Nucleoli and nucleolus‐associated chromatin (NAC) of radicle cells have been three‐dimensionally reconstructed from serial ultrathin sections during early germination of Zea mays. As a preliminary, the effect of 5 methods of fixation on the ultrastructure of the active NAC were tested qualitatively and quantitatively. It appeared that paraformaldehyde best preserved the fibrillar centres (FCs) and was consequently used for the 3‐D reconstructions. In quiescent cells, the NAC forms either 2 short internal strands about 0.7 μm thick running within the nucleolus or 2 peripheral knobs of the same diameter. Whatever its morphology, the NAC was composed of one clear zone, i.e., secondary constriction (SC) of the nucleolar organizer region (NOR), and one electron‐opaque zone, i.e., heterochromatic segment (HS). During germination the NAC was always connected to the nuclear envelope (NE) by a bridge of dense chromatin. The NAC strands or knobs of the quiescent cells are likely to be the counterpart of the 2 NORs of this species. 10–12 hr after onset of germination, one or several networks of nucleolar vacuoles were formed within which the whole NAC was located. Chromatin fibers about 12 nm thick emerged from unfolding portions of the NAC within these “nucleolar chromatin dispersal vacuoles” (NCDV). At 24 hr, the NAC appeared as 2 dichotomous strands. Seventy‐two hr after germination both the stretching out and branching of the NAC were more pronounced. After 120 hr, the transcribing ribosomal genes for each NAC strand together with the newly synthesized RNP transcripts formed a layer of dense fibrillar component surrounding a thin axis which was composed mainly of pale material. Together these formed a typical plant nucleolonema.