Pressure-volume technique was utilized to evaluate salinity response among three populations ofSpartina patens (Ait.) Muhl. from Louisiana Gulf coast marshes. Plants were subjected to salinities of 85 and 425 mol m^-3 for 77 d in a greenhouse. Ψ_w and Ψ_π decreased in all populations in response to increases in salinity. There were 32% decrease in Ψ_sat, 42% decrease in Ψ_tlp in response to salinity changes from 85 to 425 mol m^-3 in the Ferblanc population. Similarly, there were 35% and 41% decrease in Ψ_sat in the Clovelly and Lake Tambour populations, respectively. All populations showed the ability to adapt to the increased salinity as was evidenced by osmotic adjustment. However, the Lake Tambour population appeared to have superior ability to adapt to high salinity through having a significantly lower osmotic potential at saturation (Ψ_sat), osmotic potential at turgor loss point (Ψ_tlp), and maximum turgor potential (Ψ_P(max)) compared to other populations. Ferblanc and Clovelly populations revealed the ability to adapt to saline environments to a lesser extent as compared to the Lake Tambour population. Results indicate that there is a potential for selection of superior strains ofSpartina patens for use in marsh restoration projects aiming at prevention of wetland loss in certain coastal areas.

The growth and nodulation ofTrifolium alexandrinum were compared at six levels (0 - 1.2 % NaCl) of salinity. Dry mass of shoots and roots, 14 and 20 weeks after the commencement of salinity treatment, increased at low levels of salinity (0.1 - 0.2 % NaCl) but decreased with higher NaCl concentrations (0.4 - 1.2 %). Nodulation occurred at NaCl concentrations up to 0.8 %. Nodule mass decreased with increasing salinity levels. The nodule size remained unaffected at NaCl concentrations up to 0.4 % but was reduced at higher concentrations.

Effect of two different seasons and hormones on pre- and postfertilization barriers in crossability were studied inVigna mungo, V. unguiculata and their crosses. Significant differences between the two seasons for pollen fall, pollen germination, tube growth and pod set were observed. In kharif season with an average temperature of 26 to 30 °C and 75 to 85 % humidity all the characters showed higher values than in the spring season with a higher temperature of 32 to 36 °C and low humidity of 40 to 50 %. Application of gibberellic acid (GA) alone and a combination of gibberellic acid, naphthaleneacetic acid (NAA) and kinetin (KIN) significantly increased the pollen fall by 7-13 %, pollen germination by 10-12 % and pollen tube growth by 27-30 %. More pollen tube abnormalities in interspecific crosses only indicates partly incompatible reaction of pollen tube in the stylar tisue. Hormonal treatments, especially GA, significantly increased the pod set and pod harvest by 20 % and 34 %, respectively. Higher pod harvest was seen in crosses withV. unguiculata as female parent. GA treatment enhanced pollen germination and pollen tube growth, and by partially overcoming embryo abortion for 10 to 12 d, immature embryos were successfully rescued forin vitro production of hybrid plantlets.

In viviparous hypocotyls ofRhizophora apiculata Blume the triacontanol treatment enhanced the growth of root and shoot (number of primary and secondary roots, length of roots, shoot height and biomass) protein and energy contents of leaves and roots,in vivo nitrate reductase activity, contents of chlorophylls and carotenoids in leaves as well as the amount of chlorophylls present in photosystems 1 and 2 and in the light harvesting complex of chloroplasts. These promotory effects were recorded at 40 and 80 mg m^-3 triacontanol, but they decreased with increasing growth regulator concentration.

Interspecific hybrids from the crosses betweenBrassica campestris, B. carinata, B. juncea andB. napus were obtained throughin vitro ovary and ovule culture. F₁ hybrids were studied morphologically and flow cytometry was used to estimate 2C nuclear DNA content both in parentalBrassica species and their hybrids. It was found that in comparison with the A genome, the B and the C genomes ofBrassica contained 26.9 % and 43.9 % more DNA, respectively. This finding may be used to distinguish interspecific hybrids containing various genome combinations. It was concluded that flow cytometric analysis of nuclear DNA content might be useful tool inBrassica breeding.

Sodium chloride tolerant cell lines of finger millet were isolated from embryogenic cultures growing on MS medium supplemented with picloram (2 mg I^-1), kinetin (0.1 mg l^-1) and sodium chloride (1 %) at the end of 6 passages. The sodium chloride tolerant cell lines showed better growth in comparison with control at all concentrations of sodium chloride tested, with optimum growth at 0.25 % NaCl. When the tolerant lines were grown for 3 passages in absence of NaCl, the growth was lower than that of the tolerant lines tested immediately at the end of 6 passages of selection. NaCl tolerant calli had more Na¹ in comparison with control and they regenerated plants in presence of 1 % NaCl, while the control lines failed to differentiate. When screened in a hydroponics system with 1 % NaCl, the tolerant plants grew to maturity while the control plants failed to grow.

