The basal segment from hypocotyl of Linum usitatissimum L. seedling readily regenerates, to produce a large number of shoots, in a short period of 5 [ndash ] 7 d. This response was stimulated by a low concentration (0.1 [micro ]M) of thidiazuron (TDZ). TDZ was also effective in inducing regeneration in dark. A drastic reduction in regeneration response on hormone-free as well as TDZ-supplemented medium was found after inclusion of an inhibitor of calcium-uptake, lanthanum (La³⁺). An essentiality of calcium in the regeneration was also evidenced by an increased response with increasing concentration of calcium. At Ca²⁺ concentration insufficient for regeneration, inclusion of TDZ resulted in shoot formation.

Wheat seedlings of a salt tolerant cultivar were grown hydroponically in presence and absence of 100 mM NaCl. Roots were harvested, and the plasma membrane (PM) fraction was purified. PM ATPase required a divalent cations for activity (Mg > Mn > Ca > Co > Zn > Ni > Cu), and it was further stimulated by monovalent cations (K > Rb > NH₄ > Li > choline > Cs). The pH optima were 6.0 and 5.6 in absence and presence of 25 mM KCl, respectively. The enzyme was sensitive to vanadate and DCCD but insensitive to azide, oligomycine and nitrate. The enzyme displayed a high preference for ATP but was also able to hydrolyze other nucleotide tri- and diphosphates. The enzyme activity showed a simple Michaelis-Menten kinetics for the substrate Mg²⁺-ATP in both control and salt exposed roots. The polypeptide patterns of control and salt stressed PM fractions, detected by SDS-PAGE, were very similar. NaCl substantially reduced the PM ATPase specific activity, whereas it had little effect on the apparent K_m for Mg²⁺-ATP. Since the root PM ATPase of salt sensitive and resistant genotypes responded similarly to salinity stress, it seems unlikely that the mechanism of salt tolerance in wheat is primarily based on differences in PM ATPase characteristics.

Role of lipid peroxidation and antioxidative enzymes (catalase, peroxidase, superoxide dismutase, ascorbate peroxidase and glutathione reductase) in water stress-promoted senescence of detached rice leaves was investigated. The senescence was followed by measuring the decrease in protein content. Increased lipid peroxidation was closely correlated with senescence in water stressed leaves. Decrease in superoxide dismutase activity was evident 8 h after beginning of water stress. However, decreased catalase, peroxidase, and ascorbate peroxidase activity was observed only when senescence was observed. Glutathione reductase was not affected by water stress. Free radical scavengers retarded water stress-enhanced senescence.

Seed storage proteins of ten maize inbred lines were investigated by sodium dodecyl sulfate polyacrylamide gel electrophoresis. In addition, fourteen isozyme loci representing nine isozyme systems were analysed. Salt-soluble protein fraction contained a large number of proteins (30 - 40 bands) of different sizes with genotypic differences among the ten inbred lines. The methionine-rich 10 kD zein showed differential expression in the ten inbred lines with different migration rates on the SDS-PAGE. This polypeptide was completely absent in the inbred line G221D. Among nine of the inbred lines, eight of 14 isozyme loci were polymorphic and six were monomorphic resulting in seven unique fingerprints.

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.

Field study revealed that species diversity index of the community was 0.597. The data of interspecific association index of Alhagi graecorum and each of its associates, Chenopodium murale, Glinus lotoides and Malva parviflora, were 0.35, 0.41 and 0.33, respectively. Therefore, a net negative association and low diversity among the species were the main characters of the community. Laboratory experiments verified the role played by competition and allelopathy in this community organization. The bioassay results indicated that A. graecorum exhibited phytotoxic activity on the tested species. Accordingly, water-borne allelopathic compounds may be released from A. graecorum into the environment and suppress the growth of its associates where they were not able to compete with A. graecorum in the field, so the latter species become dominant.

