Acid phosphatase isolated from low altitude grown plants of two high altitude plant species,Selinum vaginatum Clarke andAcer caesium Wall, displayed higher thermostability than that from plants of the same species grown at high altitude. The isozyme composition, however, remained unchanged inSelinum vaginatum. InA. caesium, one of four isozymes, was thermolabile in the samples from high altitude and was lost after 10 min heating of the extracts at 60 °c. In the samples from low altitude, this isozyme was not detected and a band with slightly lower Rf value was present which was thermostable. The described changes in the thermal properties of acid phosphatase reflect an adaptive step towards high temperature acclimation at low altitude.

N-malonyl-D-tryptophan (MT) and D-tryptophan added to the medium instead of auxin stimulated growth of soybean and tomato cell and tissue cultures. Effects of 50-100 μmol 1^-1 MT and 100 -300 μmol 1^-1 D-tryptophan were equal to the effect of 3-10 μmol 1^-1 IAA. Soybean cells grown in the presence of 100 μmol 1^-1 MT contained 125-170 ng IAA per 1 g fresh mass (as determined by spectrofluorimetric indole-α-pyrone method), whereas the cells grown in the presence of NAA 10. 7 μmol 1^-1 contained 50 -60 ng IAA and the cells grown in the absence of auxin failed to show endogenous IAA. MT as proposed can be hydrolyzed by plant cells with liberation of D-tryptophan, which in turn can be used in IAA synthesis. It is proposed that MT is a possible source of endogenous auxin in plants.

The effect of anaerobiosis of wheat seedling roots during 6 consecutive days on contents of ethanol, lactate and glucose in roots and shoots and on the exudation of ethanol from roots to the medium was examined. Activities of alcohol dehydrogenase (ADH) and lactate dehydrogenase (LDH) were determined. After 36 h of anaerobiosis the concentration of ethanol in roots increased temporarily about 6 times and after 6 days it decreased to the level of control plants. The exudation of ethanol from roots to the medium showed similar pattern. The content of lactate was unaffected by anaerobiosis. In contrast, the content of glucose in roots of seedlings increased already after 1 day of anaerobiosis about 2 times and this higher level of glucose was noticed during consecutive 5 days. Anaerobiosis of roots caused an increase in the activity of ADH in both roots and shoots but the increase was not related to the content of ethanol in tissues, or exudated to the medium. The activity of LDH was unaffected by this factor. The results are discussed in relation to the limitation of energy supply of plants grown under root anaerobiosis.

Like wet stigmas, the stigmatic secretions of dry stigmas ofEichhornia also have proteins, sugars, amino acids, phenols and fatty acids. No significant difference could be observed in the composition of stigmatic secretions of long and medium styled flowers except that the components were marginally higher in concentration in the former than the latter. The UV absorption profiles of the stigmatic secretions also showed no difference. Stigma surface esterases could be detected in both the stigmas from a very early stage of development.

The salt tolerance was studied according to both fresh and dry matter increases of callus cultivated on the media supplemented with various sodium chloride concentrations as well as a high amount of K⁺, Na⁺, Ca²⁺, and Mg²⁺ ions as found in the East Slovakia salt soil lowland. The cells tolerate salinity at least up to 85 mM. According to statistical evaluation the salt concentrations used did not inhibit growth rate and development of tissue cultures.

Seven day- and six week-old alfalfa (Medicago sativa L.) plants, susceptible and resistant to bacterial wilt, were inoculated withCorynebacterium michiganense pv.insidiosum (McCulloch) Dye & Kemp. Leakage of solutes absorbing UV light from leaf discs into distilled water was investigated. The bacterial infection did not affect solute leakage rate from unifoliate and trifoliate leaves of either susceptible or resistant plants at an early stage of the disease. This may indicate that cell membrane integrity in alfalfa leaf tissues was not impaired.

There are several differences between monocotyledonous and dicotyledonous plants. The sensitivity towards added galactose which inhibits auxin-induced coleoptile elongation but not stem elongation is one of the conspicuous differences between the two types of plants. InAvena coleoptile segments, galactose, probably as galactose-1-phosphate, inhibits the formation of UDP-glucose from glucose-l-phosphate. The inhibition of UDP-glucose formation due to galactose is not found inPisum epicotyl segments. InAvena UTP: α-D-glucose-1-phosphate uridyltransferase (EC 2.7.7.9) which catalyzes the reaction from glucose-1-phosphate to UDP-glucose seems to be inhibited by galactose-1-phosphate.

