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USGS1992

Monitoring radionuclide and suspended-sediment transport in the Little Colorado River basin, Arizona and New Mexico, USA

From July 1988 through September 1991, radionuclide and suspended-sediment transport were monitored in ephemeral streams in the semiarid Little Colorado River basin of Arizona and New Mexico, USA, where in-stream gross-alpha plus gross-beta activities have exceeded Arizona's Maximum Allowable Limit through releases from natural weathering processes and from uranium-mining operations in the Church Rock Mining District, Grants Mineral Belt, New Mexico. Water samples were collected at a network of nine continuous-record streamgauges equipped with microprocessor-based satellite telemetry and automatic water-sampling systems, and six partial-record streamgauges equipped with passive water samplers. Analytical results from these samples were used to calculate transport of selected suspended and dissolved radionuclides in the uranium-238 and thorium-232 decay series.

Arizona;New Mexico↗

USGS2014

Mineral resource of the month: vermiculite

Vermiculite comprises a group of hydrated, laminar magnesium-aluminum-iron silicate minerals resembling mica. They are secondary minerals, typically altered biotite, iron-rich phlogopite or other micas or clay-like minerals that are themselves sometimes alteration products of amphibole, chlorite, olivine and pyroxene. Vermiculite deposits are associated with volcanic ultramafic rocks rich in magnesium silicate minerals, and flakes of the mineral range in color from black to shades of brown and yellow. The crystal structure of vermiculite contains water molecules, a property that is critical to its processing for common uses. Using a process called exfoliation-in which vermiculite flakes are heated to 900 degrees Celsius or higher, causing water within the flakes to flash to steam and expand-crude vermiculite ore is processed into particles that are eight to 20 times larger. The resulting lightweight material is chemically inert and fire resistant, with low density and low thermal conductivity. It is also odorless, has high liquid absorption capacity and catalytic properties. Because it is lightweight and thermally insulating, vermiculite is used in general building plasters and concrete products, alone or combined with other lightweight aggregates such as perlite. Special plasters, in which vermiculite is combined with binders like gypsum or portland cement, fillers or other additives, provide fire protection and soundproofing. As insulation, exfoliated vermiculite, sometimes treated with a water repellent, is used to fill pores and cavities in masonry construction and hollow blockwork to enhance acoustic properties, fire rating and insulation performance. Exfoliated vermiculite can also be used to produce refractory and insulation concretes and mortars, and to make high-temperature binders for construction materials, gaskets, specialty papers, textiles and vehicle brake linings. Finer grades of exfoliated vermiculite can be used to produce various shapes of insulation pellets, high-temperature insulation, as a primary component in cementitious coatings, and as a filler in inks, paints, plastics and other materials. Vermiculite can absorb liquids such as fertilizers, herbicides and insecticides, which can then be transported as free-flowing solids. It is used in the fertilizer and pesticide markets because of its ability to act as a bulking agent, carrier and extender. In horticulture, exfoliated vermiculite improves soil aeration and moisture retention, and when mixed with peat or other composted materials, such as pine bark, vermiculite produces a good growing medium for plants. As a soil conditioner, exfoliated vermiculite improves aeration in clay-rich soils and water retention in sandy soils, while reducing the likelihood of compaction, cracking and crusting of the soil. For more information on the commercial use of vermiculite, visit minerals.usgs.gov/minerals/ .

Earth↗

USGS2014

Mineral resource of the month: Vermiculite

Earth↗

USGS1988

Mg/Mn partitioning as a test for equilibrium between coexisting Fe-Ti oxides

Partitioning of Mg and Mn between titanomagnetite and ferrian ilmenite of volcanic rocks provides a test for equilibrium between coexisting phases. A plot of log(Mg/Mn)-, vs. log(Mg/Mn),, for 213 homogeneous oxide pairs from volcanic rocks yields a straight line over more than two orders of magnitude variation in Mg/Mn. Analyses that plot within reasonable limits of analytical precision of this line are consistent with preservation of equilibrium compositions. The test appears to be valid for fresh volcanic rocks but may not be applicable to oxides in metamorphic, plutonic, and altered volcanic rocks in which oxide minerals typicatly have oxidized or exsolved at subsolidus temperatures. It can be used to discriminate between multiple populations of an oxide phase or to evaluate equilibration of inclusions in silicate phenocrysts for Fe-Ti oxide geothermometry and oxygen barometry.

