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T.G. Lovering

Publications and source records attributed to T.G. Lovering.

17 recordsLinked to original sources
USGS1983

The use of sagebrush (Artemisia) as a biogeochemical indicator of base-metal deposits in Precambrian rocks of west-central Colorado

The efficacy of sagebrush ( Artemisia ) as a biogeochemical indicator of base-metal mineralization in stratabound Precambrian ore deposits in west-central Colorado was investigated by collecting new (mostly flowering) growth from several sagebrush shrubs over and near five such deposits in three different areas. These are the Sedalia mine and two mines in the Turret district near Salida, and two mines in the Cochetopa district southeast of Gunnison. Two species were used, A. tridentata and A. frigida , depending on the area. Sagebrush clippings were separated into two subsamples consisting of (1) stems, and (2) leaves and blossoms stripped from the stems. These subsamples were ashed separately and the ash analyzed with an emission spectrograph for 30 elements. There appear to be no appreciable differences in the analyses of the two subsamples, indicating that composite samples would provide adequate information for further investigations. Eight of these elements, Ag, Bi, Cu, Pb, Sn, Y, Zn, and Zr, are present in notably higher concentrations in the ash of samples growing over mineralized ground than in that of control samples growing over barren ground. Although the distribution pattern, and the number of these anomalous elements, differs at each of the five localities, three of them, silver, copper, and lead, show good contrast and close association with subjacent mineralization in all five study areas.

Journal of Geochemical Exploration↗
USGS1981

Jasperoid float and stream cobbles as tools in geochemical exploration for hydrothermal ore deposits

Fragments of silicified rocks that are associated with deposits of base and precious metals may be transported as cobbles and pebbles in alluvium far downstream from the source outcrop. These rocks commonly exhibit certain characteristics which distinguish them from other detrital siliceous material, and may thus serve as a useful tool in reconnaissance geochemical exploration. The predominant characteristics of jasperoid samples, classified according to genesis, type of host rock, and proximity to base and precious metal deposits have been tabulated from a large master file containing descriptive and analytical information on jasperoid samples representing more than a hundred areas in the United States. Jasperoid that is genetically and spatially associated with ore deposits is generally dark gray or brown in color, brecciated, phaneritic, and vuggy. Jasperoids associated with lead and zinc deposits exhibit extensive halos of lead and silver anomalies, and more restricted zinc and gold anomalies. Those related to copper deposits show extensive copper, silver, and gold anomalies, and more restricted bismuth and molybdenum anomalies. Jasperoid related to gold deposits tends to exhibit extensive gold and silver anomalies and more restricted titanium, barium, vanadium, molybdenum, and rare-earth element anomalies.

Journal of Geochemical Exploration↗
USGS1978

Conceptual models in exploration geochemistry-The Basin and Range Province of the Western United States and Northern Mexico

This summary of geochemical exploration in the Basin and Range Province is another in the series of reviews of geochemical-exploration applications covering a large region; this series began in 1975 with a summary for the Canadian Cordillera and Canadian Shield, and was followed in 1976 by a similar summary for Scandinavia (Norden). Rather than adhering strictly to the type of conceptual models applied in those papers, we have made use of generalized landscape geochemistry models related to the nature of concealment of ore deposits. This study is part of a continuing effort to examine and evaluate geochemical-exploration practices in different areas of the world. Twenty case histories of the application of geochemical exploration in both district and regional settings illustrate recent developments in techniques and approaches. Along with other published reports these case histories, exemplifying generalized models of concealed deposits, provide data used to evaluate geochemical-exploration programs and specific sample media. Because blind deposits are increasingly sought in the Basin and Range Province, the use of new sample media or anomaly-enhancement techniques is a necessity. Analysis of vapors or gases emanating from blind deposits is a promising new technique. Certain fractions of stream sediments show anomalies that are weak or not detected in conventional minus 80-mesh fractions. Multi-element analysis of mineralized bedrock may show zoning patterns that indicate depth or direction of ore. Examples of the application of these and other, more conventional methods are indicated in the case histories. The final section of this paper contains a brief evaluation of the applications of all types of sample media to geochemical exploration in the arid environment of the Basin and Range Province. ?? 1978.

