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USGS1964

Minor-element composition and organic carbon content of marine and nonmarine shales of Late Cretaceous age in the western interior of the United States

The composition of nonmarine shales of Cretaceous age that contain less than 1 per cent organic carbon is assumed to represent the inherited minor-element composition of clayey sediments delivered to the Cretaceous sea that occupied the western interior region of North America. Differences in minor-element content between these samples and samples of 1. (a) nonmarine carbonaceous shales (1 to 17 per cent organic carbon), 2. (b) nearshore marine shales (less than 1 per cent organic carbon), and 3. (c) offshore marine shales (as much as 8 per cent organic carbon), all of the same age, reveal certain aspects of the role played by clay minerals and organic materials in affecting the minor-element composition of the rocks. The organic carbon in the nonmarine rocks occurs in disseminated coaly plant remains. The organic carbon in the marine rocks occurs predominantly in humic material derived from terrestrial plants. The close similarity in composition between the organic isolates from the marine samples and low-rank coal suggests that the amount of marine organic material in these rocks is small. The minor-element content of the two kinds of nonmarine shales is the same despite the relatively large amount of organic carbon in the carbonaceous shales. The nearshore marine shales, however, contain larger median amounts of arsenic, boron, chromium, vanadium and zinc than do the nonmarine rocks; and the offshore marine shales contain even larger amounts of these elements. Cobalt, molybdenum, lead and zirconium show insignificant differences in median content between the nonmarine and marine rocks, although as much as 25 ppm molybdenum is present in some offshore marine samples. The gallium content is lower in the marine than in the nonmarine samples. Copper and selenium contents of the two kinds of nonmarine rocks and the nearshore marine samples are the same, but those of the offshore samples are larger. In general, arsenic, chromium, copper, molybdenum, selenium, vanadium and zinc are concentrated in those offshore marine samples having the largest amounts of organic carbon, but samples with equal amounts of vanadium, for instance, may differ by a factor of 3 in their amount of organic carbon. Arsenic and molybdenum occur in some samples chiefly in syngenetic pyrite but also are present in relatively large amounts in samples that contain little pyrite. The data on nonmarine carbonaceous shales indicate that organic matter of terrestrial origin in marine shales contributes little to the minor-element content of such rocks. It is possible that marine organic matter, even though seemingly small in amount in marine shales, contributes to the minor-element composition of the shales. In addition to any such contribution, however, the great effectiveness in sorption processes of humic materials in conjunction with clay minerals suggests that such processes must have played an important role as these materials moved from the relatively dilute solutions of the nonmarine environment to the relatively concentrated solution of sea water. The volumes of sea water sufficient to supply for sorption the amounts of most minor elements in the offshore marine samples are insignificant compared to the volumes of water with which the clay and organic matter were in contact during their transportation and sedimentation. Consequently, the chemical characteristics of the environment in which the clay minerals and organic matter accumulated and underwent diagenesis probably were the most important factors in controlling the degree to which sorption processes and the formation of syngenetic minerals affected the final composition of the rocks.

Geochimica et Cosmochimica Acta↗

USGS2011

Geochemical and stable isotopic data on barren and mineralized drill core in the Devonian Popovich Formation, Screamer sector of the Betze-Post gold deposit, northern Carlin trend, Nevada

The Devonian Popovich Formation is the major host for Carlin-type gold deposits in the northern Carlin trend of Nevada. The Popovich is composed of gray to black, thin-bedded, calcareous to dolomitic mudstone and limestone deposited near the carbonate platform margin. Carlin-type gold deposits are Eocene, disseminated, auriferous pyrite deposits characterized by acid leaching, sulfidation, and silicification that are typically hosted in Paleozoic calcareous sedimentary rocks exposed in windows through siliceous sedimentary rocks of the Roberts Mountains allochthon. The Carlin trend currently is the largest gold producer in the United States. The Screamer ore zone is a tabular body on the periphery of the huge Betze-Post gold deposit. Screamer is a good place to study both the original lithogeochemistry of the Popovich Formation and the effects of subsequent alteration and mineralization because it is below the level of supergene oxidation, mostly outside the contact metamorphic aureole of the Jurassic Goldstrike stock, has small, high-grade ore zones along fractures and Jurassic dikes, and has intervening areas with lower grade mineralization and barren rock. In 1997, prior to mining at Screamer, drill core intervals from barren and mineralized Popovich Formation were selected for geochemical and stable isotope analysis. The 332, five-foot core samples analyzed are from five holes separated by as much as 2000 feet (600 meters). The samples extend from the base of the Wispy unit up through the Planar and Soft sediment deformation units into the lower part of the upper Mud unit of the Popovich Formation.