Growth ofCichorium intybus root explants was accompanied by an important increase of fresh mass during the course of callusing and rooting. The absence of glucose in callus forming medium was compensated for by hydrolysis of storage carbohydrates of the tissues, inducing a decrease in dry mass. Protein content showed similar slight variations in explants during the course of budding and callusing, whereas an important increase of protein content was found during the first 48 h in explants cultured on root forming medium.
Specific increase of soluble peroxidase activity during bud and root neoformation was found. A peak of peroxidase activity, proceeding the organ emergence, was always observed. This peak occurred earlier in bud forming than in root forming explants. Conversely, during callusing, the bulk peroxidase activity showed only weak variations, and no peak was detectable. Moreover one basic isoperoxidase was missing in these explants after a 6-d culture, whereas in both root and bud forming explants the isoperoxidase patterns were very similar. When explants growing on differentiation media were in darkness a supplementary basic isoperoxidase with the highest electrophoretic mobility was revealed.
The data obtained show that isoperoxidase patterns cannot be correlated to a particular organ differentiation process, but that peroxidase activity and especially the moment of peak emergence can be a reliable marker of the differentiation process. Moreover, light seems to inhibit the expression of a basic peroxidase in explants growing in media promoting organ differentiation.

The effect of glucosinolates sinigrin, progoitrin, epiprogroitrin, gluconapin, gluconapoleiferin, glucobrassicanapin, glucotropaeolin and gluconasturtiin without and with the glucosinolate-degrading enzyme (myrosinase, EC:3.2.3.1.), on the infectivity of turnip mosaic virus was studied. Little or no effect was observed when the intact glucosinolate (2.5 μmol cm^-3) was added to the suspension of turnip mosaic virus (TuMV, isolate Ruzyně; 0.2 mg cm^-3 in 0.01 M potassium phosphate buffer) at both pH 7 and pH 6. A significant decrease of virus infectivity was, however, observed when 0.25, 1.25 and 2.5 μmol cm^-3 of the glucosinolate together with 0.31, 1.56 and 3.13 mg cm^-3 of the myrosinase, respectively, was added to the virus suspension of both pH 7 and pH 6. The effect, which was greater at pH 6, was most intense with sinalbin and glucobrassicin substrates.

Molecular variability was determined between, 17Brassica napus cultivars, 8 new selections 4 F₁ hybrids, 5 cultivars ofB. oleracea, B. campestris andB. peruvianum with 4 rDNA probes fromLycopersicon esculentum, 3 probes from a PstI library ofB. oleracea, 3 probes from EcoRI libraries ofB. napus andB. oleracea and the acetolactatsynthase gene fromNicotiana tabacum. Sporadic interspecific and rare intraspecific variability was detected.

To cast light upon the role of Ca¹⁺ and calmodulin on photosynthetic rate (P_n), dark respiration (R_D) and amino acid and protein contents in salinity stressed and non-stressedChlorella cultures, the Ca²⁺ chelator EGTA [ethylene glycol-bis-(2-aminoethyl ether)-N,N- tetraacetate] and the calmodulin antagonist TFP (trifluperazine) were used. TFP markedly inhibited P_N while EGTA exerted a slight, if any, effect on P_N. NaCl tolerance, on the other side, was markedly abolished by TFP that inhibited P_N and lowered rate of proline accumulation. Calmodulin might be involved in osmoregulation and salt tolerance ofChlorella. R_D, however, was markedly enhanced by EGTA and Ca²⁺-free medium and hence the Ca²⁺ deprivation increased stress severity exerted by NaCl. Combinations of Na⁺ and Ca²⁺ enhanced P_N, decreased R_D and proline content in comparison with an osmotically equivalent reference culture containing only NaCl. Addition of Ca²⁺ to TFP treated cultures failed to reactivate calmodulin for proline synthesis. However, when Ca²⁺ was added to EGTA-treated cultures, only relatively reduced proline contents were recorded.

A disease of spiraea(Spiraea xvanhouttei) manifested in leaves by very mild, mostly hardly perceptible mosaic, was found to be caused by cucumber mosaic virus (CMV) infection. The proof was given on the basis of responce of differential plants after virus transmission, by immunosorbent electron microscopy and ELISA.

