Petunia hybrida plants were inoculated with differentAgrobacterium rhizogenes andA. tumefaciens strains and developed tumors were further cultivatedin vitro. Transformed flowering plants differentiated from tumors induced byA. rhizogenes strains 8196 and TRIOL Transformed but non-rooted plants developed also from tumors incited byA. tumefaciens T37. Cultures of roots transformed byA. rhizogenes strain 15834 did not show increased incidence of chromosomal aberrations in anaphases in comparison with untransformecl control. Permanent growth of isolated untransformedPetunia roots was not induced by addition of IAA into the medium.

An improved system of plant cultivation at stable and specific levels of polyethyleneglycol (PEG, mol. mass 1400-1600) - induced water stress has been described. To set up this system a perforated tubular glass vessel containing soil to support seedling growth was wrapped externally first with a layer of macroporous silica gel-G and then with three layers of a dialysis membrane of a lower exclusion limit (2000 mol. mass). Effects of 8 days of PEG - induced stress have been studied on uptake and translocation of N and P and growth of barley (Hordeum vulgare L. cv. KN 16) seedlings. Some of the noteworthy improvements of the system were exelusion of PEG from the plant consequent upon use of silica gel-membrane combination, shorter time (2 days) for the soil-plant-air continuum to attain steady state, and stability of the plant water potential over a period of a few days.

The rates of maintenance and growth components of leaf dark respiration of a C₃ plant (Phaseolus vulgaris L.) and C₄ plant (Zea mays L.) as affected by temperature were studied using the McCree concept. Respiration rates were measured by means of infrared gas analysis in a closed gas exchange system. In both C₃ and C₄ species R_D and R_m increased with temperature in the temperature range (15-62 °C) studied. R_G depended on temperature with an optimum near the temperature optimum of gross photosynthetic rate, P_g. Significant correlation between R_D and R_M and between R_G and P_G was found.

Using water culture technique, some experiments have been performed to investigate the effect of 60 days salinization treatments (0.0-100 meq 1^-1 NaCl) on dry weight and on the content of some nutrient elements (Na, K, Ca, Mg, P, N) in castor bean, sunflower and flax plants. In general the content of sodium increased progressively with the rise of salinity level. The relatively low and moderate salinization levels (20 and 40 meq I^-1 NaCl) resulted in a promotion rather than inhibition of the dry weight and in the content of most of the investigated elements in the different organs of the test plants. However with the rise of salinization level from 60 to 100 meq l^-1, the dry weight and the content of these nutrient elements were mostly reduced.

Flower initiation takes place during a rise of peroxidase activity following a peak of minimum activity which marked the completion of the flowering inductive phase. Since basic isoperoxidases underwent an inverse variation of activity in the course of successive inductive and initiative phases, it was hypothesized that the induction of flowering led to a temporary peak of maximum auxin level in the leaves. Our analyses and available literature data support the view. They also show the different capacity of non-induced and induced material to respond to external auxin application. Since some aspects of the physiological state characterizing induced plants can be simultaneously obtained in all plant parts as a result of rapid interorgan communication, the classical florigen theory is seriously challenged.

Chlorides, nitrates, and sulfates of alkali metals, ammonium, calcium, and magnesium inhibit P_i uptake into maize root cortex segments. The concentration 100 mM brought about 50-100% inhibition, whereas 10 mM concentration (with the exception of salts of NH₄+, Ca²⁺, Mg²⁺) about 15-55%. Also potassium benzenesulfonate (100 mM) dramatically decreases P_i uptake.
Osmotic shock also inhibits P_i uptake. Marked decrease of P_i uptake ability proceeds in concentration range 0.12-0.13 M NaCl. Concomitantly, proteins are released into rehydration medium and their amount is proportional to the degree of P_i uptake inhibition.
The effect of 0.13 M NaCl on P_i uptake and protein release is about the same in roots of intact plants, excised roots, root segments and segments of isolated cortex and stele. Roots of intact plants and excised roots are more responsive to osmotic shock than studied segments.
The degree of salt tolerance of glycophytes is in correlation with NaCl concentration, which brings about 50% inhibition of P_i uptake.

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.

During high altitude acclimatization both the number of stomata and their pore width decreased. The number of open stomata per unit leaf area in the morning and evening hours was higher as compared to that in plants grown at a lower altitude. Thickness of leaves also decreased at high altitudes but the effect on the size of epidermal, mesophyll and spongy parenchymatous cells varied from species to species. Adaptational significance of these changes are discussed.

