The modes of occurrence of extractable elements from 21 A and C horizon samples of uncultivated soils were examined using R-mode factor analysis. The extractants (DTPA, EDTA, HCl, hydroquinone, magnesium nitrate, and ammonium oxalate) cover a wide range of chemical attack. Four major elements (Ca, K, Mg, and Na) and eight trace elements (Cd, Co, Cu, Fe, Mn, Ni, Pb, and Zn) were determined in each extractant solution. A variety of chemical, mineralogical, and physical variables were also determined on each sample. Four varimax factors (clay, organic, Fe and Mn oxides, and soluble-Na) accounted for 74.2% of the total variance of the 90 variables for the A horizon. Seven varimax factors (Fe and Mn oxides, clay, CEC, soluble-Na, organic, Fe and Mn, and plagioclase) accounted for 77.2% of the total variance of the 79 variables for the C horizon. A and C horizon extractable trace elements are most generally related to Fe and Mn oxides, as indicated by loadings on the Fe and Mn oxide factor for both the A and C horizons. Each extractant generally operates on different modes of occurrence of an element in soil. For example, substantial differences occur between the HCl-, oxalate-, and hydroquinone-extractable trace elements. However, the modes of occurrence for trace elements removed by DTPA and EDTA were very similar, suggesting strong relationships between elements dissolved by these two extractants. The modes of occurrence for each individual major element are similar with each of the six extractants. A horizon Ca and Mg, and C horizon K and Mg are strongly related to a clay factor. C horizon Ca and A horizon K are strongly related to the CEC and organic factors, respectively. Both A and C horizon extractable Na are very strongly related to the soluble-Na factor. These results suggest that extractable major elements are water-soluble and are associated with the constituents that are responsible for that factor. Consequently, strong relationships should occur for any individual major element dissolved by any pair of extractants.

northern Great Plains↗

USGS1981

The distribution of uranium and thorium in granitic rocks of the basin and range province, Western United States

Some secondary uranium deposits are thought to have formed from uranium derived by the weathering of silicic igneous rocks such as granites, rhyolites, and tuffs. A regional geochemical survey was made to determine the distribution of uranium and thorium in granitic rocks of the Basin and Range province in order to evaluate the potential for secondary uranium occurrences in the area. The resulting geochemical maps of uranium, thorium, and the Th:U ratio may be useful in locating target areas for uranium exploration. The granites were sampled according to a five-level, nested, analysis-of-variance design, permitting estimates to be made of the variance due to differences between:(1) two-degree cells; (2) one-degree cells; (3) plutons; (4) samples; and (5) analyses. The cells are areas described in units of degrees of latitude and longitude. The results show that individual plutons tend to differ in uranium and thorium concentrations, but that each pluton tends to be relatively homogeneous. Only small amounts of variance occur at the two degree and the between-analyses levels. The three geochemical maps that were prepared are based on one-degree cell means. The reproducibility of the maps is U > Th ⪢ Th:U. These geochemical maps may be used in three methods of locating target areas for uranium exploration. The first method uses the concept that plutons containing the greatest amounts of uranium may supply the greatest amounts of uranium for the formation of secondary uranium occurrences. The second method is to examine areas with high thorium contents, because thorium and uranium are initially highly correlated but much uranium could be lost by weathering. The third method is to locate areas in which the plutons have particularly high Th:U ratios. Because uranium, but not thorium, is leached by chemical weathering, high Th:U ratios suggest a possible loss of uranium and possibly a greater potential for secondary uranium occurrences to be found in the area.

Arizona, California, Nevada, Utah↗

USGS1977

Availability of elements in soil to native plants, Northern Great Plains

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Open-File Report↗