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At least 811 records · Page 45Linked to original sources
USGS1989

Oxygen isotope exchange kinetics of mineral pairs in closed and open systems: Applications to problems of hydrothermal alteration of igneous rocks and Precambrian iron formations

The systematics of stable-isotope exchange between minerals and fluids are examined in the context of modal mineralogical variations and mass-balance considerations, both in closed and in open systems. On mineral-pair ??18O plots, samples from terranes that have exchanged with large amounts of fluid typically map out steep positively-sloped non-equilibrium arrays. Analytical models are derived to explain these effects; these models allow for different exchange rates between the various minerals and the external fluids, as well as different fluid fluxes. The steep arrays are adequately modelled by calculated isochron lines that involve the whole family of possible exchange trajectories. These isochrons have initially-steep near-vertical positive slopes that rotate toward a 45?? equilibrium slope as the exchange process proceeds to completion. The actual data-point array is thus analogous to the hand of an "isotopic clock" that measures the duration of the hydrothermal episode. The dimensionless ratio of the volumetric fluid flux to the kinetic rate parameter ( u k) determines the shape of each individual exchange trajectory. In a fluid-buffered system ( u k ??? 1), the solutions to the equations: (1) are independent of the mole fractions of the solid phases; (2) correspond to Taylor's open-system water/rock equation; and (3) yield straight-line isochrons that have slopes that approach 1 f, where f is the fraction reacted of the more sluggishly exchanging mineral. The isochrons for this simple exchange model are closely congruent with the isochrons calculated for all of the more complex models, thereby simplifying the application of theory to actual hydrothermal systems in nature. In all of the models an order of magnitude of time (in units of kt) separates steep non-equilibrium arrays (e.g., slope ??? 10) from arrays approaching an equilibrium slope of unity on a ??-?? diagram. Because we know the approximate lifetimes of many hydrothermal systems from geologic and heat-balance constraints, we can utilize the 18O 16O data on natural mineral assemblages to calculate the kinetic rate constants (k's) and the effective diffusion constants (D's) for mineral-H2O exchange: these calculated values (kqtz ??? 10-14, kfeld ??? 10-13-10-12) agree with experimental determinations of such constants. In nature, once the driving force or energy source for the external infiltrating fluid phase is removed, the disequilibrium mineral-pair arrays will either: (1) remain "frozen" in their existing state, if the temperatures are low enough, or (2) re-equilibrate along specific closed-system exchange vectors determined solely by the temperature path and the mineral modal proportions. Thus, modal mineralogical information is a particularly important parameter in both the open- and closed-system scenarios, and should in general always be reported in stable-isotopic studies of mineral assemblages. These concepts are applied to an analysis of 18O 16O systematics of gabbros (Plagioclase-clinopyroxene and plagioclase-amphibole pairs), granitic plutons (quartz-feldspar pairs), and Precambrian siliceous iron formations (quartz-magnetite pairs). In all these examples, striking regularities are observed on ??-?? and ??-?? plots, but we point out that ??-?? plots have many advantages over their equivalent ??-?? diagrams, as the latter are more susceptible to misinterpretation. Using the equations developed in this study, these regularities can be interpreted to give semiquantitative information on the exchange histories of these rocks subsequent to their formation. In particular, we present a new interpretation indicating that Precambrian cherty iron formations have in general undergone a complex fluid exchange history in which the iron oxide (magnetite precursor?) has exchanged much faster with low-temperature (< 400??C) fluids than has the relatively inert quartz. ?? 1989.