Nevada↗

USGS2000

Transient calcite fracture fillings in a welded tuff, Snowshoe Mountain, Colorado

The core from two boreholes (13.1 and 19.2 m depth) drilled 500 m apart in the fractured, welded tuff near the summit of the Snowshoe Mountain, Colorado (47??30'N, 106??55'W) had unique petrographic and hydrodynamic properties. Borehole SM-4 had highly variable annual water levels, in contrast to SM-1a, whose water level remained near the land surface. Core samples from both boreholes (n = 10 and 11) were examined petrographically in thin sections impregnated with epoxy containing rhodamine to mark the pore system features, and were analyzed for matrix porosity and permeability. Core from the borehole sampling the vadose zone was characterized by open fractures with enhanced porosity around phenocrysts due to chemical weathering. Fractures within the borehole sampling the phreatic zone were mineralized with calcite and had porosity characteristics similar to Unweathered and unfractured rock. At the top of the phreatic zone petrography indicates that calcite is dissolving, thereby changing the hydrogeochemical character of the rock (i.e. permeability, porosity, reactive surface area, and mineralogy). Radiocarbon ages and C and O stable isotopes indicate that calcite mineralization occurred about 30 to 40 ka ago and that there was more than one mineralization event. Results of this study also provide some relationships between primary porosity development from 3 types of fracture in a welded tuff. (C) 2000 Elsevier Science Ltd.

Applied Geochemistry↗

USGS2010

Geochemical evolution of a high arsenic, alkaline pit-lake in the Mother Lode Gold District, California

The Harvard orebody at the Jamestown gold mine, located along the Melones fault zone in the southern Mother Lode gold district, California, was mined in an open-pit operation from 1987 to 1994. Dewatering during mining produced a hydrologic cone of depression; recovery toward the premining ground-water configuration produced a monomictic pit lake with alkaline Ca-Mg-HCO 3 -SO 4 –type pit water, concentrations of As up to 1,200 μ g/L, and total dissolved solids (TDS) up to 2,000 mg/L. In this study, pit-wall rocks were mapped and chemically analyzed to provide a context for evaluating observed variability in the composition of the pit-lake waters in relationship to seasonal weather patterns. An integrated hydrogeochemical model of pit-lake evolution based on observations of pit-lake volume, water composition (samples collected between 1998–2000, 2004), and processes occurring on pit walls was developed in three stages using the computer code PHREEQC. Stage 1 takes account of seasonally variable water fluxes from precipitation, evaporation, springs, and ground water, as well as lake stratification and mixing processes. Stage 2 adds CO 2 fluxes and wall-rock interactions, and stage 3 assesses the predictive capability of the model. Two major geologic units in fault contact comprise the pit walls. The hanging wall is composed of interlayered slate, metavolcanic and metavolcaniclastic rocks, and schists; the footwall rocks are chlorite-actinolite and talc-tremolite schists generated by metasomatism of greenschist-facies mafic and ultramafic igneous rocks. Alteration in the ore zone provides evidence for mineralizing fluids that introduced CO 2 , S, and K 2 O, and redistributed SiO 2 . Arsenian pyrite associated with the alteration weathers to produce goethite and jarosite on pit walls and in joints, as well as copiapite and hexahydrite efflorescences that accumulate on wall-rock faces during dry California summers. All of these pyrite weathering products incorporate arsenic at concentrations from <100 up to 1,200 ppm. In the pit lake, pH and TDS reach seasonal highs in the summer epilimnion; pH is lowest in the summer hypolimnion. Arsenic and bicarbonate covary in the hypolimnion, rising as stratification proceeds and declining during winter rains. The computational model suggests that water fluxes alone do not account for this seasonal variability. Loss of CO 2 to the atmosphere, interaction with pit walls including washoff of efflorescent salts during the first flush and seasonal rainfall, and arsenic sorption appear to contribute to the observed pit-lake characteristics.

California↗

USGS2002

Hydrogeochemical investigations of historic mining districts, central western slope of Colorado, including influence on surface-water quality

This report describes reconnaissance hydrogeochemical investigations of 22 mining districts on the Western Slope of Colorado in the Gunnison and Uncompahgre National Forests and adjacent public lands administered by the Bureau of Land Management. Sources and fates of contaminants from historic mines, mine waste, and mill tailings are interpreted from chemical analyses for 190 samples of surface waters; 185 samples of mined rocks, mill tailings, and altered rocks; and passive leach analyses of 116 samples of those mineralized materials. Short reaches of several headwater streams show relatively low level effects of historic mining; the headwaters of the Uncompahgre River are highly contaminated by mines and unmined altered rocks in the Red Mountain district. There is encouraging evidence that natural processes attenuate mine-related contamination in most districts.

