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USGS1968

Water for the growing needs of Harrison County, Mississippi

The potential for water-supply development in Harrison County is almost unlimited. During an average year, more than 350 billion gallons of water flow into the Gulf of Mexico from the streams of the county. With storage reservoirs these streams have a potential sustained supply of hundreds of millions of. gallons per day. Recreation uses and flood-control benefits could also be considered in reservoir design. Upstream from the zones of salt-water penetration, mineral content is low and fairly constant. Water in the streams generally has high color and low pH ; treatment would be required for most municipal and industrial uses. Impoundment in reservoirs normally would have little effect on the quality of the surface water. However, impoundment would trap most of the suspended-sediment load of the streams. Flooding along the major streams of Harrison County is a minor hazard at present (1966), but with further industrial development and urbanization, flooding in these now rural areas could become serious. Intense rainfall from thunderstorms and hurricanes causes serious local flooding in the populous areas near the coast. Tidal flooding, a result of tropical storms, is an ever-present hazard in areas near the coast. The ground-water reservoir, which at present provides all fresh-water supplies, is capable of supporting many times the 25 million gallons per day withdrawal through existing wells. Fresh water occurs to depths as great as 2,500 feet in sand aquifers of Pliocene and Miocene age. Many of the aquifers have high transmissibility; most of those tested have transmissibility in the range, of 50,000-100,000 gallons per day per foot. Although few wells produce more than 1,000 gallons per minute, several of the aquifers can yield two to three times that amount to wells designed for the higher production. Artesian water levels along the coast are declining at a rate of 1 foot per year on the average; however, water levels are still above or only slightly below the land surface in most places, and considerable additional drawdown is economically available. Newly discovered deep aquifers (1,700-2,500 ft) have water levels 100 feet above the surface and probably will provide flow yields of 2,000 gallons per minute or more. The temperature of this deep water is nearly 100?F. Nearly all the ground water is of good quality and requires little or no treatment for most uses. It is soft, and total mineral content is usually less than 250 parts per million. Color is seldom a problem, although it may have to be considered in the undeveloped deep aquifers. The pH ordinarily is greater than 7.0, but it is slightly less than 7.0 in most places in the shallow aquifers.

Water Supply Paper↗

USGS1986

Petroleum associated with polymetallic sulfide in sediment from Gorda Ridge

A sediment sample, impregnated with asphaltic petroleum and polymetallic sulfide, was dredged from the southern end of Gorda Ridge (the Escanaba Trough) off northern California, within the offshore Exclusive Economic Zone of the United States. The molecular distributions of hydrocarbons in this petroleum show that it was probably derived from terrestrial organic matter in turbidite sediment filling the Escanaba Trough. Hydrothermal activity at the Gorda Ridge spreading center provided the heat for petroleum formation and was the source of fluids for sulfide mineralization.

California↗

USGS2017

Biological and ecological science for Montana—The Treasure State

Montana is rich in minerals, energy, and soils, as well as prairies, forests, mountains, rivers, lakes, fish, and wildlife. Many enterprises that drive the economy are based on natural resources, including tourism, hunting, fishing, agriculture, and energy development. The outdoor-recreation economy alone supports 64,000 Montana jobs and generates nearly \$6 billion each year in economic activity.

Montana↗

USGS2019

Geological and geophysical data for a three-dimensional view—Inside the San Juan and Silverton Calderas, Southern Rocky Mountains Volcanic Field, Silverton, Colorado

Introduction The San Juan-Silverton caldera complex located near Silverton, Colorado, in the Southern Rocky Mountains volcanic field is an ideal natural laboratory for furthering the understanding of shallow-to-deep volcanic-related mineral systems. Recent advances in geophysical data processing and three-dimensional (3D) model construction will help to characterize shallow properties important for understanding surface water and groundwater quality issues and will also improve knowledge of deep geological structures that may have been conduits for hydrothermal fluids that formed mineral deposits. The study has general applications to mineral resource assessments in other areas of the world and to identifying possible groundwater flow paths and associated geochemistry important in abandoned mine lands cleanup. Silverton, Colorado, is the site of a spectacular succession of igneous rocks that formed beginning about 35 million years ago (Ma). Base metals (copper, lead, and zinc) and precious metals (silver and gold) mined from the late 1870s to 1991 owe their existence to a 25-million-year cycle of igneous activity. The presence of economic, base, and precious metal deposits within a complex geological setting were largely responsible for stimulating studies by the U.S. Geological Survey (USGS) conducted during the early 20th century. The focus of investigations in the late 20th and 21st centuries have broadened in scope to include abandoned mine lands (AML) investigations. The legacy of hard rock mining in headwater catchment areas caused environmental challenges for local communities and downstream water resource users. The Gold King Mine, located a few kilometers north of Silverton, illustrates the potential environmental effects of abandoned mines. On August 5, 2015, during reclamation efforts at the Gold King Mine, a breach of collapsed workings sent approximately 3 million gallons of acidic and metal-rich mine water into the upper Animas River, a tributary to the Colorado River Basin. Mining-related sources of metals and acidity add to geological sources of metals in surface water and groundwater. Weathering processes of altered and mineralized rock have been a source of acid rock drainage that have been ongoing for millennia.