The decrease of peroxidase (PO) and IAA-oxidase (IAAO) activities in stem bark of intact photoperiodically neutral tobacco plants was shown both in the course of development and in an acropetal direction along the stem as related to flowering regulation. In stem expiantsin vitro, the realisation stage of floral morphogenesis is related to an increase in PO and IAAO. This correlates with low auxin concentrations in the medium as required for floral morphogenesis. The changes in both PO and IAAO are suggested to be in the opposite directions during floral induction and floral morphogenesis.

Experiments were conducted (a) to identify optimum media pH for nitrate uptake by intact corn (Zed ways L. cv. XL-81) plants grown under solution culture conditions, (b) to understand the effect of media pH on growth, nitrate uptake, water use and nitrogen accumulation. pH was maintained using carboxy cation exchange resin IRC-50. Plantswere grown in 15mM NO₃-N per litre and nitrate depleted from nutrient solution over a period of time was measured. Dry matter accumulation by the plants decreased progressively with increased pH. However, the decrease was significant only at pH 7.0 and 8.0. Data on water use showed results similar to dry matter accumulation. Correlation coefficients (r values) among nitrate uptake, dry matter production, water use, nitrate -N accumulation and reduced -N accumulation was observed to be high (above 0.99). All effects of media pH are significant only at pH range 7.0 to 8.0. Despite adequate supply of iron, the plants at pH 7.0 and 8.0 showed symptoms of iron deficiency. Thus, iron and possibly micro-nutrient deficiency could have resulted in poor plant growth. These experimental results indicate optimum pH range for nitrate uptake is 4.0-6.0. Plant growth and dry matter accumulation were directly affected by media pH. The differences in nitrate uptake, water use and total nitrogen accumulation appeared to have resulted as a consequence of differential dry matter production. Whether these differences are due to altered metabolic uptake characteristics of the loots is not known.

The mechanisms by which exogenously applied plant growth regulators act to express those genes that are selectively involved in cell and tissue differentiation are not at all well comprehended. However, the ontogenetic sequences of events that enable receptor or target cells to be activated and to undergo dedifferentiation and redifferentiation, can often be followed experimentally and can lead to a better understanding of the causal relations and control mechanisms in coordinated cell growth and development.
Cytokinins, applied either in an agar medium or as high-concentration, short-duration pulses to expiants or as high-concentration, intermittent sprays to intact plants, induce switches in the normal developmental pattern of cells of certain explanted tissues. Examples of cells that are particularly receptive are the subsidiary cells of stomatal complexes and the differentiating cells of very young presumptive leaf primordia, that is before the latter have become irreversibly determined as leaves.

Anatomical-histological investigations of slide series revealed that the secondary vascular formations appearing scattered in callus tissue culture derived from a stem piece containing mycoplasma-like organisms (MLO) (potato witches' broom agent) have no connection with the vascular tissues of the original stem piece. 77% of reconstituted tobacco plants (Nicotiana glauca Grah.) from these callus cultures were infected with MLO. When diseasedNicotiana glauca scions are grafted on healthy tomato plants as stocks, MLO transmigration into the stocks is realized in all cases ten days after grafting; at that time, the scions and stocks are united only by a zone of a few layers of parenchymatous cells without any indication of vascular tissue union between the two components. In both cases, the MLO transmigration could not be realized by passage through sieve pores in sieve tubes. Our results bring indirect evidence of MLO transmigration through parenchymatous cells and thus support the hypothesis of MLO passage through the plasmodesmata.

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.

Black currant reversion disease causes serious problems in some cultivars of black and red currant. Investigating ultrathin sections prepared from overground parts of diseased red currant plants cv. Heinemann's rote spätlesse, we observed consistently local cell wall disintegration of tracheids in vascular bundles. We have observed these changes in red currant plants showing reversion symptoms during the vegetation period from March to June. The observed phenomenoni.e. cell wall disintegration of tracheids might be utilized as an auxiliary diagnostic criterion m ident ification of red currant reversion disease in the cultivar Heinemann.

Exogenoualy applicated indol-3-ylaeetic acid (IAA) is metabolized mainly to IAA aspartate in intact plants and plant segments and to IAA glucose in suspension cultures fromBeta vulgaris andChenopodium album.
Main metabolic product of D-tryptophan is N-malonyltryptophan in both suspension cultures and hypocotyl segments of both species. The turnover rate of L-tryptophan to IAA is comparatively low (0.1 %); inBeta the turnover rate is higher than inChenopodium. In sugar beets phenmedipham leads to a decrease in the IAA. biosynthesis rate in suspension cultures of both plant species. There is, however, an increase in the IAA content in all intact plants. The metabolic activity is substantially higher in suspension cultures than in intact plants and plant segments.

