Selected characteristics and streptomycin resistance were studied in a UV radiation sensitive (UVS1) and a UV radiation resistant (UVR1) strains, and the data were compared with results obtained with an original type strain. A partial prolongation of the cell cycle in the UVR1 strain as compared with the original type strain could be observed in studying cell volume growth, cell numbers, DNA, RNA and protein synthesis during the synchronous cycle. Under these conditions, the UVS1 strain behaved as a temperature sensitive cell cycle mutant. In inducing streptomycin resistant mutants, the highest frequencies in various doses were recorded in the UVS1 strain.

In intact, decapitated and decapitated indole-3-acetic acid (IAA) treated pea seedlings the translocation of benzyl-8-^l4C-adenin (¹⁴C-BA) from the roots was studied with regard to the release of lateral buds from apex-induced inhibition. In intact plants (controls) a substantial part of the activity was found in the apical part of the epicotyl. Decapitation resulted in the initiation of growth of lateral buds. As early as 24 h after decapitation and application of¹⁴C-BA a significantly higher activity was found in growing lateral buds (cotylars) of decapitated plants than in inhibited ones of intact or IAA-treated decapitated plants. The accumulation of¹⁴C-activity in stump tops of decapitated plants treated with IAA was associated with the thickening growth.

The effect of short and long term auxin treatments on the elongation of axillary buds and³²P accumulation were studied in 2-leaf decapitated Alaska pea sailings. It was found that (1) auxin delayed the elongation of the lateral buds, (2) none of the auxin concentration applied completely inhibited the elongation of axillary buds, (3) auxin had no retarding effect on the growing buds, (4) strong polarization of 32P occurred in the parts above the treated leaf, when auxin was applied for a short period just after decapitation, (5) long term auxin treatments did not induce any such polarization of 32P to the parts above the treated leaf, (6) the root acted as an alternate accumulating organ for 32P when the apex was removed and the buds were inhibited, and (7) in decapitated plants the growing buds polarized 32P.

The results of studies performed on winter rape leaves (Brassica napus L. var.oleifera L., cv. Górczański) indicated that independently of the plant cultivation conditions and of the leaf growth rate, all leaves showed significant increase in desiccation tolerance at the beginning of leaf expansion. The increase in tolerance was correlated with the formation of a central vacuole in the mesophyll cells. Therefore, the high desiccation tolerance of vacuolised cells in comparison to the non-vacuolised ones is supposed to be due to the higher ability of the former to avoid cytoplasm dehydration. Development of frost tolerance in the leaves during autumn does not seem to be causally related to desiccation tolerance changes.

Flowering ofChenopodium rubrum seedlings fed different sugars at a concentration of 0.6 and 0.4 M, reap, during a single inductive cycle was stimulated or inhibited in dependence on the conditions of germination and initial growth. Plants allowed to germinate at alternating temperatures of 28 °C and 5 °C showed a slower initial growth and their development was stimulated by some sugars as compared to controls induced in the absence of sugars. Plants germinated at alternating temperatures of 32 °C and 5 °C exhibited a rapid initial growth and flowering was inhibited after induction in the presence of sugars. On the other hand, development proceeded more rapidly in control plants induced in the absence of sugars after germination at the higher temperature than after germination at the lower one. The differences between the two variants quoted above could be observed also after induction by two 16 h dark cycles. Glucose and sucrose were most effective in stimulating flowering under appropriate conditions of germination. Fructose was less effective and the action of maltose was very weak. Xylose, ribose and galactose were innocuous, while arabinose, glucoso-6-phosphate and mannitol were toxic to the plants. The sugars inhibited root growth in all cases and led to an increase in starch accumulation in the underground and overground plant organs. At a concentration of 0.6 M they mostly inhibited the length of the cotyledons and, especially, of the first leaf; at a concentration of 0.4 M growth of the overground organs was stimulated. The results are discussed with respect to the possible ohanges in photoperiodic sensitivity brought about by the rate of initial growth.

P-coumaric acid (HCA), 2,4-dichlorophenol (DCP) and resorcionol acted as cofactors for IAA-oxidase isolated from young wheat plants. Ferulic acid (FA) and 3,4-dihydroxybenzoic acid (DHBA) induced a lag phase prior to IAA oxidation. HCA, FA (0.2-1 mg ml^-1) and DCP (0.03-1 mg ml^-1) strongly inhibited wheat coleoptile section growth. DHBA (0.01-1 mg ml^-1) slightly stimulated it and resorcinol was without effect. HCA inhibited IAA-induced growth of coleoptile sections and FA stimulated it at low IAA levels and inhibited it at higher ones. DHBA, DCP and resorcinol did not affect IAA-induced growth of coleoptile sections.