Journal of Geochemical Exploration↗
USGS1962

The origin of jasperoid in limestone

The name jasperoid has been applied to rocks that consist mainly of silica and that have formed by replacement. This paper considers only those jasperoids formed by replacement of limestone . Major problems involved in the origin of such jasperoid include: source of the silica; nature of solutions that dissolve, transport, and precipitate silica; and the mechanism of replacement of limestone by silica. The answers to these problems are of practical as well as scientific interest because many jasperoid bodies are closely related to mineralization. Silica may be derived from: juvenile silica of magmatic origin ; silica leached from underlying rocks by hydrothermal solutions; silica locally derived from enclosing rocks by circulating solutions; and silica carried downward in ground water from the weathering of overlying rocks. The nature and the concentration of other substances in solutions influence, in a complex manner, the ability of these solutions to dissolve, transport, and precipitate silica. Nevertheless, the following generalizations can be made. The solubility and rate of solution of silica in water at moderate pressure increase slowly with temperature up to 200 degrees C.; from 200 degrees to 360 degrees C. they increase rapidly; above 360 degrees C. solubility is pressure dependent, increasing steadily at high pressure and decreasing slightly at moderate pressure due to the formation of a vapor phase. The pH has slight effect on the ionic solubility of silica in the range from pH 1 to ph 9 at low temperature. The effect of other components on the solubility of silica is probably subordinate to that of temperature above 200 degrees C., but becomes increasingly important as the temperature falls below that point. Most jasperoid bodies form by both replacement and silica deposition in voids, with replacement dominant during the early phase, and precipitation dominant during later phases. Replacement of limestone by silica is favored by relatively low temperature acid solutions, and the presence of CO 2 . As limestone dissolves, Ca ions are released to promote the precipitation of colloidal silica. Acid solutions then diffuse through this gelatinous film to continue dissolving limestone behind it; the Ca ions diffusing outward cause the precipitation of more colloidal silica at the solution-gel interface. As the gel mass ages, it shrinks, hardens, and ruptures. More silica is then deposited in the fractures. Eventually the gel crystallizes to a dense mass of aphanitic quartz and chalcedony, with shrinkage cracks and vugs filled or coated with younger coarse-grained quartz and other minerals that have been deposited directly from solution. The theory that relatively low temperature favors the formation of jasperoid replacement bodies in carbonate rocks, and high temperature inhibits their formation, offers an explanation for the gap that is observed in some districts between contact metasomatic lime silicates and siliceous replacement of limestone . This gap is characterized by the lack of any reaction between limestone and silica-bearing solutions moving through it.

Economic Geology↗
USGS1962

The effect of CO2 at low temperature and pressure on solutions supersaturated with silica in the presence of limestone and dolomite

The effect of 1 atm of CO 2 over initially neutral solutions supersaturated with silica, at room temperature, as contrasted with 1 atm of air was determined over a period of 5 months, together with changes brought about by the introduction of calcite and dolomite to these solutions in the form of either chips or finely ground powder. In the absence of CO 2 all solutions quickly reached equilibrium and no silica precipitated. In the presence of CO 2 approximately two-thirds of the silica precipitated as silica gel within the first 2 months; the amount of silica precipitated was not affected by the presence of limestone or dolomite. Silica gel precipitated as a fine powder in the presence of finely ground calcite and dolomite, but as a cloudy gelatinous mass in the presence of coarse chips of dolomite and calcite, and in the absence of either calcite or dolomite. Preferential leaching of calcium from dolomite took place, both in the presence of air and in the presence of CO 2 , but was more pronounced in the presence of air. There was no evidence of physical replacement of either limestone or dolomite by precipitated silica.

Geochimica et Cosmochimica Acta↗
USGS1961

A comparison of analytical methods used in geochemical prospecting for copper

Analytical methods used in geochemical prospecting for copper were compared by analysis of samples of residual soil collected in duplicate near a copper -bearing vein at the Malachite mine, Jefferson County, Colo. In this area barren or "background" samples have a mean copper content of 58 ppm (parts per million) and anomalous samples containing copper derived from the vein have a mean copper content of 216 ppm. Most anomalous samples are above 100 ppm and most barren samples are below. Geochemical prospecting tests, such as the spectrographic, biquinoline, dithizone and chromograph tests for copper and the citrate soluble and acid-soluble tests for total heavy metal, are almost as sensitive but are less precise and less accurate than standard quantitative trace analysis. Statistical techniques based chiefly upon the coefficient of variation show that the geochemical prospecting tests differ considerably among themselves in sensitivity, precision, and accuracy. This study indicates that the dithizone and the biquinoline tests for copper are the best for geochemical prospecting in this area.