Colorado↗

USGS1970

The mineral resources of the Sierra Nevada de Santa Marta, Columbia (Zone I)

The Sierra Nevada de Santa Maria on the north coast of Colombia is an isolated triangular mountain area that reaches altitudes of almost 19,000 feet. The exceedingly complex geology is shown on the 1:200,000 geologic map. Despite five major periods of granitic intrusion, three major periods of metamorphism, and extensive volcanic eruptions, metallic deposits are small and widely scattered. Sulfide deposits of significant economic value appear to be absent. Many small copper deposits, of chalcocite, cuprite, malachite, and azurite are found in epidotized rock in Mesozoic redbeds and intercalated volcanic rocks, but their economic potential is very small. Deposits of other common base metals appear to be absent. The most important metallic deposits may prove to be unusual bimineralic apatite-ilmenite deposits associated with gneissic anorthosite. The known magnetite deposits are too small to be exploited commercially. Primary gold deposits have not been identified and the placer deposits are uneconomic and very small. The largest and most important deposits are nonmetallic. Enormous reserves of limestone are suitable for cement manufacture and some high-purity limestone is suitable for the most exacting chemical uses. Small deposits of talc-tremolite could be exploited locally for ceramic use. The important noncoking bituminous coal deposits in the Cerrej6n area are excluded from this study. Other nonmetallic resources include igneous dimension stone in a variety of colors and textures, and agricultural dolomite. There probably are important undeveloped ground water resources on the slopes of the wide Rancheria and Cesar valleys, which separate the Sierra Nevada from the Serrania de Persia.

Open-File Report↗

USGS2001

Further examination of the ragged edge of the Herrin coal bed, Webster County, Western Kentucky coal field

The Herrin (Western Kentucky No. 11) coal bed in the Dixon 7 1/2 min quadrangle, Webster County, Kentucky, displays another manifestation of the thinning margin of the coal bed. Previous studies in adjacent Hopkins County have demonstrated that the coal is brecciated as the margin is approached. The brecciated coal is not always thin; 1.5 m of brecciated, inertinite-rich coal was previously described to the southeast of the present study area. In general, the brecciated coals are considerably thinner than the 1.5-2-m-thick, "normal" Herrin coal. Both cores studied are thin (22.6 and 33 cm) and display petrographic characteristics different from thicker Herrin coals. The cores described in the present study show some signs of brecciation; in certain cases, the fragmented macerals are cemented by exsudatinite. Multiple generations of pyrite mineralization were noted in one core, with total sulfur exceeding 13% in the upper 8.48 cm lithotype. Overall, the cores investigated in this study, along with examples from previous studies, illustrate the progression of the Herrin coal from its absence, either through nondeposition or erosion, through thin, brecciated coals, to mineable coals. No other economic coal in western Kentucky shows as many examples of the depositional edge as does the Herrin. All of the examples studied are from cores, emphasizing the need to study more than just the thick, mineable coals if the total extent of the coal body is to be understood. ?? 2001 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗

USGS2016

Geochemistry, Nd-Pb Isotopes, and Pb-Pb Ages of the Mesoproterozoic Pea Ridge Iron Oxide-Apatite–Rare Earth Element Deposit, Southeast Missouri

