Influence of inoculation with efficient rhizobia or nitrate fertilization in alleviating salinity (NaCl, CaCl₂ and Na₂SO₄) stress was investigated in sand culture experiments. Shoot dry mass declined beyond salinity level corresponding to electrical conductivity (EC) 5.6 dS m^-1 in control or in inoculated plants and after EC 7.4 dS m^-1 in nitrate fed ones. Root growth was more sensitive and decreased at EC 3.3 dS m^-1. Nitrate reductase activity in leaves reduced at EC 3.3 dS m^-1 but in inoculated and nitrate fed plants it reduced at EC 5.6 dS m^-1. Na⁺ accumulation increased at EC 5.6 and 7.4 dS m^-1 in roots and, shoots, respectively. In inoculated and nitrate fed plants Na⁺ content in roots increased at EC 7.4 dS m^-1. Content of Ca²⁺ increased slightly only in shoots and content of K⁺ was unaffected. Besides inoculation, application of small doses of nitrogen should prove beneficial for legume cultivation in saline soils.

The effects of 4 or 8 drought cycles on four grass species,Cenchrus pennisetiformis, Leptochloa fusca, Panicum turgidum, andPennisetum divisum were assessed in a pot experiment. There were significant differences between the species in biomass production under water stress.C. pennisetiformis andP. turgidum produced significantly greater fresh and dry matter thanP. divisum and especially thanL. fusca. L. fusca had the lowest andP. divisum highest osmotic potentials compared with the other species after the completion of 4 or 8 drought cycles. Osmotic adjustment (difference between osmotic potential of droughted/rehydrated plants and control plants) was highest inL. fusca. The stomatal conductance was significantly decreased with increased drought stress inC. pennisetiformis. The elasticity ofC. pennisetiformis, P. turgidum andP. divisum increased with increase in number of drought cycles, whereas that ofL. fusca remained unchanged.L. fusca andP. turgidum had the lowest leaf hydration of all species after 8 drought cycles. The chlorophyllsa andb in all species remained unaffected by drought treatments. The proline content ofC. pennisetiformis andL. fusca increased significantly with increased drought stress, whereas that ofP. turgidum remained unaffected after 4 or 8 drought cycles.L. fusca synthesized great amount of leaf soluble proteins during 8 drought cycles, whereasP. divisum had low protein content after 4 drought cycles. The protein contents ofC. pennisetiformis andP. turgidum remained unaffected after 8 drought cycles. The leaf epicuticular wax ofL. fusca increased consistently with increased drought stress, but leaf wax ofP. divisum increased only at the highest drought stress and that ofC. pennisetiformis andP. turgidum increased after 4 drought cycles. On the basis of these results it was established thatC. pennisetiformis andP. turgidum were the most tolerant,P. divisum intermediate, andL. fusca the most sensitive to drought stress. The osmotic adjustment did not positively correlate with the degree of drought resistance.

Different behaviour of small groups of stomata on a single leaf blade (stomatal patchiness) is reviewed. The occurrence of stomatal patchiness depends on plant species, age, leaf position, environmental conditions,etc. The possibility of errors in conventional evaluation of stomatal and non-stomatal (biochemical) limitations of photosynthesis resulting from patchy stomatal closure is analysed. The consequences of stomatal patchiness for leaf and plant photosynthesis and water economy are discussed. A brief survey of the techniques currently used for detection and quantification of stomatal patchiness is presented.

Limitations on photosynthesis, characterized by leaf CO₂ exchange, chlorophyll fluorescence, and thylakoid structure, were studied under environmental conditions simulating culturein vitro. These were simulated by growingPhaseolus vulgaris plants in nutrient solution under high relative humidity of air (>90%), and CO₂ concentrations (c_a) that decreased with the development of photosynthetic activities during plant ontogeny (1200 to 300 mg m^-3). The ontogeny of such model plants was more rapid, primary leaves reached photosynthetic maturity 2 to 3 d earlier and their life span was 7 to 14 d shorter than in control plants. Their photosynthetic activityin situ was limited, after reaching "photosynthetic maturity", similarly to plants grownin vitro. When measured under optimal conditions, however, 50 to 70% higher net photosynthetic rates (P_N) were found in leaves of different ages as compared with plants grown under c_a of 700 mg m^-3 and a lower air humidity (30-35%). This increase in P_N was associated with a high conductance for CO₂ transfer by adaxial and abaxial epidermes. In model plants, the dark respiration rate (R_D) was almost twice that in the control, while the photorespiration rates were similar to controls; CO₂ compensation concentration was about 50% of that in controls. The ratios P_N/R_D were similar in control and in model plants. Chlorophylla+b content in leaves of the model plants was lower than that in the control plants. Grana extent increased with plant age in the model plants while it decreased in the control ones. In both the stromal and granal membranes of the chloroplasts in model plants, a marked accumulation of carotenoids occurred independent of age. The ratio of variable to maximal fluorescence, F_v/F_m, did not differ in the model and the control plants. In the control plants, photochemical quenching (q_P) slightly increased with plant age and was not affected by CO₂ concentration present during measurement. In the model plants, q_P increased with elevated CO₂ concentration in young plants and decreased in saturating CO₂ concentrations in older plants. Nonphotochemical quenching (q_NP) was lower in the model plants and increased under CO₂ saturating conditions. Vitality index, Rfd, was markedly lower in the model plants than in the control ones and a decline was found in saturating CO₂ concentration.

