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At least 811 records · Page 45Linked to original sources
USGS2016

Rare earths: Market disruption, innovation, and global supply chains

Rare earths, sometimes called the vitamins of modern materials, captured public attention when their prices increased more than ten-fold in 2010 and 2011. As prices fell between 2011 and 2016, rare earths receded from public view—but less visibly they became a major focus of innovative activity in companies, government laboratories and universities. Geoscientists worked to better understand the resource base and improve our knowledge about mineral deposits that will be mines in the future. Process engineers carried out research that is making primary production and recycling more efficient. Materials scientists and engineers searched for substitutes that will require fewer or no rare earths while providing properties comparable or superior to those of existing materials. As a result, even though global supply chains are not significantly different now than they were before the market disruption, the innovative activity motivated by the disruption likely will have far-reaching, if unpredictable, consequences for supply chains of rare earths in the future.

Environment and Resources↗
USGS2012

Electrical structure of Newberry Volcano, Oregon

From the interpretation of magnetotelluric, transient electromagnetic, and Schlumberger resistivity soundings, the electrical structure of Newberry Volcano in central Oregon is found to consist of four units. From the surface downward, the geoelectrical units are (1) very resistive, young, unaltered volcanic rock, (2) a conductive layer of older volcanic material composed of altered tuffs, (3) a thick resistive layer thought to be in part intrusive rocks, and (4) a lower-crustal conductor. This model is similar to the regional geoelectrical structure found throughout the Cascade Range. Inside the caldera, the conductive second layer corresponds to the steep temperature gradient and alteration minerals observed in the USGS Newberry 2 test hole. Drill hole information on the south and north flanks of the volcano (test holes GEO N-1 and GEO N-3, respectively) indicates that outside the caldera the conductor is due to alteration minerals (primarily smectite) and not high-temperature pore fluids. On the flanks of Newberry the conductor is generally deeper than inside the caldera, and it deepens with distance from the summit. A notable exception to this pattern is seen just west of the caldera rim, where the conductive zone is shallower than at other flank locations. The volcano sits atop a rise in the resistive layer, interpreted to be due to intrusive rocks. The intrusive material has served as a heat source to produce enhanced hydrothermal alteration and, perhaps in the case of the west-flank anomaly, elevated fluid temperatures. While no public drill hole information is available to confirm this hypothesis, the west-flank anomaly appears to be a good geothermal target. In addition to the possibility that a region on the west side of the volcano could be favorable for prospecting, part of the resistive structure under the center of the volcano could be due to a vapor-dominated environment with temperatures above 300°C. In other parts of the Cascades, pervasive alteration has produced mixed layer clays and zeolites, resulting in low-resistivity anomalies. Low resistivities cannot be assumed to indicate high-temperature pore fluids. The use of electrical methods that measure resistivity as a function of excitation frequency, such as spectral induced polarization, may provide a way of obtaining information about the type and extent of alteration.

Journal of Geophysical Research Solid Earth↗
USGS2025

lasertram: A Python library for time resolved analysis of laser ablation inductively coupled plasma mass spectrometry data

Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) data has a wide variety of uses in the geosciences for in-situ chemical analysis of complex natural materials. Improvements to instrument capabilities and operating software have drastically reduced the time required to generate large volumes of data relative to previous methodologies. Raw data from LA-ICP-MS, however, is in counts per unit time (typically counts per second), not elemental concentrations and converting these count ratesto concentrations requires additional processing. For complex materials where the ablated volume may contain a range of material compositions, a moderate amount of user input is also required if appropriate concentrations are to be accurately calculated. In geologic materials such as glasses and minerals that potentially have numerous heterogeneities (e.g., microlites or other inclusions) within them, this is typically determiningwhether the total ablation signal should be filtered to remove these heterogeneities. This necessitates that the LA-ICP-MS data processing pipeline is one that is not automated, but is also designed to enable rapid and efficient processing of large volumes of data. Here we introduce , a Python library for the time resolved analysis of LA-ICP-MS data. We outline its mathematical theory, code structure, and provide an example of how it can be used to provide the time resolved analysis necessitated by LA-ICP-MS data of complex geologic materials. Throughout the pipeline we show how metadata and data are incrementally added to the objects created such that virtually any aspect of an experiment may be interrogated and its quality assessed. We also show, that when combined with other Python libraries for building graphical user interfaces, it can be utilized outside of a pure scripting environment. can be found at https://doi.org/10.5066/P1DZUR3Z

Applied Computing and Geosciences↗
USGS2003

Excess nitrogen in selected thermal and mineral springs of the Cascade Range in northern California, Oregon, and Washington: Sedimentary or volcanic in origin?