Iron oxide-apatite and iron oxide-copper-gold deposits occur within ~1.48 to 1.47 Ga volcanic rocks of the St. Francois Mountains terrane near a regional boundary separating crustal blocks having contrasting depleted-mantle Sm-Nd model ages (T DM ). Major and trace element analyses and Nd and Pb isotope data were obtained to characterize the Pea Ridge deposit, improve identification of exploration targets, and better understand the regional distribution of mineralization with respect to crustal blocks. The Pea Ridge deposit is spatially associated with felsic volcanic rocks and plutons. Mafic to intermediate-composition rocks are volumetrically minor. Data for major element variations are commonly scattered and strongly suggest element mobility. Ratios of relatively immobile elements indicate that the felsic rocks are evolved subalkaline dacite and rhyolite; the mafic rocks are basalt to basaltic andesite. Granites and rhyolites display geochemical features typical of rocks produced by subduction. Rare earth element (REE) variations for the rhyolites are diagnostic of rocks affected by hydrothermal alteration and associated REE mineralization. The magnetite-rich rocks and REE-rich breccias show similar REE and mantle-normalized trace element patterns. Nd isotope compositions (age corrected) show that: (1) host rhyolites have ɛ Nd from 3.44 to 4.25 and T DM from 1.51 to 1.59 Ga; (2) magnetite ore and specular hematite rocks display ɛ Nd from 3.04 to 4.21 and T DM from 1.6 to 1.51 Ga, and ɛ Nd from 2.23 to 2.81, respectively; (3) REE-rich breccias have ɛ Nd from 3.04 to 4.11 and T DM from 1.6 to 1.51 Ga; and (4) mafic to intermediate-composition rocks range in ɛ Nd from 2.35 to 3.66 and in T DM from 1.66 to 1.56. The ɛ Nd values of the magnetite and specular hematite samples show that the REE mineralization is magmatic; no evidence exists for major overprinting by younger, crustal meteoric fluids, or by externally derived Nd. Host rocks, breccias, and magnetite ore shared a common origin from a similar source. Lead isotope ratios are diverse: (1) host rhyolite has 206 Pb/ 204 Pb from 24.261 to 50.091; (2) Pea Ridge and regional galenas have 206 Pb/ 204 Pb from 16.030 to 33.548; (3) REE-rich breccia, magnetite ore, and specular hematite rock are more radiogenic than galena; (4) REE-rich breccias have high 206 Pb/ 204 Pb (38.122–1277.61) compared to host rhyolites; and (5) REE-rich breccias are more radiogenic than magnetite ore and specular-hematite rock, having 206 Pb/ 204 Pb up to 230.65. Radiogenic 207 Pb/ 206 Pb age estimates suggest the following: (1) rhyolitic host rocks have ages of ~1.50 Ga, (2) magnetite ore is ~1.44 Ga, and (3) REE-rich breccias are ~1.48 Ga. These estimates are broadly consistent and genetically link the host rhyolite, REE-rich breccia, and magnetite ore as being contemporaneous. Alteration style and mineralogical or textural distinctions among the magnetite-rich rocks and REE-rich breccias do not correlate with different isotopic sources. In our model, magmatic fluids leached metals from the coeval felsic rocks (rhyolites), which provided the metal source reflected in the compositions of the REE-rich breccias and mineralized rocks. This model allows for the likelihood of contributions from other genetically related felsic and intermediate to more mafic rocks stored deeper in the crust. The deposit thus records an origin as a magmatic-hydrothermal system that was not affected by Nd and Pb remobilization processes, particularly if these processes also triggered mixing with externally sourced metal-bearing fluids. The Pea Ridge deposit was part of a single, widespread, homogeneous mixing system that produced a uniform isotopic composition, thus representing an excellent example of an igneous-dominated system that generated coeval magmatism and REE mineralization. Geochemical features suggest that components in the Pea Ridge deposit originated from sources in an orogenic margin. Basaltic magmatism produced by mantle decompression melting provided heat for extracting melts from the middle or lower crust. Continual addition of mafic magmas to the base of the subcontinental lithosphere, in a back-arc setting, remelted calc-alkaline rocks enriched in metals that were stored in the crust. The St. Francois Mountains terrane is adjacent to the regional T DM line (defined at a value of 1.55 Ga) that separates ~1600 Ma basement to the west, from younger basements to the east. Data for Pea Ridge straddle the T DM values proposed for the line. The Sm-Nd isotope system has been closed since formation of the deposit and the original igneous signatures have not been affected by cycles of alteration or superimposed mineralizing events. No evidence exists for externally derived Nd or Sm. The source region for metals within the Pea Ridge deposit had a moderate compositional variation and the REE-rich breccias and mineralized rocks are generally isotopically homogeneous. The Pea Ridge deposit thus constitutes a distinctive isotopic target for use as a model in identifying other mineralized systems that may share the same metal source in the St. Francois Mountains terrane and elsewhere in the eastern Granite-Rhyolite province.

Missouri↗

USGS1954

The gold pan: A neglected geological tool

The gold pan is ordinarily regarded as a tool for sampling placer deposits. Another and very important application is shown to be the sampling and study of decomposed bedrock, in regions where outcrops of hardrock are scarce or lacking. This technique was proposed and used by Derby, an American geologist who worked for many years in Brazil. The importance of this method has not been generally recognized, and the writer recalls it to the attention of geologists. An important application is shown to exist in the study of the decomposed bedrock, known as saprolite, that is so widespread in the Piedmont province of the southeastern United States. Using this technique, two projects have already been successfully completed in this region, and the success attained in both sets a new standard for geological exploration and mapping in areas where saprolite constitutes the dominant type of exposure. The technique of panning for heavy and semiheavy accessory minerals is described. Types of pans, factors in panning, the operation of panning, and the processing of concentrates in the field are briefly discussed. The gold pan, in the hands of an experienced operator, is shown to be a versatile and efficient field tool, which is completely independent of laboratory facilities. © 1954 Society of Economic Geologists, Inc.

