Floral induction in the long day plant spinach (Spinacia oleracea) has been shown to be accompanied by a thickening of plasmalemma. This change was observed at early evocation, in both shoot apices and leaves, as well as after inducing GA₃ treatment. To get further information on this thickening, plasma membranes from spinach leaves were isolated, in the present study, using aqueous two phase partitioning and the effect of variousin vitro treatments on their thickness was investigated. The average plasmalemma thickness was unaffected by Na⁺ and K⁺ ions. It was increased upon the effect of either Ca²⁺ or gibberellic acid. A thickening of plasmalemma was also observed when plasma membranes from vegetative plants were incubated with a cytosolic preparation from photoinduced plants. The results were discussed in relation with the plasmalemma modifications previously reported in spinach.

SC₂ and SC₃ progenies of nineteenin vitro regenerated barley plants (SC₁) from resistant calli selected against purified culture filtrate ofHelminthosporium sativum and one parent 'Dissa' genotype were studied for stability of resistance and protein, soluble protein, maltose and saccharose contents. Cytological studies were also carried out on the SC₃ generation. Stability of resistance toHelminthosporium sativum was found in 50% of the somaclonal lines. Significant variation among different somaclonal lines and among different callus lines from which the plants were regenerated were found for yield, disease score and biochemical characters assessed except saccharose content in the somaclonal lines. Significant increase and decrease over the donor parent for most of the characters were obtained. Cytological abnormalities such as multilobed nuclei, multinucleate cells, abnormal anaphase and mixoploidy were also observed.

Investigation was made on a use of microcrystal cellulose as a new and inexpensive gelling agent instead of agar. Microcrystal cellulose in concentration 20 % forms a suitable structure of nutrient medium for in vitro cultivation. The higher humidity in the culture container with microcrystal cellulose causes partial vitrification of Nicotiana tabacum L. plants, cv. Zlatna arda. It is proved by reduced chlorophyll content, changes in protein synthesis and strongly reduced isoenzyme spectrum of peroxidase.

Increasing salinity induced a marked reduction in the plant growth, thoughPhaseolus seedlings tolerated salinity up to 120 mM NaCI. A great reduction in sugar and protein contents occurred with increasing salinity, whereas soluble nitrogen compounds and the relative contents of the photosynthetic pigments were increased in the treated plants. Increasing Ca concentration in the salinized medium appeared to improve the plant growth and to increase the contents of saccharides and proteins in the NaCl-treated plants. This suggests that Ca could be added to salinized media to overcome the deleterious effects of salinity on the growth and productivity of leguminous crop plants.

Pollen embryogenesis occurred in anther cultures of two genotypes ofBrassica carinata A. Braun. Pretreatment of anthers at 35°C for 3 or 6 days was essential for the induction of androgenesis on growth regulator-free culture medium. A combination of sucrose and glucose was better than sucrose alone. None of the pollen embryos germinated normally. Full plants were raised through adventitious bud differentiation from their hypocotyl.

Barley seedlings (Hordeum vulgare L., cv. Fatran) were pretreated with various concentrations of five heavy metal ions (Zn, Cu, Fe, Mg, Mn) for 3 d. When the subsequent heat shock was administered for 2 h, the heavy metal ions had thermoprotective effect against the sub-lethal (40 °C) and lethal (45 °C) temperature stresses, which were otherwise lethal to control (water grown) seedlings. The effectiveness of each of the heavy metal ions was different, the most effective being Cu. The level of protection provided by these heavy metal ions was dependent on both the time and the concentration that plants were exposed to them. The greatest differences were recorded in the thermotolerance mediated by applied metal ions in the shoot and root cells. Thermotolerance was exhibited by both the shoot and root of pretreated seedlings, even though the heavy metal stresses were applied solely to the roots.