Chemical Geology↗
USGS2024

Layered intrusions in the Precambrian: Observations and perspectives

Layered intrusions are plutonic bodies of cumulates that form by the crystallization of mantle-derived melts. These intrusions are characterized by igneous layering distinguishable by shifts in mineralogy, texture, or composition. Layered intrusions have been fundamental to our understanding of igneous petrology; however, it is their status as important repositories of critical metals – such as platinum-group elements, chromium, and vanadium – that has predominantly driven associated research in recent decades. Many layered intrusions were emplaced during the Precambrian, predominantly at the margins of ancient cratons during intervals of supercontinent accretion and destruction. It appears that large, layered intrusions require rigid crust to ensure their preservation, and their geometry and layering is primarily controlled by the nature of melt emplacement. Layered intrusions are best investigated by integrating observations from various length-scales. At the macroscale, intrusion geometries can be discerned, and their presence understood in the context of the regional geology. At the mesoscale, the layering of an intrusion may be characterized, intrusion-host rock contact relationships studied, and the nature of stratiform mineral occurrences described. At the microscale, the mineralogy and texture of cumulate rocks and any mineralization are elucidated, particularly when novel microtextural and mineral chemical datasets are integrated. For example, here we demonstrate how mesoscale observations and microscale datasets can be combined to understand the petrogenesis of the perplexing snowball oiks outcrop located in the Upper Banded Series of the Stillwater Complex. Our data suggest that the orthopyroxene oikocrysts did not form in their present location, but rather formed in a dynamic magma chamber where crystals were transported either by convective currents or within crystal-rich slurries. Critical metals may be transported to the level of a nascent intrusion as dissolved components in the melt. Alternatively, ore minerals are entrained from elsewhere in a plumbing system, potentially facilitated by volatile-rich phases. There are many ore-forming processes propounded by researchers to occur at the level of emplacement; however, each must address the arrival of the ore mineral, its concentration of metals, and its accumulation into orebodies. In this contribution, several of these processes are described as well as our perspectives on the future of layered intrusion research.

Precambrian Research↗
USGS2021

Petrology and geochronology of 1.48 to 1.45 Ga igneous rocks in the St. Francois Mountains terrane, southeast Missouri

The igneous geology of the St. Francois Mountains terrane in southeast Missouri is dominated by the products of 1.48 to 1.45 billion year old volcanic and plutonic magmatism but also includes volumetrically minor, compositionally bimodal contributions added during plutonism between 1.34 and 1.27 billion years ago. The 1.48 to 1.45 billion year old igneous rocks in the St. Francois Mountains terrane are bimodally distributed between volumetrically dominant felsic rocks and volumetrically minor rocks with mafic to intermediate compositions. All of these rocks are ferroan, which like most of their trace element abundances, suggests a genesis associated with farfield intraplate extensional tectonism and decompression-related magmatism. The diversity of compositions among 1.48 to 1.45 billion year old igneous rocks in the St. Francois Mountains terrane probably reflects mixtures of mantle-derived mafic inputs and low-degree partial melting of more evolved crustal protoliths. Newly determined ages define essentially continuous magmatism during the 30-million-year period between 1.48 and 1.45 billion years ago. The products of this magmatism are essentially coeval, whether intrusive or extrusive or having mafic, intermediate, or felsic compositions. In addition, the iron oxide-apatite (for example, Pea Ridge) and likely the iron oxide-copper gold (Boss) deposits in the St. Francois Mountains terrane have ages coincident with this magmatic episode. Spatial and temporal relations between 1.48 to 1.45 billion year old igneous rocks in the St. Francois Mountains terrane and the mineral deposits they host suggest the associated magmatic and mineralization processes are also genetically related. Geochemical, petrographic, geochronologic, and terrane-wide physical characteristics of the 1.48 to 1.45 billion year old igneous rocks in the St. Francois Mountains terrane are consistent with an origin involving extension well inboard from the margin of the Laurentian craton, associated mantle upwelling, lower crustal melting in response to mantle-derived thermal inputs, and mixing of mantle- and juvenile lower crustal-derived melts. Significant major and trace element compositional dispersion characteristics of these rocks likely reflect midcrustal magma reservoir fractionation of their principal rock-forming minerals. The resultant magmas constitute a series of variably hybridized reservoirs, emplaced at upper levels in the crust, that form a series of plutonic and associated eruptive products.