Economic Geology↗

USGS1968

Hypogene veins of gibbsite, pyrolusite, and lithiophorite in Nye County, Nevada

Gibbsite, lithiophorite, pyrolusite, and goethite, plus discrete mixtures of gibbsite and lithiophorite and of gibbsite and iron oxide, occur as replacement veins in limestone. Minor accessories are barite, alunite, opal. Minerals of wall-rock alteration are garnet, idocrase, K-feldspar, prehnite, sericite, and quartz. These silicates formed at higher temperature than the vein minerals, but the whole sequence is considered to be a product of the same solutions, of deep-seated origin, deposited over a long period of time.

Nevada↗

USGS1968

Distribution of minor elements in ore and host rock, Illinois-Kentucky fluorite district and Upper Mississippi Valley zinc-lead district

This paper presents data on the distribution of minor elements in ore and gangue minerals and in adjacent host rock from the Illinois-Kentucky fluorite district and Upper Mississippi Valley zinc-lead district. Comparisons are made of the minor-element abundances between districts and within the paragenetic sequence in individual districts.The ore of the Illinois-Kentucky fluorite district is characterized by greater abundance of minor elements than in other Mississippi Valley deposits, by large fractionation of silver between galena and sphalerite, and by a low ratio of antimony to silver in galena. Silver and antimony are concentrated in the galena and show a marked zonal pattern within the district. Sphalerite is high in cadmium, gallium, and germanium.The Upper Mississippi Valley zinc-lead district differs markedly from the Illinois-Kentucky fluorite district in minor-element concentrations and distribution. The minor elements are much less abundant, and silver is slightly more concentrated in sphalerite than in galena.Several analyses of minor elements in ore minerals from the Southeast Missouri lead district are given for comparison.It is concluded that the minor elements were largely leached from the basement by convective circulation of heated oilfield brine.

Illinois, Kentucky↗

USGS1988

Stable isotope geochemistry of sphalerite and other mineral matter in coal beds of the Illinois and Forest City basins

Cleat and clastic dikes of Middle Pennsylvanian-age coal beds of the Illinois and Forest City basins of Illinois, Iowa, Missouri, and Kansas locally contain appreciable amounts of sphalerite within a kaolinite-pyrite-sphalerite (+ or - pyrite)-calcite paragenetic sequence. The sphalerite and associated minerals are of interest as a partial record of the history of fluids in the sedimentary basin and as possible indicators of Mississippi Valley-type mineralization. Moreover, zinc from the sphalerite may represent an exploitable by-product of coal mining and combustion.Pyrite is abundant in these coals both as fine-grained disseminated framboids that formed during early diagenesis and as coarser grained cleat fillings, etc., that formed much later. The delta 34 S values of this later pyrite, the sphalerite, and the coal organic matter range from -12 to 19 per mil. Within individual samples, however, pyrite, sphalerite, and organic matter sulfur delta 34 S values are nearly identical. This similarity strongly suggests related origins. The delta 34 S values of pyrite, sphalerite, and organic matter from coals of the Illinois basin and the central and southern Forest City basin range from -12 to 0 per mil. This range is not unique to the sphalerite-bearing coals; pyrite and organic matter from sphalerite-free high sulfur coals have similar delta 34 S values (Price and Shieh, 1979). We believe that sulfur produced by the breakdown of organosulfur compounds in the coal is incorporated into the epigenetic sulfides. In the northern Forest City basin, however, many samples have delta 34 S values between 8 and 19 per mil. These are similar to the delta 34 S values of sphalerite and pyrite from the Upper Mississippi Valley Zn-Pb district which lies northeast of the Forest City basin and north of the Illinois basin. This similarity suggests input from a Mississippi Valley-type hydrothermal system.Cleat kaolinite has delta D values of -36 to -24 per mil and delta 18 O values of 19.2 to 20.2 per mil. Assuming that clearing postdated the lignite rank of coalification implies that kaolinite was deposited between 40 degrees and 100 degrees C. At the lower temperatures, the kaolinite fluid would have had an isotopic composition similar to seawater; at the higher temperatures, it would have had a composition similar to the sphalerite-depositing fluid. Sphalerite was deposited from a fluid that was chemically and isotopically similar to the fluids responsible for the main-stage ores of the Upper Mississippi Valley Zn-Pb district (75 degrees -113 degrees C, approximately 21 equiv wt % NaCl, delta D = -65 to -3ppm, and delta 18 O = -0.9-9.9ppm). The isotopic compositions (delta 13 C = -12.4 to -2.7ppm and delta 18 O = 21.1-25.8ppm) and paragenetic positions of the cleat calcite samples are similar to those of the late-stage calcite of the Upper Mississippi Valley Zn-Pb and Illinois-Kentucky fluorspar districts. Calcite inclusion fluids had delta D (sub H 2 O) values of -80 and -58 per mil, implying a meteoric water source. At probable temperatures of 15 degrees to 75 degrees C, this calcite formed from fluids having calculated delta 18 O (sub H 2 O) values of -9 to 1 per mil, implying slight to moderate exchange with sedimentary rocks. The diagenetic-epigenetic history of fluids recorded by the cleat minerals probably began with a slightly evolved seawater, followed by a metal-bearing deep basin brine, and concluded with a cooler, slightly evolved, meteoric-water fluid.