Fusarium oxysporum f. sp. albedinis, the bayoud disease agent of date palm, grows on a mineral medium containing the cell walls of date palm roots as a sole carbohydrate source. The growth and development of pathogen under these conditions was related to the production of extracellular cell wall-degrading enzymes (CWDE): cellulases, polygalacturonases, polygalacturonate transeliminases, and pectinmethylesterases. The mycelial growth and the sporulation of pathogen were higher in the presence of cell walls of susceptible cultivars (BFG, JHL, BSK) than in the presence of those of resistant cultivars (IKL, SLY, BSTN). After 8 d of fungal culture, the activity of CWDE was equal whatever is the origin of the cell walls (resistant or susceptible cultivars). After 16 d of culture, the activity of these CWDE was higher when the parasite was cultivated on the cell walls of the susceptible cultivars than on those of the resistant cultivars. A positive correlation was observed between CWDE activities and the growth and the sporulation of F. oxysporum after 16 d of culture. These results clearly show a relation between the susceptibility/resistance of the cell walls of the roots of the date palm to the parasitic CWDE and the susceptibility/resistance of the cultivars.

Maize (Zea mays L.) seedlings were exposed to osmotic stress, and alcohol dehydrogenase (ADH) activity and abscisic acid (ABA) concentration were determined. The osmotic stress increased ADH activities in both roots and shoots, whereas the increase was 2-fold greater in roots than the shoots. The stress also increased ABA concentration in both roots and shoots and the increase was greater in the roots than in the shoots.

In an open-top chamber experiment located in a mountain stand of 14-years-old Norway spruce (Picea abies [L.] Karst.), trees were continuously exposed to either ambient CO₂ concentration (A), or ambient + 350 µmol mol^-1 (E) over four growing seasons. Respiration rates of different woody parts (stem, branches, coarse roots) were measured during the last growing season. The calculated increase in the respiration rate related to a 10 °C temperature change (Q₁₀) was different in stem compared to branches and roots. Differences between the E and A variants were statistically significant only for roots in the autumn. Stem maintenance respiration (R_Ms) measured in April and November (periods of no growth activity) were not different. The stem respiration values (R_s) were recalculated to a standard temperature of 15 °C to estimate the seasonal course. The obtained R_s differed significantly between used variants during July and August. At the end of the season, R_s in E decreased slower than in A, indicating some prolongation of the physiological activity under the elevated CO₂ concentration. The total stem respiration carbon losses for the investigated growing season (May - September) were higher for A (2.32 kg(C) m^-2 season^-1) compared to E (2.12 kg(C) m^-2 season^-1). The respiration rates of the whorl branches (R_b) were lower compared with the stem respiration but not significantly different between the used variants. The root respiration rate was increased in E variant.

Induction of rooting in the microshoots of Plumbago zeylanica was achieved on halfstrength basal Murashige and Skoog's medium supplemented with 0.25 mg dm^-3 indole-3-butyric acid. Rooting was totally inhibited when the microshoots were cultured in vitro under continuous light, however, maximum percentage of microshoots rooted when incubated in continuous light for 4 weeks before transfer to the rooting media. Peroxidase activity increased markedly during root induction indicating a key role of peroxidase in rooting of microshoots of Plumbago zeylanica in vitro.

A simple systems for in vitro storage of health asparagus germplasm was developed. High percent (90 %) of shoots cultured in a standard multiplication medium were maintained viable in vitro at 5 °C in darkness for 12 months. This percent was decreased to 60 % when cultures were stored for 18 months. At normal temperature, shoots and callus cultures also survived for 1 year under osmotic stress on medium containing 40 g dm^-3 mannitol.

The activities of peroxidase, polyphenol oxidase and superoxide dismutase was significantly lower in roots and leaves of NaCl stressed radish (Raphanus sativus L.) plants. Addition of triadimefon to the NaCl stressed plants increased peroxidase, polyphenol oxidase and superoxide dismutase activities, and thereby ameliorated the negative effect of NaCl stress.

