Barley embryos were treated by 0.1% colchicine for 30 min. Samples of root tips were fixed after 4 h, 8 h and 12 h. In the first sample,c-metaphases, normal metaphases and anaphases were present jointly. Inc-metaphases, chromosomes sometimes tended to make two groups with 7 chromosomes in each. In anaphases, lagging chromosomes, tripolar and multipolar anaphasos were found. No chromosomal aberrations were detected in anaphases and metaphases. No chromosome disturbances were found in root tips sampled 8 h and 12 h after colchicine treatment.

The initial strain ofDioscorea cell culture is characterized by a double-peak curve of mitotic activity, by dominance in the population of meristematic cells, by a great variety in the number of chromosomes and also by polyploidization in the process of cultivation.
After treatment with different doses of N-nitroso-N-methylurea (NMU) physiological parameters of the cell populations were found to change (dynamics of mitotic activity, ratio between types of cells). On passaging, physiological differences between the strains are levelled up.
The studied strains are characterized by different directions of cell selections,i.e. the control strain - towards polyploidization, and in NMU treated strains are stabilized on di- and triploid levels.

The effect on growth of an aliphatic acid isolated fromCastanea sativa cuttings was studied as well as its interaction with IAA. TheAvena coleoptile straight growth test was used. A growth inhibition was observed in a wide range of concentrations. The compound lowered or suppressed the IAA induced elongation of theAvena coleoptilo growth sections.

Nine categories (a-i) of seeds inIpomoea pes-tigridis showed diverse germination responses at desiccating high temperatures (65 °C). These nine "generative ecotypes" have assured the persistance of their race by producing sets of seeds suitable for a set of temperature conditions in the Indian desert, where high desiccation of seeds is a major natural controlling factor.

Net photosynthetic rate decreased sharply to zero in the range of water potential- 8.0 to -10.4 x 10⁵ Pa. The observed decrease in photosynthetic rate was due not only to the decrease in epidermal conductance, but also to the decrease in intraoellular conductance. Both conductances decreased in the same range of water potential. With decreasing water potential photorespiration rate decreased whereas dark respiration rate remained rather unchanged. Simultaneously CO₂ compensation concentration increased. These facts constitute an indirect evidence that water stress inhibited not only transport of CO₂ from atmosphere to carboxylation sites in chloroplasts, but also its conversion into photosynthates.

Tuber callus by subculture ofDioscorea deltoidea Wall, was grown with different sources of nitrogen on N-free Murashige and Skoog's basal media supplemented with a high level of kinetin (1, 3, 6, 9 and 12 ml 1^-1) and low concentration of auxin (0.01 mg 1^-1 2,4-D) for shoot bud differentiation. Shoot and root differentiation was observed only in the case of ammonium nitrate. Other sources of nitrogen failed to produce shoot bud differentiation except in the case of ammonium citrate where tissues were slight green in colour and were recognizable as pro-embryo.

The method for histochemical detection of IAA oxidase proposed by Sagi was tested, based on colour reaction of natural products of IAA oxidation with Ehrlich-like reagent.

The effects of red and far red illuminations were studied in spores of the dark germinatingPteridium aquilinum and that of the light dependently germinatingDryopteris filix-mas. Proteins were analysed by electrophoresis according to their molecular weights. The isoesterases were separated by gel electrofocusing. In both species we found two newly synthesized protein bands, probably controlled by the presence of active phytochrome. One of these seems to be identical, the other is different in the two species. Phytochrome control was also detected in the esterase isoenzyme pattern.

Benzylaminopurine (BA) caused an enhancement of chlorophyll and protein content and a reduced elongation of primary barley leaves. BA did not change the rhythmic pattern of¹⁴CO₂ fixation and activities of RuBP carboxylase, RuBP oxygenase, glycolate oxidase and phosphoglycolate phosphatase, but the enzyme activities were enhanced and the level of¹⁴CO₂ fixation was reduced. Light/dark¹⁴CO₂ evolution ratio was affeoted by BA only in older leaves. BA acts sequentially on the activities of photosynthetic and photorespiratory enzymes.

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.