Economic Geology↗

USGS1989

Geology and K-Ar geochronology of the Paradise Peak Mine and the relationship of pre-Basin and Range extension to Early Miocene precious metal mineralization in west-central Nevada

The Paradise Peak mine is a major gold-silver-mercury deposit located in the southwestern part of the Paradise Range near the eastern edge of the Walker Lane in the western Great Basin, Nevada. The Tertiary volcanic rocks of the area can be divided into a sequence of 26- to 24-Ma intermediate lavas, a sequence of 24- to 22-Ma silicic ash-flow tuffs, and a sequence of 20- to 15-Ma intermediate lavas. We classify these rocks as the older, middle, and younger sequences. Sedimentary rocks, and latites and basalts 12 Ma old or younger, locally overlie the younger intermediate lavas south of the mine. Silicified rhyolite tuff in the lower part of the middle tuff sequence is the principal host of the precious metal ore. Most ore occurs under an acid-leached zone of alunitic alteration and is contained in hydrothermal breccias that crosscut early quartz-pyrite and alunite alteration.Field relations and K-Ar ages of hypogene alunite indicate that precious metal mineralization and alunitic and silicic alteration formed at about 19 to 18 Ma, several million years after eruption of the main host rock. Mineralization formed during high-angle faulting related to crustal extension. Low-angle normal faults are present 5 km northeast of the Paradise Peak mine, but they formed more than 2 Ma after formation of the Paradise Peak deposit. Silicic and alunitic alteration and precious metal mineralization are generally absent in areas of low-angle faulting.Regional stratigraphic relations and K-Ar ages indicate that volcanism changed from silicic ash-flow tuffs to intermediate lavas at about 20 to 19 Ma. Regionally extensive angular unconformities indicate that a period of "pre-Basin and Range" crustal extension occurred between about 22 to 19 Ma. This extension was penecontemporaneous with the shift in the style of volcanism and with gold-silver mineralization in the Paradise Peak mine and in the Goldfield and Tonopah districts of western Nevada. The close temporal and spatial relationships of precious metal mineralization with pre-Basin and Range extension suggest that extension was a major factor in the genesis of early Miocene precious metal deposits in the western Great Basin.

Economic Geology↗

USGS1993

Geology and genesis of the Baid Al Jimalah tungsten deposit, Kingdom of Saudi Arabia

The Baid al Jimalah tungsten deposit in Saudi Arabia (lat 25 degrees 09'N, long 42 degrees 41'E) consists predominantly of swarms of steeply dipping, subparallel, tungsten-bearing quartz veins and of less abundant, smaller stockwork veins. It is spatially, temporally, and genetically associated with a 569 Ma, highly differentiated, porphyritic, two-feldspar granite that intrudes Late Proterozoic immature sandstones.Paragenetic data from crosscutting veins demonstrate unambiguously a single cycle of magma intrusion and hydrothermal mineralization. Hypogene mineralization can be divided into three periods: (1) early quartz-molybdenite stockwork veining, (2) wolframite- and scheelite-bearing, greisen-bordered veining, and (3) late, quartz-carbonate-fluorite veining. The first two of these three periods can be further divided into several stages that are transitional to each other. The greisen-bordered veins, in particular, show replacement of earlier mineral assemblages by later ones. Precious and base metal veins at Baid al Jimalah East, approximately 1.5 km east of the Baid al Jimalah tungsten deposit, are genetically related to the tungsten deposit and probably formed contemporaneously with the greisenized tungsten-bearing veins.Fluid inclusion and oxygen isotope data indicate that the Baid al Jimalah deposit formed over a temperature range of 120 degrees to 550 degrees C, from low salinity magmatic and metamorphic fluids, and at a depth of about 4.2 km. Early stockwork veins (period 1) formed at low magmatic temperatures (ca. 550 degrees C) from magma-derived (delta 18 O = 9.6-9.7ppm), low-salinity (1-2 wt % NaCl equiv) fluid. This hydrothermal fluid was generally low density and CO 2 rich. All other veins were formed from regionally derived fluid in equilibrium with metamorphic rocks (delta 18 O = 7.9 + or - 1.0ppm at the site of deposition). This fluid probably scavenged most of the period 2 ore-mineral components from a postulated granite batholith whose existence is indicated by a 6-mGal gravity low centered on the deposit. The greisen-bordered tungsten veins (period 2) formed from fluids in the liquid state at temperatures mostly between 380 degrees and 440 degrees C with salinities between 4.5 and 10.9 wt percent NaCl equiv. Late, barren veins (period 3) formed from liquids with salinities between 0.0 and 3.5 wt percent NaCl equiv at temperatures as low as 120 degrees C. The veins at Baid al Jimalah East formed from liquids with salinities between 0 and 4.2 wt percent NaCl equiv at temperatures mostly between about 340 degrees and 390 degrees C. Important volatile constituents in some hydrothermal fluids were CO 2 and CH 4 , in addition to H 2 O and HF. The delta 18 O data on mineral separates of fresh and altered Bald al Jimalah granite, and whole-rock delta 18 O data on country-rock samples as far as 16 km from the deposit, indicate that the rocks in the Bald al Jimalah area were pervasively infiltrated by a fluid with relatively high delta 18 O values. Interaction and exchange of the country rocks with this delta 18 O fluid led to an increase in the delta 18 O values of volcanic rocks of the Jurdhawiyah Group but to a decrease in the delta 18 O values of the high value delta 18 O Murdama Group sandstones, resulting in a hydrothermal anomaly exceeding 100 km 2 in area. This fluid had an estimated delta 18 O value of about 6 to 8 per mil, essentially identical to that of the metamorphic water calculated from the vein quartz, thus strongly supporting the conclusion that all of the mineral deposits at Baid al Jimalah (except for the early-stage quartz-molybdenite veins), as well as the 12-km 2 geochemical anomaly surrounding the deposit, were from the same metamorphic fluid.Bald al Jimalah is similar in character and origin to Phanerozoic tungsten-tin greisen deposits throughout the world, especially the Hemerdon deposit in Devon, England. It is also analogous to Climax-type molybdenum deposits, which contain virtually identical mineral assemblages, but with the relative proportions of molybdenum and tungsten mineralization reversed, primarily owing to differences in oxygen fugacity. This similarity in mineralization styles and fluid histories indicates that metallogenic processes in granite-related deposits in the late Precambrian were similar to those seen in the Phanerozoic.

