Thein vitro embryoids ofEschscholzia californica do not form normal plantlets in cultures. However, 6-benzylaminopurine and gibberellic acid, when added to the medium, partially alleviate this inhibition. Experiments involving decotylization, and culture of embryoids at different stages, indicated the cardinal role of cotyledons in plumular growth.

The fungusLentinus tigrinus was cultivated in a synthetic medium. During vegetative growth of mycelium and differentiation of fruiting bodies samples serving for determination of endogenous growth regulators were collected. The material was extracted with methanol, separated by chromatography and the isolated fractions were tested. Substances of auxin type were assayed with coleoptile segments of oat plants, gibberellins by measuring the hypocotyl growth in the lettuce and cytokinins from the degree of chlorophyll decomposition in the leaf segments of barley. Very low content of auxins was found in all phases of growth and differentiation of the fungus. The content of gibberellin substances was relatively high during the whole life of the fungus. The highest content is found in the vegetative mycelium and in the differentiated fruiting body, especially in the cap; it decreases during the differentiation of fruiting bodies. The content of cytokinins is equally high and the pattern of its change resembles that of the gibberellins. Its maximum is reached in young vegetative mycelium, it decreases when fruiting bodies are formed and when they are growing. Minimum is reached in the differentiated stalk, where also the amount of inhibitions is the highest.
Experimental results show that during differentiation of fruiting bodies and their morphogenesis not only gibberellins and cytokinins are of importance, but also substances of an inhibitory character. A relatively high amounts of these substances was secreted into the cultivation medium. In a synthetic nutrient solution they may be easily demonstrated.

Trifluralin was found to induce isodiametric enlargement ofAllium cepa root tip cells in the elongation zone. It enhanced the endogenous oxygen uptake of the excised root tips. The herbicide was found to have no marked effect on the dry weight of the root tips. It is suggested that the herbicide may exert its effect onAllium cepa root tips through its enhancement of ethylene production.

Long-term callus cultures of two barley cultivars have been investigated at the cellular level. One slowly growing, root forming callus of the barley cv. Bulgarische Nackte consists of cells the majority of which contain the diploid chromosome number. Contrarily, a fast growing callus of the cv. Elgina having no regeneration potency at all, is highly polyploid and includes more than two thirds of aneuploid cells. Tn this callus strain, a great number of multinucleate cells has been found. Some problems are discussed with respect to the relationships between growth rate, karyological stability and regeneration capacity in long-term callus cultures of cereals.

The changes of kernel nitrogen (N), phosphorus (P) and dry weight (DW) were determined during the time period from 10 days after anthesis till maturity in three spring barley strains. The plants were cultivated under field conditions in Gatersleben (German D.R.) and Kroměříž (Czechoslovakia). The course of N, P and DW changes was described by Richard's comprehensive growth function dW/dt = aW^m + bW, where W is the amount of N, P or dry matter per kernel, a, b, m are coefficients. The integral of this function was used and several parameters calculated. There was a remarkable synchrony between N or P and total dry matter accumulation in the kernels. Thus, the N or P concentration per unit kernel dry weight was relatively constant during the investigated period and with few exceptions corresponded to 80% to 100% of the final value. However, considerable differences between strains, years or places of cultivation were found.

As an extension of earlier studies performed in our laboratory on enzyme localization on tissue level, the distribution of starch was examined in seedling root tips of peaPisum sativum L., broad beanFaba vulgarisMoench., maizeZea mays L., lupinLupinus albus L., and pumpkinCucurbita maximaDuch., and in tips of adventive roots of onionAllium cepa L. by means of the alcian blue /JJK procedure applied to paraffin sections. In pea, some genetic (various cultivars) and eco-physiological (different harvests, various localities, diverse way of germination, uneven seedling age, unequal stage of cell growth) factors were studied concerning the present problem. In all these cases the starch localization pattern remains constant though the amounts of starch vary in particular cell complexes. From the evaluation of the starch localization at the level of the beginning cell growth in particular species and from comparison of the findings in different species it follows that starch localization and histogenesis patterns are different. This supports the view that the two phenomena are caused or controlled by uneven factors.