Cytokinin-dependent and cytokinin-autonomous strains of tobacco callus tissue (Nicotiana tabacum L. cv. 'Wisconsin 38') were grown on media containing sucrose, glucose and fructose, respectively. The tissues were kept 14 days in darkness and then transferred for 9 days to continuous light after which time the fresh weight and chlorophyll content were estimated. The highest chlorophyll concentration was recorded at sugar levels which were either suboptimal (sucrose in the case of cytokinin-dependent strain) or supraoptimal (all other sugars for both strains and sucrose for the cytokinin-autonomous strain) for tissue growth. The chlorophyll concentration was increased when the tissue was cultured on media containing glucose or fructose,i.e. sugars whioh did not support the growth as well as sucrose. Chlorophyll synthesis in the cytokinin-autonomous strain is significantly lower than in the cytokinin-dependent strain. This difference was independent of either sugar source or concentration. These results support the observed inverse relationship between tissue growth and plastid development and the limited metabolic activity of plastids in cytokinin-autonomous tissues.

On the basis of earlier data it was suggested that the induction of cytokinin autonomy might be accompanied by disorders in plastid function and a decrease in cytokinin utilization. In the work presented below the formation of chlorophyll and the isozyme patterns of nine enzymes, some of which are known to be localized in plastids, were compared in tobacco callus tissues differing in their hormonal requirements. Tissues either not requiring cytokinin or both auxin and cytokinin for their growth, contained a lower amount of chlorophyll than the cytokinin-and auxin-dependent strain. The number of isozymes of glucose-6-phosphate and NADP-malate dehydrogenase (i.e. enzymes which are known to be located in plastids) was reduced from four in the cytokinin-and auxin-dependent strain to two and one in the two cytokinin-autonomous strains, respectively. The fully habituated tissue contained an additional isozyme of NADP-malate dehydrogenase. The total number of isozymes of the remaining enzymes (NAD-malate dehydrogenase, peroxidase, esterase and a-and β-galactosidase) either was decreased or not changed in the cytokinin autonomous strains. The exception was an additional anodic peroxidase in one strain. The number of these isozymes in tissue habituated with respect to both auxin and cytokinin either remained the same or increased. Tobacco callus strains with altered requirements for growth regulators contained some new isozymes which were not present in any other strain and some isozymes present in other strains were absent. These differences are discussed in relation to the possible role of plastid function disorder associated with habituation.

Uptake of potassium by rice plants at different stages of growth can be described by a biphasic isotherm in the range of 5 × 10^-5 M and is probably mediated bya multiphasic mechanism in the plasmalemma.

The induction of gametogenesis has its beginning in the most diluted cell suspension after the transfer of the cells to a nitrogen-less medium. Here, the highest percentage frequencies of zygotes are formed within the same period of time in comparison with the less diluted cell suspensions. The zygotes formed in the mostly diluted cell suspensions mature relatively very slowly and germinate very irregularly. The induction of gametogenesis retards in the denser cultures probably due to the strongest homeostatic forces trying to return the cell population to its initial stage. In our experiments up to now, the effects of the changing irradiance of the cells inside the suspension were not separated from the effects of the changing number of the cells in the given volume of the culture. Neither were the ratios of distilled water to the amount of the zygotes, nor to the vegetative cells constant. Thus, it is necessary to consider the mentioned effects as the result of an interaction of both factors under consideration. Each of the cell populations behaved as an autonomous whole. Also the populations, starting after the transfer to a nitrogen-less medium of the same culture density, may sometimes differ significantly in the observed characteristic features at various phases of their growth. The discontinued supply of nitrogen obviously causes a change of the cell metabolism in favour of the nitrogen-less substances, especially in the more diluted cell suspension. This work completes and explains some earlier results obtained from the study of the life cycle inChlamydomonas geitleri.

The study was concerned with the effects of irradiation of the sodium humate on its biological activity, which was assessed by the elongation of the hypocotyl and root in young plants of lettuce (Lactuca sativa L. cv. Rapid and cv. Smaragd) growing in the solution of the tested preparation. It was found that its stimulative action on hypocotyl and root elongation in lettuce was changed due to irradiation. However, the degree was dependent on concentration; stimulation mostly decreased, only at some higher concentrations did it increase. Further, experiments showed that there was some interaction between the irradiation of the humate and the cultivar used for testing, but none between the irradiation and the light exposure of plants during the test. The response of the experimental plants to the concentration of the humate depends on the light exposure.