The influence of salinity, given at germination (stage I) or 75 d after sowing (stage II), on flower production and characteristic features of male reproductive structures was studied in three promising genotypes of chickpea (Cicer arietinum L. cv. ICCV 88102, H 82-2 and C-235). In ICCV 88102 and H 82-2 salinity 20 meq 1^-1 increased the number of flowers when applied at both stages whereas in C-235 only when applied at the later stage. The salinity also delayed flowering; the higher salinity the greater was delay in flowering. In H 82-2 and C-235 salinity treatment given at stage II (when few flower buds appeared) hastened the flowering. The salinity curtailed pollen production; the reduction being minimum in C-235 and maximum in H 82-2. Germination was not significantly affected in C-235 pollen collected from plants grown under salinity conditions upto 60 meq 1^-1 applied at stage I but the tube elongation was inhibited. The inhibition of tube elongation was greatest in C-235. Salinity treatment administered at stage II did not affect significantly pollen germination excepting C-235 in which a consistent decline with increasing salinity was evident. Salinity stimulated tube growth in ICCV 88102. Na₂SO₄ in the germination medium was more detrimental for both pollen germination and tube growth than NaCl.

The actively growing stems ofSalicomia brachiata (60-d old) were dissected into three major tissue layers: vascular, spongy mesophyll and palisade. Each layer was analysed for chlorophyll, protein, amino acids, and sugar contents and the activities of ATPase and phosphatase (alkaline and acid). The differences in organic compounds and enzyme activities in these different tissues have been correlated with the ion content of the corresponding tissues.

Cell walls of two strains ofChlorella vulgaris (from fresh water, F, and saline water, S) and ofKirchneriella lunaris contained various proportion of saccharides and proteins (highest percentage in dry matter was found inK. lunaris). They differed also in presence of individual monosaccharides (5 inC. vulgaris F, 8 inC. vulgaris S and 6 inK. lunaris) and amino acids (11 in C.vulgaris F, 6 in C.vulgaris S and 7 inK. lunaris). Common substances were rhamnose, cystine, proline, glutamic acid and leucine.

Restriction fragment length polymorphism in rDNA repeat unit for eight restriction endonucleases was studied in two genotypes of barley (Hordeum vulgare L.). Both genotypes contained restriction sites for EcoRI, EcoRV, PvuII and Sau3239I in rDNA repeat unit and contained two different rDNA repeat unit length variants 9.7 kbp and 9.1 kbp.

Tissue cultures were established from hypocotyl and cotyledonary leaf segments ofGuizotia abyssinica Cass. on MS medium supplemented with various concentrations of auxins (IAA, NAA, IBA or 2,4-D) and cytokinins (KN or BA). Expiants cultured on media with cytokinins or in combination with auxins produced shoot buds. Maximum number of shoot buds (20-25 per culture) were differentiated from cotyledonary leaf segments on medium with 2 mg 1^-1 each of KN and IBA. Rooting of regenerated shoot buds was acheived on medium with NAA. The obtained plantlets were successfully transferred to soil.

The effect of crude volatile oils extracted from the young leaves ofLantana camara var.camara was studied on the parent plant itself. The contents of water and chlorophyll, of leaves apart from seed germination, seed vigour and length of seedlings of the parent plant were adversely affected with increasing concentration of theLantana oils; this indicated autotoxic potential of the oil. The correlations between oil concentration and the studied parameters were rather strong and obeyed the concentration response relationship, typical of chemical bases. The cell respiration, however, increased with increasing concentration of the oil vapours. Compared to control, less than 13 % of the seeds of the parent plant exposed to 30 cm³ m^-3 of oil showed incipient germination with no growth of radicle beyond immeasurable protuberance, and no plumule emergence.

The plant cell/microbe coincubation assay is based on employing living tobacco cells in suspension culture as the activating system for promutagens and the Ames/Salmonella cells as the genetic indicator system. In contrast to aromatic amines(e.g. 2-aminofluorene andm-phenylenediamine) that were previously reported to be activated to products mutagenic in theS. typhimurium strains TA98 or YG1024 by tobacco cells, promutagenic N-nitrosoamines (N-nitrosodimethylamine, N-nitroso-morpholine, N-nitrosopiperidine, N-nitrosomethyl-2-hydroxypropylamine) were not activated to product(s) mutagenic inS. typhimurium TA 100.