Somatic embryos were induced from immature cotyledons and immature embryonal axis ofArachis hypogaea L. on L-6 basal medium supplemented with NAA, picloram or 2,4-D at 5-50 mg 1^-1. Immature embryonal axis produced a higher number of somatic embryos in comparison with immature cotyledons. The highest number of responding cultures was produced on medium supplemented with NAA (50 mg 1^-1), while the highest average number of somatic embryos per culture was produced on medium with 2,4-D (10 or 20 mg 1^-1) and picloram (30 mg 1^-1) from cotyledons. The somatic embryos developed into plants on basal medium supplemented with activated charcoal and about 100 plants were successfully transferred to the field.

In barley genotype susceptible toErysiphe graminis f. sp.hordei 1,3-β-glucan synthase activity in whole leaf extracts was higher in comparison with healthy plants. A positive correlation was found between the activity of 1,3-β-glucan synthase and the degree of barley resistance. On the contrary, the 1,3-β-D-glucanase activity in whole leaves was negatively correlated to host plant resistance. This phenomen is evident only in the early phase of plant pathogen interaction. However, in epidermal cells the 1,3-glucanase activity was not significantly changed after attack and the 1,3-glucan synthase activity was practically zero. Chitinase activity in inoculated leaves and epidermis was higher than in healthy ones, but no unambigous correlation was found between the enzyme activity and host resistance.

Transport of ions in young maize plants was affected by the temperature gradient (gradT). This influence was dependent on the age of plants and the solute concentrations in compartments at the two sides of plants. When gradT was increased, current, volume and heat flows rose during 20 min and then declined. On the other hand, the diffusive flow only declined. The character of the flow changes was given by the changes in permeability and reflection coefficients. In young plants under low solute concentration on both sides of plants, the permeability of the plant tissues shifted from positive to negative values. Under higher solute concentrations on both sides of the plants such phenomenon was not observed. At high gradT the reflection coefficients of the plant tissues were low, but they rose during levelling the temperature in the two compartments.

The influence of salinity, given at germination (stage I) or 75 d after sowing (stage II), on flower production and characteristic features of male reproductive structures was studied in three promising genotypes of chickpea (Cicer arietinum L. cv. ICCV 88102, H 82-2 and C-235). In ICCV 88102 and H 82-2 salinity 20 meq 1^-1 increased the number of flowers when applied at both stages whereas in C-235 only when applied at the later stage. The salinity also delayed flowering; the higher salinity the greater was delay in flowering. In H 82-2 and C-235 salinity treatment given at stage II (when few flower buds appeared) hastened the flowering. The salinity curtailed pollen production; the reduction being minimum in C-235 and maximum in H 82-2. Germination was not significantly affected in C-235 pollen collected from plants grown under salinity conditions upto 60 meq 1^-1 applied at stage I but the tube elongation was inhibited. The inhibition of tube elongation was greatest in C-235. Salinity treatment administered at stage II did not affect significantly pollen germination excepting C-235 in which a consistent decline with increasing salinity was evident. Salinity stimulated tube growth in ICCV 88102. Na₂SO₄ in the germination medium was more detrimental for both pollen germination and tube growth than NaCl.

Lycopersicon esculentum cv. Linia XXIV (L) and cv. Ostravské (O) was infected withAgrobacterium tumefaciens T37 (pTiT37). 37 L tumors and 33 O tumors were isolated. 13.5 % L tumors and 3.0 % O tumors regenerated shoots producing nopaline synthase. The shoots formed roots after transfer on R3B medium without phytohormones. From 10 primary shoots 35 plants cultivated in an unsterile soil were obtained by cutting. 6 selfpollinated plants did not produce any fruits. Fruits obtained through backcrossing had dramatically reduced seed numbers. The same is true of some other transformed plants with nearly normal pollen. Most transformed plants were susceptible to superinfection withA. tumefaciens T37 and B6-806. The incorporation of T-DNA into plant genome seems to cause not only male sterility, but also some kind of female sterility.