Uridine-³H incorporation and RNA concentration were investigated in different parts of the shoot apical meristem ofChenopodium rubrum using autoradiography and cytophotometry. A single inductive cycle was sufficient to bring about postinductive first events in the shoot apex but not for complete flower differentiation. The initial activation of RNA synthesis manifested itself in all zones of the apex. The first increase was more conspicuous in the peripheral than in the central zone. The indications of the first events in the apices after a single inductive cycle disappear prior to morphological reversal to the vegetative state. Induction by three short days led to rapid flower differentiation. The increase in RNA synthesis and concentration was most conspicuous in the central zone in this case. The ratio of RNA synthesis and content between bud and leaf primordia (B/L) also change in relation to photoperiodic induction. In vegetative plants the B/L ratio was low while after induction it increased.
The shifts in activity of RNA synthesis observed in the shoot apical meristem are related to the changes in growth activity of the different parts of the apex. The growth ratios in the apices bear the character of growth correlations. The change in the growth correlations following photoperiodic induction together with the total activation of RNA synthesis are considered to represent one of the first events of the transition to the reproductive state.

Soybean (Glycine max (L.) MERR. CV. 'Amsoy') plants were grown for 40 days in nutrient solution at various concentrations of ammonium. Maximum yield of dry matter was obtained at a concentration of 715 μM. Further increase in the concentration of ammonium resulted in a reduction in growth due to ammonium toxicity which affected both root and shoot development. The pattern of nitrogen accumulation in tops was consistent with the multiphasic uptake of ammonium and can be represented by 2 phases in the range 1.78 X 10-⁵-3.57 x X 10-³ M of ammonium.

Upon rooting of poplar stem cuttiags the total inductive stimulation does not take place, but the individual root primordia maintain a relative independence. This becomes evident by various time parameters of their differentiation. Under experimental conditions, in dormant cuttings from one year individuals of the hybrid I 214 the activation of the first root primordia occurs after 24 h, the pre-emergent development of the roots formed was completed after 72 h.
The activated root primordium is divided into two regions. In the distal region with the predominating cell division the root apex with histogens is formed by the action of initials. From peripheral cell layers of the distal region the so-called "Wurzeltasche" develops which covers the root cap. Due to cell elongation in the proximal region the root apex is pushed up towards the stem surface. The beginning differentiation of the connective vascular tissue is a preparative step for the connection of the vascular system of the developing root with the secondary vascular system of the maternal stem. Following the penetration of the root through the peripheral stem tissues this connection is realized with progressing development. In the developed root the protoxylem elements differentiate continuously and acropetally in direct continuity with tracheids of the basal connective region.

Starch formation was studied by means of plant anatomy in segments of maize and pea leaves, deprived of starch, floating overnight in the dark (1) on solutions of various saccharides, (2) on sucrose solutions containing auxin-type growth regulators and (3) on suorose solutions with antibiotios (proteosynthesis inhibitors). A comparison was made of mesophyll tissues of the two species used, of spongy and palisade parenchyma in pea leaves and-especially-of mesophyll and vascular bundle sheath in the leaves of maize. Although the effects of the given treatments were striking, the response of the particular tissues was considerably uniform. If the given sugar appeared as utilizable for starch formation, it was effective equally in all tissues under study. It was not possible to distinguishin situ the different ways of staroh synthesis by means of the application of growth substanoes. No striking differences in the effect of antibiotics upon staroh formation were seen in-normally-starch containing and starch lacking tissues.

The effects of acetylcholine (Ach) on growth, the total peroxidase activity and the isoperoxidase spectrum of the roots ofLens culinaris were studied and compared with actual and earlier results obtained with an auxin (IAA) treatment. The general growth and peroxidase activity patterns of Ach treated roots and IAA treated ones showed many important similarities.

The weight of alfalfa plants, especially roots of susceptible strain, decreased when inoculated withCorynebacterium insidiosum. At the 6th week after inoculation the³²P uptake per plant and its translocation into the above-ground organs were considerably decreased in susceptible plants. On the other hand, the³²P uptake was increased and the radiophosphorus was accumulated in above-ground organs in resistant plants.

The effect of plant hormones was studied on the growth of excised coleoptile segments of wheat plantlets grown under daylight conditions. In addition to the change in growth, that in the orientation of microtubules and cellulose microfibrils was investigated in parenchyma cells. Following a 6-h treatment gibberellin, and still more kinetin, stímulated the thickening of segments, which became evident also in an altered orientation of microtubules. Whereas in the control the microtubules and wall microfibrils were oriented randomly, following gibberellin treatment they were all parallel and formed an acute angle with the longitudinal cell axis. A still more pronounced difference resulted after kinetin treatment, when microtubules were localized parallel with the longitudinal cell axis. Auxin had the opposite effect: it stimulated the elongation of the segments, which became evident in a transverse orientation of both wall microtubules and microfibrils.

