Mungbean (Vigna radiata L. Wilczek cv. Sujata and cv. K851) seedlings were grown in paper towelins in dark under 0, 0.5, 1, 2 and 3 % (m/v) NaCl salinity. Germination percentage, shoot and root length, fresh mass of both cultivars decreased with salinity. Total soluble saccharides and proline accumulated in the root and shoot of salt stressed seedlings. The proline accumulation in the root was four to five times higher than that of the shoot of NaCl treated etiolated mungbean seedlings.

Indole-3-butyric acid (IBA), phenylacetic acid (PAA) and naphthaleneacetic acid (NAA) were applied at a concentration of 10^-4 mol dm^-3 to stem cutting bases ofPopulus x canadensis Moench. During adventitious root formation, the content of indole-3-acetic acid (IAA) in cutting bases was estimated using the fluorimetric method. In the control variant, a rapid increase in endogenous IAA appeared after 24-h cultivation followed by gradual decrease during the following days. In contrast, the variants treated with IBA, PAA, and especially NAA exhibited firstly a decrease in endogenous IAA content and only afterwards an increase, reaching a maximum 48 h after excision. As root regeneration proceeded gradually, a decrease in the level of endogenous IAA occurred in all treatments. The first adventitious roots appeared in all treatments after 216-h cultivation.

The effect of the proteins extracted with 1 M LiCl from theCicer arietinum etiolated epicotyl cell walls on the degradation of polysaccharides extracted with alkali was studied. The hemicellulosic polysaccharides were fractionated into three fractions extracted with 4 % KOH, 4 % KOH containing 8 M urea, and 24 % KOH. The protein extract showed exo-glycanase activity against all three hemicellulosic fractions whilst endo-glycanase activity was shown mainly against the hemicellulosic polysaccharides extracted with 4% KOH.

The net photosynthetic rate (P_N), stomatal conductance (g_s) and transpiration (E) ofHardwickia binata Roxb. leaves were reduced due to decrease in the leaf water potential (ψ_w) from -2.0 to - 5.7 MPa. P_N partially recovered in the treated plants upon rewatering. Decrease in g_s due to water stress may be the main factor for reduction of P_N.

Single treatment of expanding radish leaves with N₁-(2-chloro-4-pyridyl)-N₂-phenylurea (4-PU-30) lead to the stimulation of root cambial tissue activity and root growth. Leaf thickness, the volume of chlorophyll (Chl) containing cells per unit leaf area, starch content in the chloroplasts, and the Chl content increased simultaneously. These alterations were associated with increased leaf net photosynthetic rate and stomatal conductance in treated plants.

Plant tissue cultures established from isolated embryos or cotyledons were used to investigate the lectin biosynthesis inCanavalia virosa. The lectin (CVL) was detected by double immunodiffusion and hemagglutination tests. CVL was present in all callus cultures. The stem and leaf of the plantlet generated from the embryo also contain CVL, but no CVL was detected in the roots. As compared to mature seeds, callus derived from cotyledon of immature seeds exhibited the largest CVL content.

The responses of barley and wheat seedlings to lead and cadmium ions in relation to the concentration and duration of treatment were studied. Both metals inhibited seed germination and growth of roots and shoots, but the toxic effect of cadmium was observed at lower concentrations. Inhibition of seedling growth was already recorded already within a day after the beginning of the treatment, and then increased further. The sensitivity of the processes studied to both the metals decreased in the order: root growth, shoot growth and seed germination. The resistance of barley and wheat to lead was similar, whereas the resistance to cadmium was higher in barley

Foliar sprays with N ⁶-(m-hydroxybenzytyadenosine, (mOH)-[9R]BAP, one of the synthetic cytokinins, were applied to field-grown sugar beet twice during the vegetation period: before full canopy closing (I), 6 weeks before harvest (II) or both. Application of (mOH)[9R]BAP retained high cytokinin content that usually declines prior to harvest. The total content of isoprenoid cytokinins at harvest was 2.6-fold higher in (mOH)[9R]BAP-treated plants as compared to the controls. Treatment I had no significant effect on contents of chlorophylls (Chl)a andb and carotenoids, nor on the rates of net photosynthesis (P_N) or photorespiration (R_l), or on CO₂ compensation concentration (Γ) measured during the whole vegetation period on detached leaves under optimum environmental conditions. Increased values in P_N, R_L and Chla andb contents were found in variantsII and I+II linked with a delay in leaf senescence before harvest. Transpiration rate and stomatal conductances of adaxial and abaxial epidermes were not significantly affected by any treatment.