The full length cDNA clone of leghemoglobin I gene fromLupinus luteus was placed under dual promoter into the plant expression vector pCB1399 and the resulting vector (pCB1415) was transfered into theAgrobacterium strain LBA4404 (pAL4404). The binary system LBA4404 (pAL4404, pCB1415) was then used for transformation ofNicotiana plumbaginifolia andLotus corniculatus. In both species kanamycin-resistant plants have been selected and regenerated. The synthesis of LbI protein in transformed plants has not been shown.

NaCl salinity affected growth, the contents of chlorophyll, carotenoids, saccharides and some minerals (Na, K, Ca, Mg, P) in wheat (Triticum vulgaris L.) plants. Irrigation of soil with CaCl₂ or KCl greatly ameliorated the adverse effects of NaCl salinity. This counteraction was associated with an increase in contents of saccharides, proteins and Ca, Mg and P which might explain their role in osmotic adjustment.

The efficiency ofAgrobacterium-based transformation technique in oilseed rape and cauliflower was influenced by cultivar specificity, donor plant age and explant type. Marked differences in demands for plant hormone contents in the regeneration medium were recorded already among different types of nontransformed explants. The highest regeneration capacity was recorded with stem and leaf segments isolated from one-month-old aseptically grown plants. The regeneration was markedly species-dependent. Regeneration of transformed plants from stem segments and thin layers isolated from field-grown oilseed rape plants (at the most 2% of regenerating explants) and from oilseed rape hypocotyls (0.8% of regenerating explants) and cauliflower (1.2% of explant regenerated transformed shoots) was achieved after disarmedAgrobacterium treatment. Hypersensitive reaction of explants could be prevented by using prolongedin vitro precultivation and delayed application of the selective agent.

The rates of canopy apparent photosynthesis (P_C) and canopy respiration (R_c) were studied during vegetation season in two erectophile and two planophile hybrids of maize (Zea mays L.) grown at two canopy densities [7.5 plants m^-2 (HD) and 4.5 plants m^-2 (LD)]. Large differences in P_C, R_c, R_C/P_C, leaf area index (LAI), dry matter accumulation and grain yield were found among hybrids and plant densities. Variations in P_C and R_C were associated mainly with changes in LAI. There was also found change in P_C per unit LAI with time. The average R_C/P_C was 28.9 % for all treatments throughout the vegetation season. P_C and R_C per unit dry matter were higher in LD than in HD and decreased throughout the measurement period. The HD stand had higher P_C and yield in hybrids with erectophile foliage, whereas LD stand had higher P_C after male tetrad and got higher yield in hybrids with planophile foliage. Only R_C in hybrids of the two foliage types was higher under HD than under LD throughout the vegetation period.

Haploid and dihaploid female and rare dihaploid male plants were produced inMelandrium album throughin vitro induced androgenesis. In the seed progeny obtained from cross-hybridization between dihaploid androgenic males (supermales) and standard females only male plants were observed. The microspores containing Y chromosome gave rise to supermales.

The transaminations of L-tryptophan (L-trp) and of L-phenylalanine (L-phe) are catalysedin vitro by the same non-specific aminotransferase. The transaminations procceed at the same pH (pH 8.5) and temperature (45 °C) optima, have parallel increases in activity with addition of the coenzyme pyridoxal phosphate (PRP) and have identical elution characteristics in gel chromatography. The enzyme from pea seedlings has a relatively weak affinity for both amino acids (K_m L-trp = 4.16 × 10^-1 mmol 1^-1; K_m L-phe = 2.10 × 10^-1 mmol 1^-1). Differences in affinity for a series of keto acids in the pea enzyme were observed, with pyruvate having the strongest and glyoxylate the weakest affinity. Transamination of L-trp and L-phe was demonstrated by enzyme extracts from pea, maize and tomato, but was not detected in kohlrabi. The amino acids L-asparagine (L-asn), L-phe, L-lysine (L-lys), L-methionine (L-met) have distinct inhibitory effects on the transamination of L-trp. Indolylacetylaspartate and tryptophol were shown to be competitive inhibitors. The regulation at the molecular level of L-trp transaminase activity is discussed.

