Explants of Chenopodium rubrum, a short-day plant, were decapitated and exposed to floral inductive treatment, and the extent of flowering of axillary buds was afterwards assessed. Isolated buds never responded to induction, whereas the presence of the petiole of the subtending leaf already assured a high degree of flowering. We may assume either that the petiole is the receptor organ of the photoperiodic signal or that its transporting role is indispensable.

Differential display of mRNA has been recently developed as a tool to detect and characterize changes in gene expression. We applied this technique to fruit trees plantlets induced to root in vitro, in order to isolate and study genes involved in root induction. A reproducible pattern of polymerase chain reaction (PCR) products was obtained, both in almond and apple, in vertical polyacrylamide gels stained with ethidium bromide. Differences in PCR fingerprinting were detected in mRNAs of basal part of either auxin induced or non induced microcuttings. Thus, we suggest that this technique can be used in woody species to detect changes among mRNA populations during root induction.

Tomato (Lycopersicon esculentum Mill. cv. PKM 1) plants growing under field conditions were exposed for 15 d to solar radiation with UV-B component (280 - 320 nm) enhanced to 6.3 kJ m-2 d-1. This simulated a 15% stratospheric ozone depletion over Madurai (9° 50' N latitude). Lipid peroxidation in the leaves of UV-B treated plants was 32% higher compared to the control. Superoxide dismutase (SOD) and catalase activities registered parallel promotion by 126 and 50 %, respectively, in the UV-B treated plants. Further, the contents of total phenols and anthocyanins in the leaves have also been enhanced by 40 and 156%, respectively. On the contrary, polyphenol oxidase activity demonstrated a 58 % inhibition in the leaves of UV-B treated plants. While anthocyanins and phenols are proposed to act as antioxidants, the reduction in polyphenol oxidase activity may maintain the turnover of phenols in the UV-B treated plants.

Normal callus and embryogenic suspensor mass (ESM) were induced from the same immature embryo of Abies alba Mill. These two tissues were found to differ in their isoenzyme patterns of peroxidase, glutamate dehydrogenaseand non-specific esterase and in their requirement for myo-inositol inculture medium.

Potted two-year-old lemon plants (Citrus limon (L.) Burm. fil.) cv. Fino, growing under field conditions were subjected to drought by withholding irrigation for 13 d. After that, plants were re-irrigated and the recovery was studied for 5 d. Control plants were daily irrigated maintaining the soil matric potential at about -30 kPa. Young leaves of control plants presented higher leaf conductance (g1) and lower midday leaf water potential (Ψmd) than mature ones. Young leaves also showed higher leaf water potential at the turgor loss point (Ψtlp) than mature leaves. In both leaf types g1 decreased with increased vapour pressure deficit of the atmosphere. From day 1 of the withholding water, predawn and midday leaf water potentials (Ψpd and Ψmd) decreased, reaching in both cases minimum values of -5.5 MPa, with no significant differences between mature and young leaves. Water stress induced stomatal closure, leaf rolling and partial defoliation. No osmotic adjustment was found in response to water stress in either leaf type, but both were able to enhance the cell wall elasticity (elastic adjustment). After rewatering, leaf water potential recovered quickly (within 2 d) but g1 did not.

Eleven species of nitrogen-fixing cyanobacteria belonging to six genera (Cylindrospermum, Anabaena, Nostoc, Calothrix, Scytonema, and Westiellopsis) tolerate different concentrations of NaCl (from 0.05 to 0.35 M). Wide variation in the chlorophyll (Chl) a content of the species of the same genus and between genera in presence of NaCl was observed. The least tolerant (Cylindrospermum sp., Cy 6), the maximum tolerant (Westiellopsis sp., We 1), and the intermediate tolerant (Westiellopsis sp., We 6) species of cyanobacteria were selected, and their response to various concentrations of NaCl (growth, nitrogen-fixing capacity, and production of extracellular substances) was studied. Nitrogen fixing capacity of both the We 1 and We 6 was greatly impaired in comparison to the decrease in their Chl a content in the NaCl containing media. Cellular and extracellular saccharide and extracellular amino acid contents of the cyanobacteria species in the NaCl supplemented cultures were increased suggesting that presence of saccharides and amino acids enabled the cyanobacterial species to thrive under salt stress. Further, the We 1 did not adapt to the salt whereas Cy 6 showed adaptation to low concentrations of NaCl suggesting that the species which tolerate high concentrations of the salt may not possess the ability to adapt to NaCl.

The experiment was made by using different concentrations of polyethylene glycol (PEG) or salt solutions to decrease the osmotic potential of the growth medium to reveal the response of mung bean (Vigna radiata) to water and salt stresses. No germination (emergence of the seedling) occurred at medium osmotic potential lower than -1.0 MPa in all treatments. It was found that the activity of α-amylase and protease, and contents of proline, saccharides and the soluble proteins decreased in the germinating seeds during 3-d stress. However, after 10-d stress, the contents of organic solutes and the activity of the hydrolytic enzymes increased. Growth, chlorophyll content and mineral uptake were also significantly reduced under stress. The seedlings under water stress induced by PEG were affected much more than under salinity. This may be due to the maintenance of a higher succulence under salt stress than under PEG-induced water stress.

