It is generally believed that cytoplasmic streamings (CSs) are characteristic of all eukaryotes, including plants [1]. CSs stir the cytoplasm, free the membrane surface of transmembrane transport products, and deliver substances, including signal molecules, to the sites where they are used. CSs are driven by the activity of the actomyosin complex using the energy of ATP [2]. The CS velocity varies from several micrometers per second in terrestrial plants to about one hundred micrometers per second in aquatic ones, such as Characea [3,4]. The parameters of CSs and cell metabolism are interrelated, so that actively metabolizing cells and cells with slack metabolism, e.g., parenchymal storage cells, should be expected to differ in CS intensity. For most living objects, however, the existence of CSs is postulated rather than substantiated by experimental data. The point is that commonly available techniques of CS measurement are based on optical methods of observation of the movement of stained organelles (usually, chloroplasts [5]) serving as natural markers of cytoplasm flow. However, the velocity of organelle movement may not correspond to the true CS intensity, because it is determined by their own propellers; in addition, the organelles are large, and their movement is retarded by cytoplasmic elements, mainly, the cytoskeleton. The movement of smaller, optically indiscernible objects (vesicles and macromolecules) does not encounter substantial obstacles and may occur at a velocity different from that of organelle movement. It is also noteworthy that optical methods are inapplicable to most of nontransparent tissues. The diffusion NMR method [6,7], which permits tracing directly the translational displacement of water molecules, offers new possibilities of recording CSs. For example, NMR experiments on CS activation by temperature or Gd 3+ ions showed that the water diffusion coefficient in the cytoplasm of the cells of the Elodea canadensis stem was higher than that of pure water [7]. Taking into account the notion that cytoplasmic water molecules are involved in CS, it is logical to explain the abnormally high diffusion coefficients by the superposition of displacement caused by the CS and diffusional water displacement. However, no attempts have been made at estimating the CS velocity by differentiation between the contributions of the displacement caused by diffusion and by CS. The goals of our study were to demonstrate experimentally the CSs were formed in the parenchyma of the storage tissue of the Malus domestica fruit and to evaluate the CS velocity by means of pulsed field gradient echo-spin NMR. The experimental procedure was based on recording the integrated displacement of cytoplasmic water followed by the correction for the contribution of the diffusional movement of water molecules.We used a 30-mm 3 sample of a ripe apple of the M. domestica cultivar Granny Smith. Parenchymal cells insignificantly vary in shape and size. Microscopic examination showed that the linear size of the cells was 150-200 µ...