Tm 1−x Mn x )MnO 3 solid solutions were synthesized at a high pressure of 6 GPa and a high temperature of about 1570-1670 K for 2 h for x = 0, 0.1, 0.2, and 0.3. Magnetic, dielectric, and neutron diffraction measurements revealed that the introduction of magnetic Mn 2+ cations into the A site leads to an incommensurate spin structure for x = 0.1 and to a ferrimagnetic structure for x 0.2. Commensurate magnetic structures have a much larger correlation length (∼400 nm for x = 0, ∼600 nm for x = 0.3) than the incommensurate magnetic structure (∼12 nm for x = 0.1). The presence of Tm 3+ and Mn 2+ (with different sizes) at the A site causes significant microstrain effects along the a direction which are absent for x = 0 and get stronger with increasing x. Magnetic ordering occurs at the Néel temperature T N = 37 K (x = 0.1) and at the ferrimagnetic Curie temperatures T C = 75 K (x = 0.2) and T C = 104 K (x = 0.3). Ordering of magnetic Mn moments triggers short-range order (for x = 0.1) and long-range order (for x 0.2) of the Tm 3+ cations at the same temperaturean unusual situation in perovskite materials with a simple GdFeO 3 -type Pnma structure. For x = 0.1, long-range IC magnetic order [with propagation vector k = (k 0 , 0, 0) and k 0 ≈ 0.40] of Mn 3+ and Mn 4+ cations at the B site coexists with short-range order of Tm 3+ and Mn 2+ moments at the A site. Short-range order is induced at the Néel temperature T N = 37 K, increases towards an additional specific heat anomaly at T = 4 K, and remains at lower temperature. The ferrimagnetic structure [with propagation vector k = (0, 0, 0)] consists of ferromagnetically ordered Mn 3+ and Mn 4+ cations at the B site which are coupled antiferromagnetically with ordered Mn 2+ moments at the A site. Tm 3+ moments adopt a zigzag magnetic structure which contains a macroscopic ferromagnetic moment that aligns with the direction of the ordered Mn 2+ moments. Towards low temperature, the ordered Tm 3+ moments strongly increase and overcome the saturated magnetic Mn moments at the B site, and this behavior results in the observation of magnetization reversal or negative magnetization phenomena with a compensation temperature of about 15 K at small magnetic fields in the x = 0.2 and 0.3 samples. This is a classical mechanism of the magnetization reversal effects for ferrimagnets. at T N,R = 2−10 K [3]. A more complex picture takes place in RMnO 3 manganites, where there are two magnetic transitions associated with the Mn 3+ at the B site (for R = Gd-Lu and Y) [4], and R 3+ cations order at relatively higher temperatures in comparison with RFeO 3 and RCrO 3 , for example, T N,Mn = 73 K and T N,Nd = 15 K in NdMnO 3 [5], and T N,Mn = 47.5 K and T N,Ho ≈ 20 K in HoMnO 3 [6]. In o-TmMnO 3 , a parent compound of this study [7], an incommensurate (IC) spin structure at the Mn site (B site) appears below T N1,Mn = 42 K and locks into a commensurate noncollinear E -type structure below T N2,Mn = 30−32 K with the appearance of spin-induced ferroelectricity. Tm 3+ cations at the A site spo...