A greenhouse experiment was conducted to investigate whether small differences in UV-B irradiance would lead to changes in competition between cocksfoot (Dactylis glomerata L. cv. Athos) and white clover (Trifolium repens L. cv. Mervi). Plants were grown in greenhouses covered with different thicknesses of UV-transmittant plexi (3 and 5 mm) resulting in 82 % and 88 % of ambient UV-B radiation. Aboveground biomass was harvested at 4-week intervals and the vertical distribution of biomass, leaf thickness and specific leaf area were determined. Tillering, stubble and root biomass and crop height were also measured. There was only one significant effect: at 88 % of ambient UV-B radiation a larger fraction of the biomass was present in the lower layers and a smaller fraction was present in the upper layers.

Effects of seawater salinity (SWS) and pure NaCl on the intracellular contents of Na⁺, K⁺, Mg²⁺, Ca²⁺, chlorophylls (Chl) and carotenoids (Car) were studied in three submerged aquatic macrophytes, Hydrilla verticillata, Najas indica and Najas gramenia, which differed in their tolerance to salinity. NaCl resulted in significant increase in Chl/Car ratio in the salt-sensitive H. verticillata and moderately salt-tolerant N. indica, but not in the salt-tolerant N. gramenia. SWS treatment did not result in any significant change in the ratio. The intracellular content of Na⁺ increased significantly in all the test plants upon exposure to both NaCl and SWS. The content of K⁺ decreased significantly in these plants upon salinity treatment, except in N. gramenia. The contents of Ca²⁺ and Mg²⁺ decreased significantly upon NaCl treatment and remained unchanged or increased upon SWS treatment. No relationship between salt tolerance and K⁺/Na⁺ ratio was observed. The maintenance of a minimal level of K⁺ was observed to be the most probable requirement of salt tolerance in aquatic macrophytes.

The contents of endogenous gibberellic acid (GA₃), sugars, and dry mass in apical parts of fertile and sterile thalli of Chara vulgaris were estimated. The GA₃ concentration in the first node of fertile thallus, determined by capillary electrophoresis, was about 70.0 mg kg^-1 of fresh mass (f.m.). Pisum sativum-bioassay showed GA₃ concentration of 80.0 mg kg^-1 (f.m.) which was about 3 times higher than in the first node of sterile thallus. The higher amount of GA₃, glucose, and the lower starch content and dry mass in fertile plants than in sterile ones suggest the interdependence between fertility and contents of studied components.

Season-dependent fluctuation of hop latent viroid in meristem tips enabled selection of viroid-free cultures from Osvald's clone 31, 72, 114, and cv. Premiant. These mericlones were used to evaluate effect of viroid infection on the composition of hop resins and essential oils in the first production year. Healthy plants were compared with naturally re-infected individuals under field conditions. On average, viroid infection decreased content of α-bitter acids by 40 %. The content of β-bitter acids, as well as the ratios of humulone/cohumulone and lupulone/colupulone was not influenced by viroid infection. The content of all monoterpenes was for 29, 37.4 and 41.6 % higher for myrcene, α- and β-pinene, respectively, in infected plants compared with the healthy controls. The contents of sesquiterpenes like β-caryophyllen α-humulene, α-copaene, γ-muurolene, β-bisabolene, γ-cadinene, and δ-cadinene decreased by 13.7, 13, 14, 18.5, 29, 21.7 and 18.5 %, respectively, due to viroid infection. The possible influence of some oxidative-reduction processes activated by viroid-caused pathogenesis was assumed to be involved in the accumulation of terpenes alcohols like geraniol and methylgeranate, and in the reduction of the contents of the majority of ketones detected in the spectra of essential oils.

Application of different concentrations of cadmium [5, 10, 15, 25 and 50 μg(CdCl₂) g^-1(soil d.m.)] markedly affected leaves of Cajanus cajan (Linn.) Huth. Due to increased Cd content in leaves, stomatal density and size on abaxial epidermis, and the size of stomatal aperture and length and density of trichomes on both leaf epidermes decreased significantly in the treated plants. Net photosynthetic rate and stomatal conductance were reduced significantly at each concentration of cadmium, whereas reduction in intercellular carbon dioxide concentration was significant at 10 μg Cd onwards. The contents of chlorophyll a, chlorophyll b and carotenoids were relatively low during early stages of plant development under the effect of Cd. Nitrate content, nitrate reductase activity and protein content were also lower in treated plants, compared with control.