The minimum length of the mitotic cycle of root meristems of cultivated barley embryos and intact seedlings was longer than that measured by the construction of the labelled mitoses curve; it was 10-12 h for intact seedlings and 16 h for cultivated barley embryos. Action of colchicine on interphase was detected. Colchicine induces the increase of the frequency of prophases starting from the fourth hour. The most probable explanation is shortening of the S-phase. As the whole mitotic cycle duration is increased in comparison with that after³H-thymidine, it is most probable that G₁ phase duration is increased by colchicine treatment. Different cytogenetic effects of colchicine were analysed in detail. A basic difference between the response of root meristems of isolated embryos and of intact seedlings was found. In isolated embryos, the effect of 0.1% and 0.4% colchicine (i.e. blockage of anaphase movement, metaphase arrest and contraction of chromosomes) disappears within 2-5 h after removing the colchicine. In intact seedlings, the effect of colchicine is maintained for a considerably longer time. It leads to gradual accumulation of metaphases over 9 h after pulse treatment and this accumulation of metaphases leads to a gradual increase of the incidence of tetraploid mitoses starting from 10th - 12th till 22nd hour after the pulse. This is the reason why maximum frequency of tetraploid cells in root meristems of cultivated isolated embryos was 16 h after the pulse (i.e. at the beginning of their incidence) and it reached the value 5.4% while in seedlings the maximum was 22 h after colchicine treatment and it reached the value 38%.

Chosen species and cultivars(Nicotiana sanderae, N. glutinosa, N. otophora, N. paniculata, N. sylvestris, N. velutina, N. tabacum cv. Samsun, N. tabacum cv. Samsun - a dihaploid line, and an amphidiploid N.sylvestris x N tomentosiformis) were treated with adequate concentration of n-buthylmethane sulphonate. The anthers of M₁ plants were cultured on the medium of NITSCH 1969 plus 0.1 mg IAA/1. Special attention was paid to quantitative characteristics of androgenesis. Androgenesis occurred more often in the treated variants. The conclusions have been confirmed of a heterosis effect of adequate chemomutagen concentration at the diploid level (an increase in the number of androgenic anthers in the treated variants, and a decrease in the mean number of haploids per androgenic anther) in the broad range of the material. We have recorded a high androgenic ability in the amphidiploidN. sylvestris x N. tomentosiformis, and androgenesis inN. velutina for the first time.

Anatomical analysis of the sugar-beet seed ball indicates two possible ways for the entrance of water and oxygen during germination: cells from the operculum periphery and cells from the basal pore characterized by absence of lignin and a thin layer of cellulose. Impermeabilisation of these zones by vaseline considerably reduces the percentage of germination and stresses the major role played by the basal pore. This can also be confirmed by variation in the germination percentage when sowing the seed ball with the basal pore up or down to the substrate.

Alcohol dehydrogenase was prepared from 2-day germinating maize and 3-day germinating broad-bean seeds by ammonium sulphate fractionation of sodium phosphate extracts, chromatography onDEAE cellulose and Sephadex G-200. The activity of the broad beanADH amounted to182 800 units per mg protein, that of maizeADH 79 000 units per mg protein. Besides oxidation of a series of alcohols at pH optimum in the alkaline region and with KM equalling 10-2M, alcohol dehydrogenases isolated from both plants catalyze the reduction of acetaldehyde, n-propanal, n-butanal, isobutanal and crotonal at pH optimum in the neutral region with KM equalling 10-3M. The inhibition studies using fatty acids and chloride ions revealed that the oxidation of alcohols is inhibited competitively by both types of inhibitors, with inhibition constants of 10-2M and 10-1M, respectively. The inhibition in the presence of acetaldehyde is non-competitive since the inhibitors do not compete with acetaldehyde and do not form an enzyme-NADH-inhibitor complex, yet they obviously react with the enzyme-NAD product only, thus giving rise to an enzyme-NAD-inhibitor complex. These differences in the behaviour of inhibitors may be interpreted in the sense that the binding sites of ethanol and acetaldehyde as substrates for broad bean and maize alcohol dehydrogenases are non equivalent. The nonequivalency discussed in the text.