The excised shoot tips of Beta vulgaris L. cvs. Ras poly, Gala and Lola were inoculated aseptically on Murashige and Skoog's (MS) medium with 0.25 mg dm-3 α-naphthaleneacetic acid (NAA) and 1.00 mg dm-3 6-benzylaminopurine (BAP). They produced multiple shoots at relatively high frequency. For shoot multiplication, a concentration of 1.00 mg dm-3 NAA and 0.25 mg dm-3 BA in the culture medium was found to be optimum for all the cultivars. MS medium supplemented with 3.0 mg dm-3 3-indolebutyric acid (IBA) and 0.02 mg dm-3 N-isopentenylaminopurine (2ip) was found most effective for rooting of micropropagated shoots. In vitro produced plantlets were successfully transferred to the soil. The percentage of survival was more than 95 % and micropropagated plants showed no morphological differences from those grown naturally.

The effect of irradiance on the expression of the Cucumis sativus pathogenesis-related (srPRX) anionic peroxidase was studied in germinating seeds at the period when seedlings start to be photosynthetically active. The diversity in the expression patterns of srPRX was observed in both dark- and light-grown seedlings using activity staining and immunoblotting: beside the three srPRX isoenzymes also other three, serologically unrelated, peroxidase isoforms were accumulated in dark-grown seedlings and one in light-grown seedlings. Furthermore, in light-grown seedlings, it was observed a marked difference in the expression of particular srPRX isoenzymes at higher irradiance (up to 260 W m-2, 400 - 700 nm) in comparison to low irradiance. By tissue printing on nitrocellulose paper it was demonstrated that irradiance during germination induced changes in the temporal and spatial distribution of the srPRX.

Shoots of Malus domestica Borkh. cv. Compact Spartan raised in vitro do not root in a single auxin medium. Components of the rooting medium were tested not only for root initiation but also for root elongation. Root emergence and further growth were inhibited by a too prolonged auxin treatment, the presence of NH4NO3 and the lack of substrate aeration. Saccharose was essential to achieve highly reproducible root growth on agar but was not necessary on watered vermiculite. Ca(NO3)2 stimulated root initiation, emergence and growth and improved their viability.

In vitro cultures of Calathea ornata Koern. cv. Sanderiana shoots were maintained on modified medium of Murashige and Skoog. With the aim to find effective micropropagation method the effects of cytokinins, paclobutrazol, saccharose, mineral salts and shoot-tip damage on the shoot growth and quality were studied. The highest number of shoots was obtained on a medium containing 2.5 mg dm-3 benzylaminopurine, 2.5 mg dm-3 kinetin, 4.5 % saccharose and raised concentrations of Ca, Mg, Fe and Mn. Shoot branching was markedly stimulated by the shoot-tip damage.

Differences in anatomy and morphology of the kiwifruit leaves and leaf petioles might play a considerable role in the sex-determination. Three months after bud break (June), the kiwifruit leaves of both male and female plants, grown on the vegetative and generative shoots showed different leaf area (128.6 ± 13.45 cm2 in male and 104.5 ± 4.02 cm2 in female plants) and shape. The most frequently leaf shape was determined as "folium cordatum" and "folium rotundato-cordatum". Higher values of total leaf thickness of the female leaves (190 ± 3.84 µm) in comparison to male leaves (174 ± 3.52 µm) were estimated, resulting in the thicker adaxial leaf epidermis and especially in thicker palisade parenchyma in female leaves (136 ± 2.76 µm in comparison to 104 ± 1.61 µm in male leaves). Typically bifacial leaves were observed in both male and female leaves. Anomocytic stomata in hypostomatic leaves were found. The reticulate venation appears to be the main type of leaf venation. Stalked stellate multicellular trichomes on the abaxial leaf side were frequently observed in the leaves of both sexes. No important differences between male and female plants were found in the structures of vascular system in leaves and leaf petioles. Thus leaf thickness and surface morphology of adaxial leaf epidermis can be considered as important structural parameters in the sex determination.

Both short-term and continuous red radiation stimulated while far red radiation inhibited growth and ethylene production in Chlorella pyrenoidosa. Kinetin and linuron also affected culture density and ethylene production, depending on their concentration. Phytochrome might participated in the regulation of growth and ethylene production.

The involvement of ethylene in shoot formation in vitro was studied in one year old lavandin (Lavandula officinalis Chaix x Lavandula latifoliaVillars) callus. A peak in ethylene evolution characterized thenon-regenerating leaf callus line, as compared to the shoot-forming calyxcallus line, on the growth medium provided with 2,4-dichlorophenoxyacetic acid (1 mg dm-3) and kinetin (0.5 mg dm-3). After one year in culture, calyxcallus attained the capacity to grow on auxin-reduced media, showing decreased ethylene production and faster shoot bud emergence, when transferred onto the regeneration medium, supplemented with 10 mg dm^-3 benzyladenine. Shoot formation was also inhibited by addition of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid, indicating an involvement of ethylene in the failure of regeneration.