The bean first internode bioassay ofMeudt andBennett (Physiol. Plant.44: 422-428, 1978) is based on the curvature of bean internode sections after unilateral application of test material near to their base. The test was also used for estimation of biological activity of brassinosteroids which enhance the effect of auxin. Sensitivity of the assay to both IAA and 24-epibrassinolide was increased 1000 and 100 times, respectively, when internode sections were incubated in morphologically inversed position. Under these conditions test material was applied to the young auxin-sensitive morphologically apical internode tissues and auxin was basipetally translocated to the zone of curvature. Using this bioassay as little as 10 fmol of IAA and 1 pmol of 24-epibrassinolide can be estimated.

The present paper deals with the hormonal regulation of reproductive development,i.e. flowering and sex manifestation. Representation of hormonal regulation of flowering is based on the concept of florigen as a two-component, complementary system of flowering hormones, which consists of gibberellins and anthesins. Data are presented on the effect of extracts of gibberellin- and anthesin-type substances from the leaves of flowering and vegetatively growing plants under non-inductive conditions of day length. Experiments with flowering of plants under the influence of graftings serve as a basis for considering the question about the common nature of one of the florigen components - anthesins, for various plant species.
The mechanism controlling tuberization in both intact and grafted plants is based on the participation of all the components of the hormonal system and constitutes one of the most vivid manifestations of integration of all the organs in the whole organism.

Pharbitis nil, strain Kidachi and Violet, were grown at 20° C under continuous light in various cases of different sizes, containing the nutrient solution or tap water. Kidachi initiated flowers when seedlings were cultured in small cases containing nutrient solution but did not flower in large cases. The application of NAA, kinetin, ABA or 5-chlorobenzoiec acidvia roots in large cases caused flowering, Floral initiation was always accompanied by the suppression of root elongation. The promotion of root elongation by aeration inhibited flowering. Root cutting inhibited flowering. On the other hand, Kidachi did not flower in tap water irrespective of vessel size. Violet did not flower in the nutrient solution even in small vessels, but initiated floral buds in tap water irrespective of vessel size, though the plants grown in large cases developed very long roots. In both types of flowering, cotyledons are necessary to induce flowering and the removal of cotyledons before the 16th day after the start of culture in Kidachi and before the 12th day in Violet completely inhibited flowering. GA₃ promoted stem elongation without preventing flowering of Kidachi.

Black currant reversion disease causes serious problems in some cultivars of black and red currant. Investigating ultrathin sections prepared from overground parts of diseased red currant plants cv. Heinemann's rote spätlesse, we observed consistently local cell wall disintegration of tracheids in vascular bundles. We have observed these changes in red currant plants showing reversion symptoms during the vegetation period from March to June. The observed phenomenoni.e. cell wall disintegration of tracheids might be utilized as an auxiliary diagnostic criterion m ident ification of red currant reversion disease in the cultivar Heinemann.

The work concerns the senescence of isolated young leaves of oats (Avena sativa) floated on water or solutions. Senescence is rapid in darkness but slow in white light; the effect of light is not due to photosynthesis, but is paralleled by stomatal opening. Closure of the stomata by osmotic or chemical means makes senescence in light proceed as fast as in darkness, while opening the stomata in darkness by cytokinins, fusicoccin,etc., delays senescence to rates typical of light. The osmotic closure in light is mediated by abscisic acid, and since this also accumulates in darkness it appears as a major factor controlling senescence. Efflux of ions into the solution; indicating increased permeability, occurs almost in parallel with senescence. Senescence in light is accelerated by 1-aminocyclopropane-l-carboxylic acid (ACC) and inhibited by cobalt, silver or aminoethoxyvinyl glycine (AVG) which interfere with ethylene production or action; however, ethylene's role is unclear because some reagents, including kinetin, that delay senescence, actually increase ethylene production. At the endogenous level, therefore, ethylene may not be a limiting factor. Finally, a new ethylene-generating system is described in which the dehydrogenation of linoleic acid is coupled through manganese to the oxidation of ACC; it is probably activein vivo.

Evidence is presented to support the generalization that gibberellin A₁ is the main 'gibberellin hormone' that is activeper se in the control of elongation growth in higher plants. The evidence is based on a combination of chemical and genetic studies using single gene mutants of maize, pea and rice.