Supply of 100 μM spermidine (Spd) in the nutrient solution containing 10 mM nitrate as the sole nitrogen source, increased growth of roots and shoots, total nitrogen content andin vivo orin vitro nitrate reductase (NR) activity of leaves of 10-d oldLeucaena leucocephala seedlings. Spd and the cytokinins benzyladenine or kinetin also increased growth, total nitrogen andin vivo NR activity of isolated cotyledons. The synergistic effects of nitrate, kinetin and Spd in increasing NR activity, indicate that the Spd acted at different level than the nitrate or cytokinin.

The addition of NaCl to cadmium had significant synergistic effect on the wheat root and shoot fresh mass, relative growth rate and net assimilation rate, while showed no significant effects on the dry mass production, leaf area, leaf area ratio, leaf mass ratio and specific leaf area. Additive depression of the rate of photosynthesis and the stomatal conductance was recorded, while no significant effect on the transpiration rate was observed. The Cd stress disturbed the mineral nutrition of the wheat plants either directly or indirectly, NaCl markedly reduce the uptake and internal concentration of K and Ca in the shoot. The combination of cadmium and NaCl showed no additive effects on the content of ions in the root as well as in the shoot of wheat plants.

Hybridization between the nearly extinct speciesDiplotaxis siettiana andBrassica juncea is prevented because of strong prefertilization barriers. Use of mentor pollen ofD. siettiana irradiated with 1000 Gy gamma radiation before the incompatible pollination led to fertilization. 5 d after pollination 17% ovules showed entry of pollen tubes, 10 d after pollination 27% ovules showed small globular embryos which grew no further. No embryos were found in control pollinations. Thus , use of irradiated mentor pollen brings about fertilization in this difficult cross and hybrids can be obtained if embryos are rescued.

The short term uptake of phosphate involving 10 min absorption followed by 5 min desorption, both at 30 °C, in the concentration range 1.0×10^-9 to 7.5×10^-2 M KH₂PO₄ by fresh and washed maize (Zea mays L. cv. Ganga Safed-2) roots can be described by a single isotherm having five phases (0 and I-IV) with regularly spaced kinetic constants. Almost identical kinetics were observed in both fresh and washed maize roots. The kinetics of phase 0 in the concentration range 1.0×10^-9-3.0×10^-5 M. was sigmoidal in fresh maize roots, however, in washed tissue exhibited 2 phases termed here as 0a and 0b. 0a covered the concentration range 1.0×10^-9-5.0×10^-6 M and 0b 6.0×10^-6-3.0×10^-5 M. In the concentration range 1.0×10^-4-7.5×10^-2 M four distinct phases, termed as I, II, III and IV were evident in both fresh and washed maize roots. Each phase obeyed Michaelis-Menten kinetics. The values of K_m and V_max have been estimated for each phase. The uptake isotherm was accompanied by discontinuous transitions.

Triazine treatment of thylakoid membranes isolated from the primary leaves ofZea mays L. showed an 80% inhibition of photosystem (PS) 2 activity. No detectable change of PS 1 activity was found. The inhibited membranes showed a selective reduction of the most unsaturated linolenic acid (C_18∶3) biosynthesis by about 15% coupled with a corresponding increase in stearic (C_18∶0), oleic (C_18∶1) and linoleic (C_18∶2) acids. Thus the inhibition of electron transfer of PS 2 induced by triazine treatment was followed by lipid peroxidation and changes in the thylakoid membrane fluidity.

Low molecular mass humic acid fractions caused a decrease in the germination rate. Only the highest concentration of humic acid solution decreases the soaking of fruits. Neither sodium content nor water and osmotic potential can account for that decrease.
Seed respiration was increased in the presence of humic acids and their medium molecular mass fraction. This increase did not produce an increment in embryonic growth possibly as a result of interference in the respiration chain or decoupling in the oxidative phosphorylation.

