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T. S. Lovering

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

At least 19 recordsLinked to original sources
USGS1963

Epigenetic, diplogenetic, syngenetic, and lithogene deposits

Much of the disagreement over " epigenetic " And " Syngenetic " Deposits Is Semantic; Some Ores And altered rocks are in part syngenetic and in part epigenetic and for them the term " diplogenetic " is proposed. All these terms are primarily time terms related to the contemporaneity of the deposit and the enclosing rock, but in a secondary sense they are space terms; they do not, however, imply process of formation or source of the chemical constituents. Process or source terms such as "magmatic," "hydro-thermal," "sedimentary" are generally satisfactory, but the process term "lateral secretion" is now vague in meaning. A more precise term is needed for the process of mobilization of elements from a solid rock and their transportation and redeposition elsewhere; for this process I propose the term " lithogene " ("stone-born"), to stress the source and process as do "magmatic" and "sedimentary." Such deposits could be derived from syngenetic , diplogenetic , or epigenetic deposits through the action of metamorphic, hydrothermal, supergene or other solutions. If one wishes, however, to emphasize the distance the mobilized elements have moved from the source rock, the resulting deposit can be described best as a locally derived lithogene deposit ("lateral secretion"), or as a regionally derived lithogene deposit ("product of regional metamorphism"). The classification of many deposits such as epigenetic replacement bodies of magnetite in limestone, and syngenetic gold in recent placers is not controversial; however, where large parts of the mineral deposit are made up both of syngenetic elements and introduced elements, the term " diplogenetic " is appropriate. Examples include mineral deposits in which syngenetic cations are united with epigenetic anions, as in fluorite replacements in limestones, or where the reverse relationship holds and epigenetic cations are united to syngenetic sulfur or other anions-as may be true of certain black cupriferous shales of the Mansfeld type. Guides for distinguishing the various types of mineral deposits are discussed at length and include: mineralogy; texture; isotopic composition of hydrogen, carbon, oxygen, sulfur, and perhaps other elements; form; age relations; alteration; zoning; position and quantitative adequacy of supposed source rocks; lithology; structural geology; paleogeography; and regional geologic relations. The criteria developed are used in a critical review of several examples of controversial deposits -including the African Copper-belt deposits and those of the graphitic schists of Fenno-Scandia.

Economic Geology↗
USGS1961

Sulfide ores formed from sulfide-deficient solutions 1

Assuming that many hydrothermal ore deposits are formed from emanations given off from a magma at depth while it cools through the interval in which latent heat of crystallization is generated, it is shown that this cooling interval for magmatic bodies of moderate size must be measured in tens or hundreds of thousands of years. Emanations from such a magma should change at the source with time: relatively insoluble volatiles should depart early and the more soluble ones late; the general order is probably sulfur gases and oxides of carbon, water, chlorides, and fluorides. Experimental and field evidence indicates that this order approximates the increasing solubility of these gases in natural magmas. Theoretical considerations show that within a hydrothermal conduit a relatively small gradient would soon be established between the magma and the surface. A small gradient suggests that temperature drop is a minor factor in precipitating substances in solution , whereas a drop in pressure and reaction with wall rocks or with material precipitated from earlier emanations would be of major importance. The sulfur-rich early emanations tend to react with indigenous iron of the country rock, or with iron carried by carbon dioxide-rich solutions to where a marked pressure drop occurs; either of these reactions will form abundant early iron sulfide . Later sulfur-deficient emanations, which then carry soluble halides of ore metals, react with this early iron sulfide to precipitate the ore mineral sulfides by replacement and deposition with loss of iron to the solution . Precipitation of much sulfide ore is thus commonly accomplished by sulfur that was fixed near the site of the ore body by earlier emanations from the magmatic source; a large amount of ore , however, may be precipitated from late-stage magmatic solutions where they mingle with early-stage sulfur-bearing solutions from a different magmatic source.