Two maize lines differing in drought resistance were grown at different drought stress induced by polyethylene glycol (PEG 10 000) solutions with osmotic potentials of -0.20, -0.40 and -0.80 MPa in the semipermeable membrane system. During the five days soil water content decreased (from 0.43 to 0.29, 0.25 and 0.23 g cm^-3 for three PEG solutions, respectively) as well as leaf water potentials (ψ_w; from - 0.54 to -0.76, -1.06 and -1.46 MPa). These values were not significantly different between the investigated lines, indicating that a controlled and consistent soil moisture stress was achieved. Soil drying induced an increase in the ABA content of leaves and xylem of both lines and the effects on stomatal conductance were greater in drought susceptible line (B-432) compared to drought resistant line (ZPBL-1304). To test possible difference in stomatal sensitivity to xylem ABA between lines and to assess any ABA vs. ψ_w interaction, roots were fed with 10, 50 and 100 mmol m^-3 ABA solutions in another set of experiments. These results showed that manipulation of xylem ABA affected stomata of both lines similarly. Comparison of stomatal sensitivity to drought-induced and applied ABA demonstrated that drought treatment affected stomata of investigated lines by differentially increasing their sensitivity to xylem ABA, thus confirming an interaction between chemical signalling and hydraulic signalling.

The effect of foliar-applied glycinebetaine (GB) on chloroplast ultrastructure, the amount of chlorophyll and proteins and ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) activity in stressed tomato leaves were analysed. Initial, and total activity and activation state state of RuBPCO were also measured. RuBPCO activities, chloroplast area, and the number of plastoglobuli remained unaffected, while the relative area of starch granules increased in GB-treated, salt-stressed tomato leaflets. Under drought-stress, the relative area of plastoglobuli increased upon GB application. The primary effect of GB was, however, the increased protein and chlorophyll content.

Field experiments with Glycine max (L.) Merr. cv. Ludou 11 and Ludou 4 were conducted to evaluate changes in photosynthetic rate, antioxidative enzyme activity, soluble protein, chlorophyll (Chl) and carotenoid (Car) contents in relation to leaf senescence during seed filling period. Photosynthetic rate, soluble protein content, catalase and peroxidase activities were the highest at 25 days after flowering (DAF). Chl a, Chl b and Car contents reached the maximum at 15 DAF and rapidly decreased after 33 DAF.

Watermelon (Citrullus lanatus [Trumb.] Mansfeld cv. Early Star), was used as scion grafted onto three cultivars of pumpkin (Cucurbita pepo L. cvs. Brava, Shintoza and Kamel) used as rootstocks and ungrafted Early Star plants were used as control. The rootstocks showed a high capacity for N uptake and transport to the scion where N reduction and assimilation improved growth of the scion in grafted plants with respect to the control.

Plant dormancy and dormancy breaking depend, at least partially, on close relationships between buds and tissues underlying bud (bud stands). In Prunus persica, the dormancy was related to high nutrient absorption in bud stands linked to high plasmalemma ATPase (EC 3.6.1.3) activity. Two plasmalemma fractions was isolated from peach vegetative buds and bud stands using aqueous phase partitioning and ultracentrifugation. Results of markers enzyme assays indicated that both plasmalemma enriched fractions obtained were highly purified. During the dormancy period plasma membrane ATPase amount and activity were higher in bud stands than in buds. Moreover, assays performed at different temperatures (4, 18, 30 °C) indicated modifications of kinetic parameters (K_m, V_m) in both tissues during dormancy release. In buds, from November to February, K_m declined at 4°C and increased at 30 °C whereas no changes was measured at 18 °C and V_m increased at all temperature. In bud stands, no changes of K_m was measured at 4 °C and 18 °C whereas an increase occurred at 30 °C and V_m decreased at all temperature. According to the results, it can be postulated that dormancy release in peach-tree could be related to modifications of plasma membrane ATPase properties, in buds and bud stands, during winter time.

Two-days-old protonemata of Funaria hygrometrica Hedw. growing in in vitro conditions were treated with 4 μM PbCl₂ for 48 h. After this time grey or brown colour thickenings of the cell wall appeared in protonemata cells. They were then localized in tip parts of apical cells. Electron microscopical (TEM) observations showed that the thickenings were structurally connected with the wall and sometimes they included lead deposits. Cytochemically it was found that they contained pectic polysaccharides, callose, lipid substances (probably suberin or sporopollenin) and only few cellulose. Other compounds of cell wall, e.g. lignin and cutin were not detected.