The localization was studied of α- and β-galactosidases in frozen sections of Ca-formol fixed root tips using simultaneous azocoupling reaction. In all species studied (Allium cepa,Cucurbita maxima, Lupinus albus, Pisum sativum, Vicia faba, Zea mays) positive results were obtained, the localization being ubiquitous (according to localization typology given here).
InVicia faba andZea mays the isoenzymes of α- and β-galactosidases were revealed by means of acrylamide gel electrophoresis, using authors' modification of Reisfeld method, in whole root tips, particular growth zones and separately in cortex and central cylinder. No differences were observed comparing stele and cortex. Whereas characteristic isoenzyme patterns were found in individual growth zones in maize, no differences appeared in broad bean.
A comparison was made of thein situ localization and of the isoenzyme patterns of α- and β-galactosidases with α- and β-glucosidases. In the case of galactosidases, positive results appear with both α- and β-galactoside. The rising of pH to neutrality leads to considerable decrease in the activity of both galactosidases.

The culture filtrates of the rhizosphere fungi of broad bean (Vicia faba L.) and cotton (Gossypium barbadense L.) were analysed for the presence of plant growth substances of auxin and gibberellins nature. Bioassay test and chromatographic analysis indicated that these fungi, each synthesized different auxins in their culture medium. These auxins were indole compounds. Similarly the rhizosphere fungi produced in their culture medium some gibberellins and gibberellin-like substances.

Cell division contributing to longitudinal growth of the shoot apex was investigated inChenopodium rubrum in segments marked by the axils of leaf primordia. Plants treated with two short days (16h of darkness and 8h of light) were compared with two non-induced controls (cultivated in continuous light or treated by alternations of 8 h of darkness and 4 h of light for two days). During the short-day treatments the rate of cell division contributing to the longitudinal growth decreases in all segments of the shoot apex irrespective of whether the darkness was given in inductive or non-inductive photoperiods. The rate of cell division contributing to longitudinal growth increases in the upper internodes of the shoot apex after the termination of the photoperiodic treatment and transfer of the plants to continuous light. However, cell division remains inhibited in the lowest segment of the shoot apex. This inhibition in the differentiating parts of the shoot apical meristem is a direct consequence of photoperiodic induction. It is supposed that this inhibition is related to evocation similarly as the well-known phenomenon of stimulation of cell division in the apical dome.

Cytokinin activity was demonstrated in the Baltic sea waters. This activity was always higher in the near-bottom water, taken from theFucus vesiculosuszone, than in the superficial zone. A cytokinin-like substance showing properties typical of 6-(3-methyl-2-butenylamino)purine (2iP) was also present in extracts from the thallus ofFucus. It was found that exogenously applied cytokinins, in some concentration ranges, markedly increased the number of adventitious branches formed on the cut surface of the thallus fragments. The growth responses of the investigated plant tissues to the different cytokinins varied according to season and kind of cytokinin applied. The possibility of exudation of some cytokinin like substances by the algal cells into the surrounding waters was considered.

The effects of soaking seed in 2-chloroethylphosphonic acid (CEPA) for 24 or for 48 h on the cumulative 5-day seedling growth ofCucumis sativus L. (cucumber) andPisum sativum L. (peas) were studied. Each cucumber seed absorbed an average of 0.015 ml of CEPA solution, while pea seed absorbed 0.365 ml, over a 24 h period.
In cucumber, 240 mg l^-1 CEPA concentration decreased radicle length by 23%, regardless of soaking duration. The same concentration increased radicle weight in a 24 h soaking duration, but decreased radicle weight when soaking was for 48 h. At 48 h, CEPA concentrations of 0.24 and 2.4 mg l^-1 increased plumule growth by 26%. In peas, the 240 mg l^-1 decreased the length and the weight of both the radicle and the plumule in a 48 h soaking duration, but had no significant effect at a 24 h soaking. At the low concentration of 0.24 mg l^-1, seedling growth was stimulated by over 30%.
Cucumber was 3 times more efficient than peas in the utilization of CEPA for seedling growth, in terms of total fresh weight of seedling per microgram of CEPA absorbed: 1 127 and 274 mg μg^-1 CEPA in cucumber and peas respectively. Extrapolative calculation, using cucumber responses as standard, suggests from this seedling study that about 12 mg l^-1 CEPA is likely to stimulate growth and/or yield in sprayed pea plants.