Carbohydrate requirement for the growth of the cells and accumulation of polyphenols in culturedCassia fistula L. andDatura metel L. tissues were examined. Superiority of suerose over other carbohydrates was observed both for the growth of the cells and for the maximum production of phenolic compounds; and its availability was found to be a limiting factor for the synthesis of phenolic compounds.
Progressive changes in the pattern of peroxidase and phenylalanine ammonia-lyase (PAL) activities were followed and the relationship between the development of the enzyme activities and synthesis of polyphenols was further examined. The significance of peroxidase and PAL in the regulation of phenolic production is discussed in the light of recent findings.

Penicillin caused elongation inhibition of mungbean (Phaseolus aureus L.) seedlings at concentrations above 100 mgl^-1. Inhibition of hypocotyl could be reduced to different degrees by manganese, pyruvate, succinate, fumarate, malate, GA₃, purines, pyrimidines and nucleosides, whereas the amino acids except cysteine were not effective. Penicillin inhibited neither elongation of wheat coleoptile sections nor the cell enlargement induced by IAA in this tissue. Thus penioillin inhibits intact seedling elongation probably through an Effect on cell division apparently without inhibiting cell enlargement.

N-Methyl-N-nitrosourea and N-methyl-N-nitrosourethane at concentrations of 0.1 mM to 1 mM inhibited the growth of tissue cultures ofNicotiana tabacum L. The inhibitory effect was proportional to the mutagen concentration applied. The primary expiants (pith slices) and a 3-year tissue culture strain exhibited a different sensitivity to the same mutagen concentrations. The variability in sensitivity of tissue culture inocula to mutagen effects was reduced by previous fractionation of the culture and by standardization of the age and size of inocula. The changes investigated in the ratio of relative growth rates between the controls and treated cultures give evidence of a fluctuating expression of mutagen effect in the course of the subculture interval and may demonstrate a recovery of the cultures from the mutagen effect.

Benzylaminopurine (BA) caused an enhancement of chlorophyll and protein content and a reduced elongation of primary barley leaves. BA did not change the rhythmic pattern of¹⁴CO₂ fixation and activities of RuBP carboxylase, RuBP oxygenase, glycolate oxidase and phosphoglycolate phosphatase, but the enzyme activities were enhanced and the level of¹⁴CO₂ fixation was reduced. Light/dark¹⁴CO₂ evolution ratio was affeoted by BA only in older leaves. BA acts sequentially on the activities of photosynthetic and photorespiratory enzymes.

Two typical dark-responses namely the excessive elongation of sprouts and the formation of sprout hook, are adversely affected by chloroflurenol. It also affects the polarity of sprouts and the formation of roots on tubers, the effect varying with the concentration and the light condition. The significance of these effects of chloroflurenol used in potato production has been discussed.

Tissue culture was isolated from the stem ofPopulus alba L. 'pyramidalis'. Callus formation was observed since November till March (1974),i.e. till the formation of calluses suitable for further subeultivation. The most vigorous growth was obtained with the callus culture cultivated on the nutrient medium of DIAZ-COLONet al. (1972) on which more than 11 g of fresh matter was produced after 30 d at the end of the first year of cultivation in darkness, with inoculum weight 1.5-1.8 g. A mild decrease in growth rate of the tissue culture was observed after the first year of cultivation. When illuminated, the originally yellow calluses turned green. The morphological and anatomical structure of the callus culture is also described and cell shape and cell size evaluated.

Excised tomato cotyledonswere subjected to mannitol induced water stress solutions for three days. Extracts of proteins and the enzyme peroxidase were made and separated with polyacrylamide gel electrophoresis. The water stress injury caused increases in bigger protein molecules but decreases in smaller protein molecules. The small fastest moving peroxidase isozyme was almost completely eliminated. Applications of growth regulators to the stress solutions indicated that the protein and peroxidase changes could be explained on the basis of reduction in endogenous cytokinin activities by the water stress.

