Abstract. -The electron spin resonance (ESR) spectroscopy was employed to investigate the spin dynamics in triangular lattice antiferromagnets CuCr1−xMgxO2 with x = 0 and 0.02. All spectra can be well fitted by a single Lorentzian lineshape. The analysis of the g factor, the linewidth △H, and the ESR intensity I as a function of temperature suggests the development of significant antiferromagnetic (AFM) spin fluctuations at temperature well above TN in both samples. However, the evolution of the AFM spin fluctuations is different for each sample. For undoped sample the ESR intensity I is almost temperature independent between ∼ 100 K and 50 K and then drops rapidly below 50 K. But for x = 0.02, the I monotonously increases with cooling and reduces rapidly only below TN . These results indicate that the AFM spin fluctuations are extremely strong in the undoped sample and appear to be suppressed upon Mg doping.Introduction. -Triangular lattice antiferromagnets (TLAs) have attracted considerable interests because geometrical spin frustration inherent to these systems results in exceptionally rich physical properties ranging over spin liquid, [1, 2] quantum phase transition, [3] anomalous large thermoelectric response, [4] superconductivity, [5] and magnetoelectric properties. [6][7][8] A typical example of TLAs is CuCrO 2 ; it has a delafossite structure, which can be viewed as the alternate stacking of edge-shared CrO 6 octahedral layers and Cu layers along the [001] axis (see the inset to Fig. 1). Cr ions form an antiferromagnetic (AFM) triangular sublattice, and the compound enters a long range AFM ordered state below the Néel temperature T N ∼ 26 K.[9] Previous powder neutron diffraction study proposed that the ground state has an out-of-plane incommensurate spiral-spin structure with an in-plane wave vector q = (0.329, 0.329, 0) below T N .[10] In this spiral-spin ordered phase, the compound exhibits ferroelectricity driven by the magnetic order, [8] whose polarization P can be tuned by using both magnetic and electric fields. [11] In addition, for CuCrO 2 the temperature dependence of magnetization starts to devi-