Colorado↗

USGS2003

Preliminary geologic map of the Winchester 7.5' quadrangle, Riverside County, California

The Winchester quadrangle is located in the northern part of the Peninsular Ranges Province within the central part of the Perris block, a relatively stable, rectangular in plan view, area located between the Elsinore and San Jacinto fault zones (see location map). The quadrangle is underlain by Cretaceous and older basement rocks. Cretaceous plutonic rocks are part of the composite Peninsular Ranges batholith, which indicates wide variety of granitic rocks, ranging from granite to gabbro. Parts of three major plutonic complexes are within the quadrangle, the Lakeview Mountains pluton, the Domenigoni Valley pluton and the Paloma Valley ring complex. In the northern part of the quadrangle is the southern part of the Lakeview Mountains pluton, a large composite body, most of which lies in the quadrangle to the north. In the center part of the quadrangle is the eastern part of the Domenigoni Valley pluton, which consists of massive biotite-hornblende granodiorite and tonalite; some tonalite in the southern part of the pluton has a relatively pronounced foliation produced by oriented biotite and hornblende. Common to abundant equant-shaped, mafic inclusions occur through out the pluton except in the outermost part where inclusions are absent. The pluton was passively emplaced by piecemeal stoping of a variety of older rocks and the eastern contact is well exposed in the quadrangle. Associated with the Domenigoni Valley pluton is a swarm of latite dikes; the majority of these dikes occur in the Winchester quadrangle, but they extend into the Romoland quadrangle to the west. The latite dikes intrude both the pluton and adjacent metamorphic rocks, most are foliated, and most have a well developed lineation defined by oriented biotite and/or hornblende crystals. Dikes intruding the pluton were emplaced in northwest striking joints; and dikes intruding the metamorphic rocks were emplaced along foliation planes. In the eastern part of the quadrangle a Cretaceous age suture juxtaposes low-metamorphic grade Mesozoic rocks against high-metamorphic grade gneissic-textured Mesozoic rocks. Juxtaposition occurred when the high-metamorphic grade rocks were at upper amphibolite grade temperatures, and produced a steep thermal gradient in the low-metamorphic grade Mesozoic rocks. Age of suturing and attendant metamorphism, based on metamorphic mineral ages, is about 100 Ma (L. Snee, personal communication, 2002). The suture zone appears to vary in thickness, and includes within it a number of metadunite bodies and related rocks. Prebatholithic rocks of Mesozoic age include a wide variety of sedimentary rocks of greenschist or lower metamorphic grade, in the western and central part of the quadrangle, and upper amphibolite grade near the eastern edge of the quadrangle. The metamorphic grade increases from greenschist to upper amphibolite grade over a distance of less than two miles; andalusite and sillimanite isograds are closely spaced near the suture. Metamorphism was Buchan type of relatively high temperature and relatively low pressure (Schwarcz, 1969). Common lithologies of the low metamorphic grade suite include phyllite, lithic greywacke, impure quartzite, meta-arkose, and interlayered quartzite and phyllite. Most of the layering and foliation in the metamorphic rocks is the result of intense structural transposition. Relic bedding appears to be restricted to very local occurrences in hinges of slip folds. The upper amphibolite grade, gneissic-textured Mesozoic rocks consist of sillimanite-biotite gneiss, black amphibolite, and impure quartzite. Anatectic gneiss containing igneous textured segregations of quartz and feldspar is commonly inter leaved with biotite gneiss.

Open-File Report↗

USGS1951

Indian Creek uranium prospects, Beaver County, Utah

The secondary uranium minerals metatorbernite (?) and autunite (?) were discovered at Indian Creek in the spring of 1950. The deposits, in sec. 26, T. 27 S., R. 6 T., Beaver County, Utah, are 20 miles west of Marysvale, and about three-eighths of a mile east of a quartz monzonite stock. The uranium minerals are sparsely disseminated in argillized and silicified earlier Tertiary Bullion Canyon latite and related volcanic rock beneart, but close to, the contact of the overlying later Tertiary Mount Belknap gray rhyolite. The prospects are in a landslide area where exposures are scarce. Therefore, trend and possible continuity of the altered and the uraniferous zones cannot be established definitely. The occurrence of secondary uranium minerals in beidellite-montmorillonite rock, formed by alteration of earlier Tertiary rocks near a quartz monzonite stock, is similar to that in some of the deposits in the Marysvale uranium district.