The growth of tobacco tissue on the medium with α-naphtylacetic acid (NAA) is accomplished as an increase in cell number and on medium without NAA as an increase in cell size. CCC and B-995 at concentrations from 50 to 500 mg 1^-1 inhibited tissue growth on both media. Growth inhibition on NAA-medium was caused by the suppression of cell multiplication and it was accompanied by a 2.5-fold increase in the cell size at the 250 mg 1^-1 concentration of retardants. Growth inhibition on the medium without NAA resulted from the suppression of cell enlargement and, to a lesser extent, from the suppression of remained cell divisions. CCC on the NAA-medium induced a sharp increase in the content of carotenoids, mainly at the expense of a lycopene-like pigment which was absent in the variant without CCC. B-995 failed to influence the composition of carotenoids in a similar manner.

On cutting off one cotyledon from decapitated pea seedlings cultivated in the dark, the apical dominance is restored, as is well-known, by the growth of the bud of the removed cotyledon. As early as 12 h following cotyledon amputation(i.e. at the time when buds of both cotyledons-remaining and removed-are not yet differentiated in size), a decrease in the level of endogenous abscisic acid can be demonstrated in the bud of the removed cotyledon.

The growth of root, hypocotyl and cotyledons was measured in apple seedlings cultured for nine days from embryos isolated from seeds after various periods of after-ripening. Greening of the cotyledons was taken into account and the chlorophyll content determined as well.
Embryonal dormancy results in anomalies already appearing in the early stage of development. They are manifested by differentiated greening and uneven growth of cotyledons, as well as by hypotrophy of root or hypocotyl. The frequency of those anomalies in the population decreases during the removal of dormancy, and therefore it may be accepted as the criterion of its depth.

The growth of callus tissue cultures and the infectivity of twenty fiveSolanum laciniatum Ait. plants and of sixteenNicotiana tabacum L. cv. Samsun plants were investigated. The plants were obtained from callus tissue cultures derived from stem pieces of the respective plants infected with a mycoplasma-like organism (MLO) evoking potato witches' broom. The tissues were cultivated on synthetic nutrient medium with kinetin and IAA. Allde novo obtainedS. laciniatum plants were healthy. On the contrary twelve of the sixteen reconstituted tobacco plants showed MLO presence.
Summarizing these and previous results, the authors suppose that the most important factor influencing MLO persistence in callus tissues cultivated on the applied nutrient medium may be the callus growth rate and the organogenesis set. Both these conditions are determined by the metabolism of the investigated plant species.

The endogenous auxin-like substances were analyzed in the shoot extracts of young spinach seedlings, exposed to photoperiodic induction. At least eight indole auxins were found. One of them was identified as tryptophan, the other one is most probably IAA. The plants grown in long days had a higher level of ether soluble auxins than the controls in short days. Separate extractions of plants after each of the eight inductive days showed that the auxin content was not constant, but subjected to irregular oscillations. However, parallel oscillations were also found in control plants grown in short days. Staminate plants were found to contain more endogenous auxins than the pistillate ones. It is concluded that the quantitative changes in auxins during the photoperiodic induction are probably not related to flowering, but to some other growth process, common to all plants in that phase of growth. The higher level of auxins in staminate plants may be the cause of their faster elongation before the onset of flowering.

Gamma radiation in doses 0.13 to 0.77 C kg^-1 (0.5 to 3.0 kR) significantly (P ≥ 0.01) stimulated seed germination, seedling height, and length of primary leaves of French bean cv. 'Blue Lake'; these doses did not affect chlorophyll content per leaf area unit. Doses of 1.16 to 1.93 C kg^-1 (4.5 to 7.5 kR) induced inhibition of the four parameters studied.