Missouri↗
USGS1990

Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc to back-arc volcanism in southern South America. The "cratonic" basalts do not contain the slab-derived components that impart the higher Ba/La, Ba/Nb, La/Nb, Cs/Rb, 87Sr/86Sr at a given 143Nd/144Nd, 207Pb/204Pb at a given 208Pb/204Pb, and ??18O to Andean orogenic arc basalts. Instead, these basalts are formed by relatively low degrees of partial melting of heterogeneous lower continental lithosphere and/or asthenosphere, probably due to thermal and mechanical pertubation of the mantle in response to subduction of oceanic lithosphere below the western margin of the continent. The "transitional" basalts do contain components added to their source region by either (1) active input of slab-derived components in amounts smaller than the contribution to the mantle below the arc and/or with lower Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios than below the arc due to progressive downdip dehydration of the subducted slab; or (2) subarc source region contamination processes which affected the mantle source of the "transitional" basalts earlier in the Cenozoic. ?? 1990 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1987

Summary mineral resource appraisal of the Richfield 1° x 2° quadrangle, west-central Utah

The mineral resource potential of the Richfield 1° x 2° quadrangle, Utah, has been appraised using geological, geophysical, geochemical, and remote-sensing techniques. These studies have led to many publications giving basic data and interpretations; of these, a series of 18 maps at 1:250,000 and 1:500,000 scales summarizing aspects of the geology, geophysics, geochemistry, and remote sensing is designated the CUSMAP (Conterminous United States Mineral Appraisal Program) folio. This circular uses the data shown on these maps to appraise the mineral resource potential of the quadrangle. The oldest rocks exposed in the Richfield quadrangle are small patches of Early Proterozoic (1.7 billion years old) gneiss and schist on the west side of the Mineral Mountains. These rocks presumably formed the basement on which many thousands of meters of Late Proterozoic, Paleozoic, and lower Mesozoic sedimentary strata were deposited. These rocks were deformed during the Late Cretaceous Sevier orogeny when Precambrian and Paleozoic strata in the western part of the quadrangle were thrust relatively eastward across Paleozoic and Mesozoic strata in the eastern part of the quadrangle. Late Cretaceous and early Tertiary highlands above the overthrust belt were eroded and much of the debris was deposited in broad basins east of the belt. Volcanism in Oligocene and earliest Miocene time formed an east-northeast-trending belt of calcalkalic volcanoes across the southern half of the quadrangle. In early Miocene time, the composition of the volcanic rocks changed to a bimodal assemblage of mafic rocks and high-silica alkali rhyolite that has been erupted episodically ever since. Syngenetic mineral resources developed during formation of both sedimentary and volcanic rocks. These include limestone and dolomite, silica-rich sandstone, metalliferous black shale, evaporite deposits, zeolite deposits, pumice, cinders and scoria, and evaporitic or diagenetic deposits in playa environments. Most of these deposits need to have markets established, or extraction and fabrication techniques developed, for them to be utilized. Most epigenetic deposits are of volcanogenic-hydrothermal origin. Deposits associated with calc-alkalic igneous activity largely contain Cu, Pb, Zn, Au, and Ag, and occur in a variety of types zoned around core intrusions. Younger deposits are mostly associated with silicic igneous centers belonging to the bimodal mafic-silicic igneous association. Resources associated with this latter group are likely to contain one or more of the elements Mo, W, U, Sn, Be, and F, as well as Pb, Zn, Au, and Ag. Alunite and kaolinite deposits are found at many mineralized centers. Most epigenetically mineralized areas expose only the upper, near-surface parts of the different hydrothermal systems; most of whatever mineral deposits formed in these systems probably still exist at depth, awaiting discovery. Our conclusion is that many mineralized areas have excellent possibilities for the occurrence of mineral resources. Each of the many identified centers of mineralization is discussed briefly in this report and an estimate made of its resource potential.