Colorado↗
USGS1956

Preliminary study of radioactive limonite localities in Colorado, Utah, and Wyoming

Nine radioactive limonite localities of different types were sampled during the spring and fall of 1953 in an effort to establish criteria for differentiating limonite outcrops associated with uranium or thorium deposits from limonite outcrops not associated with such deposits. The samples were analyzed for uranium and thorium by standard chemical methods, for equivalent uranium by the radiometric method, and for a number of common metals by semiquantitative geochemical methods. Correlation coefficients were then calculated for each of the metals with respect to equivalent uranium, and to uranium where present, for all of the samples from each locality. The correlation coefficients may indicate a significant association between uranium or thorium and certain metals. Occurrences of specific that are interpreted as significant very considerably for different uranium localities but are more consistent for the thorium localities. Samples taken from radioactive outcrops in the vicinity of uranium or thorium deposits can be quickly analyzed by geochemical methods for various elements. Correlation coefficients can then be determined for the various elements with respect to uranium or thorium; if any significant correlations are obtained, the elements showing such correlation may be indicators of uranium or thorium. Soil samples of covered areas in the vicinity of the radioactive outcrop may then be analyzed for the indicator elements and any resulting anomalies used as a guide for prospecting where the depth of overburden is too great to allow the use of radiation-detecting instruments. Correlation coefficients of the associated indicator elements, used in conjunction with petrographic evidence, may also be useful in interpreting the origin and paragenesis of radioactive deposits. Changes in color of limonite stains on the outcrop may also be a useful guide to ore in some areas.

Colorado;Utah;Wyoming↗
USGS1954

Radioactive deposits of Nevada

Thirty-five occurrences of radioactive rocks had been reported from Nevada prior to 1952. Twenty-five of these had been investigated by personnel of the U. S. Geological Surveyor of the U. S. Atomic Energy Commission. Of those investigated, uranium minerals were identified at 13 sites; two sites contained a thorium mineral (monazite); the source of radioactivity on nine properties was not ascertained, and one showed no abnormal radioactivity. Of the other reported occurrences, one is said to contain uraniferous hydrocarbons and nine are placers containing thorian monazite. Pitchblende occurs at two localities, the East Walker River area, and the Stalin's Present prospect, where it is sparsely disseminated in tabular bodies cutting granitic rocks. Other uranium minerals found in the state include: carnotite, tyuyamunite, autunite, torbernite, gummite, uranophane, kasolite, and an unidentified mineral which may be dumontite. Monazite is the only thorium mineral of possible economic importance that has been reported. From an economic standpoint, only four of the properties examined showed reserves of uranium ore in 1952; these are: the Green Monster mine, which shipped 5 tons of ore to Marysvale, Utah, during 1951; the Majuba Hill mine; the Stalin's Present prospect; and the West Willys claim in the Washington district. No estimate has been made of thorium reserves and no commercial deposits of thorium are known.

Bulletin↗
USGS1953

Radioactive deposits of Nevada

Thirty-five occurrences of radioactive rocks had been reported from Nevada prior to 1952. Twenty-five of these had been investigated by the U. S. Geological Survey and the U. S. Atomic Energy Commission. Of those investigated, uranium minerals were identified in 13; two contained a thorium mineral (monazite); the source of radioactivity on 7 properties was not ascertained; and one showed no abnormal radioactivity. Of the other reported occurrences, one is said to contain uraniferous hydrocarbons and 9 are placers containing thorian monazite. Pitchblende occurs at two localities; the East Walker River area, and the Stalin's Present prospect, where it is sparsely disseminated in tabular bodies cutting granitic rocks. Other uranium minerals found in the state include: carnotite, tyuyamunite, autunite, torbernite, gummite, uranophane, kasolite, and an unidentified mineral which may be dumontit. Monazite is the only thorium mineral of possible economic importance that has been reported. From an economic standpoint 9 only 4 of the properties examined showed reserves of uranium ore in 1952; these are: the Green Monster mine, which shipped 5 tons of ore to Marysvale, Utah, during 1951, the Majuba Hill mine, the Stalin's Present prospect, and the West Willys claim in the Washington district. Reserves of ore grade are small on all of these properties and probably cannot be developed commercially unless an ore-buying station is set up nearby. No estimate has been made of thorium reserves and no commercial deposits of thorium are known.

Nevada↗