American Mineralogist↗

USGS2016

Geochemistry of host rocks in the Howards Pass district, Yukon-Northwest Territories, Canada: implications for sedimentary environments of Zn-Pb and phosphate mineralization

Detailed lithogeochemical data are reported here on early Paleozoic sedimentary rocks that host the large Howards Pass stratiform Zn-Pb deposits in Yukon-Northwest Territories. Redox-sensitive trace elements (Mo, Re, V, U) and Ce anomalies in members of the Duo Lake Formation record significant environmental changes. During the deposition of lower footwall units (Pyritic siliceous and Calcareous mudstone members), bottom waters were anoxic and sulphidic, respectively; these members formed in a marginal basin that may have become increasingly restricted with time. Relative to lower members, a major environmental change is proposed for deposition of the overlying Lower cherty mudstone member, which contains phosphorite beds up to ∼0.8 m thick in the upper part, near the base of the Zn-Pb deposits. The presence of these beds, together with models for modern phosphorite formation, suggests P input from an upwelling system and phosphorite deposition in an upper slope or outer shelf setting. The overlying Active mudstone member contains stratabound to stratiform Zn-Pb deposits within black mudstone and gray calcareous mudstone. Data for unmineralized black mudstone in this member indicate deposition under diverse redox conditions from suboxic to sulphidic. Especially distinctive in this member are uniformly low ratios of light to heavy rare earth elements that are unique within the Duo Lake Formation, attributed here to the dissolution of sedimentary apatite by downward-percolating acidic metalliferous brines. Strata that overlie the Active member (Upper siliceous mudstone member) consist mainly of black mudstone with thin (0.5–1.5 cm) laminae of fine-grained apatite, recording continued deposition on an upper slope or outer shelf under predominantly suboxic bottom waters. Results of this study suggest that exploration for similar stratiform sediment-hosted Zn-Pb deposits should include the outer parts of ancient continental margins, especially at and near stratigraphic transitions from marginal basin facies to overlying slope or shelf facies.

Mineralium Deposita↗

USGS2002

Dinosaurs that did not die: Evidence for Paleocene dinosaurs in the Ojo Alamo Sandstone, San Juan Basin, New Mexico

Palynologic and paleomagnetic data confirm a Paleocene age for the Ojo Alamo Sandstone (and its contained dinosaurs) throughout the San Juan Basin of New Mexico. The recently reported discovery of 34 skeletal elements from a single hadrosaur in the Ojo Alamo provides unequivocal evidence that these bones were not reworked from underlying Cretaceous strata. Geochemical studies of samples from several single-dinosaur-bone specimens from the Paleocene Ojo Alamo Sandstone and the underlying Late Cretaceous (Campanian) Kirtland Formation show that mineralized bones from these two rock units contain distinctly different abundances of uranium and rare-earth elements and demonstrate that Cretaceous and Paleocene bones were mineralized at different times when mineralizing fluids had distinctly different chemical compositions. These findings indicate that the dinosaur bone from the Paleocene Ojo Alamo is indigenous and not reworked. These data show that a relatively diverse assemblage of dinosaurs survived the end-Cretaceous asteroid-impact extinction event of 65.5 Ma. The San Juan Basin’s Paleocene dinosaur fauna is herein named the Alamoan fauna. Magnetic-polarity chronology shows that these survivors lived for about one million years into the Paleocene and then became extinct around 64.5 Ma. We suggest that a plausible survival mechanism for this Lazarus fauna may have been the large numbers of buried dinosaur eggs, laid just before the asteroid impact occurred. These buried eggs would have provided a safe haven for developing dinosaur embryos for the first one to two years after the impact, thereby making it possible for them to survive the worst of the impact’s early devastation.

Colorado, New Mexico↗

USGS2018

Compositional variation in the chevkinite group: new data from igneous and metamorphic rocks

Electron microprobe analyses are presented of chevkinite-group minerals from Canada, USA, Guatemala, Norway, Scotland, Italy and India. The host rocks are metacarbonates, alkaline and subalkaline granitoids, quartz-bearing pegmatites, carbonatite and an inferred K-rich tuff. The analyses extend slightly the range of compositions in the chevkinite group, e.g. the most MgO-rich phases yet recorded, and we report two further examples where La is the dominant cation in the A site. Patchily- zoned crystals from Virginia and Guatemala contain both perrierite and chevkinite compositions. The new and published analyses are used to review compositional variation in minerals of the perrierite subgroup, which can form in a wide range of host rock compositions and over a substantial pressure- temperature range. The dominant substitutions in the various cation sites and a generalized substitution scheme are described.