Economic Geology↗

USGS1999

Design approaches in quarrying and pit-mining reclamation

Reclaimed mine sites have been evaluated so that the public, industry, and land planners may recognize there are innovative designs available for consideration and use. People tend to see cropland, range, and road cuts as a necessary part of their everyday life, not as disturbed areas despite their high visibility. Mining also generates a disturbed landscape, unfortunately one that many consider waste until reclaimed by human beings. The development of mining provides an economic base and use of a natural resource to improve the quality of human life. Equally important is a sensitivity to the geologic origin and natural pattern of the land. Wisely shaping out environment requires a design plan and product that responds to a site's physiography, ecology, function, artistic form, and publication perception. An examination of selected sites for their landscape design suggested nine approaches for mining reclamation. The oldest design approach around is nature itself. Humans may sometimes do more damage going to an area in the attempt to repair it. Given enough geologic time, a small-site area, and stable adjacent ecosystems, disturbed areas recover without mankind's input. Visual screens and buffer zones conceal the facility in a camouflage approach. Typically, earth berms, fences, and plantings are used to disguise the mining facility. Restoration targets social or economic benefits by reusing the site for public amenities, most often in urban centers with large populations. A mitigation approach attempts to protect the environment and return mined areas to use with scientific input. The reuse of cement, building rubble, macadam meets only about 10% of the demand from aggregate. Recognizing the limited supply of mineral resources and encouraging recycling efforts are steps are steps in a renewable resource approach. An educative design approach effectively communicates mining information through outreach, land stewardship, and community service. Mine sites used for art show a celebration of beauty and experience -- abstract geology. The last design approach combines art and science in a human-nature ecosystem termed integration. With environmental concerns, an operating or reclaimed mine site can no longer be considered isolated from its surroundings. Site analysis of mine works needs to go beyond site-specific information and relate to the regional context of the greater landscape. Understanding design approach can turn undesirable features (mines and pits) into something perceived as desirable by the public.

Book↗

USGS2016

High spatial resolution U-Pb geochronology and Pb isotope geochemistry of magnetite-apatite ore from the Pea Ridge iron oxide-apatite deposit, St. Francois Mountains, southeast Missouri, USA