Open-File Report↗

USGS1987

The U.S. Midcontinent: a new frontier for mineral exploration.

The north-central US Midcontinent is underlain by a considerable thickness of sedimentary rocks, mostly Paleozoic, which lie upon a heterogeneous basement of Precambrian granitoid and metamorphic rocks. This article describes a representative sample of Midcontinent geology and explains why the authors believe this region is a 'new frontier' for mineral exploration and discovery. -Authors

Episodes↗

USGS1964

Nickeliferous laterites in southwestern Oregon and northwestern California

Deposits of ferruginous nickeliferous lateritic soils formed by weathering in place of ultramafic rocks occur at several places in northwestern California and southwestern Oregon, mostly in the Klamath Mountains province. Most of the deposits have been derived from relatively fresh peridotite, although at least one deposit was formed on serpentinite. The accumulations of lateritic soil are on flat-lying to gently sloping surfaces in a terrain that has been extensively dissected and deeply entrenched.The thickness of the deposits ranges from a few feet to more than 50 feet, and may vary widely in any given deposit, for the bedrock surface is commonly highly irregular. The deposit at Nickel Mountain, Oregon, is unique, because it is the only one in which the nickel silicate, garnierite, is plentiful. At Nickel Mountain, garnierite, accompanied by abundant microcrystalline quartz, occurs in veinlike bodies and boxworks that lie at the base of the soil zone and persist in depth along joints and fractures into the underlying slightly weathered or fresh peridotite.Mineralogical studies and chemical analyses show that weathering of the ultramafic rocks destroyed olivine and much of the orthopyroxene and serpentine minerals. Secondary minerals formed are predominantly hydrated ferric oxides (goethite); minor amounts of a montmorillonite mineral, chlorite, and talc were also identified. The kaolin group and bauxite minerals were not found. Except for garnierite at the Nickel Mountain deposit, no nickel-bearing mineral was identified. Nickel may occur, however, in montmorillonite, chlorite, and talc where it substitutes for Mg to a limited extent; in serpentine minerals that were not destroyed by weathering; and possibly in combination with ferric hydroxides. Cobalt may also occur in the clay minerals and probably is associated with trace amounts of manganese oxide or hydroxides.The lateritic soils in northwestern California and southwestern Oregon are similar to soils formed by lateritic weathering of ultramafic rocks in Cuba, the Philippines, New Caledonia, and other tropical regions of the world. They have, however, a higher content of SiO 2 and MgO, and a lower content of Fe 2 O 3 than deposits formed in tropical climates. The California and Oregon deposits are considerably smaller and lower in average metal content which, because they are widely scattered in a rugged, relatively isolated terrain, makes them unpromising as likely reserves for commercial exploitation in the foreseeable future.Most of the deposits are regarded as having been formed by chemical weathering in a climate having alternating wet and dry seasons, probably similar to that prevailing today. Their age is uncertain but may range from post-Miocene to Pleistocene.

California, Oregon↗

USGS2007

Major Crustal Fault Zone Trends and Their Relation to Mineral Belts in the North-Central Great Basin, Nevada

The Great Basin physiographic province covers a large part of the western United States and contains one of the world's leading gold-producing areas, the Carlin Trend. In the Great Basin, many sedimentary-rock-hosted disseminated gold deposits occur along such linear mineral-occurrence trends. The distribution and genesis of these deposits is not fully understood, but most models indicate that regional tectonic structures play an important role in their spatial distribution. Over 100 magnetotelluric (MT) soundings were acquired between 1994 and 2001 by the U.S. Geological Survey to investigate crustal structures that may underlie the linear trends in north-central Nevada. MT sounding data were used to map changes in electrical resistivity as a function of depth that are related to subsurface lithologic and structural variations. Two-dimensional (2-D) resistivity modeling of the MT data reveals primarily northerly and northeasterly trending narrow 2-D conductors (1 to 30 ohm-m) extending to mid-crustal depths (5-20 km) that are interpreted to be major crustal fault zones. There are also a few westerly and northwesterly trending 2-D conductors. However, the great majority of the inferred crustal fault zones mapped using MT are perpendicular or oblique to the generally accepted trends. The correlation of strike of three crustal fault zones with the strike of the Carlin and Getchell trends and the Alligator Ridge district suggests they may have been the root fluid flow pathways that fed faults and fracture networks at shallower levels where gold precipitated in favorable host rocks. The abundant northeasterly crustal structures that do not correlate with the major trends may be structures that are open to fluid flow at the present time.