Anomalous N 2 /Ar values occur in many thermal springs and mineral springs, some volcanic fumaroles, and at least one acid-sulfate spring of the Cascade Range. Our data show that N 2 /Ar values are as high as 300 in gas from some of the hot springs, as high as 1650 in gas from some of the mineral springs, and as high as 2400 in gas from the acid-sulfate spring on Mt. Shasta. In contrast, gas discharging from hot springs that contain nitrogen and argon solely of atmospheric origin typically exhibits N 2 /Ar values of 40–80, depending on the spring temperature. If the excess nitrogen in the thermal and mineral springs is of sedimentary origin then the geothermal potential of the area must be small, but if the nitrogen is of volcanic origin then the geothermal potential must be very large. End-member excess nitrogen (δ 15 N) is +5.3‰ for the thermal waters of the Oregon Cascades but is only about +1‰ for fumaroles on Mt. Hood and the acid-sulfate spring on Mt. Shasta. Dissolved nitrogen concentrations are highest for thermal springs associated with aquifers between 120 and 140°C. Chloride is the major anion in most of the nitrogen-rich springs of the Cascade Range, and N 2 /Ar values generally increase as chloride concentrations increase. Chloride and excess nitrogen in the thermal waters of the Oregon Cascades probably originate in an early Tertiary marine formation that has been buried by the late Tertiary and Quaternary lava flows of the High Cascades. The widespread distribution of excess nitrogen that has been generated in low to moderate-temperature sedimentary environments is further proof of the restricted geothermal potential of the Cascade Range.

Cascade Range↗
USGS1987

Mineralogy and petrology of the Cretaceous- Tertiary boundary clay bed and adjacent clay-rich rocks, Raton Basin, New Mexico and Colorado.

The Cretaceous-Tertiary (K-T) boundary is preserved in a sequence of coal-bearing, fluvial rocks in the lower part of the Raton Formation (Late Cretaceous and Paleocene) at several sites in the east-central part of the Raton Basin. The K-T boundary occurs at the top of a kaolinitic claystone layer, commonly referred to as the "boundary clay layer," in an interval of coal and carbonaceous shale. The boundary is defined by the disappearance of certain fossil-pollen taxa. The boundary clay layer also contains shocked quartz grains and abundance anomalies of iridium, chromium, and other elements. Each of these characteristics support the hypothesis of an asteroid impact at the end of the Cretaceous. Small goyazite spheres were also found in the boundary clay bed; however, their origin is uncertain. X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and thin-section petrography have shown that the boundary clay bed exhibits unique mineralogic and petrologic characteristics not possessed by other clay-rich beds in coal-bearing rocks of the Raton Basin. The boundary clay bed is composed primarily of well-crystallized kaolinite but also contains subordinate, randomly interstratified, mixed-layer illite/smectite, both of which appear to have been formed by the alteration of vitreous material in a coal-swamp environment. The bulk mineralogy of the boundary clay bed is similar to that of other kaolinite-rich clay beds (tonsteins) that altered in coal swamps from airfall volcanic ash. The alteration process and diagenetic products of the host material in the boundary clay bed, however, differed from those of the tonsteins, resulting in a unique petrographic fabric. The boundary clay bed is characterized by an overall imbricate fabric that may reflect an original vitreous material that included shards, bubbles, and spheres. The original fallout material of the boundary clay bed first altered to "cabbage-like" microspherules, indicating a halloysite or allophane precursor, and then to well-crystallized kaolinite; the well-crystallized kaolinite is the diagenetic stable phase for these rocks at their maximum burial conditions. In comparison, the vitreous components of the tonsteins were altered directly to coarse vermicular and platey kaolinite. Alteration of the original fallout material in the boundary bed was probably rapid, leading to hydrated, disordered, fine-grained clay minerals that formed into curled spherical or tubular shapes. The factors that produced these unique fabrics in the boundary clay bed existed at all K-T sites in the Raton Basin and were much different from those that formed the coarse platey and vermicular fabrics of ordinary tonsteins. The distinctive character of the boundary clay may be due to the unique nature and chemistry of the fallout material and (or) physical or chemical conditions existing shortly after its deposition.