Two selected strains ofSilene armeria L. were used: S_1-2 (GA-line, not induced to flowering by GA₃ in SD of 8 h) and S_2-1 (GA+ line which reacts to GA₃ with flowering in non-inductive photoperiod). Moreover S_1-2 and S_2-1 differ in their critical daylength 14.5 and 8.0 h, respectively. Changes in the mitotic index and DNA content of cells in the various zones of the apical meristem during GA₃ treatment were described. At the start of the experiment, the functioning of the apex was characterized by a predominance of G₁ phase in the two strains. Therefore S_2-1 differed by a higher mitotic activity specially in the central zone. In S_1-2, GA₃ acted mainly on the rib-meristem cells, which resulted in stem elongation. Lack of response in the cells of the central zone explains why GA₃ fails to induce flowering in this strain. In S_2-1, GA₃ acted mainly on the central zone where a gradual increase in mitotic acitivity and in the percentages of nuclei at the (S + G₂) level was recorded. This stimulation brought the meristems into the prefloral stage. The differences between the two strains are discussed according to the status of control meristems. The reactions induced by GA₃ were compared with the pattern of changes during induction, in LD.

The inhibitor of microsomal monooxygenase activities 9-hydroxyellipticine markedly inhibited the frequency of embryonic and chlorophyll mutations induced by the metabolism-requiring mutagen dimethylnitrosamine (DMN) in a higher plantArabidopsis thaliana, but had no effect on the frequency of mutations induced by the direct-acting mutagen N-methyl-N-nitrosourea (MNU). The presence of thiol containing compounds thiourea and cysteine before and during DMN or MNU treatment resulted in a decline of mutation frequency as compared to treatment with either nitroso compound alone. In contrast, the mutagenicity of DMN and. MNU was not altered in the presence of two other thiol compounds, thiouracil and glutathion and by six naturally occurring phenolic acids: ellagic. vanillic, cinnamic, coumaric, caffeic and ferulic acids.

Occurrence and operation of sucrose synthetic system in randomly selected callus cultures such as persimmon, soybean and poplar cultures were examined by¹⁴C-tracer analysis and determining enzyme activities involved in sucrose metabolism. All the enzymes examined were present and¹⁴C-glueose was transformed into¹⁴C-sucrose in every callus. Sucrose synthetic capacity appears to be widely distributed in cultured plant tissues.

IAA synthesis proceeding by indol-3-ylpyruvate (IPyA) pathway seems to be regulated in two steps. In the first the L-trp conversion into IPyA is reduced by a low affinity of L-trp to the unspecific aminotransferase, by competition of L-trp with some aminoacids (e.g. L-asp) and indoles (e.g. indol-3-ylacetylaspartate). Simultaneously, a specific L-trp-dehydrogenase in dependence on the NAD(P)/NAD(P)H ratio regulates by its reversible effect the level of IPyA, connecting photosynthesis with growth. A second more "delicate" regulation of IAA level is carried out by the indol-3-ylacetaldehyde system. In pea plants two indol-3-ylacetaldehyde oxidases with pH optima 4.5 and 7.0 were found. The oxidases are differentially inhibited by an excess of IAA, different indoles as indol-3-ylacetylaspartate and aminoacids as L-asp. GA₃ and kinetin stimulate the conversion of indol-3-ylacetaldehyde to IAA.

The possibility that some of the variation in callus cultures involves epigenetic changes is examined in cultures established from the hypoootyls and roots ofEuphorbia heterophylla. It is shown that the responses of the cultures are affected by the light regimes under which they are grown and that in the dark and under short photoperiods, there are differences between the two types of culture with respect to pigmentation, auxin requirement, capacity to regenerate buds and roots and in certain isozyme patterns, whereas the two cultures are similar from the first passage under continuous light. However, these differences are only maintained for 2-3 passages, after which the root callus becomes similar to the hypoc otyl callus. Evidence is presented that these differences between cultures are epigenetic. Callus cultures established from the apical meristems of shoots and roots ofE. hetero phylla show similar differences to those observed between hypocotyl and root cultures and these differences are also lost after 3 passages. These results indicate that the cells of apical meristems are not totally uncommitted, but are determined as 'shoot' and 'root' meristem colls, respectively. The practical importance of a better understanding of epigenetic effects in plant cells is strassed.