The changes of kernel nitrogen (N), phosphorus (P) and dry weight (DW) were determined during the time period from 10 days after anthesis till maturity in three spring barley strains. The plants were cultivated under field conditions in Gatersleben (German D.R.) and Kroměříž (Czechoslovakia). The course of N, P and DW changes was described by Richard's comprehensive growth function dW/dt = aW^m + bW, where W is the amount of N, P or dry matter per kernel, a, b, m are coefficients. The integral of this function was used and several parameters calculated. There was a remarkable synchrony between N or P and total dry matter accumulation in the kernels. Thus, the N or P concentration per unit kernel dry weight was relatively constant during the investigated period and with few exceptions corresponded to 80% to 100% of the final value. However, considerable differences between strains, years or places of cultivation were found.

Penicillin caused elongation inhibition of mungbean (Phaseolus aureus L.) seedlings at concentrations above 100 mgl^-1. Inhibition of hypocotyl could be reduced to different degrees by manganese, pyruvate, succinate, fumarate, malate, GA₃, purines, pyrimidines and nucleosides, whereas the amino acids except cysteine were not effective. Penicillin inhibited neither elongation of wheat coleoptile sections nor the cell enlargement induced by IAA in this tissue. Thus penioillin inhibits intact seedling elongation probably through an Effect on cell division apparently without inhibiting cell enlargement.

During the germination of fenugreek (Trigonella foenum graecum L.) sulfhydryl groups rapidly declined in cotyledon and seedling axis, while peroxidase activity increased. Studies on purified isoenzymes showed that GSH was oxidized by the isoenzymes and was accomplished in presence of cofactors, Mn²⁺ and DCP along with H₂O₂ (0.01 mM). This reaction was found to be peroxidatic in nature. The oxidation was inhibited by catechol but was enhanced by malic acid.

Fusarium moniliforme var.subglutinansWr. etRg. causes malformations of mango inflorescences that finally fail to fruit. The host-cultivar Himsagar showed higher contents of total saccharides, chlorophyll and protein than the cultivar Bombai. Considerable loss in saccharides and chlorophyll contents and increase in protein content as a result of malformation of inflorescence was recorded in both the host-cultivars which progressed with time.

Rhynchosia capitata possesses a hard seed coat dormancy. Three types of seeds were marked out of this species on the basis of colour and mottling on the seed coat. The three different types behave differently when they were tested for germination.

On cutting off one cotyledon from decapitated pea seedlings cultivated in the dark, the apical dominance is restored, as is well-known, by the growth of the bud of the removed cotyledon. As early as 12 h following cotyledon amputation(i.e. at the time when buds of both cotyledons-remaining and removed-are not yet differentiated in size), a decrease in the level of endogenous abscisic acid can be demonstrated in the bud of the removed cotyledon.

In the cultivar ofPhaseolus vulgaris L. cv. Vainica Saavegra B a protein was found in the seeds having a more or less reduced electrophoretic mobility on the cathodic side in comparison with standard cultivars. This protein which has phytohaemagglutinating activity loses this property at a greatly decreased mobility, whereas at partially reduced mobility the phytohaemagglutinating activity is maintained. The protein with a partially decreased mobility is immunochemically identical with the protein having normal mobility, whilst the protein with strongly reduced mobility is immunochemically only partly similar.

Kinetin and auxin when applied to excised segments of wheat coleoptiles bring about changes in chloroplast structure and chlorophyll content of parenchymatous cells. Auxin (IAA) alone at a concentration of 10^-5M stimulated the elongation (growth), but the chloroplast membrane system was less developed and the chlorophyll content was lowest in comparison with control and other variants. Kinetin (KIN) exhibited various effects depending on the concentration used. 10^-6M KIN somehow stimulated the elongation and enhanced the amount of grana coming to one chloroplast section, but the individual grana were relatively small and the chlorophyll content a little higher than in the control. On the other hand 10^-5M KIN which did not promote the elongation of wheat coleoptiles, had the maximum stimulatory effect on the chloroplast membrane system, especially on the occurrence of large grana, and the chlorophyll content was highest in comparison with the other variants. The occurrence of starch grains in chloroplasts was lower than in the other variants. The effect of a joint treatment of KIN and IAA did not exceed that of KIN (10^-5M) alone. Thus the development of chloroplasts and the accumulation of chlorophyll in wheat coleoptiles are stimulated by the concentration of KIN which does not promote the elongation of coleoptiles.