Utah↗
USGS2001

Geology and mineral deposits of the Minnie Moore and Bullion mineralized areas, Blaine County, Idaho

In the early 1880?s the discovery of rich ores in the Minnie Moore and Bullion mineralized areas sparked a rush to settle and develop the Wood River valley. Silver and lead discoveries in these areas spurred the boom in mining after completion of the Oregon Short Line Railroad to Hailey in 1883. In both areas the ore comprises galena, sphalerite, and tetrahedrite in a gangue of siderite, calcite, or quartz. Minor goldbearing quartz veins are also present. The ore is in fissure and replacement veins along fracture systems that formed in Late Cretaceous time, after intrusion of nearby granodiorite or quartz diorite stocks. The ore formed under mesothermal conditions and heat was supplied by the nearby plutons. In the Minnie Moore area, the mineralized veins are cut by low-angle normal faults that are of probable Eocene age. In the Minnie Moore mineralized area, the host rock is the middle part of the Devonian Milligen Formation, (the informal Lucky Coin limestone and Triumph argillite), which is the same stratigraphic level as the host ore in the rich Triumph mine northeast of Hailey. In the Bullion mineralized area, the ore is hosted by the lower member of the Middle Pennsylvanian to Lower Permian Dollarhide Formation. Rich ore was mined in several tunnels that reached the Mayflower vein, a northwest-striking mineralized shear zone. The deposits are thought to be mainly mesothermal veins that formed in association with Cretaceous magmatism. The syngenetic stratiform model of ore formation has often been applied to these deposits, however, no evidence of syngenetic mineralization was found in this study. Faulting has displaced most of the major orebodies and thus has made mining these deposits a challenge.

Bulletin↗
USGS1984

MINERALOGICAL STUDIES OF THE HYDROTHERMAL SYSTEM IN NEWBERRY VOLCANO DRILL HOLE 2, OREGON.

Studies of secondary mineral distribution, whole-rock chemical compositions, isotopes, and fluid inclusions are being conducted on the core from Newberry Volcano drill hole 2. Rocks from the drill core are divided into 3 major intervals on the basis of their alteration pattern, which is controlled by rock permeabilities, primary lithologies, and temperatures. Incomplete alteration of pumice-rich lithic tuff layers in the upper part of the altered section and lack of self-sealing in fractures of most lava flows suggest that the hydrothermal system is young. Most of the secondary minerals could have been formed at temperatures near those present today; maximum measured temperature was 265 degree C at the bottom of the hole. Fluid inclusions indicate that past temperatures in the deeper part of the drill hole may have been as much as 100 degree C hotter than presently measured temperatures.

Conference Paper↗
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↗
USGS1998

Geochemical and isotopic (Nd-Pb-Sr-O) variations bearing on the genesis of volcanic rocks from Vesuvius, Italy