In mustard(Brassica juncea L.) addition of 20 mM nitrogen (in the form of NaNO₃) inhibited after 50 d the activities of carbonic anhydrase and nitrate reductase and net photosynthetic rate. However, when nitrogen was applied in association with the foliar spray of gibberellic acid, the inhibition was reversed and the above parameters and also leaf area index and dry mass were enhanced.

Anin vitro procedure for large scale multiplication ofBoswellia serrata Roxb. has been developed using cotyledonary node segments. In average 4 shoots per node were obtained on Murashige and Skoog's (MS) medium containing 0.5 mg dm^-3 6-benzylaminopurine (BAP) and 0.05 mg dm^-3 napthaleneacetic acid (NAA) within 22 d. By repeated subculture technique 90-100 shoots per node could be obtained after 88 d of initial culture. Shoots could be rooted on MS medium containing 1/4 salts, 1% saccharose, and a combination of 0.5 mg dm^-3 indole-3-butyric acid (IBA) and 0.25 mg dm^-3 indole-3-acetic acid (IAA). Addition of antioxidants like polyvinylpyrrolidone (PVP-50 mg dm^-3) and ascorbic acid (100 mg dm^-3) in both multiplication and rooting media prevented browning of cultures. Approximately 80% of shoots rooted within 8-10 d. Rooted plantlets were kept for 15 d in culture bottles containing Soilrite^TM irrigated with a nutrient solution containing 1/4 MS salts and finally transferred to pots containing soil: Soilrite^TM (1∶1), mixture with 70% transplantation success.

Leaves of micropropagated highbush blueberry (Vaccinium corymbosum) cv. 'Bluetta' have been observed during the acclimatization phase. In vitro-developed leaf cells were circular and small, the spongy parenchyma was discontinuous and disorganized and formed by 1-2 layers of cells with large intercellular spaces and the palisade to spongy mesophyll thickness ratio was 1:1.5. After rooting ex vitro, the first leaves formed under natural conditions showed substantial changes in the anatomical characteristics. After 6 months, the plants produced leaves similar to those in field-grown plants. The palisade cells were rectangular, the spongy parenchyma was formed by 3-4 layers of cells and the intercellulars were around the stomata. Leaves from field-grown plants lost 24 % of water during 150 min after excision while leaves from in vitro shoots lost about 50 % of water in the same time. Leaves from in vitro shoots showed a higher number of smaller stomata (361 per mm²), with the guard cells forming a circular ring; the stomata frequency in field-grown leaves was 241 per mm² and the guard-cells were elliptical.

Investigations were carried out to determine the sites of lead uptake within the frond and the root ofLemna minor. With the sodium rhodizonate four regions favoured in lead uptake were distinguished: the frond region between the base and the node, the basal part of the root, and the regions at the proximal and distal ends of the root cap. For analysis in electron microscope only the root regions were chosen. The highest rate of lead uptake was found in the basal part of the root. Lead was present in the apoplast of this region after 5 min of exposure and was observed in the stelar cells after 30 min of incubation. Lead deposits were detected mostly in the cell walls adjacent to the plasma membrane and in the lumen of several endomembrane compartments - the endoplasmic reticulum (ER), dictyosomal vesicles, nuclear envelope and the vacuoles. Lead induced changes of cell ultrastructure; an increase in the number of membraneous structures, swelling of ER cisternae and distortion of the dictyosomal cisternae were observed after 2 to 6 h of exposure.