Genetically identical mirror-imaged left and rightLemna minor plants were treated using the stereomers of arginine, asparagine and atebrine (mepacrine). In contrast with the stereomers of arginine and asparagine, those of atebrine were found to be isoeffective throughout the dosage range from the ineffective dose to the lethal one. All indices used (rate of reproduction, length of a frond and sensitivity to the treatments) pointed to the absence of any difference between left and right plants. The left or right handedness inLemna cannot be explained bv assuming the existence of any stereochemical difference between left and right plants.

Pharbitis nil, strain Kidachi and Violet, were grown at 20° C under continuous light in various cases of different sizes, containing the nutrient solution or tap water. Kidachi initiated flowers when seedlings were cultured in small cases containing nutrient solution but did not flower in large cases. The application of NAA, kinetin, ABA or 5-chlorobenzoiec acidvia roots in large cases caused flowering, Floral initiation was always accompanied by the suppression of root elongation. The promotion of root elongation by aeration inhibited flowering. Root cutting inhibited flowering. On the other hand, Kidachi did not flower in tap water irrespective of vessel size. Violet did not flower in the nutrient solution even in small vessels, but initiated floral buds in tap water irrespective of vessel size, though the plants grown in large cases developed very long roots. In both types of flowering, cotyledons are necessary to induce flowering and the removal of cotyledons before the 16th day after the start of culture in Kidachi and before the 12th day in Violet completely inhibited flowering. GA₃ promoted stem elongation without preventing flowering of Kidachi.

The current status of our knowledge of auxin effects on floral induction is summarized. The most general effect is inhibition, although the concentration of synthetic auxins added to. plants tends to be too high for us to be certain that the inhibitory effects are truly physiological. Studies of endogenous levels of auxin have focused almost entirely on IAA-like bioassay activity. Chemical identifications of endogenous IAA are needed and feasible. In addition, a search for-other auxins involved in vegetative to floral transitions, their chemical identification, and measurement of their changing levels in the plant are urgently needed.

IAA synthesis proceeding by indol-3-ylpyruvate (IPyA) pathway seems to be regulated in two steps. In the first the L-trp conversion into IPyA is reduced by a low affinity of L-trp to the unspecific aminotransferase, by competition of L-trp with some aminoacids (e.g. L-asp) and indoles (e.g. indol-3-ylacetylaspartate). Simultaneously, a specific L-trp-dehydrogenase in dependence on the NAD(P)/NAD(P)H ratio regulates by its reversible effect the level of IPyA, connecting photosynthesis with growth. A second more "delicate" regulation of IAA level is carried out by the indol-3-ylacetaldehyde system. In pea plants two indol-3-ylacetaldehyde oxidases with pH optima 4.5 and 7.0 were found. The oxidases are differentially inhibited by an excess of IAA, different indoles as indol-3-ylacetylaspartate and aminoacids as L-asp. GA₃ and kinetin stimulate the conversion of indol-3-ylacetaldehyde to IAA.

Current knowledge about effects of exogenous PGR on cone initiation in coniferous trees is briefly reviewed. Long life-cycles, large tree size and great irregularity in coning have imposed severe restraints, but experimental study of reproduction can now be achieved in small plants of some species. In adult, clonal cuttings ofThuja plicata, standard injections of 50-250 (μg GA₃ induce substantial male and female coning, and have been used to test effects of other PGR on cone initiation and development. In thePinaceae, propagation of naturally heavily-coning genotypes has facilitated research on the effects of PGR.

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 low frequency androgenesis was inducedin vitro in all experimental variants ofCapsicum anthers cultured in standard and minimalized media. The embryogenic frequency was stimulated by the presence of activated charcoal which also prolonged the vitality of the culture. The percentage of embryoids growing to complete plants increased, if the embryoids were removed from the anthers and cultured separately. The morphogenic initiation of globular embryoids was conditioned by the presence of FeEDTA in the culture medium. The stimulation of androgenesis initiation can be explained by the same change in the decisive factor caused by various effects. In long-term embryoid cultures, which stagnated in growing and seemingly necrotized, a second somatic embryogenesis occurred. About 10% of obtained androgenic plants were fertile and even gave progenies. The process can be recommended for breeding.

