The paper deals with problems associated with preparation and collection of samples when estimating the production of ethylene and content of ACC (1-aminocyclopropane-1-carboxylic acid) in plants by means of gas chromatography. A proper method of sampling can significantly influence not only the reliability of obtained data but also their interpretation. Attention was paid to cultivation of plant material, sampling vessels, conditions of ethylene production, sampling procedure, and storage of gaseous samples. The estimation of ACC as a precursor of ethylene is more laborious but it supplements the information about the endogenous level of ethylene in a given part of the plant organism. The authors describe the sampling procedure, methods of sample preservation, extraction and purification, and also the method of oxidation of ACC to ethylene. In the final part of this study the authors evaluate the time consumption and difficulty of individual methods and describe their advantages and disadvantages as compared with other, alternative methods.

This paper deals with apical dominance using a dicotylar model obtained after decapitation of pea seedlings with two shoots -one dominant and the other inhibited. When the dominant shoot was decapitated the inhibited one is released from inhibition and after 24 to 72 h begins to grow. However, the levels of trans-zeatin and production of ethylene increase within 4 and 6 hours respectively after release from inhibition, and within an interval of 72 h the levels of both phytohormones begin gradually to decrease. This indicates that also in this model, the release from apical dominance is associated with an increase in the level of cytokinin zeatin and, thereafter, also with an increased production of ethylene. If indolyl-3-acetic acid (IAA) is applied on the decapitated main stem after decapitation of the dominant shoot, the growth of the initially inhibited one is very strongly retarded; if, however, IAA is applied on the decapitated dominant shoot, this inhibition is significantly weaker. This means that the inhibiting effect of IAA on the inhibited shoot originates to a greater degree from the main stem rather than from the dominant shoot. The effect of benzyladenine (BA) is transferred equally from the decapitated main stem and from the decapitated dominant shoot because the initially inhibited shoot begins to grow as well as also other shoots from serial cotyledonary buds.