Alcohol dehydrogenase (ADH), its isozyme profiles and ethanol concentration in lettuce (Lactuca sativa L.) seedlings subjected to flooding stress were determined. Flooding stress caused increases in ADH activity and ethanol concentration. By 48 h, ADH activity and ethanol concentration in the flooded seedlings increased 3.2- and 7.0-fold, respectively, in comparison with those in non-stressed seedlings. Five electrophoretically separable ADH bands were found in extract of the flooded seedlings, whereas only two or three ADH bands were found in extract of non-stressed seedlings. These results indicate that lettuce ADH may have a system of three-gene and six-isozyme, and the increase in ADH activity in the flooded seedlings may be due to increased synthesis of the enzyme.

With the aim to effectively minimise the browning of tissue cultures of different Piper species (P. longum, P. attenuatum, P. betle, P. nigrum) explants from stem (nodal and internodal segments), petiole, and leaf were planted on Murashige and Skoog's basal medium supplemented with activated charcoal (AC). AC in the concentration of 200 mg dm^-3 proved to be the best. Among the taxa studied, P. longum showed the least browning whereas, wild P. nigrum showed maximum browning.

The contents of gibberellic acid (GA₃), glucose and starch, and dry mass in four nodes of apical parts of male and female thalli of Chara tomentosa were measured. The GA₃ concentration was about 4 times higher in male than in female thallus and about 10 times higher in the first node than in the next three nodes of both thalli. The apical part of male thallus contains 2.5 times less glucose and 1.7 times less starch than female one. The average amount of dry mass of male and female thallus was similar: 9.9 and 9.8 % of fresh mass. The findings of this investigation demonstrate the interdependence of gibberellic acid and sugars in development of male and female Chara tomentosa thalli.

In vitro culture of Chenopodium murale L. (ecotype 197) green and herbicide SAN 9789 - treated "white" plants was established and the effects of benzylaminopurine (BAP), indole-3-acetic acid (IAA) and gibberellic acid (GA₃) on growth and flowering were tested. Green plants did not flower on glucose free media, while 17 % of plants flowered on 5 % glucose-containing medium. SAN 9789 (10^-5 M) inhibited growth and flowering. BAP and IAA (0.1 - 5 mg dm^-3) also inhibited growth and flowering of green and "white" plants. GA₃ (10 mg dm^-3) stimulated leaf development in green plants, but had no significant effect on "white" plants, and stimulated flowering of green (41 %) and "white" (33 %) plants.

Growth of tobacco (Nicotiana tabacum L.) pollen tube is controlled by post-transcriptionally regulated protein synthesis. Stored mRNA was found to be present in the form of messenger ribonucleoprotein particles (mRNPs) in both maturing and germinating pollen. During pollen dehydration in the anthers content of mRNPs strongly increased during dissociation of polysomes suggesting a transfer of mRNA liberated from polysomal structures into mRNP particles. Pollen germination and initial pollen tube growth characterized by rapid reassociation of ribosomes was accompanied by decrease of mRNPs indicating an involvement of mRNA of these particles in the formation of polysomes. Distribution of the particular mRNAs during the pollen activation preceeding tube growth suggests that other mechanisms along with pollen rehydration are engaged in this process and that the continuous exploitation of stored mRNPs during pollen tube growth is precisely regulated.

The effect of aluminium (0.5 -1.0 mM) on contents of phosphorus, pigments, and pigment-protein complexes was studied in soybean (Glycine max Merril.) grown in different nutrient medium with and without P. Increased Al concentrations led to the decrease in the contents of chlorophylls (Chl) a and b, and carotenoids (Car) in soybean leaves, but Chl a/b ratio did not vary significantly. In long-term experiments, P ameliorates the negative effects of Al.

Alterations in free and conjugated polyamines (PAs) and the enzymes involved in their biosynthesis, namely arginine decarboxylase, ornithine decarboxylase and S-adenosyl methionine decarboxylase have been reported to occur during cell division, growth, embryogenesis and rhizogenesis in an array of plant materials. However, the relationship, if any, between them and all these processes has not yet been established. It seems that specific PAs at specific concentration ranges are required during critical stages of growth and morphogenetic events. Furthermore, the effects of PA biosynthesis inhibitors vary considerably at different developmental stages of the same tissue. The present review deals with the available information about the possible role of PAs in aforesaid physiological processes.