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The radium isotopes 226Ra and 228Ra were analyzed in surface water at six points in the neighborhood of a mine of phosphate, associated with uranium, in the region of Santa Quiteria, state of Ceara, Brazil. Water samples were collected during twenty months, filtered and the concentrations of activity determined in the soluble and particulate phases. The results were analyzed using the Principal Component Analysis (PCA) for ordination of environmental data, and also by ANOVA, Tukey and Z tests to compare sets of data considering the radionuclides, the two analyzed phases and the six collecting points. The PCA identified four groups that included all collecting points, using aggregation features such as radionuclide and analyzed phase. The first group is composed by the samples of 226Ra in the soluble phase; the second group by samples of 226Ra in the particulate phase; the third one by 228Ra in the soluble phase, and finally, the fourth group by 228Ra in the particulate phase. This last group has two discrepant points (01 and 06). Statistical analysis identified differences between the concentrations of activity of radionuclides (228Ra higher than 226Ra) and in analyzed phases (soluble phase higher than the particulate one) but showed no differences between sampled points.

This study aims to assess the behavior of the release of Unat (i.e. uranium isotopes in natural relative abundance) from the release of water treated by the Ore Treatment Unit (UTM) in Caldas, state of Minas Gerais, Brazil, during the years 1999 to 2009. During this period, the unit showed no industrial activity, except between 2004 and 2005, when UTM operated 400 tons of monazite in a process to obtain rare earths. Unat was analyzed by spectrophotometry once per week in the effluent waters at sampling point 014. Two fractions were considered for analysis: the soluble one (that passes through a 0.45 μm filter) and the particulate one (retained on a 0.45 μm filter). Statistical analyses were performed: the “Z” test and Pearson’s r2 correlation index. The values for the soluble fraction were consistently lower than those of the particulate fraction and no statistically significant correlation was observed between the soluble and particulate fractions. However, the particulate and the total fractions (the sum of soluble and particulate) strongly correlated.