Open-File Report↗

USGS2024

Apatite and monazite geochemistry record magmatic and metasomatic processes in rare earth element mineralization at Mountain Pass, California

The largest rare earth element (REE) deposit in the United States is a carbonatite intrusion at Mountain Pass in the Mojave Desert, California. Despite a clear spatiotemporal association of alkaline silicate and carbonatite intrusions at Mountain Pass, a genetic model of their mutual formation has not been resolved. The Mountain Pass carbonatite has long been upheld as an example of a primary magmatic body, but recent work has suggested it could be fluid-derived. This study investigates the geochemistry of apatite and monazite grains from the alkaline silicate and carbonatite stocks and dikes of the Mountain Pass district, to elucidate the magmatic history of the intrusive suite and identify the role of fluids in rare earth element mineralization. Three apatite populations are identified in the alkaline silicate rocks. A primary magmatic apatite group supports intrusion of the stocks as separate pulses of magma derived from a spatially extensive metasomatized mantle source region. The second group implicates the role of a regional fluid that mobilized light rare earth elements from apatite grains. A minor group of inherited apatite cores, identified by low Sr and negative Eu anomalies, supports assimilation of crustal material in the formation of the intrusive suite. Analyses of monazite and apatite grains from the carbonatite orebody also reveal a mix of primary magmatic and metasomatic (fluid-related) minerals. Compositional similarities between primary phosphates in the carbonatite and alkaline silicate rocks support a genetic link between the intrusive suites. The presence of fluids regionally and within the carbonatite orebody indicates the Mountain Pass carbonatite should not be classified as a purely magmatic REE deposit.

Arizona, California, Nevada↗

USGS2012

Alaska Geochemical Database - Mineral Exploration Tool for the 21st Century - PDF of presentation

The U.S. Geological Survey has created a geochemical database of geologic material samples collected in Alaska. This database is readily accessible to anyone with access to the Internet. Designed as a tool for mineral or environmental assessment, land management, or mineral exploration, the initial version of the Alaska Geochemical Database - U.S. Geological Survey Data Series 637 - contains geochemical, geologic, and geospatial data for 264,158 samples collected from 1962-2009: 108,909 rock samples; 92,701 sediment samples; 48,209 heavy-mineral-concentrate samples; 6,869 soil samples; and 7,470 mineral samples. In addition, the Alaska Geochemical Database contains mineralogic data for 18,138 nonmagnetic-fraction heavy mineral concentrates, making it the first U.S. Geological Survey database of this scope that contains both geochemical and mineralogic data. Examples from the Alaska Range will illustrate potential uses of the Alaska Geochemical Database in mineral exploration. Data from the Alaska Geochemical Database have been extensively checked for accuracy of sample media description, sample site location, and analytical method using U.S. Geological Survey sample-submittal archives and U.S. Geological Survey publications (plus field notebooks and sample site compilation base maps from the Alaska Technical Data Unit in Anchorage, Alaska). The database is also the repository for nearly all previously released U.S. Geological Survey Alaska geochemical datasets. Although the Alaska Geochemical Database is a fully relational database in Microsoft® Access 2003 and 2010 formats, these same data are also provided as a series of spreadsheet files in Microsoft® Excel 2003 and 2010 formats, and as ASCII text files. A DVD version of the Alaska Geochemical Database was released in October 2011, as U.S. Geological Survey Data Series 637, and data downloads are available at http://pubs.usgs.gov/ds/637/ . Also, all Alaska Geochemical Database data have been incorporated into the interactive U.S. Geological Survey Mineral Resource Data web portal, available at http://mrdata.usgs.gov/ .

Alaska↗

USGS1982

Geochemical orientation for mineral exploration in the Hashemite Kingdom of Jordan