Bacteria of the speciesPseudomonas putida andPseudomonas fluorescens isolated from the rhizosphere of maize and bean plants produce indol-3-ylacetic acid and some other auxins when grown in suspension cultures. IAM and ILA were also found besides IAA and its degradation product IAH by means of HPLC and MS methods. This finding indicates the involvement of two different metabolic pathways in IAA synthesis in bacteria. The amounts found varied between 1.6 and 3.3 μg IAA per ml of media which corresponded to 100-200 μg per gram of bacterial dry mass. The effect of IAA production by rhizosphere bacteria on IAA level in the plant is discussed.

After infection ofNicotiana tabacum cv. Samsun with tobacco mosaic virus (TMV) crude extracts from dark-green spots of upper leaves had a more strongly marked inhibitory effect upon TMV addedin vitro than crude extracts from the surrounding light-green tissue. Likewise, crude extracts from leaves ofNicotiana tabacum cv. Samsun showing recovery after infection with tobacco ringspot virus (TRV) were seen to have a marked inhibitory effect on TMV addedin vitro. The results obtained suggest that virus inhibitors are produced after virus infections not only in hypersensitive hosts but also in systemic hosts. Necrotizing processes are not an indispensable prerequisite of the production of virus-induced virus inhibitors.

Under increasing water saturation deficit of leaves of young bailey plants, the proportion of the cuticular transpiration may be higher than 10%, as usually anticipated. In this case the calculation of the intercellular CO₂ concentration on the basis of the premise, usually employed, that the resistance of stomata equals that of the leaf, is affected by a considerably high error.

Rapid multiplication of axillary shoots of oak and linden has been achieved on broad-leaved tree medium (BTM) and woody plant medium (WPM) containing low level of cytokinin (BAP 0.2-1.0 mg l^-1). High rooting percentages (80-95%) were obtained on low salt, low sucrose media, containing low level of auxins. Rooted plants were transplanted into pots containing a mixture of peat and perlite. Most of the plants (90-95%) survived the transfer. After the hardening off period the new plants were planted in the field.

Cholinesterase activity was studied in 2 to 10-week-old pea plants cultivated under artificial illumination. Free and membrane-bound forms of the enzyme were separated by extracting the enzyme from pea shoots with buffers differing in ionic strength. The ratio of the free cholinesterase to the membrane-bound one fluctuated between 1 : 1 and 1 : 2.5. The free cholinesterase was inhibited by neostigmine (0.1mmoll^-1) by 50%, the membrane-bound enzyme by 90%. The pH optimum of cholinesterase activity was 8.5, the temperature optimum 37 °C. The enzyme activity was increased by some cations in this order: Mg²⁺ < < K⁺. The K^m value for the substrate S-acetylthiocholine iodide was 250 μmoll^-1, the enzyme activity being inhibited by concentrations higher than 3 mmoll^-1 of this substrate.
The activity of the membrane-bound enzyme was demonstrated in the roots, leaves, stems, fruits, seeds and carpels, but could not be reliably detected in the blossoms. The highest activity expressed per fresh matter was found in older leaves and in the fruits, the lowest in the roots and stems. Cholinesterase activity in plant parts markedly varied during the investigated growth period.

At pollination of maize plants, the old leaves, those of medium age, and young leaves, cut into segments transversally (10 segments) and longitudinally (8 segments and main vein), were sampled and concentrations of N, P, K, Ca, and Mg were determined. Then concentration gradients of these elements in maize leaves of different age were evaluated. The results obtained show that concentration gradient of N was the most evident in transversal segments of leaves of different ages, in particular in young leaves, that of K in the old leaves, and the Ca concentration gradient in leaves of medium age. The phosphorus concentration gradient was weakly expressed and in the young leaves not recorded at all. In longitudinal segments, concentration gradients of elements varied in leaves of different ages.

Crown galls induced onArabidopsis thaliana plants by octopine or nopaline strains ofAgrobacterium tumefaciens were grownin vitro on different media. Dark growth of all tumor tissues was strictly hormone-dependent. In contrast, hormonal autonomy was observed in the light where crown gall calli readily differentiated into teratomas and (sometimes fertile) plants. Differentiating tissues always grew more vigorously than subtended calli. The growth of transformed calli was stimulated by vitamins and partly inhibited by growth regulators in concentrations used for the maintenance of untransformed calli. Crown gall calli, teratomas and sometimes regenerated plants were shown to express lysopine or nopaline dehydrogenase activities.