When flax seedlings are decapitated above cotyledons and three days later one of the two cotyledons is removed then the remaining cotyledon stimulates in four to five days growth of its axillary bud. It has been found that content of endogenous cytokinins was higher in the stimulated bud as compared with the other one already 12 h after the cotyledon removal.
Flax seedlings decapitated under cotyledons regenerate adventitious buds on thy hypocotyl stump during 5-6 days. The endogenous fytohormonal preparation of this regeneration was investigated in the 20 mm apical part of the hypocotyl stump. Decrease in auxin and increase in gibberellins was already found during the first day after decapitation while the level of cytokinins increased as late as three days after the apex removal.

Anomocytic stomata and stomata with single subsidiary cells are commonly observed Sometimes a stoma appears anisocytic. Double cytoplasmic connections between nearby stomata and division of guard cells with persistent or degenerating nuclei are seen in GA. One or more divisions of guard cells, displaced guard cells and single guard cells with or without pore are noticed in SUC. Formation of single guard cells is a common feature in TIBA. Paracytic stomata, one and a half stomata and persistent stomatal initials are seen in SUL. COUM seems to be not inhibitory inCucumis sativus. In COL stomata with unequal guard cells, unequal stomatal cells with thickening in between but without intervening pore, stoma with double pores, persistent stomatal initials which may be solitary or in groups with varying shapes and with one or two nuclei of different shapes are noticed. The growth regulators affect the frequency of stomata, epidermal cells; stomatal index; size of guard and epidermal cells.

Barley plants were grown until day 21 under conditions which were different in relation to photon flux density, carbon dioxide concentration and temperature. Dry weight and leaf area increase from day 7 until day 21, shoot apex development between day 15 and day 47, and yield of each treatment group were considered. Photon flux density was demonstrated to have a greater influence on net assimilation rate (NAR) of young plants than has carbon dioxide enrichment. High temperature treatment seems to influence NAR less than growth and developmental processes. Grain yield of high temperature treated plants was significantly lower than that of the other treatment groups. Significant correlations have been found between growth analysis values of young plants and some yield components of each treatment.

Following moderate water stress in the cortical cells of theZea mays primary roots, the condensation of the nuclear chromatin, a higher density of free ribosomes and a reduction of polyribosomes, the reduction of mitochondrial cristae, elongation of ER elements, less compact dictyosomes and inhibited production of the Golgi vesicles were observed. Severe water stress would cause more severe structural damage in the cortical cells. The more differentiated cortical cells showed more expressive ultrastructural damage when compared with the meristematic nonvacuolated cells. Similarly, the cells of the peripheral layers of the cortex suffered more from water deficit than the cells of the layers situated closer to the central cylinder.

The effect of various sodium salts at the early developmental stages of wheat cultivars was studied. Germination was not affected by the presence of salts but cv. H-68 was more tolerant than Mexipak during later growth. The roots were more sensitive than the shoots. The salts under study could be divided into two groups. Bicarbonate, carbonate, acetate and citrate were more toxic for growth than sulphate, nitrate, phosphate and chloride of sodium. The individual members of each group did not vary much from one another.

The time course of the changes in the level of endogenous growth regulators was followed during the stratification at 5 °C of the seeds of 'Panenské české' apples. An increase in the endogenous gibberellin activity was found already during the first and the second week of stratification which is according to it decisive for the release of dormancy in the seeds, as it precedes with the anticipation of approximately two weeks the curve of the release of dormancy in the seeds. The rise in the level of endogenous cytokinins in the seeds is belated one to two weeks behind the rise in gibberellin activity in them and thus approximately coincides with the release of dormancy. The rise in auxin level occurs approximately 4 weeks after the increase in cytokinin level. The increase in auxin level, which is accompanied by an increase in inhibitions, is apparently not connected with the release of dormancy in the seeds during the stratification.

Ethanol-soluble and insoluble nitrogen and protease activity in maize seeds during imbibition period of 6 to 60 h at 30 ± 2 °C were determined both in light and in the dark. In light, soluble and insoluble nitrogen in the embryo were similar to that in the dark. But the increase in soluble nitrogen in the endosperm up to 38 h was higher in light than in the dark. Decrease in insoluble nitrogen was correlated with increase in soluble nitrogen, the level always being higher in the dark. Light increased protease activity also in the endosperm. Among various light qualities, red light was most effective in inducing proteolysis, and loss of nitrogen from the endosperm. Further, the growth and organic nitrogen of primary leaves from seedlings raised from light pretreated seeds were better than those from dark pretreated ones.