Journal of Sedimentary Petrology↗
USGS2012

Porphyry copper assessment of the Mesozoic of East Asia: China, Vietnam, North Korea, Mongolia, and Russia: Chapter G in Global mineral resource assessment

The U.S. Geological Survey (USGS) collaborated with the China Geological Survey (CGS) to conduct a mineral resource assessment of Mesozoic porphyry copper deposits in East Asia. This area hosts several very large porphyry deposits, exemplified by the Dexing deposit in eastern China that contains more than 8,000,000 metric tons of copper. In addition, large parts of the area are undergoing active exploration and are likely to contain undiscovered porphyry copper deposits. Three tracts were delineated to be permissive for Mesozoic porphyry copper deposits in East Asia: the Manchuride, Coastal Pacific, and East Qinling tracts, all Jurassic through Cretaceous in age. The tracts are based on mapped and inferred subsurface distributions of igneous rocks that define areas where the occurrence of porphyry copper deposits is possible. These tracts range in area from about 170,000 to about 1,400,000 km 2 . Although maps at a variety of scales were used in the assessment, the final tract boundaries are intended for use at a scale of 1:1,000,000. These Mesozoic deposits in East Asia all formed in post-subduction environments, environments newly recognized as permissive for the occurrence of porphyry copper deposits. Based on the grade, tonnage, and geologic characteristics of the known deposits, two tracts, Manchuride and Coastal Pacific, were evaluated using the general (Cu-Mo-Au) porphyry copper grade and tonnage model. The East Qinling tract was evaluated using the molybdenum-rich (Cu-Mo) model. Assessment participants estimated numbers of undiscovered deposits at different levels of confidence for each permissive tract. These estimates were then combined with the selected grade and tonnage models using Monte Carlo simulation to generate quantitative probabilistic estimates of undiscovered resources. Resources in future extensions of deposits with identified resources were not specifically evaluated. Assessment results, presented in tables and graphs, show mean amounts of metal and rock in undiscovered deposits at different quantile levels, as well as the arithmetic mean for each tract. This assessment estimated a mean total of about 44 undiscovered porphyry copper deposits within the assessed permissive tracts in East Asia. This represents nearly 4 times the 12 known deposits. Predicted mean (arithmetic) resources that could be associated with these undiscovered deposits are about 198,000,000 metric tons (t) of copper and about 3,900 t of gold, as well as byproduct molybdenum and silver. The reported identified resources for those 12 known deposits total about 23,000,000 t of copper and about 850 t of gold. The assessment area is estimated to contain nearly nine times as much copper in undiscovered porphyry copper deposits as has been identified to date. This report includes an overview of the assessment results and summary tables. Descriptions of each tract are included in appendixes, with estimates of numbers of undiscovered deposits, and probabilistic estimates of amounts of copper, molybdenum, gold, and silver that could be contained in undiscovered deposits for each permissive tract. A geographic information system that accompanies the report includes tract boundaries and a database of known porphyry copper deposits and prospects.

Scientific Investigations Report↗
USGS2017

Soils mediate the impact of fine woody debris on invasive and native grasses as whole trees are mechanically shredded into firebreaks in piñon-juniper woodlands

To stem wildfires, trees are being mechanically shredded into firebreaks with the resulting fine woody debris (FWD) potentially exerting immense control over soil and plants. We linked FWD-induced changes in microbial activity and nutrient availability to the frequency of Bromus tectorum and three native, perennial grasses across 31 piñon-juniper woodlands, UT, USA. Using a series of mixed models, we found that FWD increased the frequency of three of the four grasses by at least 12%. Deep, as opposed to shallow, soils mediated frequencies following FWD additions but only partially explained the variation in Bromus and Pseudoroegneria spicata . Although fertile areas associated with tree-islands elicited no response, FWD-induced increases in nitrogen mineralization in deep soils (15–17 cm) caused the frequency of the exotic and Pseudoroegneria to rise. Higher phosphorus availability in FWD-covered surface soils (0–2 cm) had no impact on grasses. FWD altered deep soil respiration, and deep and shallow microbial biomass structuring Pseudoroegneria frequencies, suggesting that microorganism themselves regulated Pseudoroegneria . The positive effects of FWD on grass frequencies intensified over time for natives but diminished for Bromus . Our results demonstrate that microorganisms in deeper soils helped mediate species-specific responses to disturbance both facilitating exotic invasion and promoting native establishment.