This report is a supplement to previous accounts of geochemical exploration conducted in the Hashemite Kingdom of Jordan by the Natural Resources Authority of the Royal Government of Jordan and the U.S. Geological Survey. The field work on which this report is based was sponsored by the U.S. Agency for International Development, U.S. Department of State. Procedures used in collecting various kinds of rocks, ores, slags, eluvial and alluvial sediments, heavy-mineral concentrates, and organic materials for use as geochemical sample media are summarized, as are the laboratory procedures followed for the analysis of these sample materials by semiquantitative spectrographic, atomic absorption, fluorometric, and X-ray diffraction methods. Geochemical evaluations of the possibilities for economic mineral deposits in certain areas are presented. The results of these preliminary investigations open concepts for further use in geochemical exploration in the search for metallic mineral deposits in Jordan. Perhaps the most desirable new activity would be hydrogeochemical exploration for uranium and base metals, accompanied by interpretation of such remote-sensing data as results of airborne radiometric surveys and computer-enhanced LANDSAT imagery. For more conventional approaches to geochemical exploration, however, several fundamental problems regarding proper choice of geochemical sample media for different geologic and geographic parts of the Country must be solved before effective surveys can be made. The present results also show that such common geochemical exploration techniques as the determination of the trace-element contents of soils, plant ash, and slags have direct application also toward the resolution of several archaeological problems in Jordan. These include the relation of trace-elements chemistry of local soils to the composition of botanic remains, the trace-elements composition of slags to the technological development of the extractive metallurgy of copper and iron in the region, and the use of charcoal from slags for the C-14 dating of periods of archaeometallurgical activity. Less directly, interpretations based on the distribution in time and space of the archaeometallurgical activities of the region might add to the knowledge of early climatic conditions and vegetative cover of the area.

Open-File Report↗

USGS2010

Polybaric evolution of phonolite, trachyte, and rhyolite volcanoes in eastern Marie Byrd Land, Antarctica: Controls on peralkalinity and silica saturation

In the Marie Byrd Land volcanic province, peralkaline and metaluminous trachytes, phonolites, and rhyolites occur in 18 large shield volcanoes that are closely associated in time and space. They are arrayed radially across an 800 km wide structural dome, with the oldest at the crest and the youngest around the flanks. Several lines of evidence suggest that these rocks evolved via opensystem, polybaric fractionation. We have used mass balance modeling of major elements together with trace-element data and mineral chemistry to help explain the evolution of this diverse suite of felsic rocks, which appear to have been generated coevally in isolated magma chambers, and erupted close to each other in patterns related to tectonic uplift and extension within the West Antarctic rift system. Isotopic and trace-element data indicate that this occurred with only minimal crustal contamination. We focus on volcanoes of the Executive Committee Range and Mount Murphy, where we find good representation of basalts and felsic rocks within a small area. Our results suggest that the felsic rocks were derived from basaltic magmas that differentiated at multiple levels during their passage to the surface: first to ferrogabbroic compositions near the base of the lithosphere, then to intermediate compositions near the base of the crust, and finally to felsic compositions in mid- to upper crustal reservoirs. The high-pressure history has been largely masked by low-pressure processes. The best indications of a high-pressure history are the mineral phases in cumulate nodules and their correlation with modeling results, with REE anomalies, and with the composition of an unusual gabbroic intrusion. Silica saturation characteristics are believed to have originated in magma chambers near the base of the crust, via fractionation of variable proportions of kaersutite and plagioclase. Development of peralkalinity in felsic rocks took place in upper crustal reservoirs by fractionating a high ratio of plagioclase to clinopyroxene under conditions of low pH 2 O. With increasing pH 2 O, the ratio plagioclase/clinopyroxene in the fractionated assemblage decreases and metaluminous liquids resulted. Crustal contamination seems to have had a role in suppressing peralkalinity , and was probably a factor in the origin of high- silica metaluminous rhyolite , but metaluminous rocks are uncommon. The volume and diversity of felsic rocks were probably enhanced by the structure of the lithosphere, the persistence of plume activity, and the immobility of the Antarctic plate. Mechanical boundaries at the base of the lithosphere and crust, and within the crust, appear to have acted as filters, trapping magmas at multiple levels, and prolonging the fractionation process. Final volumes would have been further enhanced by repeated refluxing of the same magma chambers, controlled by plume activity and plate immobility.

International Geology Review↗

USGS2007

Barite-forming environments along a rifted continental margin, Southern California Borderland

