We have investigated the variation of induced ferroelectric polarization under magnetic field with various directions and magnitudes in a staggered antiferromagnet Ba2CoGe2O7. While the ferroelectric polarization cannot be explained by the well-accepted spin current model nor exchange striction mechanism, we have shown that it is induced by the spin-dependent p-d hybridization between the transition-metal (Co) and ligand (O) via the spin-orbit interaction. On the basis of the correspondence between the direction of electric polarization and the magnetic state, we have also demonstrated the electrical control of the magnetization direction.Electrical control of magnetism has long been an important subject in condensed-matter physics as well as an urgent issue in contemporary spin-electronics. One of the promising ways toward this goal is to make use of magnetoelectric effect (change of magnetization by electric field, or reciprocally, change of electric polarization by magnetic field) in magnetic dielectrics [1][2][3][4][5]. The electric-field control of magnetism in terms of the magnetoelectric effect is much less dissipative in energy than the current control of magnetism in itinerant ferromagnets. While the magnetoelectric effect was thought to be quite small, the magnetically-induced ferroelectrics (multiferroics) and their giant magnetoelectric effect have recently been discovered and are now attracting much attention.There are several microscopic mechanisms for the magnetically-induced ferroelectricity. The most prevailing mechanism is the spin current mechanism[6], or equivalently the inverse Dzyaloshinskii-Moriya mechanism [7,8]. In the transverse-helical (cycloidal) spin structure, the spin chirality can induce the polarization P ∝ i,j e ij × (S i × S i ) in terms of the spin current mechanism, where e ij denotes the unit vector connecting the interacting neighbor spins S i and S j . In the crystal which contains multiple inequivalent magnetic sites, even the collinear spin structure may also induce ferroelectricity with use of magnetostriction caused by the symmetric exchange interaction [15]. In these materials, the ferroelectricity can be caused by the transition metal-ligand (p-d) hybridization depending on the spin direction [16,17]. Owing to the hybridization relevant to the spin-orbit interaction, the ionic charge ρ of the ligand can vary depending on the angle η between the spin of the transition metal and the vector e connecting the transition metal and the ligand, i.e. ∆ρ ∝ (S · e) 2 . Therefore, the local electric polarization ∆P ∝ (S · e) 2 e exists between the transition metal and the ligand. The induced charge of the local dipoles, when summed up over the whole crystal, may induce the ferroelectricity. To examine the mechanism in more detail, a more simple spin structure is desirable because this is a single ion problem rather than a spin correlation (S i × S j , S i · S j , etc.) one. In this paper, we show the ferroelectricity and its magnetic-field dependence in a simple staggered antif...