon was decapitated. In this case the axillary of the remaining cotyledon grows in the plants where the root has been left, but in those deprived of the root, there appears a serial of the amputated cotyledon (Dostál, Biol. Plant. 9 : 330, 1967). When GA was supplied to the plants treated in this way, the coty lary of the remaining cotyledon grew even in the plants deprived of the root.

The effect of glycine on the growth of isolated tomato roots in White's nutrient solution was studied. It is obvious that the root tips grow better in the medium without glycine, because increasing rates of glycine produce inhibition. The growth of root explantates in nutrient media indicates a high synthetic ability of isolated roots. Optimal concentrations of humus acids in White's nutrient solution without glycine and with glycine stimulate the growth of root explantates. It cannot be decided which of the two substances affects the root directly and which acts as a chelating agent in the medium. The effect of glycine varied, depending on the origin of sucrose used. It appears that in media containing beet sucrose, glycine is unsuitable but in media containing cane sucrose it is necessary.

Changes in the percentage of seed germination, the growth and respiration rate of the seedlings were observed at 15-day intervals from the stage of the full germination capacity of rice (Oryza saliva L.) seeds till they became non-viable. At the beginning, the respiration rate changed but little, but afterwards, with the approach of non-viability, the rate declined sharply. A positive correlation of respiration with a decrease in the germination percentage and the length of seedlings and a negative correlation with days of storage were also established. A strong correlation existed between catalase and peroxidase activity with respiration, indicating that the activity of these enzymes can be used as an indicator of metabolism, and therefore can be considered as part of the respiratory mechanism of rice seedlings.

The influence of photoperiodic induction on the incorporation of uridine-³H into the shoot apices ofChenopodium rubrum was studied using the technique of autoradiography. No increase in uridine incorporation was detected either during induction lasting three days or immediately after its termination. Pyroninophylia likewise did not rise. However, changes in uridine incorporation related to morphogenetic activity during leaf formation and later during differentiation of inflorescences were well marked. The distribution of label in the nucleus immediately after three inductive cycles shows the ratio of extranucleolar to nucleolar incorporation to be higher in non-induced control plants than in induced ones.
Data from literature pointing to an activation of RNA synthesis during transition to flowering are discussed and compared with other systems where ontogenetic changes are accompanied by marked changes in RNA synthesis. It is assumed that the activation of RNA synthesis after induction is connected mainly with the activation of growth. However, inChenopodium rubrum photoperiodic induction proceeds together with limited growth and without activation of RNA synthesis.

The nucleic acid fractions in cotyledons of young Chenopodium rubrum plants exposed to continuous light, continuous darkness and short (8 h) day, respectively and labelled with³²P 24 h prior to harvesting were studied by means of chromatography on MAK columns. Some parameters of cotyledon growth (dry weight, cotyledon area, occurrence of mitoses) were also investigated.
The changes in the nucleic acid fractions agreed with the dynamics of cotyledon growth. In continuous light the content of all fractions increased. The radioactivity of DNA and s-RNA did not undergo any great changes and only r-RNA increased. The specific activity of r-RNA increased slightly, that of soluble RNA and DNA was reduced. In continuous darkness the content of all the fractions did not undergo any great changes. The radioactivity as well as the specific activity of all fractions decreased. In short day the content of the nucleic acid fractions did not change conspicuously. Only the specific activity of s-RNA increased in a noticeable way while the radioactivity of r-RNA and the specific activity of DNA decreased and this of r-RNA did not change. The changes in nucleic acid metabolism were partially connected with changes in³²P uptake which depended upon light conditions but they were not merely a consequence of this fact. Obviously, there also exists a more direct relationship between nucleic acid synthesis and growth.