The relationships among 20 samples belonging to 6 subspecies of Vicia sativa based on the variability of seed storage proteins and esterase isozyme electrophoretic patterns was discussed in relation to variation in their morphology and chromosome characters. Electrophoretic protein profiles of different accessions of the same subspecies showed identical (e.g. macrocarpa and cordata) or similar (e.g. amphicarpa) patterns, confirming the stablity of seed storage proteins within these subspecies. However, considerable variation of protein patterns were observed within accessions of both nigra and sativa subspecies, which could be correlated to different geographical origins. Esterase pattern revealed a sharp distinction for each subspecies according to the number and loci of allelic bands. The dendrogram delimited the subspecies incisa and sativa as two separate groups, while the other subspecies were grouped together in another group.

Shoots of rose cultivars Super Star and Sonia were multiplied for ten subcultures at 4-week intervals on solidified Murashige and Skoog's medium supplemented with 22.19 μM benzylaminopurine + 1.07 μM napthalene acetic acid + 0.05 μM gibberellic acid. Addition of anti-auxins 2,3,5-triiodobenzoic acid (TIBA; 2.0 μM) and 2,4,6-trichlorophenoxy-acetic acid (2,4,6-T; 0.39 μM) into proliferation medium increased number of shoots per explant and length of shoots in both cultivars. Treatment with TIBA increased also number of leaves per shoot and leaf chlorophyll content.

Cytokinin-like activity of orotic acid and its 1-cyclohexyl and 1-phenyl derivatives was tested estimating the anthocyanin accumulation and inhibition of root formation in isolated buckwheat cotyledons (Fagopyrum esculentum Moench.). The anthocyanin content was stimulated most by 1-phenylorotic acid. Strong synergetic effect of the phenylurea cytokinin 4PU-30 was found.

Solanum nigrum is a model system especially for newcomer to the subject of plant tissue culture. Shoot culture has been easily established from shoot cutting of germinated seeds on Gamborg (B5), or Murashige and Skoog (MS) medium without phytohormones. Direct regeneration was possible using basal media B5, B5C (B5 supplemented with 5 % coconut endosperm milk), Schenk and Hildebrandt (SH), and MS, leaf, stem, shoot tip as explants, cytokinins benzylaminopurine (BAP) or kinetin (KIN) at concentrations from 0.25 to 2 mg dm^-3, and different light treatments (dark, dim and normal light). The best culture condition for shoot formation was the culture of stem internode segments on B5 medium supplemented with 0.5 mg dm^-3 BAP at 16-h photoperiod (irradiance of 100 µmol m^-2 s^-1). Also, root formation was possible under different culture conditions. The best culture condition was the culture of microshoot segments on half strength MS medium supplemented with 1 mg dm^-3 isobutyric acid. Induction of callus formation from young and mature tissues on MS medium supplemented with 0.5 mg dm^-3 BAP, 0.1 mg dm^-3 2,4-dichlorophenoxyacetic acid and 1 mg dm^-3 naphthalene acetic acid, and subsequent plant regeneration on B5C medium supplemented with 0.5 mg dm^-3 BAP was easy. Regeneration of protoplasts isolated from shoot tips and fully expanded leaves was also simple. Finally, the transfer of rooted plantlets to the soil was successful.

The trace metal (Fe, Mn, Zn, Cu, Ni, Pb, Cd, Sr, and Cr) contents in the most common submerged and floating aquatic plants Ceratophyllum demersum L., Myriophyllum spicatum L., and Nymphoides flava Hill. of Provala Lake were evaluated. Considerable higher contents of iron, manganese, zinc, nickel, lead and strontium were found in submerged species than in the floating ones. The presence of cadmium and lead in plant tissues points to a certain degree of lake water pollution.