Oscillation movements of primary roots of pea seedlings were investigated after low- and high-energy irradiation (10^-2 and 10⁶ W m^-2) which was applied continuously and in pulses at intervals of 3 and 30 min. Oscillation amplitudes of control roots grown in darkness were lower (1 mm) than those of irradiated ones recorded in our previous experiments. The elongation rate of roots grown under scattered and low-energy irradiation as well as their mean oscillation amplitude (2.6 mm) and frequency (8 h) correspond to the standard values recorded in previous experiments. The same effects on root growth and oscillations had scattered electronic flash irradiation.
Side-irradiation did not influence the oscillation movements of growing roots. Their frequency and oscillation amplitudes were not changed. Their longitudal axis was, however, deflected 2.75° from the vertical one due to the negative phototropic response of the root.
The growth oscillations may be, according to present results, interpreted as consequences of tropic growth controlling system. External factors, like irradiation, may influence oscillation parameters,i.e. their amplitudes and after application of side-irradiation also the direction of longitudinal axis of oscillation spirals. The resultant trajectory is composed from movements which resulted from geotropic and phototropic responses of the roots.

Biologioal activities of humic acid (Na salt), hymatomelanic acid (Na salt), lignofulvic acid and of fulvic acids isolated from peat were studied by means of the auxin-, gibberellin-, and cytokinin- bioassays. All the four tested fractions showed higher or lower stimulating activity in these bioassays. However, the stimulating effect is considerably lower and cannot be interpreted as phytohormone activity. Some fractions in some concentrations also showed inhibitory effects. The manner of biological action of the studied fractions might bo the result of interaction of their respective components.

The action of exogenously applied hormones in the induction of morphogenesis inLimnophila chinensis (Osb.) Merr. tissue culture has been demonstrated. Stem expiants were grown on Murashige and Skoog's medium containing various levels of kinetin, gibberellic acid and indole-3-acetic acid. Formation of roots, shoots (normal or abnormal), plantlets and friable, hard or nodulated calluses depended largely on the hormone levels used. The formation of normal shoots and roots were stimulated by treatment with kinetin. GA₃ treatment stimulated the bud differentiation but inhibited the root initiation. A combination of kinetin and GA₃ gave variable results.

Mycoplasma-like organisms (MLO) spread from the infectious grafts intoSolanum laciniatumAit. stock plants relatively slowly. MLO were present in all sprouts ofS. laciniatum four weeks after grafting, but the infected plants remained under glasshouse conditions mostly symptomless and flowered normally and formed fruits like healthy plants. The growth of plants with infectious tomato grafts was identical with the controls but that of plants with infectious tobacco (Nicotiana glaucaGrah.) grafts was expressively stimulated. The first flower symptoms appeared onS. laciniatum plants with tomato grafts after five and half months and on.S. laciniatum plants with tobacco grafts after seven months of graft symbiosis. Electron micrographs of ultrathin sections showed the presence of MLO in sieve tubes of potiols and midribs of the infected but symptomless plants. In the phloem parenchyma cells of the witches' broom diseased plants, highly ordered crystals were occasionally found lying in a microbody surrounded by a membrane. The possible reasons of the disease latency are discussed.

The influence of gibberellic acid (GA³) and kinetin (6-furfurylaminopurine) on the regeneration ability of the basal and apical thallus fragments ofFucus vesiculosus L. was examined. The naturally occurring gibberellin and kinetin-like substances in these thallus fragments were also studied. It was found that exogenously applied GA³ markedly increased the number of adventitious branches formed on the cut surface of the thallus fragments taken from the apical parts of plants. The concentration of 0.001 mg GA³ I-1 proved to be the most effective. The growth promoting effect of GA³ was increased by simultaneous action with kinetin. In experiments in which the fragments of the basal parts of the thallus were treated with GA³, as a rule a slight growth inhibition was observed. The growth responses of the investigated plant tissues to gibberellin and kinetin varied according to season. Usually their susceptibility to the applied plant hormones was greater in spring than is summer. The shifts in growth reaction were related to the seasonal changes in the content of endogenous gibberellin and kinetin-like substances in the investigated parts of the thallus. It is suggested that growth regulators of the gibberellin and cytokinin type are involved in the regeneration processes inFucus.