The Southern California Continental Borderland (SCCB) is part of the broad San Andreas transform-fault plate boundary that consists of a series of fault-bounded, petroleum-generating basins. The SCCB has high heat flow and geothermal gradients produced by thinned continental crust and Neogene volcanism. Barite deposits in the SCCB occur along faults. Barite samples from two sea-cliff sites and four offshore sites in the SCCB were analyzed for mineralogy, chemical (54 elements) and isotopic (S, Sr) compositions, and petrography. Barite from Palos Verdes (PV) Peninsula sea-cliff outcrops is hosted by the Miocene Monterey Formation and underlying basalt; carbonate rocks from those outcrops were analyzed for C, O, and Sr isotopes and the basalt for S isotopes. Cold-seep barite from Monterey Bay, California was analyzed for comparison. SCCB offshore samples occur at water depths from about 500 to 1800 m. Those barites vary significantly in texture and occurrence, from friable, highly porous actively growing seafloor mounds to dense, brecciated, vein barite. This latter type of barite contrasts with cold-seep barite in being much more coarse grained, forms thick veins in places, and completely replaced rock clasts in breccia. The barite samples range from 94 to 99 wt% BaSO4, with low trace-element contents, except for high Sr, Zr, Br, U, and Hg concentrations compared to their crustal abundances. δ34S for SCCB offshore barites range from 21.6‰ to 67.4‰, and for PV barite from 62‰ to 70‰. Pyrite from PV sea-cliff basalt and sedimentary rocks that host the barites averages 7.8‰ and 2.2‰, respectively. Two offshore barite samples have δ34S values (21.6‰, 22.1‰) close to that of modern seawater sulfate, whereas all other samples are enriched to strongly enriched in 34S. 87Sr/86Sr ratios for the barites vary over a narrow range of 0.70830–0.70856 and are much lower than that of modern seawater and also lower than the middle Miocene seawater ratio, the time of deposition of the host rocks for the PV samples. This indicates that the mineralizing fluids were not unaltered seawater. We develop a model in which the barites precipitated both below the sediment–water interface and at the seafloor from low-temperature fluids that circulated along faults. The isotopic, chemical, and textural data indicate that the barites formed by several processes. Mesozoic and Cenozoic basement rocks (crystalline and overlying sedimentary rocks), Quaternary basin fill, turbidite fans, and seawater provided various elements for the barites in different environments. The fluids had a deep-seated source and were hydrothermal in the deeper parts of the system for all the barite types, including the seafloor cold-seep deposit, based on Sr isotopes and regional geothermal gradients. These deep-seated fluids mixed with other fluids as they ascended, including seawater at and near the seafloor. The high δ34S values may have resulted from extreme Rayleigh fractionation during bacterially mediated (semi)closed-system sulfate reduction, probably driven by the flux of methane- and hydrocarbon-bearing fluids through basement rocks and basin sediments. Early diagenetic dolomite and pyrite in the host Monterey Formation in the PV Headland also formed in a zone of sulfate reduction, but within sediment buried only centimeters to a few meters and with a predominantly seawater source for the sulfur. Dolomite occurring with vein barite in the PV Headland formed at temperatures in the range of 40–90 °C. The cold-seep barites have δ34S values near that of modern seawater, although still somewhat fractionated. The barites that precipitated below the sediment–water interface have higher δ34S values, suggesting that the fluids were relatively reduced with molar dissolved barium in excess of dissolved sulfate. Those samples were exposed at the seafloor by uplift along faults and are composed predominantly of massive, brecciated, and vein barite.

California↗

USGS1989

Sulfide mineralization and magnetization, Cement oil field, Oklahoma

Geochemical, petrographic, and rock-magnetic studies were undertaken to investigate possible sources for reported positive aeromagnetic anomalies over the Cement oil field, Oklahoma. Ferrimagnetic pyrrhotite (monoclinic, Fe 7 S 8 ), intergrown with more-abundant, nonmagnetic pyrite (FeS 2 ), is present in well-cutting, core, and quarry samples at Cement, and it is the only identified source of possible enhanced magnetization in rocks over the field. Magnetite, found only in well cuttings from Cement, is contamination from drilling. Magnetite was considered previously by others to be the source of magnetic anomalies at Cement.

Oklahoma↗

USGS2024

Onset and tempo of ignimbrite flare-up volcanism in the eastern and central Mogollon-Datil volcanic field, southern New Mexico, USA