Changes in growth characteristics and photochemical activities inVigna unguiculata L. Walp seedlings maintained at constant temperature of 10, 20, 30 and 40 ‡C under control and ultraviolet-B enhanced radiation (UV-B) were investigated. UV-B retarded the shoot elongation and also leaf expansion to a great extent at 30 ‡C but produced only marginal changes at 20 and 40 ‡C. Similar response was also observed with respect to changes in leaf fresh and dry masses and total chlorophyll (Chl) content under these temperatures. At 10 ‡C the total Chl content was 3-fold higher under the treatment than under control conditions. In seedlings growing at 20 and 30 ‡C the overall photosynthetic electron transport (H₂O -> methyl viologen) showed a significant enhancement during the 36-h UV-B treatment and thereafter a gradual reduction. Although a similar trend was found in photosystem 1 (PS1), the inhibition even after 60 h of UV-B treatment was not statistically significant. Photosystem 2 (PS2) activity was inhibited in seedlings treated for 60 h by UV-B at 20 and 30 ‡C. However, no inhibition was observed at 40 ‡C. No detectable photochemical activity was found in seedlings grown at 10 ‡C under either control or UV-B enhanced irradiation although the chloroplasts contained Chl.

The content of abscisic acid (ABA) in abaxial leaf epidermis of the host (Capsella bursa pastoris) and the unattached hemiparasiteMelampyrum arvense showed diurnal changes. ABA content increased during the light period and declined rapidly upon the darkening of leaves. In an attached hemiparasite the content of ABA in the epidermis was maintained at an almost constant level irrespective of the diurnal cycle. As compared with the maximum level in the host, at the end of the light phase the content of ABA in abaxial epidermis constituted about 70 % and 164 % in the unattached and attached hemiparasite, respectively. No significant changes in ABA content were recorded in adaxial epidermis. In all the samples abaxial/adaxial epidermis ABA content ratio was about 3.6:1 in light phase. In darkness this ratio decreased to about 1.1:1 in the host and the unattached hemiparasite and did not show significant change after attachment. ABA content ratio in mesophyll was 1:0.7:1.5 for the host, the unattached, and attached hemiparasite, respectively. In comparison with the host the concentration of ABA in xylem sap of the hemiparasite constituted about 31 % and 152 % for the unattached and attachedM. arvense, respectively.

The distribution of the stress-related anionic peroxidase (srPRX) activity was investigated in various organs of cucumber (Cucumis sativus L. cv. Laura) during their development by activity staining and immunoblotting. In shoots, including cotyledon, leaf, stem and tendril, three stress-related peroxidase isoenzymes were present, particularly in old ones. The PRX1 was the only srPRX isoenzyme found in both young and old roots. As fruits became mature, srPRX activity increased dramatically and was particularly enriched in the external parts of the fruit. The PRX1 isoenzyme was highly accumulated in the course of seed germination, while the absence of other two srPRX isoenzymes (PRX2 and PRX3) was recorded. The possible function of the srPRX is discussed, with respect to this spatio-temporal distribution.

Cadmium, copper and zinc ions at high concentrations partially released scarified freshly-harvested seeds ofStylosanthes humilis from physiological dormancy. This response to toxic metals increased along with seed postharvest ageing. Cobalt and silver ions, and abscisic acid impaired metal-promoted germination.

Paclobutrazol (PB), a triazole growth retardant and an inhibitor of gibberellin biosynthesis, reduced at 17 μM concentration the adventitious root formation of bean primary leaf cuttings. Treatments with 5 μM ABA or 4 μM Ethrel, an ethylenereleasing compound, restored the rooting of PB-treated cuttings. Ethylene production and the content of the precursor 1-aminocyclopropane-l-carboxylic acid (ACC) were enhanced in root-forming tissues of PB-treated petioles 48 h after ABA application. The effect of ABA could be abolished by 10 μM CoCl₂, an inhibitor of ACC oxidase. Thus, ABA might stimulate rooting through its effect on ethylene release. 2 mM silver thiosulphate, an inhibitor of ethylene action, decreased the rooting of PB-treated cuttings similarly to Co²⁺, but failed to negate the ABA effect. These data indicate that the effect of PB on rhizogenesis is not associated directly with the inhibition of the biosynthesis of gibberellins

The rate of germination, radicle and plumule length, fresh and dry mass of maize seedlings were increased as Ca²⁺ was added to the nutrient solution, which contained different levels of Cd²⁺, especially at low concentration of Ca²⁺ (5 mM) and high concentrations of Cd²⁺ (1.4 and 1.8 mM). The biosynthesis of pigments, respiration rate and content of soluble saccharides in endosperm were reduced sharply as the concentration of Cd²⁺ in the medium increased. This effects was alleviated by Ca²⁺ addition. Cd²⁺ content in seedlings was increased as the Cd²⁺ concentration in medium was increased and decreased sharply as Ca²⁺ was present in the culture medium. The study suggests liming of soil with CaCO₃ to improve the yield of many crops.