Journal of Arid Environments↗
USGS2012

Porphyry copper assessment of the Tibetan Plateau, China: Chapter F in Global mineral resource assessment

The U.S. Geological Survey collaborated with the China Geological Survey to conduct a mineral-resource assessment of resources in porphyry copper deposits on the Tibetan Plateau in western China. This area hosts several very large porphyry deposits, exemplified by the Yulong and Qulong deposits, each containing at least 7,000,000 metric tons (t) of copper. However, large parts of the area are underexplored and are likely to contain undiscovered porphyry copper deposits. Three tracts were delineated as permissive for porphyry copper deposits on the Tibetan Plateau—the Yulong (Eocene and Oligocene), Dali (Eocene through Miocene), and Gangdese (Oligocene and Miocene) tracts. The tracts were defined based on mapped and inferred subsurface distributions of igneous rocks of specific age ranges in which the occurrence of porphyry copper deposits is possible. These tracts range in area from about 95,000 to about 240,000 square kilometers. Although maps of different scales were used in the assessment, the final tract boundaries are intended for use at a scale of 1:1,000,000. The deposits on the Tibetan Plateau all formed in a post-subduction environment, one newly recognized as permissive for the occurrence of porphyry copper deposits. Based on the grade, tonnage, and geologic characteristics of the known deposits, two tracts, Yulong and Gangdese, were evaluated using the general (Cu-Mo-Au) porphyry copper grade and tonnage model. The Dali tract was evaluated using the gold-rich (Cu-Au) submodel. Assessment participants estimated numbers of undiscovered deposits at different levels of confidence for each permissive tract. These estimates were then combined with the selected grade and tonnage models using Monte Carlo simulation to generate quantitative probabilistic estimates of undiscovered resources. Additional resources in extensions of deposits with identified resources were not specifically evaluated. Assessment results, presented in tables and graphs, show mean expected amounts of metal and rock in undiscovered deposits at different quantile levels, as well as the arithmetic mean for each tract. This assessment estimated a mean of 39 undiscovered porphyry copper deposits within the assessed permissive tracts on the Tibetan Plateau. This represents nearly four times the number of known deposits (11) already discovered. Predicted mean (arithmetic) resources that could be associated with the undiscovered deposits are about 145,000,000 t of copper and about 4,900 t of gold, as well as byproduct molybdenum and silver. Reliable reports of the identified resources in the 11 known deposits total about 27,000,000 t of copper and about 800 t of gold. Therefore, based on the assessments of undiscovered Tibetan Plateau resources in this report, about six times as much copper may occur in undiscovered porphyry copper deposits as has been identified to date.

Tibetan Plateau↗
USGS1990

Recent geophysical and geological research in Antarctica related to the assessment of petroleum resources and potential environmental hazards to their development

During the 6-year negotiation of and adoption of the Convention on the Regulation of Antarctic Mineral Resources Activities on June 2, 1988, various countries have increased their attention to the possibility of exploitation of Antarctica's petroleum resources, which are covered by this treaty. However, there are no known petroleum resources in Antarctica, and scientific information is lacking to adequately assess any undiscovered resources or the possible environmental hazards to their development. Scientific research carried out in Antarctica since the International Geophysical Year (1957-1958) has provided a great deal of information on the geological framework of this ice-covered continent and its margin and has found general indications of the types of hazards that must be considered. Antarctica covers a vast area, and likely supergiant oil fields of the type to be exploited would be tiny (e.g., a few tens of kilometers across) in comparison. Any petroleum resources located in Antarctica will be found by applying the knowledge, techniques, and experience gained developing oil fields in other parts of the world and would, therefore, be other examples of general cases; in contrast, the Antarctic environment and its associated hazards must be considered unique.

Book chapter↗
USGS2015

Global patterns and environmental controls of perchlorate and nitrate co-occurrence in arid and semi-arid environments