Alkaline volcanism produced by Monte Somma-Vesuvius volcano includes explosive plinian and subplinian activity in addition to effusive lava flows. Pumice, scoria, and lava (150 samples) exhibit major- and trace-element gradients as a function of SiO2 (58.9-47.2 wt%) and MgO (0-7.8 wt%); Mg value are ???50. Internally gradational chemical groups or cycles are distinguished by age: (1) 25 000 to 14 000 yr B.P.; (2) 8000 yr B.P. to A.D. 79; and (3) A.D. 79 to 1944. A small number of lavas, dikes and scora were also analysed from the Somma formation (~ 35 000 to 25 000 yr B.P.). Within each group, contents of Na2O + K2O increas with decreasing MgO along distinct rocks. Nb/Y values are variable from 0.66 to 3.14 (at SiO2 ??? 50 wt%) generally in the range of alkaline and ultra-alkaline rocks. Variations in contents of some majro elements (e.g., P and Ti), and trace elements (e.g., Th, Nb, Ta, Zr, Hf, Pb, La, and Sc), as well as contrasting trends in ratios of various elements (e.g., Ta/Yb, Hf/U, Th/Ta, Th/Hf, Th/Yb, etc.) are also generally consistent with the group subdivisions. For example, Th/Hf increases from ??? 5 to ??? 10 with decreasing age for the Vesuvius system as a whole, yielding similar compositions in the least evolved rocks (low-silica, high-MgO, imcompatible element-poor) erupted at the end of each cycle. Internal variations within individual eruptions also systematically changed generally towards a common mafic composition at the end of each cycle, thus reflecting the dominanit volume in the magma chamber. At the start of a new eruptive cycle, the rocks are relatively enriched in incompatible elements; younger groups also contain higher abundances than other groups. N-MORB-normalized multielement diagrams exhibit selective enrichments of Sr, K, Rb, Th, and the light rare-earth elements; deep Nb and Ta negative anomalies commonly seen in rocks generated at orogenic margins are absent in the light rare-earth elements; deep Nb and Ta netgative anomalies commonly seen in rocks generated at orogenic margins are absent in our samples. Sr isotopic compositions are known to be variable within some of the units, in agreement with our data (87Sr/86Sr ~ 0.70699 to 0.70803) and with contributions from several isotopic components. Isotopic compositions for ??18O (7.3 to 10.2%), Pb for mineral separates and whole rocks (206Pb/204Pb ~ 18.947 to 19.178, 207Pb/204/Pb ~ 15.617 to 15.769, 208Pb/204Pb ~38.915 to 39.345), and Nd (143Nd ~ 0.51228 to 0.51251) also show variability. Oxygen isotope data show that pumices have higher ??18O values than cogenetic lavas, and that ??18O values and SiO2 are correlated. Radiogenic and stable isotope data plot within range of isotopic compositions for the Roman comagmatic province. Fractional crystallization cannot account for the radiogenic isotopic compositions of the Vesuvius magmas. We favor instead the combined effects of heterogeneous magma sources, together with isotopic exchange near the roof of the magma chamber. We suggest that metasomatized continental mantle lithosphere is the principal source of the magmas. This kind of enriched mantle was melted and reactivated in an area of continental extension (incipient rift setting) without direct reliance on contemporaneous subduction processes but possibly with input from mantle sources that resemble those that produce ocean island basalts.

Journal of Volcanology and Geothermal Research↗
USGS2017

Mobilization of mercury and arsenic from a carbonate-hosted ore deposit, central Idaho, U.S.A.

The Cinnabar and Fern mine sites in central Idaho are primary source areas for elevated mercury and arsenic entering the South Fork of the Salmon River, which provides critical spawning habitat for bull trout and Chinook salmon. Mercury mineralization is hosted by carbonate rocks, which generate waters dominated by Ca2+ and HCO3 - at pH 7 to 9. A synoptic sampling was conducted on headwater tributaries to determine geologic background concentrations and quantify trace metal concentrations in stream water associated with historical mining. Geologic background concentrations in unfiltered Cinnabar Creek water were 8 - 14 ng Hg L-1 and 4.8 - 9.5 µg As L-1. Immediately downstream from the mine site, concentrations increased to 257 ng Hg L-1 and 20.6 µg As L-1. Groundwater inflow diluted these concentrations by approximately half before the confluence of Cinnabar Creek with Sugar Creek. As expected, mercury and arsenic concentrations increased downstream in Sugar Creek below the confluence with Cinnabar Creek. However, the final downstream reach on Sugar Creek showed an increase in unfiltered mercury, methylmercury, and iron concentrations relative to the upstream reach. This increase is associated with historical mining activity in a mineralized area of carbonate rock that intersects the reach.