Economic Geology↗
USGS1960

The chief oxide-burgin area discoveries, East Tintic district, Utah; A case history

In 1955 exploration for base and precious metals was undertaken by Bear Creek Mining Company immediately north of the Main Tintic district , Utah . During the course of this work Bear Creek became interested in the East Tintic district , primarily as a result of the activities of the U.S. Geological Survey in that area . Data published on the East Tintic district by the Survey and others were studied and map data made available from various mining companies were compiled. Preliminary economic studies were made to determine the present day value of the type of ore body discovered previously in the district . Encouraging results from these investigations led to the selection of specific targets for exploration. Recommendations for a project program were made and approved. Negotiations were successfully concluded in mid-1956 for a unit lease agreement on lands in the East Tintic district owned by the Tintic Standard and Chief Consolidated mining companies and their subsidiaries. Of the targets selected for exploration, the Chief Oxide area seemed to be one of the most prominent. Our preliminary work in the Chief Oxide area corroborated the findings of the U.S. Geological Survey described in Part I of this paper. After careful consideration it was decided to gamble the cost of an exploration shaft in this area for the purpose of providing an underground drilling platform. We also hoped by means of underground workings to establish the existence and nature of the postulated fault. A limited amount of surface drilling was done prior to shaft sinking in order to locate a shaft site and also to obtain additional information of subvolcanic structure and alteration. Underground exploration in the Chief Oxide area was started in January, 1957. The Burgin shaft was sunk to a depth of 1,100 feet and by August, 1959, lateral development on the 1050 level totaled 4,721 feet and underground diamond drilling totaled 15,480 feet. Results of the work done to date are as follows: ( a ) Identification of the sedimentary rock section and an interpretation of the structure in the Burgin mine area . (b) Discovery by penetration of the previously postulated East Tintic thrust fault. (c) Discovery of large zones of manganese oxides and carbonates, which were found to be closely related to silver-lead-zinc mineralization. (d) Discovery of ore-grade lead-zinc mineralization within the footwall rocks of the East Tintic thrust. (e) Discovery of high-grade silver-lead ore within the thrust zone. Insofar as ore localization is concerned the most important structural feature in the Burgin mine area is the East Tintic thrust fault- a fact that opens up new ore potential over a large part of the East Tintic district not previously explored. Although the discoveries to date must be attributed essentially to the application of geology to exploration, the tools of geochemical prospecting and geophysics were also used, and the geochemical work, in particular, was found to be a definite aid in the selection of areas for further exploration.

Utah↗
USGS1960

The chief oxide-burgin area discoveries, East Tintic district, Utah; A case history

The Burgin shaft is in the Chief Oxide area of the E. Tintic district, Utah, and is about a mile E. of any previously known ore bodies; workings from it are currently developing a substantial amount of commercial Pb-Zn ore in several blind ore bodies that lie in folded Paleozoic carbonate rock concealed beneath a blanket of Eocene lava. This area was mapped by Tower and Smith of the U.S. Geological Survey in 1897 and again by Lindgren and Loughlin in 1911, but no detailed work was done until after 1943 when a field party headed by T.S. Lovering began a study of the entire E. Tintic district. The history of the development of exploration concepts is summarized under Historical Summary. The E. Tintic mining district is in the E.-central part of a N.-trending fault-block mountain range near the eastern margin of the Great Basin; dominant structures of the range are a N.-trending syncline on the W. and a less well exposed anticline on the E. Both folds are cut by an intersecting system of transcurrent strike-slip faults and by minor thrust faults and normal faults of moderate displacement. A strong W.-dipping thrust fault cuts the anticline a short distance E. of the fold axis, but is hidden by Eocene lava throughout the E. Tintic district. The pre-Tertiary rocks range from Lower Cambrian to Upper Mississippian and exceed 7,000 ft. in total thickness; they are dominantly marine limestone and dolomite except for a thick basal Cambrian quartzite. The Tertiary rocks are chiefly dacitic lavas and pyroclastic deposits that are intruded by moderately persistent dikes and irregular bodies of monzonite and quartz porphyry. Nearly all the faulting and folding took place before the extrusion of the lavas on a rugged Eocene erosion surface. At about the time of the intrusion of monzonitic magma, many of the faults in the Paleozoic rock were re-opened and in the overlying lava some fracturing took place which was later accented by hydrothermal alteration. Most of the ore mined in the E. Tintic district has come from Pb-Zn-Ag replacement bodies in shattered Jasperoidized hydrothermal dolomite at the intersection of low angle faults and steep mineralized NE.-trending cross fractures. The U.S. Geological Survey studies of 1943 to 1957 concentrated on detailed mapping of geology and alteration in the E. Tintic district, together with field and laboratory studies of the relation of alteration to stages of mineralization and ore deposition. Trenching and core drilling were carried on after World War II to aid in interpreting the subrhyolite geology, and the Chief Oxide area was 1 of 4 localities tested by drilling. Study of the fossils, lithology, and alteration shown here in a deep drill core, together with the knowledge of the regional geology, led to an essentially correct interpretation of subrhyolite structure in the strongly discordant underlying Paleozoic rocks in which a mineralized tear fault cuts a strong thrust fault, and to the conclusion that ore stage mineralization was present in substantial amounts in the Paleozoic rocks below the Chief Oxide alteration patch in the quartz latite lava. Subsequent geothermal and geochemical work strengthened this conclusion, and the recent development work of the Bear Creek Mining Company, which sank the Burgin shaft, has shown the presence of Pb-Zn-Ag ore of commercial grade in substantial amount in blind ore bodies below the lava blanket in the Chief Oxide area.