Supply of 1, 2, 5, 10 or 20 mM nitrate to detached roots, scutella or shoots from 5- to 6-d-old Zea mays L. seedlings increased in vitro nitrate reductase (NR) activity in all the organs and NADPH specific NR (NADPH:NR) activity in roots and scutella but not in the shoots. Usually 2 to 5 mM nitrate supported maximum enzyme activity, the higher concentration did not increase it further. The protein content in the roots, scutella and shoots increased up to 5, 2 and 20 mM medium nitrate, respectively. Nitrate uptake also increased with increasing nitrate concentration in roots and shoots, but it increased only slightly in the scutella. In both roots and scutella, methionine sulfoximine had no effect, while cycloheximide and tungstate abolished nitrate induced NADH:NR activity completely and NADPH:NR partially. Methionine sulfoximine increased nitrate uptake by roots and scutella slightly, but other inhibitors had no effect. The depletion of dissolved oxygen from the medium was lower in the presence of nitrate than in its absence or in the presence of ammonium, especially in the scutella.

Five sets of synthetic oligonucleotide (20-to 24-mers containing no intenal repeats) primers of known gene sequences [yellow lupin nodule specific (hydroxyl) proline-rich protein, pearl millet alcohol dehydrogenase, Pisum sativum heat shock proteins, Drosophila homeobox, and tRNA] were used to differentiate 73 soybean accessions, including 56 Glycine max (L.) Merr. and 17 G. soja Zucc. & Sieb. The amplified genetic markers revealed polymorphic bands for most genotypes studied. The χ²-analyses of the results showed that several fragments produced with these gene primers were associated non-randomly with resistance to Phytophothora, maturity, seed size, flower colour, seed coat colour, seed hilum colour, growth type, and leaf shape. These markers appear to be valuable for differentiation of G. max and G. soja species and genotypes within these species.

Membrane lipid peroxidation, activity of free radical scavangers and ethylene evolution of Amaranthus lividus seedlings were used to determine the lead and cadmium (1, 10, 100 and 1000 µM) induced phytotoxicity. Malondialdehyde (MDA) accumulation and higher lipoxygenase activity (LOX) was found in the 7-d-old treated seedlings. The activities of free radical scavangers like peroxidase, catalase and superoxide dismutase declined considerably with the concomitant rise in hydrogen peroxide level. Heavy metal treatment also caused decline in ethylene evolution in germinating seedlings.

A floating green alga Ulva pertusa Kjallman was grown in the laboratory under various irradiations: "white light" (as reference, broad spectral band, WLC), red radiation (600-700 nm, RRC) and blue radiation (400-500 nm, BRC). During 15 d of culture, the specific growth rate of WLC varied highly when compared to BRC and RRC. The contents of chlorophyll (Chl) and proteins, and the nitrate reductase (NR) activity were significantly higher in BRC than in RRC while the content of saccharides was slightly higher in RRC than BRC. U. pertusa in WLC had the highest contents of saccharides, proteins, and Chl, and the highest NR activity. In the WLC, closely arranged well organized thylakoids were seen whereas in the BRC, although the number of thylakoid layers was similar to WLC, they were widely separated from each other. In contrast to this, in the RRC, the thylakoids were less prominent and were also densely covered with ribosomes.

Cytokinin-like effects of pure caffeine were tested in bioassays specific for this hormonal activity [radish cotyledon growth and chlorophyll (Chl) biosynthesis in cucumber cotyledon and tobacco cell suspension] and in cell elongation bioassays [elongation of segments from soybean internode and internode elongation in dwarf cultivars of guandu (Cajanus cajan) and mucuna (Mucuna deeringiana)]. 6-Benzyl-aminopurine and kinetin (KIN) were used for comparison with caffeine. Although weaker than those given by cytokinins, positive responses were observed in all specific bioassays and in elongation of soybean internodes. A remarkable synergistic effect between caffeine and KIN was observed for the synthesis of Chl in the tobacco cell suspension bioassay, in which different concentrations of the alkaloid were combined with a single concentration of KIN. The hormone-like effect of caffeine might be related to the resemblance between caffeine and adenine derivatives.

The effect of concentration of zinc ions on chlorophyll (Chl) and dry matter contents in Senna occidentalis (L.) Link plants was studied under various availability of soil water. Diurnally, the internal Zn2+ content was predominantly affected by supplied Zn2+ and by daytime (Tm). Chl content, Chl a/b ratio, and Chl stability to heat were mainly affected by soil water content, and the dry matter content depended mostly on Tm.

5-Aminolevulinic acid synthase (ALAS) has been detected in a normal (auxin- and cytokinin-dependent) green sugar beet callus under light and under darkness. ALAS activity was lower when the callus was grown under light. The supply of precursors of the Shemin pathway (glycine and succinate) to dark-grown callus enhanced considerably the capacity of the 5-aminolevulinic acid (ALA) formation. Glutamate, γ-aminobutyrate or α-ketoglutarate also increased ALA accumulation. Such an accumulation was also obtained after inhibition of polyamine synthesis. The results show that glutamate or its derivatives might feed the Shemin pathway in conditions preventing glutamate to be used through the Beale pathway.