The Cenozoic ignimbrite flare-up (40–18 Ma) generated multiple volcanic fields in the southwestern United States and northern Mexico resulting from asthenospheric mantle upwelling after removal of the Farallon slab. The correlation of tuffs to one another and to source calderas within these volcanic fields is essential for determining spatiotemporal patterns in volcanism and magma geochemistry, which have been used to deduce migration of the Farallon slab at depth and associated mantle melting. However, the correlation of Eocene–Oligocene tuffs in the southwestern U.S. is difficult because of post-emplacement erosion and faulting. This study focuses on spatiotemporal patterns of the initial episode of ignimbrite flare-up activity (ca. 36.5–33.8 Ma) in the Mogollon-Datil volcanic field in south-central New Mexico, USA. We show that alkali feldspar major and trace element geochemistry is an effective tool for correlating tuffs when combined with high-precision, single-crystal 40 Ar/ 39 Ar geochronology and bulk-rock geochemistry. Using these data, we correlate several tuff units and differentiate other tuffs that have the same eruption age but very different geochemistry, and we conclude that there was a broadly northwestward migration in volcanism over time. The new tuff correlations are used to investigate spatiotemporal variations in magma geochemistry, erupted volumes, and recurrence intervals during the initial episode of Mogollon-Datil volcanic field volcanism. Early-erupted tuffs restricted to the eastern Mogollon-Datil volcanic field share similarities with western U.S. topaz rhyolites, which suggests that the silicic magmas were generated by partial melting of mafic lower crustal rocks. We also find differences in the compositions, crystallinities, and mineral assemblages between the early- and late-erupted tuffs. The early-erupted tuffs tend to have single-feldspar mineralogies, lower feldspar Or contents, large negative Eu anomalies, and low-whole–rock Ba concentrations. Conversely, late-erupted tuffs have two feldspar plus quartz assemblages, lesser Eu anomalies, higher whole-rock Ba concentrations, and feldspars have higher Or contents. Thus, we suggest that for some of the early eruptions, after magmas underwent crystal fractionation in the crust, the silicic melt largely separated from the crystalline mush prior to eruption, whereas late-erupted tuff magmas underwent crystal fractionation at near the eutectic minimum and were remobilized and erupted with a larger proportion of their crystalline mush. Using our new ages, correlations, and previously published data, we find that the initial phase of Mogollon-Datil volcanic field volcanism produced at least 15 eruptions between 36.5 Ma and 33.8 Ma, with a minimum total erupted volume of ~1350 km 3 and an average recurrence interval of 170 k.y. However, eruptions were generally smaller in volume (most <15 km 3 ) than in other coeval fields, and most eruptions (n = 11) occurred in the first 1.2 m.y. (ca. 36.5–35.3 Ma) of activity. Altogether, our work sheds new light on variations in the composition, timing, and migration of volcanism during the initial phase of Mogollon-Datil volcanic field activity and highlights the utility of feldspar geochemistry in both “fingerprinting” tuffs and elucidating magma evolution.

New Mexico↗

USGS2019

Tourmaline boron and strontium isotope systematics reveal magmatic fluid pulses and external fluid influx in a giant iron oxide-apatite (IOA) deposit

Tourmaline is a common boron-bearing mineral in hydrothermal system and has been widely used as a mineral probe to reconstruct geological processes because of its broad range in composition and resistance to metasomatic alteration. The origin of Kiruna-type iron oxide-apatite (IOA) deposits, commonly linked to andesitic subvolcanic or volcanic rocks, is highly controversial. Constraints on the evolution of these mineralizing systems are needed to advance understanding of the ore-forming process. In this study, we apply in situ elemental and combined B-Sr isotopic analyses of tourmaline to elucidate the nature and evolution of the subsurface hydrothermal system associated with IOA mineralization in the giant Taocun deposit, eastern China. Taocun is hosted at the top of a diorite intrusion and exhibits three stages of hydrothermal alteration that contain tourmaline: pre-ore Na alteration (Tur I), syn-ore magnetite formation and associated Ca-Fe alteration (Tur II), and post-ore Ca-Mg alteration with sulfide veins (Tur III). Compositional data for each stage of tourmaline plot along the “oxy-dravite”–povondraite join, which is indicative of precipitation from relatively oxidizing fluids. Ranges of Sr-isotopic compositions in Tur I (0.7065–0.7078) and Tur II (0.7068–0.7076) are identical to those of the igneous host rocks, indicating precipitation from magmatic-hydrothermal fluids. The range of B-isotopic compositions in Tur I (δ 11 B values of −6.3‰ to −1.2‰) is also consistent with a magmatic source. Higher δ 11 B values (−2.4‰ to 5.4‰) obtained from Tur II are mainly ascribed to Rayleigh fractionation in the magmatic-hydrothermal system as tourmaline precipitated. Post-ore Tur III has a wide range of mostly lower B-isotopic compositions (−8.5‰ to 0.8‰) that record another pulse of magmatic fluid input. This interpretation is supported by the enrichment of Na, Li, Be, W, Sn, V, and Ti in Tur III, relative to Tur I and II. However, the higher Sr-isotope composition (0.7076–0.7086) of Tur III and available O-isotope composition (−7‰ to 3.5‰) of fluids of this stage record the infiltration of meteoric ground water from adjacent sedimentary country rocks. The results suggest that the Taocun IOA deposit formed in a magmatic-hydrothermal system characterized by two (or more) pulses of magmatic fluid discharge from subvolcanic diorite intrusions, followed by the influx of external ground water as the system waned. This study highlights the utility of tourmaline as a robust geochemical and isotopic monitor of ore-forming processes in such systems.

Ningwu IOA district↗