Natural perchlorate (ClO 4 − ) is of increasing interest due to its wide-spread occurrence on Earth and Mars, yet little information exists on the relative abundance of ClO 4 − compared to other major anions, its stability, or long-term variations in production that may impact the observed distributions. Our objectives were to evaluate the occurrence and fate of ClO 4 − in groundwater and soils/caliche in arid and semi-arid environments (southwestern United States, southern Africa, United Arab Emirates, China, Antarctica, and Chile) and the relationship of ClO 4 − to the more well-studied atmospherically deposited anions NO 3 − and Cl − as a means to understand the prevalent processes that affect the accumulation of these species over various time scales. ClO 4 − is globally distributed in soil and groundwater in arid and semi-arid regions on Earth at concentrations ranging from 10 −1 to 10 6 μg/kg. Generally, the ClO 4 − concentration in these regions increases with aridity index, but also depends on the duration of arid conditions. In many arid and semi-arid areas, NO 3 − and ClO 4 − co-occur at molar ratios (NO 3 − /ClO 4 − ) that vary between ∼10 4 and 10 5 . We hypothesize that atmospheric deposition ratios are largely preserved in hyper-arid areas that support little or no biological activity (e.g. plants or bacteria), but can be altered in areas with more active biological processes including N 2 fixation, N mineralization, nitrification, denitrification, and microbial ClO 4 − reduction, as indicated in part by NO 3 − isotope data. In contrast, much larger ranges of Cl − /ClO 4 − and Cl − /NO 3 − ratios indicate Cl − varies independently from both ClO 4 − and NO 3 − . The general lack of correlation between Cl − and ClO 4 − or NO 3 − implies that Cl − is not a good indicator of co-deposition and should be used with care when interpreting oxyanion cycling in arid systems. The Atacama Desert appears to be unique compared to all other terrestrial locations having a NO 3 − /ClO 4 − molar ratio ∼10 3 . The relative enrichment in ClO 4 − compared to Cl − or NO 3 − and unique isotopic composition of Atacama ClO 4 − may reflect either additional in-situ production mechanism(s) or higher relative atmospheric production rates in that specific region or in the geological past. Elevated concentrations of ClO 4 − reported on the surface of Mars, and its enrichment with respect to Cl − and NO 3 − , could reveal important clues regarding the climatic, hydrologic, and potentially biologic evolution of that planet. Given the highly conserved ratio of NO 3 − /ClO 4 − in non-biologically active areas on Earth, it may be possible to use alterations of this ratio as a biomarker on Mars and for interpreting major anion cycles and processes on both Mars and Earth, particularly with respect to the less-conserved NO 3 − pool terrestrially.

Geochimica et Cosmochimica Acta↗
USGS1998

Chemical weathering in a tropical watershed, Luquillo Mountains, Puerto Rico: II. Rate and mechanism of biotite weathering

Samples of soil, saprolite, bedrock, and porewater from a lower montane wet forest, the Luquillo Experimental Forest (LEF) in Puerto Rico, were studied to investigate the rates and mechanisms of biotite weathering. The soil profile, at the top of a ridge in the Rio Icacos watershed, consists of a 50–100-cm thick layer of unstructured soil above a 600–800 cm thick saprolite developed on quartz diorite. The only minerals present in significant concentration within the soil and saprolite are biotite, quartz, kaolinite, and iron oxides. Biotite is the only primary silicate releasing significant K and Mg to porewaters. Although biotite in samples of the quartz diorite bedrock is extensively chloritized, chlorite is almost entirely absent in the saprolite phyllosilicates. Phyllosilicate grains are present as 200–1000 μm wide books below about 50 cm depth. X-ray diffraction (XRD) and electron microprobe analyses indicate that the phyllosilicate grains contain a core of biotite surrounded by variable amounts of kaolinite. Lattice fringe images under transmission electron microscope (TEM) show single layers of biotite altering to two layers of kaolinite, suggesting dissolution of biotite and precipitation of kaolinite at discrete boundaries. Some single 14-Å layers are also observed in the biotite under TEM. The degree of kaolinitization of individual phyllosilicate grains as observed by TEM decreases with depth in the saprolite. This TEM work is the first such microstructural evidence of epitaxial growth of kaolinite onto biotite during alteration in low-temperature environments. The rate of release of Mg in the profile, calculated as a flux through the soil normalized per watershed land area, is approximately 500 mol hectare −1 yr −1 (1.6 × 10 −9 mol Mg m soil −2 s −1 ). This rate is similar to the flux estimated from Mg discharge out the Rio Icacos (1000 mol hectare −1 yr −1 , or 3.5 × 10 −9 mol Mg m soil −2 s −1 ), indicating that scaling up from the soil to the watershed is possible for Mg release. The rate of Mg release from biotite, normalized to Brunauer-Emmett-Teller (BET) surface area, is calculated using a mass balance equation which includes the density and volume of phyllosilicate grains, porewater chemistry and flux, and soil porosity. The mean rates of biotite weathering calculated from K and Mg release rates are approximately 6 and 11 × 10 −16 mol biotite m biotite −2 s −1 respectively, significantly slower than laboratory rates (10 −12 to 10 −11 mol biotite m biotite −2 s −1 ). The discrepancy in scaling down from the soil to the laboratory is probably explained by (1) differences in weathering mechanism between the two environments, (2) higher solute concentrations in soil porewaters, (3) loss of reactive surface area of biotite in the saprolite due to kaolinite and iron oxide coatings, and/or (4) unaccounted-for heterogeneities in flow path through the soil.

