6-benzylaminopurine (BAP), β-indolylbutyric acid (IBA), phenylacetic acid (PAA) and a triazine herbicide (TH) affected the development of vascular bundles both in coleoptiles and the last intemodium below the ear of wheat plants. These substances were applied before the conductive tissues in the organs investigated were fully differentiated, the degree of their effect being dependent not only on the concentration, but also on the developmental stage of the plants and on cultivation conditions. In coleoptiles the area of vascular bundles was increased especially in the dark. In the stalk, BAP, PAA, IBA and IBA + TH increased the area of phloem. BAP also stimulated the activity of parenchymatous cells of xylem. TH had the same effect only on xylem, which became evident by an increase in vascular bundle area, but not in that of phloem. These anatomical aberrations were confirmed by cytological analysis which revealed that the stimulatory effect of the substances investigated consisted in activation both of companion cells of phloem and parenchymatous cells of xylem, whose function is analogous. As a result, both types of cells contained numerous organelles characteristic of meristematic cells, which suggests protein synthesis and an active transport of substances.

The radiotracer technique is described for transport and metabolic studies in latex producing bark. This technique provided further evidence that carbohydrates are supplied to latex vessels as sucrose and that sucrose is readily used for rubber synthesis. Bark treatment with ethylene resulting in latex flow stimulation is shown to activate within a few hours sucrose and water transport into the latex vessels. The available knowledge suggests an implication of an energy-dependent process of proton excretion which could explain the earlier observed ethylene induced alkalization of latex cytosol enhancing invertase and sucrose utilization.
An increase of tapping intensity decreases the level of latex sucrose and changes its distribution pattern in drained bark. There is a clonal difference in the early response to exploitation. Bark excision by conventional tapping inhibits downward sucrose translocation, the inhibition being proportional to the surface of consumed bark above the tapping cut. Seasonal variation in the level of latex sucrose is related to variations in sunshine duration and sucrose concentration rises during the process of refoliation. The results stress the importance of sucrose supply to latex vessels for latex producing potentialities and indicate an association of low sucrose availability in latex vessels with premature latex vessel degeneration and bark dryness.

Lemna gibba G3 is an ideal system for studying the chemical control of flowering in a photoperiodic plant due to its small size and aquatic growth habit which allow substances to be taken up continuously and rapidly distributed throughout the plant. Each of the known plant growth regulators has been tested onL. gibba G3 and only the gibberellins appear to be important for flowering, although they are not the limiting factor for flowering on short days. Salicylic acid (SA) and ferricyanide will both induce flowering inL. gibba G3 with ferricyanide being most effective on short days where flowering is daylength limited and SA most effective where flowering is limited by factors other than daylength. The ferricyanide action is probably due to HCN and it may act during photoperception or photoinduction. SA is most effective when reversing the inhibition caused by various parameters including copper and agar, and its effect is always strongly daylength dependent. It is postulated that SA may interact with the flowering stimulus to promote flowering and thus that SA acts at some point following photoinduction and the formation of the flowering stimulus.

Agrobacterium tumefaciens C58M (a nopaline strain) was used for induction of crown gall tumors inCentaurium umbellatum Gilib. The formation of tumors is very rare. After elimination of bacteria the tumor tissues grow in the light on R3B medium without growth regulators. They are positive in nopaline synthase.

Populations ofAllium montanum from 6 localities in Czechoslovakia show a certain variability, but no correlation between their mutual affinity and geological substrate, climate or altitude above sea level.

When the wheat germ cytokinin-binding protein (CBF-1) is isolated from excised wheat embryos only one group of polypeptides near 54 000 is observed as opposed to three polypeptide groups reported for CBF-1 from commercially milled wheat germ. The other two lower molecular mass polypeptide groups previously reported are probably proteolytic degradation products of the 54 000 species resulting from excessive heat or physical damage during milling. The CBF-1 polypeptide accumulates rapidly in the embryo after 20 days post-anthesis. A larger set of polypeptides near 66 000 - 68 000 appears during embryo development and also reacts with anti-CBF-1 serum. These polypeptides are also observed upon immunoprecipitation of 20-day embryo polyadenylated RNA translation products although the data are not definitive enough to prove a precursor relationship to the CBF-1 54 000 polypeptide. The new findings are discussed in regard to previous characterizations of CBF-1.

³H-labelled zeatin riboside (ZR) was applied to pod walls of intactLupinus luteus L. plants. Metabolites present in mature, dry seeds were zeatin nucleotide (ZNT), zeatin riboside (ZR) and zeatin (Z), zeatin O-glucosides and lupinic acid (LA), and the corresponding dihydro-derivatives of the cytokinins listed. Endogenous cytokinins were rapidly metabolised in germinating seeds. In seeds labelled with [³H]ZR for 90 min following a 2 h period of imbibition in water, ZR was actively converted to ZNT and dihydro-ZNT but the prevailing CTK was Z in cotyledons and ZR in embryo axes (EA); later LA and dihydro-LA, and O-glucoside metabolites accumulated. When [³H] zeatin was introduced into imbibing seeds, it was converted to dihydro-ZNT, ZNT, dihydro-ZR, ZR and dihydro-Z; in EA of the Z-labelled seeds, dihydro-ZR and ZR were the main cytokinins. After incubation of the Z-labelled seeds for 6 h in water, the ratios of dihydro-ZNT: ZNT and dihydro-ZR: ZR were, respectively, 20: 1 and 3.4: 1 in EA, and 3.5: 1 and 1.4: 1 in cotyledons.

