ECXXI V.-The Radioactivity of Tkorium Compounds-11-The Cause and Nature of Radioactivity. By E. RUTHERFORD and FREDERICK SODDP. AT the close of the first paper on this subject (tbis vol., p. 321), it was shown that a constituent responsible for part of the radiohtivity of thorium could be separated from its compounds by chemical means. TWO methods were given. In one, a thorium solution was precipitated by ammonia, and the thorium hydroxide precipitate showed only about one-third of the normal activity, whilst the filtrate, on evaporation and removal of the ammonium salts by ignition, left a very active residue i n some cases more than a thousand times as active as an equal weight of thoria. In the other method, thorium oxide was washed repeatedly with large quantities of water. The washings, on evaporation, deposited very active residues, whilst the radioactivity of the thoria was appreciably diminished by the process. In both these methods, the active residues are extremely small, and the view was put forward that even the most active specimens consisted largely of accidental impurities, ThX, the active constituent of thorium, being only present in minute amount. By the kindness of Dr. KnGfler, of Berlin, who in the friendliest manner placed at our disposal a large specimen of his purest thorium nitrate, we were a t once able to confirm this opinion, This specimen, which had been purified by many processes, did not contain any of the impurity precipitable by sodium phosphate after the removal of the thorium with ammonia, which was present in the commercial nitrate previously used. The radioactivity and emanating power of Dr. Kniifler's specimen were, however, at least as great aa any other in our possession, and the residuerJ obtained from the filtrate after precipitating with ammonia were no less active.