El Yunque, Luquillo Experimental Forest, Luquillo ↗
USGS1959

Some aspects of the origin of the Ironwood iron-formation of Michigan and Wisconsin

The Ironwood iron-formation of the Gogebic Range of Michigan and Wisconsin is made up of several rock types, each of which is characterized by a different iron-rich mineral: hematite, magnetite, pyrite, iron carbonate, or iron silicate (minnesotaite, stilpnomelane). Where the Ironwood iron-formation is relatively unaltered the Plymouth, Norrie, and Anvil members consist of wavy-bedded magnetite and silicate-rich rocks, whereas the Yale and Pence members consist of even-bedded carbonate, silicate, magnetite, and pyrite-rich rocks. These rock types represent primary facies of the iron-formation that were deposited under differing physical and chemical conditions during a period of continuous iron-rich sedimentation. Animikie sedimentation in the Gogebic district began with the deposition of sandstone and dolomitic limestone in a shallow sea advancing over a low-lying land mass of lower Precambrian granite and green-stone. Continued advance of the sea, with effective separation of clastic material near shore, permitted the dominantly chemical sedimentation of the iron- formation in somewhat deeper water. The development of an off-shore basin with partially restricted circulation would have facilitated such deposition. Minor fluctuations in the physical and chemical conditions within the depositional environment are reflected in the differing facies of the iron-formation. Deposition of the iron and silica-rich chemical sediments was terminated by increased tectonism and the deposition of the thick sequence of slates and graywackes of the Tyler formation.

Michigan, Wisconsin↗
USGS2012

Quick-start guide for version 3.0 of EMINERS - Economic Mineral Resource Simulator

Quantitative mineral resource assessment, as developed by the U.S. Geological Survey (USGS), consists of three parts: (1) development of grade and tonnage mineral deposit models; (2) delineation of tracts permissive for each deposit type; and (3) probabilistic estimation of the numbers of undiscovered deposits for each deposit type (Singer and Menzie, 2010). The estimate of the number of undiscovered deposits at different levels of probability is the input to the EMINERS (Economic Mineral Resource Simulator) program. EMINERS uses a Monte Carlo statistical process to combine probabilistic estimates of undiscovered mineral deposits with models of mineral deposit grade and tonnage to estimate mineral resources. It is based upon a simulation program developed by Root and others (1992), who discussed many of the methods and algorithms of the program. Various versions of the original program (called "MARK3" and developed by David H. Root, William A. Scott, and Lawrence J. Drew of the USGS) have been published (Root, Scott, and Selner, 1996; Duval, 2000, 2012). The current version (3.0) of the EMINERS program is available as USGS Open-File Report 2004-1344 (Duval, 2012). Changes from version 2.0 include updating 87 grade and tonnage models, designing new templates to produce graphs showing cumulative distribution and summary tables, and disabling economic filters. The economic filters were disabled because embedded data for costs of labor and materials, mining techniques, and beneficiation methods are out of date. However, the cost algorithms used in the disabled economic filters are still in the program and available for reference for mining methods and milling techniques included in Camm (1991). EMINERS is written in C++ and depends upon the Microsoft Visual C++ 6.0 programming environment. The code depends heavily on the use of Microsoft Foundation Classes (MFC) for implementation of the Windows interface. The program works only on Microsoft Windows XP or newer personal computers. It does not work on Macintosh computers. This report demonstrates how to execute EMINERS software using default settings and existing deposit models. Many options are available when setting up the simulation. Information and explanations addressing these optional parameters can be found in the EMINERS Help files. Help files are available during execution of EMINERS by selecting EMINERS Help from the pull-down menu under Help on the EMINERS menu bar. There are four sections in this report. Part I describes the installation, setup, and application of the EMINERS program, and Part II illustrates how to interpret the text file that is produced. Part III describes the creation of tables and graphs by use of the provided Excel templates. Part IV summarizes grade and tonnage models used in version 3.0 of EMINERS.

Open-File Report↗
USGS2011

Trace metals related to historical iron smelting at Hopewell Furnace National Historic Site, Berks and Chester Counties, Pennsylvania