Experiments were made with the uptake of 35-S sulphate along the axis of the intact seminal root of maize seedlings.
Using short exposures the most intensive sulphur uptake was found in the apical 10 mm long region of the root. In the differentiating cells the maximum of sulphur uptake was in the first two 1-mm segments of the elongation zone immediately behind the meristem and then in the zone of the root hairs. Apart from the high activity in the area of the root hairs, two and three peaks, respectively, of increased sulphur accumulation were found in the area of the formation of laterals in case of longer exposure.

The effect of 0.1% Metation E 50 (fenitrothion) and Fosfotion 50 (malathion) on the level of total nitrogen and that of free amino acids was investigated in juvenile and mature leaves of apple seedlings in the course of six days following treatment. Fosfotion affected both nitrogen and amino acid content to a higher degree than Metation. Fosfotion increased the total nitrogen content in all leaves, but Metation induced the change only in the leaves which were at the end of the logarithmic growth phase at the time of treatment. The level of amino acids increased on the whole, with the exception of a temporary decline in the youngest leaves as well. The treatment with both insecticides affected most the content of amides: the greatest decrease of glutamine occurred in young leaves, the highest increase in asparagine content was recorded in both juvenile and mature leaves.

The seeds ofFraxinus excelsior L. were stratified at 17-20 °C (warm stratification), at 4-6 °C (cold stratification) and at alternating temperature (warm - cold stratification). The seeds subjected to warm stratification only, remained dormant. The seeds stratified only at 4-6 °C germinated gradually during a long period of time. The seeds subjected to warm - cold stratification, however, germinated with great intensity within a relatively short period of time.
GA₃ was shown to stimulate the growth of embryos markedly, and its effect on the germination of seeds depended on the temperature of stratification. GA₃ applied during the cold stratification accelerated the removal of dormancy by shortening the period of stratification and by influencing the germination of seeds. The results obtained indicate a similarity between the effect of temperature 17-20 °C during the warm stratification and that of gibberellic acid. Both those factors applied separately affect favourably after-ripening of the embryos and accelerate the germination of seeds.

The formation of polysomes in relation to RNA synthesis was investigated in tobacco (Nicotiana tabacum L.) pollen cultivated submersely for a period of 12 h. The percentage of polysomes was estimated by determining the number of ribosomes carrying nascent polypeptides using RNase and 0.8 M KC1 treatment of the ribosomal preparation. This approach showed that the proportion of ribosomes "active" in protein synthesis amounts to about 12 % in dry pollen rising to 46 % within 10 min of imbibition and to 66 % during the period 1-4 h of cultivation. The latter increase is accompanied by a rapid incorporation of uridine-¹⁴C into polysome-as-sociated RNA and is sensitive to actinomycin D.
The rapidly labelled RNA isolated from the ribosomal preparation sedirnented in the range from about 5S to 30S. Longer labelling periods led to a gradual shift of the major peak of this heterogeneous RNA from about 11.5S and 14S to about 7.5S and the development of radioactivity peaks in the position of 18S and 28S RNA. Uridine incorporated both into the active ribosomes and into the subunits of inactive ribosomes at a more or less constant rate during the whole 12-h period of cultivation.
These results present evidence that in addition to the initial combination of the existing ribosomes with the stored mRNA following imbibition, an activation of pollen tube genome and its implication in directing protein synthesis take place during the early phases of pollen tube growth. From the results on kinetics of labelling of ribosomes it appears that in pollen tubes new synthesized ribosomal subunits enter polysomes directly, the entry of 40S subunits being more rapid than that of 60S subunits.

The blue-green algaeChroococcus, Oscillatoria and Nostoc, excrete vitamin B₁₂ and pantothenic acid in the culture filtrates during the phase of active growth. The excretion has an ecological significance.