Soluble sugars, proline, total chlorophyll contents and electrolyte leakage were measured in two wheat (Triticum aestivum L.) cultivars KRL 1-4 and HD 2009 at different growth stages [crown root initiation (CRI), flowering, and soft dough] under short term salinity (NaCl, CaCl₂ and Na₂SO₄). In control plants sugar contents were maximum at flowering stage. Proline and sugar concentrations increased in both cultivars under salinity with a maximum increase at CRI. Electrolyte leakage increased and chlorophyll content decreased with the plant age. A sharp increase of electrolyte leakage was noticed at salinity of 10 and 15 dS m^-1 in HD 2009 and KRL 1-4, respectively. The short-term salinity at CRI stage proved more detrimental as compared to salinity at flowering and soft dough stages in term of all biochemical changes induced. In wheat, plant resistance to salinity increased with the age of plant. The cultivar KRL 1-4 performed better under salinity as compared to HD 2009.

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.

Acceptor sites of unlinked transposed Ds element from two T-DNA loci in tomato were mapped. Experimental data obtained from TC₁ progeny testing were employed for estimation of germinal excision frequency (GEF) of Ds element and frequency of its reinsertion (FR). The donor T-DNAs 1481J and 1601D, containing a 35S:NPT transformation marker, a 35S:BAR or nos:BAR excision marker conferring phosphinothricine resistance and a Ds element in the 5' untranslated leader of the nos (or 35S): BAR gene, were located on chromosome 7 and 8, respectively. Ds transposition was induced by 105121 T-DNA carrying stabilized Ac (sAc) which provides a source of transposase and 2':GUS marker conferring β-glucuronidase activity. Tomato plants harbouring the Ds in 1481J or 1601D locus and sAc were crossed and F₁D, were crossed individually as seed parents to wild-type plants to generate TC₁ progenies. TC₁ seed was germinated on phosphinothricine (Basta)-containing medium, and individual seedlings carrying a transposed Ds and lacking sAc were identified by PCR (to detect the Ds) on phosphinothricine resistant individuals that lacked β-glucuronidase activity. From segregation ratio in TC₁ the germinal excision and reinsertion frequencies of the Ds element were estimated for individual F₁ plants. A total of 14560 TC₁ seedlings of 1481J and 16195 TC₁ seedlings of 1601D was analyzed. We observed high variation between individual plants as regards both GEF and FR despite of donor locus (1481J or 1601D), however, the average germinal excision frequencies as well as average frequencies of reinsertion were very similar for both donor loci: GEF_1481J = 24 %, GEF_1501D = 25 %, FR_1481J = 42 %, FR_1601D = 46 %.

The megagametophytes of the European black pine (Pinus nigra Arn.) were cultured on modified MS medium. After 10 d, protein bodies showed well-marked degradation on freeze-etched replicas and in preparations observed by scanning electron microscopy. After 20 d of cultivation, the megagametophyte cells were completely empty. Proteins secreted into the agar medium were determined by electrophoresis and 15 different proteins, in the range of 6.5 to 71 kDa, were identified.

Young plants of Lotus creticus creticus growing in a hydroponic culture were submitted to 0, 70 and 140 mM NaCl treatments for 28 d and the growth and ecophysiological characteristics of these plants have been studied. The growth of Lotus plants was not affected by salinity when applied for a short period (about 15 d); however, 140 mM NaCl induced a decrease in shoot RGR at the end of the treatment. The root growth was not decreased, even it was stimulated by 140 mM NaCl. The osmotic adjustment of Lotus plants at 70 and 140 mM NaCl maintained constant pressure potential, avoiding the visual wilting. For a similar leaf water potential, cuticular transpiration of salinized plants was lower than in control plants due to the salinity effect on the cuticle. Moreover, the presence of hairy leaves (60 and 160 trichomes per mm² in young and adult leaves, respectively) allows keeping almost 81 % of sprayed water and absorbing the 9 % of the water retained, decreased the epidermal conductance to water vapour diffusion.

Polyphenol oxidase activity was higher in resistant wheat cultivar ACC-8226 than in susceptible cultivar MP-845 in control sets and after inoculation of Alternaria triticina. However, similar polyphenol oxidase isozyme pattern was found in control and inoculated sets of both the cultivars, but the band intensity was higher after inoculation. Three and four peroxidase isozymes were found in ACC-8226 and MP-845, respectively. An extra peroxidase isozyme band was observed in both the cultivars after inoculation. The results suggest an active role of peroxidase and polyphenol oxidase in defence mechanism of wheat plants.

