The ion-exchange ability of a soil is an important factor in soil fertility. Van Bemmelen [1] discovered that the absorption and exchange of ions in soils pertain to colloidal particles. Gedroits [2] showed that the absorbent complex of soils consists of mineral, organomineral, and organic colloidal particles.It is commonly accepted that these particles occur in soils in the form of a sol in the soil solution and in the form of thick gel films. The films form as a result of direct contact between colloidal particles and coat coarse soil particles [3,4].It was inferred more than half a century ago [5] that not only can sols and thick gels form in the water-colloidal particles system but periodic colloidal structures can also appear due to the long-range, contactless interaction between colloidal particles, also referred to as long-range aggregation [6].It was demonstrated recently [7-12] that various phenomena observed in soils find explanation if the soils are treated from the standpoint of the existence of organomineral colloidal structures in the soils, more exactly, in the soil solution. However, the arguments cited in those works were circumstantial.Here, we have shown using electron microscopy that the soil solution has a colloidal structure. This structure is formed through the long-range aggregation of colloidal particles (their anchorage at a distance from one another).The electron microscopic investigation was carried out on a Leo Supra 50VP (Carl Zeiss, Jena) scanning electron microscope equipped with an autoemission source operated at accelerating voltages of 3-10 kV and an InLens secondary electron detector. The primary signal processing involved the accumulative averaging over the scan line.For better illustration, the electron microscopic images were inverted. X-ray electron probe microanalysis (EPMA) was carried out on an INCA Energy + energy dispersive spectrometer (from Oxford Instruments) attached to the Leo Supra 50VP microscope operated at an accelerating voltage of 20 kV in a particular region.The samples studied were soil solutions that were separated from a greenhouse substrate [7] under a pressure of 10 atm.In the investigations of the colloidal structure, the soil solution was allowed to settle for 24 h; then, it was diluted 1000-fold with water and applied to a fresh fracture of natural mica.After the water evaporated, the samples were sputtered with carbon using a Univex-300 Leybold thermal evaporator.From the electron micrograph in Fig. 1, one can see that the starting soil solution before dilution contained a large amount of colloidal particles of various sizes. EPMA showed C, O, Ca, Si, Al, Mg, and Fe in the colloids. These results correlate with the suggestion [7][8][9][10][11][12] CHEMISTRY 1 µ m Fig. 1. Electron micrograph of the soil solution separated from the greenhouse substrate and applied to a copper substrate. 50000 × .