Transport of¹⁴C-IAA was studied in apple spurs of a 20-year-old McIntosh with one fruit and one shoot. Water solutions of IAA were applied to intact, pricked or scratched leaf blades, to decapitated shoots or to petioles (leaf-blade removed) at the end of June, July and August.¹⁴C-IAA (in an unknown form) was transported from intact leaves and shoots to pedicel, pericarp and seeds. Radioactivity of the pedicels increased every month while that of seeds reached maximum at the end of July and then markedly decreased in August. Total radioactivity of whole fruit doubled, at least, with every month due to enlargement of the pericarp. Pedicels deprived of fruits had their retention prolonged on spurs with leaves or shoots treated with 1% IAA in lanoline. It is assumed that auxin delivered from shoots or still growing leaves at the time of its deficiency in seeds, restrains fruits from premature dropping. At the same time seeds seem to be protected by a regulatory system in pedicel against too massive flow of auxin from outside.

Callus formation by fragments of cauliflower hypocotyls was favoured by raising culture medium osmolarity above -0.38 MPa. Increase in sucrose concentration while diminishing macronutrients inhibited callus initiation and growth. Root formation by the same material required a low medium osmolarity (-0.19 MPa). Reducing sucrose concentration in the classical Murashige and Skoog rooting culture medium favoured root formation. Adventitious bud formation was also depending upon medium osmolarity besides the need for a cytokinin. Reducing too much the osmotic potential of the medium had an unfavourable effect on bud neoformation. The importance of sucrose in all these processes is pointed out.

We followed the effect of storage conditions on the serological activity of the potato virus A (PVA) in the ELISA test. Storage of the purified PVA in 0.05 M borate buffer, pH 8.3 at -70°C represents the optimum conditions. The activity decreased 40% in comparison to the original activity after four months. Lyophilization of infected leaves or the leaf homogenate in the extraction buffer were found to be the best methods for the storage of the PVA in natural conditions. After 12 months, the activity of PVA decreased to 80% and 50% of the original activity in the case of lyophilized leaves and leaf homogenates, respectively.

The rates of canopy apparent photosynthesis (P_C) and canopy respiration (R_c) were studied during vegetation season in two erectophile and two planophile hybrids of maize (Zea mays L.) grown at two canopy densities [7.5 plants m^-2 (HD) and 4.5 plants m^-2 (LD)]. Large differences in P_C, R_c, R_C/P_C, leaf area index (LAI), dry matter accumulation and grain yield were found among hybrids and plant densities. Variations in P_C and R_C were associated mainly with changes in LAI. There was also found change in P_C per unit LAI with time. The average R_C/P_C was 28.9 % for all treatments throughout the vegetation season. P_C and R_C per unit dry matter were higher in LD than in HD and decreased throughout the measurement period. The HD stand had higher P_C and yield in hybrids with erectophile foliage, whereas LD stand had higher P_C after male tetrad and got higher yield in hybrids with planophile foliage. Only R_C in hybrids of the two foliage types was higher under HD than under LD throughout the vegetation period.

Sugar uptake by potato tuber discs was studied. Discs were used "fresh" or after a 24-h ageing period. It was shown that ageing increases (by 3 to 4 times) the rate of glucose and sucrose uptake. Sucrose uptake by fresh tissues was insensitive to the presence of glucose or fructose while a competitive effect was observed after ageing. This indicates the development of an invertase activity, which was inhibited by tris-buffer. Sucrose and glucose uptake by aged discs was dependent on cellular metabolism as shown by the sensitivity to low temperature and metabolic inhibitors (NaCN, DNP, CCCP). Involvement of thiol groups was demonstrated by the inhibition with NEM and PCMBS. Orthovanadate, which decreases phosphate uptake by 85 % (Poderet al. 1986) did not produce any effect on glucose and sucrose uptake by aged tissues. Fusicoccin produced only a slight stimulation (15 %). These results argue in favour of the involvement of specific ATPases in ion and sugar uptake. No involvement of a redox system was observed. ABA and BAP inhibited the uptake induced by ageing but had no effect on the endogenous sugar content. BAP would act by its effect on the amount of ATP while ABA would act at the membrane level. The results are discussed in relation to the mechanisms of transfer of glucosyl groups and to the transport of sucrose by the symplasmic pathway. Reçule

SC₂ and SC₃ progenies of nineteenin vitro regenerated barley plants (SC₁) from resistant calli selected against purified culture filtrate ofHelminthosporium sativum and one parent 'Dissa' genotype were studied for stability of resistance and protein, soluble protein, maltose and saccharose contents. Cytological studies were also carried out on the SC₃ generation. Stability of resistance toHelminthosporium sativum was found in 50% of the somaclonal lines. Significant variation among different somaclonal lines and among different callus lines from which the plants were regenerated were found for yield, disease score and biochemical characters assessed except saccharose content in the somaclonal lines. Significant increase and decrease over the donor parent for most of the characters were obtained. Cytological abnormalities such as multilobed nuclei, multinucleate cells, abnormal anaphase and mixoploidy were also observed.