Utah↗
USGS1952

Supergene and hydrothermal dispersion of heavy metals in wall rocks near ore bodies, Tintic district, Utah

Part I, T. S. Lovering. Preliminary work in the Tintic district , Utah , determined the relative distance of migration of ore metals in moist carbonate and silicic wall rocks near ore , and in ground water having a very sluggish circulation through mineralized ground. The analyses of efflorescences in the Tintic Standard mine openings at suitable localities indicated that under the conditions existing during the past 25 years lead has not moved perceptibly; gold has migrated only a few inches; copper has moved a few score feet at most and only in acid solutions; and zinc has traveled hundreds of feet, but not as far as some silver. Silver may travel far in the oxidized zone, but if it comes in contact with sulfides its migration is quickly halted. The chief chemical factors that influence the migration of metals in supergene solutions are the hydrogen ion concentration (pH) of hydrolysis of the metal ion, the solubility of sulfates of the metals , and the position of the metals in Schuermann's series if the solutions are in contact with sulfides for a considerable time.

Utah↗
USGS1950

Dispersion of copper from the San Manuel copper deposit, Pinal County, Arizona

At San Manuel, near Tucson, Arizona, recent churn drilling has blocked out large reserves of low-grade "porphyry copper" ore. This virgin deposit has a small outcrop and seems ideally suited for a geochemical study of the dispersion pattern produced by weathering in a desert climate. Samples of soils, alluvium, ground water, and vegetation were analyzed for copper. To avoid grinding, to accentuate differences in copper concentration, and to decrease sampling error, sampling was confined to the silt and clay fraction of the soil and alluvium. A sensitive field test for copper, using hydrochloric acid for a digestant and dithizone for copper determination, proved both quick and reliable. The results of the study show that at present little copper from the ore body dissolves in the ground water or runoff, and also that very little is taken up by plants growing on the ore outcrop. For this reason, prospecting for similar deposits by the sampling and analysis of ground water or vegetation is unlikely to be fruitful. A study of plant ecology, however, shows that certain plant species grow preferentially on outcrops of copper ore and may be useful as indicators of ore. Chrysocolla along joints carries most of the copper in the oxidized zone. The chrysocolla is slowly disintegrated mechanically as the rock weathers and enters the fine fraction of the soil. Slope wash and soil creep carry the copper along with the other soil materials into the nearby washes, where they are incorporated in the alluvium and swept downstream during floods. Abrasion probably continues to concentrate the copper in the fines, but the net change downstream is a decrease in copper content caused by dilution. As copper can now be readily determined by chemical analysis in the field, analysis of soil and alluvium seems to be one of the best geochemical methods of prospecting for copper in a desert environment. Wherever appreciable copper is found in alluvium or soils, upstream or upslope sampling can be used to trace the copper back to its source.

Arizona↗