Mineralogical Magazine↗

USGS2025

Petrogenesis and mineralization potential of spinifex komatiitic basalts in the Bradley Peak greenstone terrane, Wyoming Province

Komatiitic volcanic rocks are important hosts of Ni sulfide mineralization and record early Earth evolution; however, those in the well-studied Archean Wyoming Province have received little attention. Here, we elucidate the timing and petrogenesis of the Bradley Peak komatiitic volcanic rocks using field and textural observations, geochronology, and geochemistry. Detrital and igneous zircon U-Pb ages for two samples from previously undated units support published age determinations, placing the eruption age at 2.72 Ga. Stratigraphy of the volcanic flows was mapped and 36 samples including cumulates, greenschists, and spinifex-textured rocks were collected. Whole-rock geochemistry was used to classify the spinifex-textured samples as Al-undepleted komatiitic basalts (11–17 wt% MgO). Platinum-group element concentrations (n = 25) are like those in global Al-undepleted komatiitic basalts, and PGE/Ti ratios do not indicate the volcanic flows likely host sulfide mineralization. Initial ε Nd values of −0.5 to +4.7 (n = 16), indicate that these lavas were derived from a depleted mantle source and have negligible evolved crust contamination. The primary magma to the komatiitic basalt flows is estimated to have had 19 wt% MgO and be derived from ∼15 to 25 % mantle partial melting at 3–4 GPa. Trace element chemistry and thermodynamic modeling suggest the primary melt assimilated local banded iron formation. Although the Bradley Peak komatiitic basalts do not contain positive evidence of magmatic sulfide deposits, depleted Au in the flows suggests they could be source rocks for nearby orogenic gold deposits.

Wyoming↗

USGS2023

A review of geology and mining in the Marble Mountains, southeastern California

Mining in the Marble Mountains of southeastern California was active in the earliest 1900s and gradually declined to very few active mines by 1959. Most mining consisted of hard-rock prospects and mines, with a few soft-rock prospects and one mine. The Marble Mountains are a 10 km by 30 km, gently NE-dipping dipping structural block composed of Proterozoic plutonic and metamorphic rocks, Paleozoic sedimentary rocks, and Jurassic granitoids exposed along the western anti-dip slopes, and Miocene volcanic and sedimentary rocks exposed along the crest of the range and eastern dip slopes. Mineralization occurred in metamorphic aureoles of intrusions, along dikes, as contact metasomatic replacement bodies in carbonate rocks, or adjacent to or along thrust faults. Mineralization locally formed gold, copper, malachite, azurite, bornite, chalcopyrite, magnetite, specularite, limonite, quartz, epidote, actinolite, and garnet. Hard-rock prospects and mines are clustered into five locations. The mines are small open pits, a few consist of a shaft or two with a few adits, most are just a single shaft or adit. There are a few small open-pit marble mines, and one is an open pit fossil mine. Eight prospects were developed in the Miocene tuffaceous deposits; three in the northwest and five prospects, and a single adit, in the south. Most of the Marble Mountains are now in the Trilobite Wilderness or adjacent Areas of Critical Environmental Concern, and the area of the Golden Cycle district (Castle Mine area) and prospect areas in the southern part of the range are in the Mojave Trails National Monument. The Iron Hat mine, several nearby areas, and the Trilobite mine area are privately owned. No rock or mineral mines are currently active, but the Trilobite mine in the south end of the range is still open to the public.