Electrophoretic separation of seed alcohol dehydrogenase (ADH) fromNicotiana tabacum on 12% starch gels at pH 7.8 produced only one band with an apparent R_f of 0.65, which confirmed earlier reports. The same was found with pollen ADH. However, in polyacrylamide gel isoelectric focusing, seed ADH separated into three distinct bands with apparent pI of 5.33, 5.42 and 5.50. The pI 5.33 isoenzyme was found to be the essential form inN. sylvestris seeds. The analysis of charge properties ofN. tomentosiformis seed ADH showed only one isoenzyme with pI of 5.56. These results present further evidence thatN. tabacum has arisen from a cross between aN. sylvestris predecessor and an ancestral type ofN. tomentosiformis. The presence of the pI 5.42 form inN. tabacum is consistent with the reported formation of heterodimeric ADH in tobacco hybrids.

The constitutive expression of peroxidase isoenzymes which are capable of oxidizing 4-hydroxystilbenes was studied during the growth cycle of suspension cell cultures from grapevine (Vitis vinifera L. cv. Monastrell) berries. the results showed that the growth of suspension cell cultures is accompanied by the constitutive expression of the peroxidase isoenzymes HSPrx 1 and HSPrx 2, previously characterised by their properties for oxidizing 4-hydroxystilbene, the expression of these isoenzymes being characteristic of Monastrell vines brought to a resistant state. However, although the differential catalytic properties of these grapevine isoenzymes are also shown by the horseradish peroxidase, no immunological relationships have been found between the peroxidases from either source.

The influence of N, P, K supply on the contents of dry mass, chlorophyll (a+b), vitamin C, saccharides and the activities of peroxidase (E.C. 1.11.1.7), catalase (E.C. 1.11.1.6), and acid phosphatase (E.C.3.1.3.2) in leaves of celery plants during their growth stages was investigated. A correlation between the amount of N, P, K and the chemical composition and catalytic activities of enzymes was found.

Cell nuclei were isolated from leaf tissues of wild banana (Musa balbisiana, M. acuminata ssp.banksii andM. acuminata ssp.errans) and of the two vegetative clones of diploid cultivar "Pisang Mas". Relative fluorescence intensity was measured on propidium iodide-stained nuclei by flow cytometry. Nuclei isolated fromGlycine max with known nuclear genome size were used as internal standard to determine nuclear DNA content ofMusa in absolute units. The results of the study showed that the size of nuclear genome ofMusa is smaller than previously estimated. In general, it is smaller in comparison with many other angiosperms. Furthermore, it was found that nuclear DNA content ofM. balbisiana (genome BB) is significantly lower than that ofM. acuminata subspecies and cultivars (genome AA). This finding should permit estimation of genome composition in triploidMusa clones with expected hybrid composition. Flow cytometry is proposed as a useful technique with potential applications in taxonomy, breeding and biotechnology ofMusa.

Crenatin (3, 4, 5, tri-hydroxybenzyl alcohol, 4-glucoside) isolated from chestnut, was studied for its ability for improvement of rooting in the bean rooting test. Crenatin itself had a positive effect on number of roots. Moreover it enhanced the number of IAA-induced roots. In addition, a retardation of the apical bud growth was observed.

The relative efficiency of incorporation of the exogenously supplied primary precursors [2-¹⁴C]acetate, [U-¹⁴C]glucose and [U-¹⁴C]sucrose into essential oil was determined in the immature leaves of threeCymbopogon species(C. martinii,C. winterianus andC. flexuosus). Acetate was most efficiently incorporated into essential oil inC. winterianus andC. flexuosus, whereas glucose was the best precursor inC. martinii. The observations are consistent when expressed as radioactivity [Bq] of essential oil per leaf, as percent incorporation or moles of precursors utilized for essential oil synthesis. Thus, there is selectivity in the efficiency of precursor utilization for the oil synthesis inCymbopogon species.

A salt mixture resistant (SMR) cell line ofVigna radiata (L.) Wilczek was isolated by selection on agar solidified PC-L2 medium supplemented with NaCl, KCl and Na₂SO₄ (8∶1∶1) equimolar to 300 mol m^-3 NaCl, a concentration inhibitory to the wild-type non-selected cells (salt mixture sensitive, SMS). This line retained its resistance after subculture for 3 passages (3 months) on normal medium. The SMR line grew significantly better than SMS line at all the levels of salts, though less in saline medium than the SMR on normal medium. The growth of SMR line was significantly higher than that of SMS line under KCl stress. However, both the lines responded similarly to Na₂SO₄ at a concentration higher than 100 mol m^-3. The SMR line was found to be more sensitive to NaCl than SMS line. The SMR line under salt mixture stress maintained lower levels of Na⁺ and higher levels of K⁺ than SMS line. The SMR line failed to regenerate shoots, although rhizogenesis was observed on PC-L2 medium containing salt mixture (300 mol m^-3).