Epidermal strips from well-watered faba-bean plants were subjected to a range of abscisic acid (ABA) and indolyl-3-acetic acid (IAA) concentrations (10^-5 to 1 mM) in the presence or absence of CO₂ in light or dark. ABA had inhibitory effect on abaxial stomatal apertures in all the concentrations studied and retained them closed even after addition of KCl (SO and 100 mM) to the incubation medium. It also influenced stomatal responses to CO₂. In the presence of CO₂ apertures were greater than in its absence in light as well as in darkness. This relationship remained unchanged also after addition of KCl. The action of ABA inhibited accumulation of potassium in the guard cells. IAA stimulated stomatal opening and its effect was quite opposite to ABA; in the presence of CO₂ the apertures were smaller than in its absence. IAA, however, was able to inhibit the closing effect of darkness, CO₂, and ABA, and stimulated potassium accumulation in the guard cells. Simultaneous action of ABA+IAA manifested effects of both substances.

During 195-min light exposure following 5 d in dark, nitrate content was studied in different organs of lucerne plants in early bud stage. Nitrate content varied considerably especially in stems. Rapid diurnal variations in nitrate content were found in lower and upper halves of stems, in petioles and in leaf blades. The results reflected discontinuous nitrate movement in lucerne shoots. The positive correlation between the diurnal course of the nitrate and potassium contents in different plant organs showed that the K⁺ transport followed the NO₃ ^- transport. Similar diurnal changes were found also in Na⁺ and Ca²⁺ contents. Discontinuous salt movements occurring in xylem sap flow were in contrary to continuous transpiration stream and could be a consequence of temporary adsorption or binding of salts in xylem vessels.

The effect of CCC treatment on the GA and IAA contents of the hypocotyls of green and etiolated bean plants and on their distribution was studied. In the treated plants the GA content of the hypocotyls was higher than that of the control. On the application of CCC the distribution of the hormone content within the organ altered: in the basal part of the hypocotyls of the treated plants the hormone content increased. In the hypocotyls of the treated plants the IAA content was less than in the controls and it was accumulated in the basal part. The ethylene production of the aplcal and basal parts of the hypocotyls proved to be correlated with their IAA content.

Winter barley (Hordeum vulgare L. cv. Efra) plants were grown till the stage of the fourth leaf under controlled conditions at constant temperatures 26.0 °C, 21.8 °C, 19.6 °C and 15.3 °C. The relationships between the sheath and blade growth was studied. The leaf sheath began to be discernible when it was 0.1 mm long and the blade length was 20 mm. In this stage a correlation (r = 0.812) was found between the length of blade and that of shearth. The sheath length in 20 mm long leaf increased in dependence on leaf insertion. At the time of the beginning of sheath discernibility the elongation growth of the subsequent leaf was initiated. In this stage the sheath length and the length of the subsequent leaf were correlated (r = 0.911). At the beginning of the growth of the subsequent leaf the length of the preceding sheath increased in dependence on insertion. Other relations were derived graphically and a hypothetical model of relationships between the cereal leaf growth and development was formulated.

Salinity had generally little influence on the water content of different parts of cowpea(Vigna sinensis L.), calabrese(Brassica oleracea L. var.botrylis) and red radish(Raphanus salivus L.) plants. Salinity showed a promotive effect on the growth of cowpea, while in calabrese the effect was either promotive or depressive depending upon the concentration of the NaCl, and in red radish plants salinity progressively suppressed growth.
Total nitrogen, phosphorus, potassium and sodium contents of cowpea leaves were not affected by salinity treatments, while in calabrese and red radish leaves the contents of N, P and K were generally decreased as the salinity level increased. Gibberellin (GA₃) applied to salt-treated plants had either a stimulatory or inhibitory effect on the growth, water content and contents of N, P, K and Na in the leaves depending upon the plant type, the concentration of GA₃ and level of salinity.