The decrease of peroxidase (PO) and IAA-oxidase (IAAO) activities in stem bark of intact photoperiodically neutral tobacco plants was shown both in the course of development and in an acropetal direction along the stem as related to flowering regulation. In stem expiantsin vitro, the realisation stage of floral morphogenesis is related to an increase in PO and IAAO. This correlates with low auxin concentrations in the medium as required for floral morphogenesis. The changes in both PO and IAAO are suggested to be in the opposite directions during floral induction and floral morphogenesis.

Curves relating net photosynthetic rate to irradiance [P(I) curve relation] were estimated and analysed inMercurialis perennis L. plants stemming from three forest (spruce, beech and ash) stands with different tree leaf canopy development and different light regime.
The saturating irradiance (I_s) reached the highest values in plants of all three stands in spring (spruce forest: 438 W m^-2, beech forest: 440 W m^-2 and ash forest: 367 W m^-2), it declined sharply in the middle of the growing season (283, 285 and 297 W m^-2, respectively) and this I_s level persisted until autumn. A pronounced dynamics in plants from spruce and beech forests made itself manifest also in the adaptation (I_a) and compensating (I_c) irradiances, respectively. After a sudden decline in summer, values in autumn were close to those of the vernal season.
The most pronounced parameter, which optimally expressed the adaptation ofMercurialis perennis to various light conditions, was the photosynthetic efficiency (α) calculated as the slope of the linear part of the curve relating net photosynthetic rate to irradiance.
At the time of the highest P_{N sat.} value in course of the growing season (August) (spruce forest: 100, beech forest: 98.7 and ash forest: 85.8 μg CO₂ m^-2 s^-1), R_D was in its minimum; in autumn P_{N sat.} reached the lowest values which corresponded to the most intensive R_D.
It was found thatMercurialis perennis plants stemming from forest stands with different light conditions did not make use equally of the altering light conditions in the course of the growing season. By the underlying analysis of P(I) curves this rhizomatous perennial herb (geophyte) may be characterized as a shade tolerant species.

A possible involvement of the alternative oxidase pathway in proton translocation was investigated. Net H⁺ efflux- and elongation-rates were simultaneously and continuously measured by means of a pH-stat and an angular position transducer. Disulfiram, an inhibitor of the alternative path, reduces the IAA- and Fusicoccin-induced as well as endogenous proton secretion and growth. Fusicoccin-induced H⁺ secretion is very sensitive to reduced oxygen concentration values far apart from the K_m of cytochrome oxidase. The sensitivity of non stimulated proton secretion to reduction of oxygen concentration depends on the age of plant material. It is proposed that more than one system is responsible for proton translocation across the plasmalemma. One of them has a high sensitivity to reduced oxygen concentration which is within the same range of the high K_m value of the alternative oxidase.

Evidence for the existence of a neutral inhibitor specific for auxin has been in the literature for 45 years. The inhibitor is demonstrable by its effect in causing positive curvature of theAvena coleoptile. The growth of the mesocotyl of oat and corn seedlings in darkness and its inhibition by light are determined by the neutral inhibitor as is the phototropic response of the sunflower stem. Production of the inhibitor is promoted by red and fluorescent light. Irradiance at 730 nm promotes auxin production while irradiance at 660 nm promotes production of the inhibitor. The positive curvature induced by 2,3,5-triiodobenzoic acid can be used to quantify the neutral inhibitor. Since the benzoic acid is more effective than iodoacetate in reacting with the sulfhydryl of cysteine, a sulfhydryl group is indicated to bo one reaction site for auxin and to be the basis of polar transport.

The current status of our knowledge of auxin effects on floral induction is summarized. The most general effect is inhibition, although the concentration of synthetic auxins added to. plants tends to be too high for us to be certain that the inhibitory effects are truly physiological. Studies of endogenous levels of auxin have focused almost entirely on IAA-like bioassay activity. Chemical identifications of endogenous IAA are needed and feasible. In addition, a search for-other auxins involved in vegetative to floral transitions, their chemical identification, and measurement of their changing levels in the plant are urgently needed.

Inhibition of root growth was observed inChenopodium rubrum under photoperiodic conditions inducing flowering. That this inhibition is mediated by the cotyledons was shown directly by the effect of their excision, which changes the responsiveness of the roots to photoperiodic treatment. On the other hand, decapitation did not lead to such an effect. Some evidence is put forward suggesting that changes in IAA may be involved in these correlations. The existence of two different mechanisms of photoperiodic action in flowering and in root growth is proposed to explain these differences.