Idaho↗
USGS2015

Detailed interpretation of aeromagnetic data from the Patagonia Mountains area, southeastern Arizona

The induced magnetic field and the remanent magnetic field of rock masses are important to geologic modeling based on Earth&rsquo;s magnetic field data. The orientation of the induced magnetic field is approximately parallel to the orientation of Earth&rsquo;s geomagnetic field and its intensity can be derived from measured magnetic susceptibilities of rocks in a study area. The orientation and intensity of the natural remanent magnetic field is much harder to determine; therefore, few investigators have included magnetic remanence as a contributing factor to studies of continental magnetic anomalies. All rocks have remanent magnetism and, in intrusive or volcanic rocks, this component of the total magnetic intensity of the Earth&rsquo;s magnetic field can be as large as or larger than the induced component. The Patagonia Mountains in southeastern Arizona were selected to produce a subsurface geologic model from aeromagnetic data by incorporating physical properties of rock including measured magnetic susceptibilities, estimated remanent magnetic field orientations and intensities, a known association of intrusive events, and information from existing geologic mapping. The result is a model of geology at depth that may better represent reality than previous poorly substantiated cross sectional models. This new model includes concealed intrusive rocks and defines areas where concealed mineral deposits may be found. It also shows that volcanic rocks might occupy basins at relatively shallow depths in basins with low aeromagnetic anomalies. Euler deconvolution depth estimates derived from aeromagnetic data with a structural index of 0 show that mapped faults on the northern margin of the Patagonia Mountains generally agree with the depth estimates in the new geologic model. The deconvolution depth estimates also show that the concealed Patagonia Fault southwest of the Patagonia Mountains is more complex than recent geologic mapping represents. Additionally, Euler deconvolution depth estimates with a structural index of 2 locate many potential intrusive bodies that might be associated with known and unknown mineralization.

Arizona↗
USGS2008

Geochemical data for samples collected in 2007 near the concealed pebble porphyry Cu-Au-Mo deposit, southwest Alaska

In the summer of 2007, the U.S. Geological Survey (USGS) began an exploration geochemical research study over the Pebble porphyry copper-gold-molydenum (Cu-Au-Mo) deposit in southwest Alaska. The Pebble deposit is extremely large and is almost entirely concealed by tundra, glacial deposits, and post-Cretaceous volcanic and volcaniclastic rocks. The deposit is presently being explored by Northern Dynasty Minerals, Ltd., and Anglo-American LLC. The USGS undertakes unbiased, broad-scale mineral resource assessments of government lands to provide Congress and citizens with information on national mineral endowment. Research on known deposits is also done to refine and better constrain methods and deposit models for the mineral resource assessments. The Pebble deposit was chosen for this study because it is concealed by surficial cover rocks, it is relatively undisturbed (except for exploration company drill holes), it is a large mineral system, and it is fairly well constrained at depth by the drill hole geology and geochemistry. The goals of the USGS study are (1) to determine whether the concealed deposit can be detected with surface samples, (2) to better understand the processes of metal migration from the deposit to the surface, and (3) to test and develop methods for assessing mineral resources in similar concealed terrains. This report presents analytical results for geochemical samples collected in 2007 from the Pebble deposit and surrounding environs. The analytical data are presented digitally both as an integrated Microsoft 2003 Access? database and as Microsoft 2003 Excel? files. The Pebble deposit is located in southwestern Alaska on state lands about 30 km (18 mi) northwest of the village of Illiamna and 320 km (200 mi) southwest of Anchorage (fig. 1). Elevations in the Pebble area range from 287 m (940 ft) at Frying Pan Lake just south of the deposit to 1146 m (3760 ft) on Kaskanak Mountain about 5 km (5 mi) to the west. The deposit is in an area of relatively subdued topographic relief with an elevation of around 300 m (1000 ft). This portion of Alaska is part of the subarctic regime mountains division, Yukon intermontane plateaus-tayga-meadow province ecoregion, as defined by Bailey (U.S. Forest Service, 2007). Between June 28th and July 12th, 2007, scientists from the USGS collected soil, water, stream sediment, vegetation, heavy-mineral concentrate, till, and rock samples from the deposit area. This report contains analytical results for soil, water, stream sediment, and vegetation samples. Analyses for the heavy-mineral concentrate, till, and rock samples are still in progress. The sampling was undertaken during relatively dry and stable weather conditions. Only minor scattered rain showers occurred during the sampling period, so surface conditions were largely unaffected by weather. The predominant sample media collected were soils and surface waters. Soil and water (mostly from ponds and springs, some from small creeks) samples were collected along a single 7.8 km-long (4.8 mi) east-west traverse across the Pebble East and Pebble West zones and from more distal background areas around Koktuli and Kaskanak Mountains. Sample sites are shown on figure 2 and plate 1, and locality coordinates are provided in the accompanying Access and Excel files named FieldSite. Water samples were analyzed by USGS laboratories with one subset analyzed by Activation Laboratories (Actlabs), as indicated below. Soils and stream sediments were analyzed for their total content by SGS Minerals Services under a contract with the USGS. Soil samples were also leached by selected partial-extraction leaching procedures and then analyzed by several commercial laboratories, as described below. Vegetation samples were analyzed as indicated below.