California↗

USGS2008

User's Guide to Handlens - A Computer Program that Calculates the Chemistry of Minerals in Mixtures

HandLens is a computer program, written in Excel macro language, that calculates the chemistry of minerals in mineral mixtures (for example, in rocks, soils and sediments) for related samples from inputs of quantitative mineralogy and chemistry. For best results, the related samples should contain minerals having the same chemical compositions; that is, the samples should differ only in the proportions of minerals present. This manual describes how to use the program, discusses the theory behind its operation, and presents test results of the program's accuracy. Required input for HandLens includes quantitative mineralogical data, obtained, for example, by RockJock analysis of X-ray diffraction (XRD) patterns, and quantitative chemical data, obtained, for example, by X-ray florescence (XRF) analysis of the same samples. Other quantitative data, such as sample depth, temperature, surface area, also can be entered. The minerals present in the samples are selected from a list, and the program is started. The results of the calculation include: (1) a table of linear coefficients of determination (r2's) which relate pairs of input data (for example, Si versus quartz weight percents); (2) a utility for plotting all input data, either as pairs of variables, or as sums of up to eight variables; (3) a table that presents the calculated chemical formulae for minerals in the samples; (4) a table that lists the calculated concentrations of major, minor, and trace elements in the various minerals; and (5) a table that presents chemical formulae for the minerals that have been corrected for possible systematic errors in the mineralogical and/or chemical analyses. In addition, the program contains a method for testing the assumption of constant chemistry of the minerals within a sample set.

Open-File Report↗

USGS1959

Geology and uranium-vanadium deposits of the slick rock district, San Miguel and Dolores counties, Colorado

Sedimentary rocks known in the Slick Rock district in southwestern Colorado range in age from Devonian (?) to Cretaceous, and aggregate about 13,000 feet in maximum thickness. Important uranium-vanadium production has come from deposits in the Salt Wash member of the Morrison formation of Late Jurassic age. The sedimentary rocks are gently folded in the Dolores and Glade anticlines and the Disappointment syncline, and are cut by the Dolores fault zone in the north part of the district and by the Glade fault zone in the south part of the district . Principal fracture sets are oriented approximately parallel to the major faults. Detrital hematite, magnetite, and ilmenite in rocks of the Morrison formation not affected by epigenetic alteration contain appreciable amounts of several of the elements found in the ore deposits . Epigenetic alteration processes have bleached large volumes of rock and largely destroyed these minerals. Such alteration is spatially associated with the Dolores fault zone. Most of the known ore deposits are in the north part of the Slick Rock district in a belt called the Dolores ore zone. The zone lies along the Dolores fault zone but is wider than the fault zone. All known deposits are associated with abundant carbonaceous plant material. Uranium-vanadium deposits in the district are chiefly tabular to lenticular and are roughly parallel to the sedimentary bedding. Some ore bodies, however, are narrow, elongate, and curve sharply across bedding; these bodies have been called "rolls" by the miners. Mineral zoning is evident in some roll bodies; carbonates, goethite (altered from pyrite), selenides, and sulfides are commonly found in concentric layers at the concave edge of rolls. This zoning, and the relationship of roll ore bodies to sedimentary structures and lithology, suggest that ore was deposited at an interface between two solutions, possibly cool connate water and a warmer ore solution. On a district scale, copper and lead are distinctly most abundant in the ore deposits within and immediately adjacent to the Dolores fault zone, and less abundant in deposits toward the edge of the zone. Uranium-vanadium deposits in the district occur only in sandstone that is considered to be epigenetically altered, and the most extensive epigenetic changes have occurred close to ore bodies. It is concluded that ground water, heated and set into circulation near the end of Cretaceous time by igneous intrusions in the La Sal and other centers on the Colorado Plateau, picked up elements from sedimentary rocks where they had been faulted and fractured, and deposited the elements at solution interfaces where accumulations of carbonaceous material provided favorable chemical conditions for precipitation.

Colorado, Utah↗

USGS2006

Geology and reconnaissance stable isotope study of the Oyu Tolgoi porphyry Cu-Au system, South Gobi, Mongolia