The effect of shortwave (250 nm) UV radiation (UV-C) on the level of peroxidase activity and peroxidase isoenzyme patterns in leaves of resistant ([Vitis vinifera x Viris riparia] x Vitis rupestris andVitis rupestris) and susceptible (Vitis vinifera) grapevine species toPlasmopara viticola (downy mildew) was studied. The results show that although UV-C did not produce significant changes in peroxidase activity in susceptible species, and only minor changes in resistant species, treatment with UV-light induces an acidic isoperoxidase (isoperoxidase A₁), capable of oxidising 4-hydroxystilbenes in resistant species. It was named HSPrx 2. Since peroxidase is apparently the enzyme responsible for ε-viniferin synthesis from resveratrol in grapevines, a close relationship between this peroxidase isoenzyme and ε-viniferin synthesis which occurs in grapevine leaves after UV-C treatment must be expected.

In the topmost leaves of low-irradiance (LI) tolerant CO 43 and LI susceptible IR 20 rice cultivars, the contents of chlorophyll (chl)a andb and carotenoids and the Hill reaction activity increased under LI. The increase was greater in cv. CO 43 than that in cv. IR 20, and in Chlb than in Chla. The contents of soluble proteins and reducing sugars and nitrate reductase activity of the leaves decreased while the content of non-reducing sugars increased due to shading. The decrease in reducing sugars was greater in cv. CO 43 than in cv. IR 20. On the other hand, the decrease in soluble proteins and nitrate reductase was much less in cv. CO 43 as compared with cv. IR 20.

Phosphorylase from tubers ofDioscorea dumentorum was fractionated by (NH₄)₂SO₄ precipitation and further purified to apparent homogeneity. Two forms of phosphorylase, Dd₁ and Dd₂ were obtained with different K_m, optimum temperatures and pH values. They obeyed Michaelis-Menten kinetics, they were activated by AMP, Mg²⁺ and Ca²⁺ but inhibited by ATP, ADP, ADP-glucose and Na₂SO₄. The molecular masses found for Dd₁ and Dd₂ were 102 000 and 195 000 respectively. SDS gel electrophoresis indicated that Dd₂ is a dimer and Dd₁ is a monomer. Both phosphorylase forms contained pyridoxal-5'-phosphate as their prosthetic group, which was essential for their activity. Dd₂ is more active in starch synthesis while Dd₁ is more active in starch degradation. The affinity of the enzyme forms for P_i is not a measure of the rate of glucan degradation. The decline in activities of the enzymes between pH 5.5 and 7.5 was due to unsuitable ionic forms of the enzymes and not due to irreversible denaturation. Both forms of phosphorylase showed double displacement reaction mechanism in direction of phosphorolysis, while in direction of synthesis, sequential mechanism was indicated. Indoleacetic acid activated the enzyme forms in direction of starch degradation but acted as an inhibitor in direction of glucan synthesis. The results of this study suggest that Dd₂ may have some synthetic function while Dd₁ has a degradative role. The effect of pH on the phosphorylase activity suggests histidine as the amino acid residue around the active site that might be involved in enzyme catalysis.

Sclerotium rolfsii andSclerotium bataticola could utilize protein and produce extracellular proteinase. In protein-deficient media no extracellular proteinase was detected. In protein-containing media addition of glucose stimulated enzyme synthesis; in absence of glucose addition of ammonium to the protein-media decreased enzyme activity. The rate of protein hydrolysis was higher in media contained glucose but not ammonium. The rate of glucose depletion from the culture filtrates was faster in treatments received protein with glucose or with glucose and ammonium, and addition of sulphur showed slight decrease in glucose utilization.

Methylmethanesulfonate induced chromosomal aberrations in callus culture ofCrepis capillaris. The clastogenic effect was markedly decreased when calli were pretreated with dimethylsulfoxide.

Chloris barbata Sw. andCyperus rotundus L. from a mercury contaminated site near a chloralkali plant were tested for relative tolerance to Hg by root-elongation method. The above two species from the Hg-contaminated site exhibited high tolerance to Hg compared to the same species from a non-contaminated site. Tolerance to Hg was higher inChloris barbata than inCyperus rotundus.

Addition of either abscisic acid (ABA) or kinetin at 10^-6 M to salinized media (20-120mM NaCl) induced remarkable effects on growth ofPhaseolus vulgaris plants. Whereas ABA inhibited the plant growth and the rate of transpiration, kinetin induced stimulation of both parameters. Moreover, ABA increased proline and phosphorus concentrations in the salinized plants whilst kinetin decreased them.
ABA induced stimulation of the transport of K, Ca and Cl from root to shoot, accumulation of K, Na and Cl in root cells and inhibits the transport of Na and accumulation of Ca. Kinetin appeared to inhibit the transport and accumulation of Na and Cl, transport of K, and stimulates the accumulation of K and Ca as well as the transport of Ca. The highest influence of both ABA and kinetin was mostly observed when these hormones were used in combination with the highest concentration of NaCl (120 mM) in the medium.