Diurnal changes in K content in leaf blades, petioles, stems and roots of eleven lucerne genotypes were followed. Significant positive correlations between changes in K content in petioles and upper half of stems and significant negative correlations between changes of K content in leaf blades and lower half of stems reflected rapid K movement. The velocity - up to 60 μmol g-1 (f.m.)h-1 - of changes in K content from leaf blades to lower part of stems and the other way round showed that long distance phloem transport occurred. Only moderate increase of K content contemporarily took place in roots. When total K amount in the whole plant was calculated then K uptake alternatively with K release were noticed during the day. Average K release reached 1.48 μmol g-1 (f.m.) h-1. The rate of K movement correlated with irradiance and physiological activity of plants. The time course of K movement was uniform in plants of the same strain and it differed partially in different strains.

The partitioning of¹⁴C-assimilates was studied in pigeonpea(Cajanus cajan L.) at vegetative and flowering stages (40 and 70 d after sowing, respectively) exposed to moderate and severe drought induced by withholding the irrigation. At vegetative stage, the ethanol soluble fraction in shoot decreased from 99 to 43.16 % between 0 and 120 h, whereas in underground part it increased from 1% to 56.84 % with maximum amount in nodules (35.51 %). Similar trend was observed in ethanol insoluble fraction. At moderate drought, a significant increase in soluble fraction (11.31 %) in nodules was observed. Stem showed significant reduction of assimilates (13.09 %). After flowering, the assimilates produced in leaves were exported to reproductive parts, especially under drought. In plants recovering from severe drought, 14C in soluble and insoluble fractions in reproductive parts was reduced to 85 % and 43 %, respectively, whereas leaf and nodules showed a significant increase. Thus the assimilate partitioning to different plant parts was dependent on growth stage and affected by drought.

Cytological and cytophotometric analysis of root tips of regenerated plants, derived from rhizome expiant ofKniphofia nelsonii andKniphofia uvaria, revealed marked difference in behaviour of chromosomes and level of 4C nuclear DNA content. Karyotypic stability could be retained in all 52 regenerants of K. nelsonii whereas inK. uvaria out of 75 regenerants analysed, 12 plants were exclusively diploid and the rest 63 plants were predominantly diploid comprising variable amount of aneuploid and tetraploid cells. Cytological data was further confirmed by nuclear DNA content estimation. Alteration in the structure of chromosomes could also be noted in 57 regenerants ofK. uvaria giving rise to two new karyotypes. The use of polysomatic tissue for securing variantsin vitro inK. uvaria has been suggested.

The main scientific results achieved in individual departments of the Institute of Experimental Botany during 30 years of its existence are briefly summarized. They include methods of studying photosynthesis, ontogenetic changes of photosynthetic characteristics, stress factors affecting photosynthetic activities, photosynthesis of transgenic plants and duringin vitro cultivation, roles of auxins and cytokinins in plant growth and development, development and testing of new plant growth regulators, models of organogenesisin vitro, metabolic and mutagenic activities of phenolic substances, hormonal regulation of flowering, activities of promutagens (nitrosamines, 7,12-dimethylbenzanthracene), model systems of genetic damage, repair synthesis and post-replication repair, developmental pollen biology and biotechnology, extracellular nucleolytic activity of pollen, selection of apple scab immune cultivars of apple tree, chemotaxonomy ofFabaceae andAllium species, selection pressures in embryoids, somatic embryogenesis and nuclear genome changes in plant cell and callus cultures, discoveries of new plant viruses, virus spread and persistence in crops, development of polyclonal and monoclonal antibodies, role of oxidative pentosephosphate cycle in biosynthesis of viral RNA, and virus diseases of forest trees.