The -Fe 2 O 3 magnetic structure has been analyzed using the synchrotron radiation source. Time spectra of nuclear forward scattering for isolated nanoparticles with an average size of 8 nm immobilized in a xerogel matrix have been recorded in the temperature range of 4-300 K in applied magnetic fields of 0-4 T in the longitudinal direction at the European Synchrotron Radiation Facility (ESRF, Grenoble, France). It has been found that the external magnetic field does not qualitatively change the H hf (T) behavior, but makes a strong opposite impact on the hyperfine fields in the nonequivalent iron sites, leading to the divergence of H hf polar angle dependences below 80 K. A complete diagram of the -Fe 2 O 3 magnetic structure in the temperature range of 4-300 K is proposed. At 300 K, the -Fe 2 O 3 compound is confirmed to be a collinear ferrimagnet. The experimental results show that the magnetic transition at 150-80 K leads to the formation of a noncollinear magnetic structure. Furthermore, in the range of the 80-4 K, the ground state of a magnetic spiral is established. The experimental results are supplemented by the analysis of the exchange interactions and temperature dependence of the magnetization in a magnetic field of 7 T.