Elevation in the cytosolic free calcium is crucial for plant growth, development and adaptation. Calcium influx into plant cells is mediated by Ca<sup>2+</sup> depolarisation-activated, hyperpolarisation-activated and voltage-independent Ca<sup>2+</sup>-permeable channels (DACCs, HACCs and VICCs respectively). These channels are encoded by the following gene families: (1) cyclic nucleotide-gated channels (CNGCs), (2) ionotropic glutamate receptors (GLRs), (3) annexins, (4) ‘mechanosensitive channels of small (MscS) conductance’-like channels (MSLs), (5) ‘mid1-complementing activity’ channels (MCAs), Piezo channels, and hyperosmolality-induced [Ca<sup>2+</sup>]<sub>cyt.</sub> channel 1 (OSCA1). Also, a ‘tandem-pore channel1’ (TPC1) catalyses Ca<sup>2+</sup> efflux from the vacuole in response to the plasma membrane-mediated Ca<sup>2+</sup> elevation. Recent experimental data demonstrated that <i>Arabidopsis thaliana</i> (L.) Heynh. CNGCs 2, 5–10, 14, 16 and 18, GLRs 1.2, 3.3, 3.4, 3.6 and 3.7, TPC1, ANNEXIN1, MSL9 and MSL10,MCA1 and MCA2, OSCA1, and some their homologues counterparts in other species, are responsible for Ca<sup>2+</sup> currents and/or cytosolic Ca<sup>2+</sup> elevation. Extrusion of Ca<sup>2+</sup> from the cytosol is mediated by Ca<sup>2+</sup>-ATPases and Ca<sup>2+</sup>/H<sup>+</sup> exchangers which were recently examined at the level of high resolution crystal structure. Calcium-activated NADPH oxidases and reactive oxygen species (ROS)-activated Ca<sup>2+</sup> conductances form a self-amplifying ‘ROS-Ca<sup>2+</sup>hub’, enhancing and transducing Ca<sup>2+</sup> and redox signals. The ROS-Ca<sup>2+</sup> hub contributes to physiological reactions controlled by ROS and Ca<sup>2+</sup>, demonstrating synergism and unity of Ca<sup>2+</sup> and ROS signalling mechanisms.