The Pea Ridge iron oxide-apatite (IOA) deposit is one of the major rhyolite-hosted magnetite deposits of the St. Francois Mountains terrane, which is located within the Mesoproterozoic (1.5–1.3 Ga) Granite-Rhyolite province in the U.S. Midcontinent. Precise and accurate determination of the timing and duration of oreforming processes in this deposit is crucial for understanding its origin and placing it within a deposit-scale and regional geologic context. Apatite and monazite, well-established U-Pb mineral geochronometers, are abundant in the Pea Ridge orebody. However, the potential presence of multiple generations of dateable minerals, processes of dissolution-reprecipitation, and occurrence of micrometer-sized intergrowths and inclusions complicate measurements and interpretations of the geochronological results. Here, we employ a combination of several techniques, including ID-TIMS and high spatial resolution geochronology of apatite and monazite using LA-SC-ICPMS and SHRIMP, and Pb isotope geochemistry of pyrite and magnetite to obtain the first direct age constraints on the formation and alteration history of the Pea Ridge IOA deposit. The oldest apatite TIMS 207 Pb*/ 206 Pb* dates are 1471 ± 1 and 1468 ± 1 Ma, slightly younger than (but within error of) the ~1474 to ~1473 Ma U-Pb zircon ages of the host rhyolites. Dating of apatite and monazite inclusions within apatite provides evidence for at least one younger metasomatic event at ~1.44 Ga, and possibly multiple superimposed metasomatic events between 1.47 and 1.44 Ga. Lead isotop analyses of pyrite show extremely radiogenic 206 Pb/ 204 Pb ratios up to ~80 unsupported by in situ U decay. This excess radiogenic Pb in pyrite may have been derived from the spatially associated apatite as apatite recrystallized several tens of million years after its formation. The low initial 206 Pb/ 204 Pb ratio of ~16.5 and 207 Pb/ 204 Pb ratio of ~15.4 for individual magnetite grains indicate closed U-Pb system behavior in this mineral and are consistent with derivation of the Pb from a mantle-like source.

Missouri↗

USGS1985

A reconnaissance Rb-Sr, Sm-Nd, U-Pb, and K-Ar study of some host rocks and ore minerals in the West Shasta Cu- Zn district, California

The Copley Greenstone, Balaklala Rhyolite, and Mule Mountain stock in the West Shasta Cu-Zn district, California, have Rb-Sr, Sm-Nd, U-Pb, and K-Ar systematics that indicate they are a cogenetic suite of ensimatic island-arc rocks about 400 m.y. Pervasive alteration and mineralization of these rocks, for the most part, was syngenetic and the major component of the mineralizing fluid was Devonian seawater. K-Ar ages of quartz-sericite concentrates from ore horizons and Rb-Sr systematics of a few rock and ore specimens record a later thermal and mineralizing event in the district of about 260 m.y. Contamination of some rocks with pelagic sediments is indicated by the Sm-Nd data.

Economic Geology↗

USGS2019

Magmatic-hydrothermal gold mineralization at the Lone Tree Mine, Battle Mountain district, Nevada

The Lone Tree deposit is located in the northern Battle Mountain mining district, Nevada. Prior to mine closure in 2006, Santa Fe Pacific Gold and Newmont produced 4.2 Moz of gold at an average grade of 2.06 g/t at Lone Tree, primarily from the N-S– to NNW-SSE–striking Wayne zone. The ore is located between the Roberts Mountain and Golconda thrusts in siliciclastic rocks of the Ordovician Valmy Formation and in the Pennsylvanian-Permian Battle Mountain and Edna Mountain Formations, and above the Golconda thrust in siliciclastic and carbonate rocks of the Mississippian to Permian Havallah sequence. Ore is also hosted by rhyolitic dikes that were emplaced at 40.95 ± 0.06 Ma based on zircon U-Pb chemical abrasion-thermal ionization mass spectrometry. The gold is associated with sericitic and argillic alteration of the siliciclastic rocks and dikes and with decarbonatization and Fe carbonate alteration of the carbonate-bearing units, as well as in Fe-As sulfide and finegrained quartz alteration of all rock types. Oxidation affects 30 to 45% of the deposit, penetrating into the stratigraphy along numerous steeply dipping north-south, east-west, and north-northeast–south-southwest structures. Gold is positively correlated with Ag, As, Hg, and Sb. The highest Au grades occur in quartz-sulfide ore hosted in siliciclastic and carbonate sedimentary rocks and rhyolitic intrusions. In this ore style, fine-grained quartz and sericite are intergrown with disseminated sulfide minerals (quartz-sericite-pyrite alteration), constituting cores of weakly mineralized pyrite or marcasite, which are surrounded by fuzzy arsenopyrite rims that contain up to ~2,000 ppm Au. Low gold grades occur in late-stage banded pyrite breccias consisting of a finely zoned Au-poor pyrite matrix surrounding jigsaw-fit clasts of quartz-, illite-, barite-, and adularia-altered siliciclastic rock. The timing of main-stage mineralization is bracketed between the emplacement of the dikes and an adularia 40 Ar/ 39 Ar age of 40.14 ± 0.74 Ma. Sericite intergrown with arsenopyrite-rimmed pyrite in phenocrysts of the rhyolite dikes gave δ 18 O values of 1.6 to 9.5‰ and δ D values of –105 to –145‰. For temperatures of 300 ± 100°C, the calculated fluid isotopic compositions are consistent with felsic magmatic water and minor modifications by mixing with meteoric water and exchange with wall rocks. In the silica-sulfide ore, in situ isotopic laser ablation-multicollector-inductively coupled plasma-mass spectrometry (LA-MC-ICP-MS) analyses of pyrite cores yielded δ 34 S values ranging from 3.4 to 7.7‰, with average values of 5.6‰ in the felsic dikes, 4.5‰ in the siliciclastic rocks, and 5.3‰ in the carbonate rocks. These values match conventional pyrite δ 34 S data reported for Eocene porphyry systems elsewhere in the district. Nanoscale secondary ion mass spectrometry analyses show that gold and associated trace elements occur in submicron-scale zones within arsenopyrite rims on pyrite. The average δ 34 S values of the arsenopyrite rims are 5.3 to 6.5‰ heavier than the pyrite cores, indicating cooling and an increasing H 2 S/SO 2 ratio. The highest grades resulted from episodic pulses of a gold-rich fluid that was partly derived from, or exchanged with, the sedimentary host rocks. In situ LA-MC-ICP-MS δ 34 S values for the late-stage banded pyrite breccia become progressively lighter from veinlet margin to center, reaching a low of –32‰. These veinlets indicate a shift from main-stage quartz-sericite-pyrite and intermediate argillic alteration to more neutral pH and oxidizing conditions during late-stage mineralization, indicating either increasing interaction between the fluid and sedimentary sulfur sources in the host-rock package or bacterial sulfate reduction and supergene sulfide precipitation.