Anin vitro procedure for large scale multiplication ofBoswellia serrata Roxb. has been developed using cotyledonary node segments. In average 4 shoots per node were obtained on Murashige and Skoog's (MS) medium containing 0.5 mg dm^-3 6-benzylaminopurine (BAP) and 0.05 mg dm^-3 napthaleneacetic acid (NAA) within 22 d. By repeated subculture technique 90-100 shoots per node could be obtained after 88 d of initial culture. Shoots could be rooted on MS medium containing 1/4 salts, 1% saccharose, and a combination of 0.5 mg dm^-3 indole-3-butyric acid (IBA) and 0.25 mg dm^-3 indole-3-acetic acid (IAA). Addition of antioxidants like polyvinylpyrrolidone (PVP-50 mg dm^-3) and ascorbic acid (100 mg dm^-3) in both multiplication and rooting media prevented browning of cultures. Approximately 80% of shoots rooted within 8-10 d. Rooted plantlets were kept for 15 d in culture bottles containing Soilrite^TM irrigated with a nutrient solution containing 1/4 MS salts and finally transferred to pots containing soil: Soilrite^TM (1∶1), mixture with 70% transplantation success.

Binding protein for N-1-naphthylphthalamic acid (NPA), an auxin transport inhibitor, was studied by analysis of the effects of reactions which modify particular amino acid side chains upon their binding activity. Na₂SO₃, N-ethylmaleimide (NEM) and dithiobisnitrobenzoic acid all inhibited the specific binding of NPA to its binding protein fromAcer pseudoplatanus L. cells. The presence of 10^-6 M Na₂SO₃ in the binding assay reduced the affinity of the binding protein to NPA from K_d of 1.5 £ 10^-8 M to K_d of 2.1 £ 10_-8 M, while concentration of the binding protein was not significantly changed. When the same analysis was applied to NPA binding to the NEM-treated membrane particles, it was found that NEM inactivated binding without changing the affinity for NPA. This study revealed the importance of sulphydryl group(s) in the maintenance of NPA binding protein activity.

The plants of mustard (Brassica juncea L.) were treated with 0, 25 and 50 ΜM gibberellic acid (GA₃) at three fully developed leaf stage (30 d after sowing). Effect of GA₃ on carbonic anhydrase activity, photosynthetic rate, leaf area index and dry mass was studied at 50, 70 and 90 d after sowing. At harvest 1000 seed mass, pod number and seed yield were recorded. GA₃ treatment (50 ΜM) enhanced all the characteristics studied.

The detrimental effect of NaCl was found at the oxidation site of photosystem 2 (PS2). An impairment of PS2 was caused by damage of the oxygen evolving polypeptides (33, 23 and 20 kDa) of thylakoid membranes as well as by changes in the unsaturated and saturated fatty acids. Application of triacontanol, TRIA (1 mg kg^-1) ameliorated the effect of NaCl and promoted the ratio of unsaturated to saturated fatty acids, the rate of¹4CO₂ fixation and the activity of ribulose 1,5-bis-phosphate carboxylase.

Echinochloa colona regeneration via organogenesis in callus cultures derived from leaf base and mesocotyl expiants andin vitro flowering were achived. Shoot bud regeneration was achieved on Murashige and Skoog's (MS) basal medium supplemented with 6.66 μM 6-benzylaminopurine (BAP), 2.68 μM 1-naphthalene acetic acid (NAA) and 3 % (m/v) saccharose. Regenerated shoots were rooted on half strength basal MS medium with 2 % (m/v) saccharose devoid of growth regulators. About 90 -95 % of rooted plantlets survived in the greenhouse.In vitro flowering was induced in the regenerated shoots derived from callus on half strength MS medium supplemented with 4.4 μM BAP, 74.07 μM adeninesulphate, 0.72 μM gibberellic acid, and 3 % (m/v) saccharose. The frequency ofin vitro flowering was 80 - 90 % in three repeated experiments. Fertile seeds were recovered fromin vitro grown plantlets which were subsequently germinated into plants.