Individual molecular orbital (MO) contributions to the magnetic shielding of atoms as well as to the nucleus-independent chemical shifts (NICS) of aromatic compounds can be computed by the widely used gauge-including atomic orbital (GIAO) method. Detailed analyses of magnetic shielding MO-NICS contributions provide interpretive insights that complement and extend those given by the localized MO (“dissected NICSâ€�, LMO-NICS) method. Applications to (4n + 2) Ï€-electron systems, ranging from [n] annulenes to D_nh S₃, S₅, and N₆H₆²⁺ rings as well as to D_2h cyclobutadiene, show the extent to which their diatropic character results from the σ framework and from the Ï€ orbitals. The diatropicity of both these contributions decreases with the number of nodes of the wave function around the ring. The highest-energy orbitals can become paratropic. This is generally the case with the σ orbitals, but is found only for “electron-richâ€� Ï€ systems such as sulfur rings. MO-NICS contributions, which can be interpreted using London−Hückel theory, correlate with inverse ring size.