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.

Two maxima in flowering response to one inductive dark period of 13 h were found in the short day plant Chenopodium rubrum within three weeks of cultivation under continuous illumination either in vitro or in vivo. These maxima correlated with the number of leaf primordia and their relation to the size of the apical meristem. The first maximum in flowering responsivity corresponded with the stage when primordia of the second leaf pair had not yet overtopped the apical meristem, the second one when the primordia of the fourth leaf overgrew the meristem. Maximum responsivity to flowering reached by a mother plant was reflected in explants derived from it. The above morphological markers of responsiveness to floral induction were not linked to plant age and/or to general growth habit. The explants flowered only when part of the stem was present.

In vitro culture of long-day plant Chenopodium murale L was established. The effects of photoperiod, glucose and gibberellic acid (GA₃) on flowering and growth in vitro were investigated. Oscillatory changes of photoperiodic sensitivity were noticeable with regard to plant age. The plants induced at the phase of the 1^st and the 3^rd pair of leaves flowered to higher degree than those induced at the phase of 2^nd pair. Plants induced at the phase of the 1^st pair of leaves flowered to 17 % on 5 % glucose-containing medium and the addition of 5 mg dm^-3 GA₃ resulted in maximum flowering (43 %). Neither glucose nor GA₃ were able to compensate for photoperiodic requirements for flowering. Hypocotyl growth was decreased and the 1^st internode elongation and development of leaves were increased due to inductive photoperiodic conditions, as compared to non-inductive ones.

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.

The effects of water stress on the contents of proline, ornithine, arginine and glutamic acid in detached rice leaves were examined. In water stressed leaves, the content of proline was elevated to a content approximately 8-, 14- and 17-fold higher than in control leaves after 4, 8 and 12 h, respectively. We also observed that omithine and arginine contents were much higher under water stress than in control leaves. However, the content of glutamic acid in water stressed leaves was higher after 4 and 8 h and lower after 12 h than that in control leaves.

We induced an oxidative stress by means of exogenous hydrogen peroxide in two wheat genotypes, C 306 (tolerant to water stress) and Hira (susceptible to water stress), and investigated oxidative injury and changes in antioxidant enzymes activity. H₂O₂ treatment caused chlorophyll degradation, lipid peroxidation, decreased membrane stability and activity of nitrate reductase. Hydrogen peroxide increased the activity of antioxidant enzymes, glutathione reductase and catalase. These effects increased with increasing H₂O₂ concentrations. However, no change was observed in the activity of superoxide dismutase and proline accumulation.

Two genotypes of mungbean differing in the leaf shape, K-851 (trifoliate) and a mutant (pentafoliate), were exposed to salinity (0, 2.5, 5, 10 dS m^-1) for 3, 6 and 9 d at flowering stage (40 - 45 d after sowing) to see the effect of salinity on nodule functioning. In both the genotypes, osmotic potential (ψ_s) and relative water content (RWC) of nodules decreased significantly, and proline content increased with increasing the salinity. The ψ_s of nodules was more decreased in the mutant than in genotype K-851, while reverse was true for RWC and proline accumulation. A remarkable increase in ethylene evolution was noticed from nodulated roots with the increasing level and duration of salinity and was much higher in K-851. A sharp decline in leghemoglobin content and acetylene reduction assay (ARA) of the nodules was observed with the salinity and this decrease was more marked in K-851 than the mutant. N content declined while Na⁺/K⁺ ratio and Cl^- content increased significantly. The mutant maintained better N status but lower Na⁺/K⁺ ratio and Cl^- content in nodules than K-851. Nodule dry matter also declined with salinity and the decrease was more expressed in K-851. Thus the functioning of nodules in the mutant was better than in the genotype K-851 under stress conditions.

