The growth of vapour-deposited silver nanoparticles on α-Al₂O₃ was studied in situ from 190 to 675 K by surface differential reflectivity spectroscopy in the UV-visible range. Changes in size, shape and density were derived from the plasmonic response modelled in the framework of interface susceptibilities by assuming that supported clusters were in the form of truncated spheres. The sticking coefficient of silver on alumina is close to one up to T ≃ 575 K before entering a regime of incomplete condensation. The Arrhenius dependence of the saturation density indicates a nucleation on defects at low temperature (T ≤ 300 K) and detrapping above. The particle size D evolution follows temporal power laws, independent of temperature and flux, which characterize the growth (D ∼ t(0.31)) and coalescence (D ∼ t(0.55)) of the film. These are indicative of the growth of isolated particles at constant density and dynamic coalescence, respectively. The wetting angle of the silver clusters is shown to increase during the growth regime, which is assigned to a combination of surface stress and mismatch-induced strain, and to decrease upon coalescence, which is attributed to plastic relaxation. For particles larger than 10 nm in size, the values of contact angle and adhesion energy level off with asymptotic limits (θ(c) = 127.5° ± 1° and 0.48 ± 0.02 J m⁻²) that nicely agree with tabulated data. This work highlights the ability of nanoplasmics to monitor in situ the growth kinetics of thin supported films.