Iron ore containing elevated concentrations of trace metals was smelted at Hopewell Furnace during its 113 years of operation (1771-1883). The ore used at Hopewell Furnace was obtained from iron mines within 5 miles of the furnace. The iron-ore deposits were formed about 200 million years ago and contain abundant magnetite, the primary iron mineral, and accessory minerals enriched in arsenic, cobalt, copper, lead, and other metals. Hopewell Furnace, built by Mark Bird during 1770-71, was one of the last of the charcoal-burning, cold-blast iron furnaces operated in Pennsylvania. The most productive years for Hopewell Furnace were from 1830 to 1837. Castings were the most profitable product, especially the popular Hopewell Stove. More than 80,000 stoves were cast at Hopewell, which produced as many as 23 types and sizes of cooking and heating stoves. Beginning in the 1840s, the iron industry shifted to large-scale, steam-driven coke and anthracite furnaces. Independent rural enterprises like Hopewell could no longer compete when the iron and steel industries consolidated in urban manufacturing centers. The furnace ceased operation in 1883 (Kurjack, 1954). The U.S. Geological Survey (USGS), in cooperation with the National Park Service, completed a study at Hopewell Furnace National Historic Site (NHS) in Berks and Chester Counties, Pennsylvania, to determine the fate of toxic trace metals, such as arsenic, cobalt, and lead, released into the environment during historical iron-smelting operations. The results of the study, conducted during 2008-10, are presented in this fact sheet.

Pennsylvania↗
USGS2007

Observations of magnetite dissolution in poorly drained soils

Dissolution of strongly magnetic minerals is a common and relatively rapid phenomenon in poorly drained soils of the central United States, resulting in low magnetic susceptibility (MS). Low Eh reducing conditions are primarily responsible for magnetic mineral dissolution; a process likely mediated by iron-reducing bacteria in the presence of soil organic matter. Based on transects across drainage sequences from nine sites, natural magnetic minerals (>5 ??m) extracted from surface soil consist of 54% ?? 18% magnetite, 21% ?? 11% titanomagnetite, and 17% ?? 14% ilmenite. Magnetite and titanomagnetite dissolution, assessed by scanning electron microscopy on a 0-to-3 scale, inversely correlates with surface soil MS (r = 0.53), a proxy for soil drainage at studied transects. Altered magnetite typically displays etch pits <1-??m diameter, whereas titanomagnetite exhibits a latticework pattern of alteration along planes of crystallographic weakness (<1-??m spacing). Ilmenite, containing solely ferrous iron, is unaffected by reducing conditions, portraying mainly smooth-textured grains. Magnetic fractions (>5 ??m) include 26% ?? 18% anthropogenic fly ash that also exhibits greater dissolution in low MS soils (r = 0.38), indicating detectable alteration can occur within 150 years in low Eh soils. Laboratory induced reduction of magnetite, titanomagnetite, and magnetic fly ash, with a citrate-bicarbonate- dithionite solution, resulted in dissolution textures similar to those of in situ soil particles. Although experiments indicate that reductive dissolution of magnetite can occur abiotically under extreme conditions, bacteria likely play an important role in the natural environment. ?? 2007 Lippincott Williams & Wilkins, Inc.

Soil Science↗
USGS1946

Preliminary chemical correlation of chromite with the containing rocks

Chromite investigations of the U. S. Geological Survey since 1939 indicate that economic deposits of chromite rich in normative spinel ((Mg, Fe)Al 2 O 4 ) occur in peridotites which are closely associated with gabbro; high-chrome chromites occur in feldspar-free peridotites; and chromites rich in both normative chromite ((Mg, Fe)Cr 2 O 4 ) and magnetite (FeFe 2 O 4 ) are found in the pyroxene-rich stratiform complexes. Reaction of high-alumina chromite with diopsidic gabbro to form anorthite, olivine, and enstatite is described, and some probable equilibria between chromite and silicate minerals are discussed. A plot of 63 complete analyses on a triangular prism of composition shows that chromites from different geologic provinces in the Western Hemisphere vary consistently and fall in overlapping, but distinct, fields. The chromites of the Caribbean Province, which occur in dunite and troctolite, have the general formula Cr (sub 25-80) Al (sub 15-75) Fe (sub 1-5) (Mg (sub 65-75) ) and average about Cr 50 Al 47 (Mg 70 ). The chromites of the Pacific Coast, which occur in dunite and saxonite, average about Cr 70 Al 24 (Mg 60 ) in the range Cr (sub 60-77) Al (sub 16-35) Fe (sub 3-12) (Mg (sub 45-75) ). The stratiform deposits of the Stillwater and Bushveld complexes occur in harzburgite and bronzitite, and are very much alike, averaging Cr 60 Al 32 (Mg 52 ) and Cr 58 Al 34 (Mg 44 ) respectively. Chromites from gabbroic facies of the Bushveld complex are much richer in normative magnetite, presumably reflecting a higher CaO: Al 2 O 3 ratio in the silicate environment.