Lines of winter hexaploid Triticale and their F₁ and F₂ hybrids differing in morphological structure, pigment contents, photosynthetic productivity, and grain crops were studied. F₁ hybrids received by crossing of Triticale lines contrasting in pigment contents showed in some cases a heterosis effect for chlorophyll (Chl) content per unit leaf area. Variation analysis demonstrated a polygenic control of Triticale pigment contents, and different rate of increase in F₂ generation. We found maternal type of heritability of Chl b content and Chl content in light-harvesting complex of photosystem 2.

This study evaluates the impact of cadmium and zinc interaction on the amount of soluble proteins, CO₂ fixati stomatal conductance and intercellular CO₂ contents in regenerants of B. monniera. The regenerants were grown 16 weeks on MS medium containing cadmium and zinc in various concentrations. Cadmium decreased the stom conductance, photosynthetic rate and root growth but increased the protein content. Additional supply of zinc in medium reduced the adverse effects of cadmium on these parameters.

A small population (16 individuals) of Orchis × colemanii Cortesi, a natural hybrid between O. mascula (L.) L. and O. pauciflora Ten. was sampled from a locality near Sassano (National Park of Cilento, province of Salerno, Southern Italy) in order to assess its genetic structure. Filter hybridizations of O. × colemanii, O. mascula and O. pauciflora DNAs against a PCR-amplified ribosomal fragment indicated that all the hybrid individuals in study have the ribosomal repeats of both parents, even if not always combined in equal proportions, and that no specimen morphologically identified as O. mascula or O. pauciflora possessed detectable rDNA of the other species. The majority of the hybrid specimens (12 individuals) showed a preponderance of O. mascula rDNA, three had approximately equal proportions of parental repeats and one had a preponderance of O. pauciflora rDNA. As the parental species have different amounts of rDNA, as inferred from dot blot hybridization, it has been deduced that the 12 specimens may represent F₁ or successive, presumably non-recombinant progenies, while the last four specimens may represent either F₂ genotypes or backcrosses with O. pauciflora.

In 10-d-old soybean seedlings, the growth of roots and shoots was significantly inhibited at 50 and 100 μM and more Cd²⁺, respectively, and by 50 μM or more Ni²⁺. Although total protein content of roots exposed to 200 μM Cd²⁺ or Ni²⁺ was similarly decreased compared to the control, the activity of nitrate reductase was much more inhibited by Cd²⁺. Ni²⁺-treatment (200 μM) induced an accumulation of all free amino acids in roots associated with a decrease in alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities reflecting the accumulation of both alanine and aspartic acid, respectively. Cd²⁺-treatment (200 μM) decreased the amount of all free amino acids. In addition, cysteine which is the main amino acid consisting the phytochelatin complexes constituted about 17.5 % of total free amino acids. The activities of both ALT and AST in Cd²⁺-treated roots were higher than in Ni²⁺-treated roots suggesting higher conversion of alanine and aspartate to pyruvate and oxaloacetate. Primary leaves excised from either Cd²⁺ or Ni²⁺-treated seedlings showed similar pattern of enzyme activities as roots.

Primers with higher G+C content produced better random amplified polymorphic DNA (RAPD) profiles in Nepenthes. The occurrence of clustered G's and C's in the center of the primer seemed also to influence the banding patterns. It was also observed that for certain polymerases, the use of different buffers other than that recommended by the manufacturer provided a better amplification profile for Nepenthes.

In vitro proliferated shoot culture of six grape genotypes (Vitis vinifera L.) were screened for tolerance to NaCl (0 to 200 mM). The cv. Perlette was found to tolerate 175 mM NaCl followed by cvs. Pusa Seedless and Beauty Seedless 150 mM NaCl. Na, K, Cl, Ca and Mg content increased upto 100 mM NaCl in most of the genotypes. Total sugar and proline content of stem tissue gradually increased under NaCl stress while leaf chlorophyll a+b content declined. Studies suggest that the in vitro screening procedure can be used for ranking the grape genotypes for salinity tolerance.