Densities of aqueous solutions of K4Fe(CN)(6), K3Fe(CN)(6), K3Co(CN)(6), K-2,Ni(CN)(4), and KAg(CN)(2) have been measured with a vibrating-tube densimeter at temperatures from 293.15 to 343.15 at 5 K intervals over the approximate concentration range 0.02 to 0.4 mol.kg(-1). Apparent molar volumes, V-phi, calculated from these data were fitted with an extended form of the Redlich-Rosenfeld-Meyer equation to obtain the standard partial molar quantities, V degrees. The V-phi, and V degrees values for all the salts are in reasonable agreement with literature data at all temperatures. Deviations of the V-phi, values from the Debye-Huckel limiting law were found to increase considerably with increasing anion charge. Values of V degrees for the cyanometallate anions were obtained using an appropriate extrathermodynamic assumption and were found to increase with increasing crystallographic size or ionic charge except for Fe(CN)(6)(4-), which shows a remarkable contraction of more than 35 cm(3).mol(-1) relative to Fe(CN)(6)(3-). The origins of this anomaly are unclear. Isobaric expansivities, alpha, of all the salt solutions show the greatest increase with solute concentration, but the smallest dependence on the nature of the anion, at lower temperatures. These effects are consistent with the dissolved ions changing from water-structure breaking to net structure making with increasing temperature.