The Oyu Tolgoi porphyry Cu-Au system in the South Gobi desert, Mongolia, comprises five deposits that extend over 6 km in a north-northeast-oriented zone. They occur in a middle to late Paleozoic are terrane and are related to Late Devonian quartz monzodiorite intrusions. The Hugo Dummett deposits are the northernmost and deepest, with up to 1,000 m of premineral sedimentary and volcanic cover rock remaining. They are the largest deposits discovered to date and characterized by high-grade copper (>2.5% Cu) and gold (0.5-2 g/t) mineralization associated with intense quartz veining and several phases of quartz monzodiorite intruded into basaltic volcanic host rocks. Sulfide minerals in these deposits are zoned outward from a bornite-dominated core to chalcopyrite, upward to pyrite ?? enargite and covellite at shallower depth. The latter high-sulfidation-state sulfides are hosted by advanced argillic alteration mineral associations. This alteration is restricted mainly to dacitic ash-flow tuff that overlies the basaltic volcanic rock and includes ubiquitous quartz and pyrophyllite, kaolinite, plus late dickite veins, as well as K alunite, Al phosphate-sulfate minerals, zunyite, diaspore, topaz, corundum, and andalusite. A reconnaissance oxygen-hydrogen and sulfur isotope study was undertaken to investigate the origin of several characteristic alteration minerals in the Oyu Tolgoi system, with particular emphasis on the Hugo Dummett deposits. Based on the isotopic composition of O, H, and S (??18O(SO4) = 8.8-20.1???, ??D = -73 to -43???, ??34S = 9.8-17.9???), the alunite formed from condensation of magmatic vapor that ascended to the upper parts of the porphyry hydrothermal system, without involvement of significant amounts of meteoric water. The isotopic data indicate that pyrophyllite (??18O = 6.5-10.9???, ??D = -90 to -106???) formed from a magmatic fluid with a component of meteoric water. Muscovite associated with quartz monzodiorite intrusions occurs in the core of the Hugo Dummett deposits, and isotopic data (??18O = 3.0-9.0???, ??D = -101 to -116%o) show it formed from a magmatic fluid with water similar in composition to that which formed the pyrophyllite. Mg chlorite (??18O = 5.5???, ??D = -126???) is a widespread mineral retrograde after hydrothermal biotite and may have formed from fluids similar to those related to the muscovite during cooling of the porphyry system. By contrast, paragenetically later and postmineralization alteration fluid, which produced dickite (??18O = -4.1 to +3.3???, ??D = -130 to -140???), shows clear evidence for mixing with substantial amounts of meteoric water. Relatively low ??D values (-140???) for this meteoric water component may indicate that its source was at high elevations. The geologic structure, nature of alteration, styles of mineralization, and stable isotope data indicate that the Oyu Tolgoi deposits constitute a typical porphyry system formed in an island-arc setting. The outward zonation of sulfide minerals for the Hugo Dummett deposits, from a bornite-dominated core to chalcopyrite and pyrite-enargite, can be interpreted to be related to a cooling magmatic hydrothermal system which transgressed outward over enclosing advanced argillic alteration. This resulted in some unusual alteration and sulfide parageneses, such as topaz, or pyrite, enargite, and tennantite, entrained by high-grade bornite. ?? 2006 by Economic Geology.

Economic Geology↗

USGS2010

Legacy of the California Gold Rush: Environmental geochemistry of arsenic in the southern Mother Lode Gold District

Gold mining activity in the Sierra Nevada foothills, both recently and during the California Gold Rush, has exposed arsenic-rich pyritic rocks to weathering and erosion. This study describes arsenic concentration and speciation in three hydrogeologic settings in the southern Mother Lode Gold District: mineralized outcrops and mine waste rock (overburden); mill tailings submerged in a water reservoir; and lake waters in this monomictic reservoir and in a monomictic lake developing within a recent open-pit mine. These environments are characterized by distinct modes of rock-water interaction that influence the local transport and fate of arsenic. Arsenic in outcrops and waste rock occurs in arsenian pyrite containing an average of 2 wt% arsenic. Arsenic is concentrated up to 1300 ppm in fine-grained, friable, iron-rich weathering products of the arsenian pyrite (goethite, jarosite, copiapite), which develop as efflorescences and crusts on weathering outcrops. Arsenic is sorbed as a bidentate complex on goethite, and substitutes for sulfate in jarosite. Submerged mill tailings obtained by gravity core at Don Pedro Reservoir contain arsenic up to 300 ppm in coarse sand layers. Overlying surface muds have less arsenic in the solid fraction but higher concentrations in porewaters (up to 500 μg/L) than the sands. Fine quartz tailings also contain up to 3.5 ppm mercury related to the ore processing. The pH values in sediment porewaters range from 3.7 in buried gypsum-bearing sands and tailings to 7 in the overlying lake sediments. Reservoir waters immediately above the cores contain up to 3.5 μg/L arsenic; lake waters away from the submerged tailings typically contain less than 1 μg/L arsenic. Dewatering during excavation of the Harvard open-pit mine produced a hydrologic cone of depression that has been recovering toward the pre-mining groundwater configuration since mining ended in 1994. Aqueous arsenic concentrations in the 80 m deep pit lake are up to 1000 μg/L. Redistribution of the arsenic occurs during summer stratification, with highest concentrations at middle depths. The total mass of arsenic in the pit lake increases coinciding with early winter rains that erode, partially dissolve, and transport arsenic-bearing salts into the pit lake. Arsenic concentration, speciation, and distribution in the Sierra Nevada foothills depend on many factors, including the lithologic sources of arsenic, climatic influences on weathering of host minerals, and geochemical characteristics of waters with which source and secondary minerals react. Oxidation of arsenian pyrite to goethite, jarosite, and copiapite causes temporary attenuation of arsenic during summer, when these secondary minerals accumulate; subsequent rapid dissemination of arsenic into the aqueous environment is caused by annual winter storms. As the population of the Mother Lode area grows, it is increasingly important to consider these effects during planning and development of land and groundwater resources.