In young sugar beet plants cadmium suppressed the activity of nitrate reductase, glutamine synthetase and glutamate dehydrogenase, whereas sulphur exhibited a protective role towards activity of these enzymes, except of glutamine synthetase. Protein synthesis was suppressed in the absence of S in nutrient medium; the lowest level was at 10^-3 M Cd²⁺. Chloroplast pigment contents were increased by S while Cd²⁺, even in the lowest concentration, (10^-5 M) showed a repressive effect. The highest concentrations of Cd²⁺ (10-3 M) caused a decrease in dry mass, whereas S induced its increase. Nitrate content was increased in the presence of Cd²⁺ and decreased by increased concentration of S.

Induced mutagenesis in callus tissues was studied in the medicinal plant Scilla indica irradiated with different doses of γ-radiation ranging from 2.5 to 20 Gy. Low doses accelerated the cell division and growth rate of the tissues whereas high doses repressed growth rate and resulted in lethality of tissues. Various cytological and chromosomal abnormalities were observed in the irradiated calli, the degree of which depended upon the dosage. Low doses of irradiation also promoted the regenerating capacity of the calli tissues and plants regenerating from them exhibited better growth and vigour compared to normal plants. High doses led to loss of regenerating capacity and promoted formation of malformed and stunted plants. Cytological study of regenerants revealed both diploid and mixoploid plants but no tetraploids were obtained.

Two successive cycles of mature embryo-derived callus culture separated by one cycle of sexual reproduction of R₀ regenerated plants were performed using two rice (Oryza sativa L.) cultivars in order to gain information upon the nature of somaclonal variation in this species. Plants regenerated after one cycle of tissue culture exhibited higher variability and lower performances than those of initial cultivar. A second cycle performed using R₁ embryos as explants showed that the cellular component of salt resistance in terms of growth and regenerating abilities selected during the first cycle could be transmitted to the progenies. The extent and the nature of somaclonal variation depended on the identity of R₀ mother plant and culture conditions, somaclonal variation being strongly reduced in some families obtained from salt-treated calli.

Zea mays ssp. mays (2n=40) and Z. mays ssp. parviglumis (2n=20) were crossed to obtain hybrid plants by embryo rescue. Hybrid embryos were isolated and cultured on García et al. (1992) basic medium supplemented with 2,4-dichlorophenoxyacetic acid and/or kinetin in different concentrations. Caryopses harvested 23 d after pollination (DAP) were turgid, with 0.3 to 0.5 mm long embryos, while those harvested 30 DAP were shrunken, with 1 to 1.5 mm long embryos. Twenty days after plating, 100 % of the younger embryos gave rise to white, compact embryogenic calli. Subsequently, coleoptiles, leaf-like structures, shoots and roots originated from them and 35 hybrid plants were regenerated from 60 embryos. Embryogenic or organogenic calli frequencies did not differ among hormonal treatments, but they decreased, on average, from 90.5 to 44.3 %, comparing 50 and 120-d-old cultures. The older embryos regenerated plants only by germination, although they gave rise to organogenic callus with low frequencies. Regenerated plants showed a somatic chromosome number of 2n=30, pollen fertility of 40 to 80 % and 15 % viable naked caryopses.