Buckwheat cotyledons were induced to form callus tissuein vitro, in which shoots or roots could be regenerated, by changing the hormonal composition of the medium. The effect of gibberellic acid (GA₃) was studied in these processes. Addition of GA₃ to cell division medium during the first 5 days after inoculation did not interfere either with the induction of cell division, or with the subsequent organogenesis. However, GA₃ had a very pronounced effect on organogenesis when added immediately upon the transfer of expiants to organ induction medium. While root initiation was accelerated and root number increased, bud induction was inhibited. An initial GA₃ treatment had a long-lasting effect on bud induction and the tissue recovered from inhibition only in the fifth subculture.

Chromosomal variability in callus culture ofAsparagus racemosus was comparatively higher in the presence of 2,4-D than of NAA. The frequency of polyploid cells was enhanced with the increase in the concentration of 2,4-D or with the addition of coconut water. Gradual polyploidization with increasing age of the callus has been recorded.

Endogenous concentrations of indol-3-ylacetic acid (IAA) in auxin-autotrophio crown gall tissue cultures are presented in relation to culture growth rate and to tissue IAA levels in auxin-dependent cultures maintained on IAA as auxin source. Cellular levels of synthetic auxins absorbed from culture media were monitored in auxin-dependent cell cultures exhibiting selectivity in growth response to exogenous auxins. The results are used in modelling culture growth patterns and changes in intracellular auxin content.

Germination and seedling growth of rice was studied in NaCl and PEG 6000 solutions having osmotic potentials -0.2, -0.4, -0.6 and -0.8 MPa.
At isoosmotic concentrations, the NaCl proved more harmful to germination, seedling growth, per cent moisture content of seedling organs as well as mobilization of food matter from seed to the growing seedlings. This fact suggested that in rice, at least in the early stage, a specific ion effect rather than osmotic effect is the prime cause of salt injury. Compared to susceptible cultivar, the tolerant one was less inhibited by salinity.

Treatment of etiolated and excisedCucurbita cotyledons with exogenous cytokinin (benzyladenine) in darkness or light results in a marked stimulation of Rubisco activity, content of enzyme protein, and incorporation of labelled precursors into it, indicating cytokinin-stimulatedde novo synthesis of the enzyme. Cell-free translations of RNA in the wheat germ andE. coli systems show an increase in both large and small subunit mRNA amounts relative to the increase of total RNA under the influence of the phytohormone and light. This increase in the level of translatable RNA is confirmed by RNA hybridization with the Rubisco large subunit gene of spinach. In addition, our results demonstrating additive effects of benzyladenine and light in cotyledon and chloroplast development suggest that the two factors co-act independently in the causal sequence of Rubisco gene expression. The data are discussed in a general view of cytokinin action in gene expression steps.

The auxin transport inhibitor TIBA strongly influences meristem structure and activity in the unistratose gemmaling ofRiella. The gradient of cell cycle duration, essential for normal morphogenesis, is abolished and the cell cycle is reversibly arrested during exposure to light. At the same time starch accumulation in the light is inhibited. Possibly, these effects are the consequencc of the inactivation of sulfhydryl-containing proteins by TIBA.

Leaf expiants from vegetative plants of the short-day plantStreptocarpus nobilis (C. B. Clarke) developed flower budsin vitro when cultured in 8 h photoperiods. Tn non-inductive photoperiods only vegetative buds were formed.In vitro photoinduction was demonstrated by giving the expiants short-day (SD) cycles and then transferring them to non-inductive photoperiods for expression of flowering. On medium containing 6-benzylaminopurine (BAP) organogenesis was initiated during the photoinductive treatments. Photoinduction of leaf tissue without adventitious bud development was obtained on medium without BAP. The photoinductive state of the leaf tissue was fairly stable, being expressed after 2-3 weeks in non-inductive photoperiods when adventitious buds were formed. The quantitativein vitro flowering response to the endogenous floral stimuli, resulting from photoinduction, could provide the basis of a bioassay for presumptive flower inducing chemicals.

A specific, high affinity, IAA binding site was demonstrated in both a cytosolic fraction, and in isolated nuclei, fromNicotiana tabacum cv. Wisconsin No. 38 cells grown in suspension culture. The amount of the binding site detected in both these fractions changed during the culture cycle according to a strict pattern. The molecular mass of the binding site was estimated by gel filtration to be approximately 175 000 and it appears to be a protein. When partially purified by affinity chromatography and allowed to pre-incubate with IAA, the site had a significant stimulatory effect on total RNA synthesis, as measured by a cell-free assay system. Unpurified extracts had no such effects. The system behaves rather like the steroid hormone-receptor system in animals.

A range of endogenous cytokinins have been identified inDatura crown-gall tissue by GC-MS. Incorporation of [³H]adenine into zeatin riboside, zeatin and its nucleotide(s) is also shown. Metabolism studies usingcis- andtrans-isomers of zeatin riboside indicate that interconversion of the two isomers does not occur in this tissue. Data on the identity of major endogenous cytokinins in a genetic tumour line of tobacco is also provided.

The influence of different organs on flowering of photoperiod- or temperature-dependent plants and of neutral plants is described. Special attention is given to the influence of roots which generally inhibit flowering. High or low temperatures applied to the roots ofChenopodium polyspermum, a quantitative short day plant, induce flowering. Vernalizing treatment of roots ofCichorium intybus suppresses the inhibition of flowering arising from the tissues immediately underlying the terminal bud. Other plants such as coniferous trees can flower more intensively if the growth of their roots is reduced. After a short presentation of the very complex situation concerning the regulation of floweringvia the presently known hormones, the methodological limitations of our understanding of the precise hormone mechanism of flowering will be discussed. One example of an immunologica 1 approach to localize endogenous hormones inside tissues is given, using abscisic acid.