California↗

USGS2014

Rare chemical constituents of amelia (Virginia) pegmatite dikes, and their mineral sources

Students of Igneous phenomena have long since become familiar with the occurrence of rare minerals in pegmatitic bodies. The great local concentration of rare elements in pegmatite minerals provides a remarkably good opportunity for the Investigation of deep-seated rock constituents, for it is reasonable to suppose that these same elements are widely distributed in minute amounts through the parent rocks to which they are genetically related; but their concentration in pegmatite bodies affords a record of their presence that is lacking in other rocks. The unusual number of rare minerals of the Amelia, Virginia, pegmatites has long attracted attention, and the rare elements of the more abundant minerals which have been investigated in the laboratories of the United States Geological Survey afford an unusual opportunity to study the rare constituents of a pegmatite. This famous locality for rare minerals is situated 38 miles southwest of Richmond, just south of Appomattox River, on the Piedmont plateau.

Eos, Transactions, American Geophysical Union↗

USGS2024

Lead isotopes in New England (USA) volcanogenic massive sulphide deposits: Implications for metal sources and pre-accretionary tectonostratigraphic terranes

Lead isotope values for volcanogenic massive sulfide (VMS) deposits provide important insights into metal sources and the nature of pre-accretionary tectonostratigraphic terranes and underlying basements. Deposits of this type in New England formed in diverse tectonic settings including volcanic arcs and backarcs, a supra–subduction zone arc, a rifted forearc foreland basin, and a rifted continental margin. Following VMS mineralization on or near the seafloor, components of the tectonostratigraphic assemblages—volcanic ± sedimentary rocks, coeval intrusions, sulfide deposits, and underlying basements—were diachronously accreted to the Laurentian margin during the Paleozoic. Lead isotope data for galena show relatively large ranges for 206 Pb/ 204 Pb, 207 Pb/ 204 Pb, and 208 Pb/ 204 Pb. Evaluation of potential lead sources, using for comparison Pb-isotope data from modern and ancient settings, suggests that principal sources include the mantle, volcanic ± sedimentary rocks, and deeper basement rocks. Integration of the Pb-isotope values with published data such as Nd isotopes for the volcanic rocks and from deep seismic reflection profiles points to the involvement of several basements, including those of Grenvillian, Ganderian, Avalonian, and West African (and (or) Amazonian) affinity. Clustering of Pb-isotope data for VMS deposits within individual Cambrian and Ordovician volcanic and volcanosedimentary settings, delineated by differences in 206 Pb/ 204 Pb and µ ( 238 U/ 204 Pb) values, are consistent with lead derivation from at least four and possibly five different tectonostratigraphic assemblages with isotopically distinct basements. Collectively, our Pb-isotope data for New England VMS deposits provide a novel window into the nature of subarc basement rocks during pre-accretionary sulfide mineralization outboard of Laurentia during early Paleozoic time.

Canadian Journal of Earth Sciences↗

USGS2002

Argon thermochronology of mineral deposits; a review of analytical methods, formulations, and selected applications

40Ar/39Ar geochronology is an experimentally robust and versatile method for constraining time and temperature in geologic processes. The argon method is the most broadly applied in mineral-deposit studies. Standard analytical methods and formulations exist, making the fundamentals of the method well defined. A variety of graphical representations exist for evaluating argon data. A broad range of minerals found in mineral deposits, alteration zones, and host rocks commonly is analyzed to provide age, temporal duration, and thermal conditions for mineralization events and processes. All are discussed in this report. The usefulness of and evolution of the applicability of the method are demonstrated in studies of the Panasqueira, Portugal, tin-tungsten deposit; the Cornubian batholith and associated mineral deposits, southwest England; the Red Mountain intrusive system and associated Urad-Henderson molybdenum deposits; and the Eastern Goldfields Province, Western Australia.