Effects of high temperature on the activity of photosynthetic enzymes and leaf proteins were studied in mulberry (Morus alba L. cv. BC2-59). A series of experiments were conducted at regular intervals (120, 240 and 360 min) to characterize changes in activities of ribulose-1,5-bisphosphate carboxylase (RuBPC) and sucrose phosphate synthase (SPS), photosystem 2 (PS 2) activity, chlorophyll (Chl), carotenoid (Car), starch, sucrose (Suc), amino acid, free proline, protein and nucleic acid contents in leaves under high temperature (40 °C) treatments. High temperature markedly reduced the activities of RuBPC and SPS in leaf extracts. Chl content and PS 2 activity in isolated chloroplasts were also affected by high temperature, particularly over 360 min treatment. Increased leaf temperature affected sugar metabolism through reductions in leaf starch content and sucrose-starch balance. While total soluble protein content decreased under heat, total amino acid content increased. Proline accumulation (1.5-fold) was noticed in high temperature-stressed leaves. A reduction in the contents of foliar nitrogen and nucleic acids (DNA and RNA) was also noticed. SDS-PAGE protein profile showed few additional proteins (68 and 85 kDa) in mulberry plants under heat stress compared to control plants. Our results clearly suggest that mulberry plants are very sensitive to high temperature with particular reference to the photosynthetic carbon metabolism.

The effects of Cr and Co supplied either individually or mixed together in the nutrient solution on seed germination, enzyme activities, photosynthesis, metabolic products, and yield were investigated. Cr and Co reduced germination percentage only at the highest concentration used but markedly decreased radicle growth which might be attributed to depressive effect of Cr and Co on the activity of amylases and subsequent transport of sugars to the embryo axes. Protease activity, on the other hand, increased with the metal treatment. The highest concentration (10^-2 M) tested of both metals was harmful on plant growth, while the low and moderate concentrations (10^-6 and 10^-4 M) enhanced the contents of chlorophylls and sugars, and activity of Hill reaction. Fresh mass of the produced pods increased at low and moderate concentrations of Cr and at Cr+Co treatment, but decreased in plants treated with Co.

Plasticity of the tobacco genome was studied by testing the DNAs of protoplast-derived regenerants with three different repetitive DNA sequences by the method of quantitative DNA/DNA hybridizations. A large population of 91 regenerants belonging to 35 different protoclones was analysed and a high degree of heterogeneity in the contents of the different DNA repeats was detected. The contents of middle repetitive sequences of two types were more stable or changed in the same direction, while the highly repetitive sequence varied independently and displayed a significant reduction in comparison with the two other sequences. Comparing the variation within the subpopulations of plants of the same clonal origin and the variation among the protoclones led to a conclusion that the pre-existing DNA variability in the starting plant material and/or thein vitro stress during the very early stages of protoclone regeneration played a decisive role in the formation of modified genomes in regenerants.

The protein profile of cells of control somatic embryos was compared to that of embryos that have become selected and maintained on 200 mM NaCl in order to detect salt inducible proteins. Two proteins (60 and 51.5 kDa) were more abundant in the selected embryos and one protein with molecular mass 18 kDa was unique to the selected embryos. Enhanced content of 27 kDa protein was observed in all somatic embryos indicating its involvement in the embryonal state. Similar pattern of salt inducible proteins in selected somatic embryos and the plantlets regenerated from such embryos was found.

Changes in the starch and sucrose contents, and the sucrose phosphate synthase, acid invertase, and starch phosphorylase activities were studied in the seedlings of salt sensitive and salt tolerant rice cultivars growing under two NaCl concentrations (7 and 14 dS m^-1) for 20 d. Under salinity, the starch content in roots declined more in salt sensitive cvs. Ratna and Jaya than in salt tolerant cvs. CSR-1 and CSR-3 and was unchanged in shoots. The contents of reducing and non-reducing sugars, and the activity of sucrose phosphate synthase was increased more in the sensitive than in the tolerant cultivars. Acid invertase activity decreased in shoots of the salt tolerant cultivars, whereas increased in salt sensitive cultivars. Starch phosphorylase activity decreased in all cultivars.

Genomic instability of protoplast-derived tobacco plants was studied by means of phenotypic evaluation, karyological analysis, and Southern blot experiments. Of the total number of 91 regenerants belonging to 35 different protoclones 57 plants displayed various morphological and/or functional aberrations, some of them being inherited into the progeny. A karyological study of 20 randomly chosen plants revealed 15 tetraploid and 5 diploid chromosome sets. A Southern blot hybridization analysis of three regenerants displayed some DNA polymorphism (RFLP) and thus confirmed that in such plants alterations in the genome structure could be found and that genotypes of protoplast-derived plants frequently differ from the parental genotype.