Alaska↗
USGS2001

Preliminary lithogeochemical map showing near-surface rock types in the Chesapeake Bay watershed, Virginia and Maryland

This preliminary experimental lithogeochemical map shows the distribution of rock types in the Virginia and Maryland parts of the Chesapeake Bay watershed. The map was produced digitally by classifying geologic-map units according to composition, mineralogy, and texture; rather than by age and stratigraphic relationships as shown on traditional geologic maps. This map differs from most lithologic maps in that the lithogeochemical unit classification distinguishes those rock units having key water-reactive minerals that may induce acid neutralization, or reduction, of hosted water at the weathering interface. The validity of these rock units, however, is independent of water chemistry, because the rock units are derived from geologic maps and rock descriptions. Areas of high soil carbon content, and sulfide metal deposits are also shown. Water-reactive minerals and their weathering reactions yield five lithogeochemical unit classes: 1) carbonate rock and calcareous rocks and sediments, the most acid-neutralizing; 2)carbonaceous-sulfidic rocks and sediments, oxygen-depleting and reducing; 3) quartzofeldspathic rocks and siliciclastic sediments, relatively weakly reactive with water; 4) mafic silicate rocks/sediments, oxygen consuming and high solute-load delivering; and, 5) the rarer calcareous-sulfidic (carbonaceous) rocks, neutralizing and reducing. Earlier studies in some parts of the map area have related solute loads in ground and stream waters to some aspects of bedrock lithology. More recent preliminary tests of relationships between four of the classes of mapped lithogeochemical units and ground water chemistry, in the Mid-Atlantic area using this map, have focused on and verified the nitrate-reducing and acid-neutralizing properties of some bedrock and unconsolidated aquifer rock types. Sulfide mineral deposits and their mine-tailings effects on waters are beginning to be studied by others. Additional testing of relationships among the lithogeochemical units and aspects of ground and surface water chemistry could help to refine the lithogeochemical classification, and this map. The testing could also improve the usefulness of the map for assessing aquifer reactivity and the transport properties of reactive contaminants such as acid rain, and nitrate from agricultural sources, in the Chesapeake Bay watershed.

Maryland, Virginia↗
USGS1997

Sedimentary carbonate-hosted giant Bayan Obo REE-Fe-Nb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin

Detailed, integrative field and laboratory studies of the textures, structures, chemical characteristics, and isotopically determined ages and signatures of mineralization of the Bayan Obo deposit provided evidence for the origin and characteristics favorable for its formation and parameters necessary for defining giant polymetallic deposits of hydrothermal origin. Bayan Obo is an epigenetic, metasomatic, hydrothermal rare earth element (REE)-Fe-Nb ore deposit that is hosted in the metasedimentary H8 dolostone marble of the Middle Proterozoic Bayan Obo Group. The metasedimentary sequence was deposited on the northern continental slope of the North China craton. The mine area is about 100 km south of the suture marking Caledonian subduction of the Mongolian oceanic plate from the north beneath the North China craton. The mineralogy of the deposit is very complex, consisting of more than 120 different minerals, some of which are epigenetic minerals introduced by hydrothermal solutions, and some of which are primary and secondary metamorphic minerals. The major REE minerals are monazite and bastnaesite, whereas magnetite and hematite are the dominant Fe-ore minerals, and columbite is the most abundant Nb mineral. Dolomite, alkali amphibole, fluorite, barite, aegirine augite, apatite, phlogopite, albite, and microcline are the most widespread gangue minerals. Three general types of ores occur at Bayan Obo: disseminated, banded, and massive ores. Broad zoning of these ore types occurs in the Main and East Orebodies. Disseminated ores are in the outermost zone, banded ores are in the intermediate zone, and massive ores are in the cores of the orebodies. On the basis of field relations, host rocks, textures, structures, and mineral assemblages, many varieties of these three types of ores have been recognized and mapped. Isotopic dating of monazite, bastnaesite, aeschynite, and metamorphic and metasomatic alkali amphiboles associated with the deposit provides constraints on the ages of mineralization and the history of the deposit. Textural relations, differences in chemical composition, and 232Th/208Pb internal isochron ages of monazite and bastnaesite samples indicate that many episodes of REE mineralization occurred at Bayan Obo, ranging from about 555 Ma to about 398 Ma. Initial 208Pb/204Pb ratios suggest different sources of REE's for different generations of REE minerals. Relative ages of Fe mineralization were deduced from textural relationships of Fe minerals with other, dated mineral phases in the deposit. Most Nb mineralization was in the area of the West Orebodies and resulted in disseminated ore. Aeschynite, an early stage of Nb mineralization (438+-25.1 Ma), occurs with huanghoite and alkali amphiboles in veins. The 40Ar/39Ar ages of amphiboles, as well as petrographic textures, were used to distinguish three periods of regional metamorphism in the Bayan Obo mine area: (1) Late Proterozoic, about 890 Ma, which recrystallized H8 carbonate to marble and crystallized lineated alkali amphiboles along foliation planes in the marble; (2) Caledonian, about 425-395 Ma, which resulted in metamorphic and metasomatic-metamorphic alkali amphiboles; and (3) Hercynian, about 300 Ma, based on biotite 40Ar/39Ar analyses from biotite schist and folded banded ores. The 40Ar/39Ar ages of metasomatic alkali amphiboles also place time constraints on the hydrothermal history of the ore deposit. Metasomatic amphiboles represent periods of intense hydrothermal activity, which began as early as 1.26 Ga; that date is based on the age of amphibole from a vein that crosscuts the H6 quartzite that underlies the H8 dolostone marble. Although much of the metasomatic amphibole formed during periods that overlapped the peak period of REE mineralization of banded ores, REE and alkali amphibole phases generally occur in different mineral assemblages or are of very different ages in the same assemblage and, therefore, may have been derived from

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USGS2005

Missouri magnetic and gravity maps and data: A web site for distribution of data

Magnetic anomalies are due to variations in the Earth's magnetic field caused by the uneven distribution of magnetic minerals (primarily magnetite) in the rocks that make up the upper part of the Earth's crust. The features and patterns of the magnetic anomalies can be used to delineate details of subsurface geology, including the locations of buried faults and magnetite-bearing rocks and the depth to the base of sedimentary basins. This information is valuable for mineral exploration, geologic mapping, and environmental studies. The Missouri magnetic map is constructed from grids that combine information collected in 25 separate magnetic surveys conducted between 1943 and 1987. The data from these surveys are of varying quality. The design and specifications (terrain clearance, sampling rates, line spacing, and reduction procedures) varied from survey to survey depending on the purpose of the project and the technology of that time. Every attempt was made to acquire the data in digital form.

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