Bulletin↗

USGS1984

Aeromagnetic map of the Fossil Springs Roadless Area, Yavapai, Gila, and Coconino counties, Arizona

The aeromagnetic map of the Fossil Springs Roadless Area was compiled from data collected in 1980 by Airmag Surveys, Inc., for the U.S. Geological Survey. Total magnetic intensity measurements were made along east-west flight lines about 0.5 mi apart and flown at an average altitude of 1,000 ft above the ground surface. A regional magnetic field (the International Geomagnetic Reference Field, 1975, updated to months flown) was removed from the data and a constant of 50,800 gammas was added to the adjusted total field intensity values. The roadless area includes the upper part of Fossil Creek and its northeastern tributaries in Sandrock Canyon and Calf Pen Canyon. The extremely rugged canyon of Fossil Creek is in several places more than 1,500 ft deep. Elevation of the canyon floor ranges from 4,600 ft near the mouth of Calf Pen Canyon to 3,500 ft at the southwest end of the area. Peaks and ridges on the uplands bordering the canyons range in elevation from 5,300 ft west of Fossil Springs to 6,900 ft in the northeastern part of the area. Maximum topographic relief along these uplands is less than 200 ft. The Fossil Springs Roadless Area is underlain by more than 3,000 ft of Paleozoic rocks consisting mostly of sandstone, shale, dolomite, and limestone. West of Fossil Springs and along most of the border of the area, these rocks are generally overlain by late Tertiary volcanic rocks, mainly basaltic lavas and pyroclastic deposits. Quaternary alluvial, colluvial, landslide, and travertine deposits overlie large parts of the country rock in the canyons. In the southwestern part of the area, the volcanic rocks are more than 2,000 ft thick. Along the northwest and northeast margins, these rocks are 300-400 ft thick. The prevailing dip of the Paleozoic strata is low to the north or northeast. The dominant homoclinal structure is interrupted by several fault blocks, in which the strata dip westward or southward. All the faults are high-angle normal faults and have displacements commonly ranging from about 50 to 400 ft. Although fault relations are obscure within the volcanic sequence, many faults seem to displace the volcanic rocks less than the underlying Paleozoic rocks. The volcanic rocks, which rest unconformably on the Paleozoic strata, are flat lying in the northern part of the map area, but west of Fossil Springs they dip gently southwestward. The ancestral Mogollon Rim, a north-northwest-trending escarpment of Paleozoic rocks now concealed by Tertiary volcanic rocks lies near Fossil Springs (Twenter, 1962). The magnetic anomalies and patterns on the aeromagnetic map reflect variations of magnetization in the underlying rocks. Basaltic rocks contain moderate amounts of magnetic minerals, mainly magnetite, and possess strong intensities of magnetization. The more silicic volcanic rocks have much lower magnetization intensities. Sedimentary rocks contain little or no magnetite and are virtually nonmagnetic.

Arizona↗

USGS1982

Uranium and other element geochemical covariation in a granitic host rock and in the derived sediment, Deep Creek Range, Juab County, Utah

Correlation and factor analysis of geochemical data from a Tertiary biotite quartz monzonite, the Ibapah stock, and from derived sediment shows on comparison a major shift in element covariation among uranium and 24 other elements. Samples used were collected for a 1978 study in the central part of the Deep Creek Range, Juab County, Utah. Computed correlations among elements in granitic igneous rock samples suggest a high degree of covariation among elements that compose the rock. Uranium, however, shows significant correlation with only 12 elements and almost zero correlation with thorium. Computed correlations among elements in the derived sediment suggest that major decreases have occurred in covariation of the elements in the derived sands. Uranium in the sands, however, shows 15 significant correlations compared to 12 in the igneous rock samples, and shows an extremely high correlation with thorium. Factor analysis shows three geochemical petrogenic factors and the regional Be-U mineralization factor in the igneous rocks, and two mechanical segregation and one chemical precipitation factors in the sediments.

Open-File Report↗