A sterile mutant of pea (Pisum sativum L. line HM-6) with a number of morphological alterations was found after plant regeneration via somatic embryogenesis. Embryogenic callus was derived from the whole immature zygotic embryo on medium with 2.26 μM 2,4-dichlorophenoxyacetic acid. Morphological changes included altered leaflet shape, one pair of leaflets only, altered stipule morphology, shortened internodia, irregular or opposite leaf position on the stem, shortened flower stalk, and aborted flowers resulting in complete sterility. If the isolation of the shoot apex and axillary buds from evidently sterile plant and their culture in vitro resulted in morphologically normal and fertile regenerated plants, the chimaeric nature of R₀ mutant is considered.

Study of the effects of air pollution caused by thermal power plant emissions on some foliar traits of Ruellia tuberosa L. has shown that length and width of stomata, length of stomatal pore, stomatal density, photosynthetic rate, stomatal conductance and chlerophyll content were reduced in the polluted plants in pre-flowering, flowering as well as post-flowering phases of plant growth. Intercellular carbon dioxide concentration in the palisade tissue was increased at each stage of plant development. Stomatal index remained almost unchanged at the polluted site, except on the adaxial surface during the preflowering stage where it was higher as compared to the non-polluted plants.

Tobacco plants (Nicotiana tabacum L. cv. Sevilla) were grown under controlled conditions. The leaf content of Ca²⁺, Mg²⁺ and K⁺, and the activity of the pyruvate kinase were analyzed. The increased application of Ca²⁺ diminished the content of K⁺ and Mg²⁺ in leaves, and decreased the activity of pyruvate kinase. Taking into account these results, we suggest the pyruvate kinase activity as an bioindicator of the contents of the Ca²⁺, Mg²⁺ and K⁺.

Two-year-old plants of Karwinskia humboldtiana Zucc. and Karwinskia parvifolia Rose grown from the seeds in greenhouse were transferred to the growth cabinet and cultivated for two months under different temperature regimes (35/20 °C - the summer temperature regime, SR, and 20/5 °C - the winter temperature regime, WR). These temperatures were similar to the temperature conditions in the natural areas of the species studied (Nuevo León, Mexico). The root respiration rate was higher in the plants cultivated under SR than in those under WR. Roots of K. parvifolia res faster in both temperature regimes than roots of K. humboldtiana. Starch content in roots was higher in the plan cultivated under SR, however, concentrations of the other investigated organic and inorganic compounds were higher in the plants cultivated under WR. In K. humboldtiana roots, higher concentration of reducing sugars, carbon and hydrogen were found than in K. parvifolia.

Genetic analysis with T-DNA mutants often brings difficulties resulting from instability of the transgenic phenotype. In this work three different Arabidopsis thaliana T-DNA embryonic lethals and one T-DNA morphological mutant were analyzed in F2 progeny after 15 different crosses with marker lines for individual chromosomes. F2 analysis of 44 segregation ratios revealed segregation distortion of similar character consisting in abnormal excess of nontransgenic plants to the detriment of transgenic ones. We quantified this phenotypic drift (d) on the basis of phenotypic ratios given the respective formulas. The d values indicate the rate of F1 gametes which loose the T-DNA mutation or ability of its expression. The obtained d value were relatively high, 0.4 to 0.9 for individual crosses. It makes the standard recombination analysis with insertional mutants very problematic or even impossible.