Nevada↗

USGS2017

Vanadium

Vanadium is used primarily in the production of steel alloys; as a catalyst for the chemical industry; in the making of ceramics, glasses, and pigments; and in vanadium redox-flow batteries (VRBs) for large-scale storage of electricity. World vanadium resources in 2012 were estimated to be 63 million metric tons, which include about 14 million metric tons of reserves. The majority of the vanadium produced in 2012 was from China, Russia, and South Africa. Vanadium is extracted from several different types of mineral deposits and from fossil fuels. These deposits include vanadiferous titanomagnetite (VTM) deposits, sandstone-hosted vanadium (with or without uranium) deposits (SSV deposits), and vanadium-rich black shales. VTM deposits are the principal source of vanadium and consist of magmatic accumulations of ilmenite and magnetite containing 0.2 to 1 weight percent vanadium pentoxide (V 2 O 5 ). SSV deposits are another important source; these deposits have average ore grades that range from 0.1 to greater than 1 weight percent V 2 O 5 . The United States has been and is currently the main producer of vanadium from SSV deposits, particularly those on the Colorado Plateau. Vanadium-rich black shales occur in marine successions that were deposited in epeiric (inland) seas and on continental margins. Concentrations in these shales regularly exceed 0.18 weight percent V 2 O 5 and can be as high as 1.7 weight percent V 2 O 5 . Small amounts of vanadium have been produced from the Alum Shale in Sweden and from ferrophosphorus slag generated during the reduction of phosphate to elemental phosphorus in ore from shales of the Phosphoria Formation in Idaho and Wyoming. Because vanadium enrichment occurs in beds that are typically only a few meters thick, most of the vanadiferous black shales are not currently economic, although they may become an important resource in the future. Significant amounts of vanadium are recovered as byproducts of petroleum refining, and processing of coal, tar sands, and oil shales may be important future sources. Vanadium occurs in one of four oxidation states in nature: +2, +3, +4, and +5. The V 3+ ion has an octahedral radius that is almost identical to that of (Fe 3+ ) and (Al 3+ ) and, therefore, it substitutes in ferromagnesian minerals. During weathering, much of the vanadium may partition into newly formed clay minerals, and it either remains in the +3 valence state or oxidizes to the +4 valence state, both of which are relatively insoluble. If erosion is insignificant but chemical leaching is intense, the residual material may be enriched in vanadium, as are some bauxites and laterites. During the weathering of igneous, residual, or sedimentary rocks, some vanadium oxidizes to the +5 valence state, especially in the intensive oxidizing conditions that are characteristic of arid climates. The average contents of vanadium in the environment are as follows: soils [10 to 500 parts per million (ppm)]; streams and rivers [0.2 to 2.9 parts per billion (ppb)]; and coastal seawater (0.3 to 2.8 ppb). Concentrations of vanadium in soils (548 to 7,160 ppm) collected near vanadium mines in China, the Czech Republic, and South Africa are many times greater than natural concentrations in soils. Additionally, if deposits contain sulfide minerals such as chalcocite, pyrite, and sphalerite, high levels of acidity may be present if sulfide dissolution is not balanced by the presence of acid-neutralizing carbonate minerals. Some of the vanadium-bearing deposit types, particularly some SSV and black-shale deposits, contain appreciable amounts of carbonate minerals, which lowers the acid-generation potential. Vanadium is a micronutrient with a postulated requirement for humans of less than 10 micrograms per day, which can be met through dietary intake. Primary and secondary drinking water regulations for vanadium are not currently in place in the United States. Vanadium toxicity is thought to result from an intake of more than 10 to 20 milligrams per day. Vanadium is essential for some biological processes and organisms. For example, some nitrogen-fixing bacteria require vanadium for producing enzymes necessary to convert nitrogen from the atmosphere into ammonia, which is a more biologically accessible form of nitrogen.

Professional Paper↗