Geology topics

C. V. Dutra

Publications and source records attributed to C. V. Dutra.

3 recordsLinked to original sources

USGS1960

Minor element abundance in a part of the Brazilian shield

Thirty-nine samples of granitic rocks from the Quadrilátero Ferrifero, Minas Gerais, Brazil, representing "mixed" ages and at least three distinct Pre-Cambrian ages were analysed for seventeen minor elements. The rocks are placed in five groups:, (1) 2400 million year old group;, (2) Bacao complex younger, a group of mixed rocks derived from, (1) and, (3);, (3) 1350 million year old group;, (4) a 500 million year old gneissic group;, (5) a 500 million year old silicic group, a later differentiate of a 500 million year old magma. Compared to granitic rocks elsewhere, these Brazilian rocks are about average in Ba, So, Zr, Pb, Nb, Co, Ni, Be and Mo; above average in La and Y; and below average in Cu, Sr, Ga, Sn, V and Cr. Compared to metasedimentary rocks elsewhere in the world., metasedimentary rocks of this region are about average in all seventeen minor elements. Sr has its greatest abundance in the 2400 million year old rocks; Ba, V, Co, Sc, Cr, Ni and Cu in the 1350 million year; and La, Nb, Sn, Zr, Y and Ga in the 500 million year silicic. These abundances are in accord with the petrology and chemistry of the rocks. The 1350 million year rocks are the most mafic of the group and should logically concentrate Ba, V, Co, So, Or, Ni and Cu which are most abundant in earlier crystallates. The 500 million year old silicic rocks are the most felsic and should concentrate La, Nb, Sn, Zr, Y and Ga, which are all most abundant in the latest fractions of granitic magna crystallization. The trace elements also lend support to the idea that the Bacao complex rocks developed by anatexis of 2400 million year rocks during the 1350 -pillion year orogeny. Cu, Sc, Ga, Zr, Sn and Nb have about the same magnitude in the Bagao and the 2400 million year rocks and Sr, V, Co, Or and Ni are lower in the BagAo than either the 2400 or the 1350 million yoar old rocks. This lower abundance is a probable effect of "debasif-cation" which is also brought out by the analysis of major constituents. The effects of a geochemical migration of the elements in this part of the earth's crust may be indicated by the increased abundance of Y in successivol y younger rock types. The increase of La, Nb, Pb, Sn, Y and Zr in the 1350 million year rocks compared to the 2,100 million year rocks might also be an effect of a secular migration.

southeast Brazil↗

USGS1959

Composition of monazites from pegmatites in eastern Minas Gerais, Brazil

Two zoned pegmatites in south-eastern Minas Gerais were sampled in detail for their content of monazite and xenotime and the monazite was analysed for certain of the rare-earth elements and thorium. The ratio of xenotime to monazite increases in both pegmatites from the wall toward the quartz core. The content of the less basic rare-earth elements and of thorium in monazite rises in the same direction. These variation trends suggest that during the crystallization of these pegmatites there was a fractionation of the elements leading to a more or less steady enrichment of the less basic rare-earth elements and of thorium in the residual fluids. One mode of explaining these observed effects postulates that the rare-earth elements and thorium were present in pegmatitic fluids as co-ordination complexes rather than as simple cations.

Minas Gerais↗

USGS1954

Spectrochemical determination of thorium in monazite by the powder-d.c. arc technique

Thorium in monazite is determined by a d.c. carbon-arc technique using zirconium as the internal standard. The analytical curve for Th II 2870.413 Å/Zr II 2844-579 Å is established by means of synthetic standards containing graduated amounts of thoria and 0.500 per cent zirconia in pegmatite base (60 parts quartz, 40 parts microchne, and 1 part ferric oxide). Monazite samples are diluted 14-fold with pegmatite base that contains 0.538 per cent ZrO 2 , so that the zirconia content of the resulting mixture is also 0.500 per cent. In addition, both the standards and the diluted monazites are mixed with one-half their weight of powdered graphite. Approximately 25 mg of the prepared samples are arced to completion at 15.5 to 17.5 amperes. With the 14-fold dilution employed, the accurate range of the method is 3 to 20 per cent thoria in the original monazite. The coefficient of variation for a single determination is 4 per cent at the 7 per cent thoria level. Tests with synthetic unknowns and chemically analyzed monazites show a maximum error of ±10 per cent of the thoria content. If niobium is substituted for zirconium as the internal standard, there is a loss of precision. Platinum as the internal standard gives results of good precision but introduces a marked sensitivity to matrix effects.

Spectrochimica Acta↗