Wheat plants were grown from sowing to day 18 in 26-dm³ chambers at three different CO₂ concentrations: 150 (-CO₂), 350 (C, control), 800 (+CO₂) μmol mol^-1. Afterwards, plants of the three variants were grown at the same natural CO₂ concentration. Plant characteristics were measured just before the transfer (0 days after CO₂ treatment, DAT), and at 5 - 8 DAT on the 1^st leaf, and at 12 - 22 DAT on the 4^th leaf. Decreased or increased CO₂ concentrations caused acclimations which persisted after transplantation to natural CO₂ concentration. At 5 - 8 DAT, stomatal density, stomatal conductance (g_s), CO₂ saturated net photosynthetic rate (P_Nsat0), radiation saturated net photosynthetic rate (P_Nsat1), and carboxylation efficiency (τ) were higher in -CO₂ plants and lower in +CO₂ plants than in C plants. As compared with C plants, the photochemical efficiency (α) was lower in -CO₂ and higher in -CO₂ plants, however, chlorophyll (Chl) a, Chl b, Chl a-b and carotenoid contents were lower in both -CO₂ and +CO₂ plants. On the 4^th leaf, which emerged on plant after finishing CO₂ treatments, at 12 - 22 DAT, no differences in stomatal density and g, between treatments were observed. In -CO₂ plants, pigment content and P_Nsat0 were higher, α was lower, and P_Nsat1 and τ were not different from C plants. In contrast, in +CO₂ plants, pigment content, P_Nsat1 and τ were lower, and P_Nsat0 and α were unchanged. Leaf area, dry mass, and tiller development increased in +CO₂ plants and decreased in -CO₂ plants. In the interval between 8 and 22 DAT, lower net assimilation rate in +CO₂ than in -CO₂ plants was observed.

Pea plants were more susceptible to long-wave UV-B irradiation (305 - 320 nm, 7.7 kJ m^-2 d^-1, 4 weeks) in comparison with the triticale. This difference was more apparent from the changes in total area of leaves and dry mass of shoots, rather than from the parameters of chlorophyll fluorescence and net photosynthetic rate.

The medium forin vitro culture of green and SANDOZ herbicides-treatedChenopodium rubrum L. plants contained saccharides and hormones in different concentrations. Five days after sowing, the plants were exposed to non-inductive (15 long days-LD) or inductive (6 short days-SD + 9 LD) photoperiodic conditions. The length of hypocotyl and cotyledon blade were measured and percentage of flowering was scored. Gibberellic acid (GA₃) stimulated hypocotyl growth of green and photobleached plants under SD and inhibited under LD conditions. Indole-3-acetic acid (IAA) slightly stimulated hypocotyl growth of green plants only under LD conditions. Benzylaminopurine (BAP) inhibited hypocotyl growth regardless of photoperiodic regime. The optimal concentration of glucose or saccharose for flowering in green and SANDOZ-treated plants was 5%. In green SAN 9785-treated plants exogenous saccharides compensated lack of photosynthates to bring about full flowering, but SAN 9789-treated plants needed in addition GA₃.

Anatomical changes of leaf epidermes of tomato plants (Lycopersicon esculentum Mill. cv. INCA 9) submitted to water stress in the preflowering stage were studied. 20 d after germination, plants were subjected to three treatments: 1) 100 % of evapotranspired water was applied every day, 2) from 100 up to 10 % of evapotranspired water was applied every day, and 3) water supply was completely suppressed. Trichome density was similar in apical, middle and basal zones, and adaxial and abaxial leaf surfaces. Stomatal density and length, and epidermal cell length and width had similar values on the same leaf surface, but the values were higher on the abaxial than on the adaxial leaf surface. The water deficit had little effect on number of trichomes, length and width of epidermal cells and length of stomata, and decreased the stomatal density especially on adaxial surface.

The effect of low temperature on the protein metabolism of wheat primary leaves was examined. In seedlings transferred from 25 to 5 °C, total soluble protein accumulation, in vivo protein synthesis and breakdown, in vitro protein breakdown, and SDS-PAGE profiles of proteinases in gelatine-containing gels were analysed. Leaf protein content increased within a 7-d period (70 % over the initial value) in plants exposed to 5 °C. The fast protein accumulation observed on days 0 - 2 was mainly attributed to a decreased breakdown. In further days, parallelly to a slowdown in the rate of protein accumulation, the leaf proteolytic activity increased. The incubation temperature also had an influence on the proteolytic activity: Q ₁₀ values for the 15 - 5 °C range were 80 - 200 % higher than those observed for the 25 - 15 °C range. On the other hand, the in vivo protein synthesis capacity, at either 25 or 55 °C, was not significantly modified in cold-treated plants. In addition to the enhanced activities of two serine-proteinases (previously found in control plants by SDS-PAGE analysis), cold-treated plants displayed a new proteinase, which had not been detected so far.