Economic Geology↗
USGS2001

Biology and conservation of the common murre in California, Oregon, Washington, and British Columbia: Vol. 1, Natural history and population trends

Over the past 30 years, the common murre ( Uria aalge californica ) has been recognized as a prominent indicator of marine conservation issues in California, Oregon, Washington, and British Columbia, especially regarding oil pollution, certain fisheries, and human disturbance. To assist the effective management of the common murre and the marine environments in which they live, this summary of available information on the biology and regional status of the common murre has been sponsored by the U.S. Fish and Wildlife Service (Division of Migratory Bird Management). In Volume 1 (Chapter 1), the natural history of the common murre is summarized, drawing heavily on breeding studies from the South Farallon Islands, California, plus a host of detailed breeding studies from the North Atlantic Ocean. Population trends of the common murre are summarized in Volume 1 (Chapter 2), focusing on changes in whole-colony counts determined from aerial photographs between the late 1970s and 1995 in California, Oregon and Washington. Historical data and human impacts to murre colonies since the early nineteenth century are also summarized. Volume 2 will summarize population threats, conservation, and management. Information presented in Volume 1 has been obtained and recorded by a large number of researchers and natural historians over two centuries. From the 1960s to 1995, most work in California, Oregon, and Washington was sponsored by the U.S. Fish and Wildlife Service, Minerals Management Service, and California Department of Fish and Game. Important breeding biology studies were conducted at the South Farallon Islands (Farallon National Wildlife Refuge) by the Point Reyes Bird Observatory, in coordination with the U.S. Fish and Wildlife Service (San Francisco Bay National Wildlife Refuge). Colony surveys in California were conducted mainly by the U.S. Fish and Wildlife Service (San Francisco Bay National Wildlife Refuge), U.S. Geological Survey (Western Ecological Research Center, Dixon Field Station), Humboldt State University, and University of California (Santa Cruz). Colony surveys in Oregon and Washington were conducted mainly by the U.S. Fish and Wildlife Service (Oregon Coast National Wildlife Refuge and Washington Maritime National Wildlife Refuges). In British Columbia, most work from the 1960s to 1995 was sponsored and conducted by the Canadian Wildlife Service and Royal British Columbia Museum.

British Columbia, California, Oregon, Washington↗
USGS1990

The geology of selected peat-forming environments in temperate and tropical latitudes

We studied peat in several geologic and climatic settings: (1) a glaciated terrain in cold-temperate Maine and Minnesota, U.S.A.; (2) an island in a temperate maritime climate in the Atlantic Ocean off the coast of Maine, U.S.A., where sea level is rising rapidly and changing the environment of peat accumulation; (3) swamps along the warm-temperate U.S. Atlantic and Gulf Coastal Plains, where sea level has changed often, thus creating sites for accumulation; and (4) in a tropical climate along the coast of Sarawak, Malaysia, and the delta of the Batang Hari River, Sumatra, Indonesia (Figs. 1 and 2). With the exception of the deposits on the Atlantic and Gulf Coastal Plains, most of the deposits described are domed bogs in which peat accumulation continued above the surface of the surrounding soil. The bogs of the U.S. Atlantic and Gulf Coastal Plains have almost level surfaces. All domed bogs are not entirely ombrotrophic (watered only from precipitation); multidomed bogs that rise from irregular or hilly surfaces may be crossed by streams that supply water to the bogs. The geologic processes or organic sedimentation, namely terrestrialization and paludification, are similar in all peat deposits considered here. Differences in geomorphology affecting the quantity and that quality of peat that has ash contents of less than 25%, which are desirable for commercial purposes, depend chiefly on: (1) high humidity, which is favorable to luxuriant growth of peat-forming vegetation; (2) a depositional setting that permits extensive accumulation relatively free from inorganic contamination from sea water and streams and from dust and volcanic ash; and (3) a stable regional water table that controls the rate of decomposition under aerobic conditions and protects the deposit against the ravages of fire. Differences in peat textures are due to the type of vegetation and to the degree of decomposition. The rate of decomposition is largely the result of the amount of oxidation and aerobic microbial activity. Stratigraphic distribution of various textures and amounts of inorganic components within a peat deposit is largely determined by the vertical positions occupied by peat-forming environments, such as pond, marsh, swamp and heath where vegetation accumulated, and the depth to zones of unoxygenated water. Peat also differs in the rate of accumulation. On the basis of carbon-14 dating, an estimated 8 m of peat in the tropical Batang Hari River deposit in Sumatra has been accumulating at the rate of about 1.5 m/1,000 yr, whereas peat in the cold-temperate deposit in Maine has been accumulating at the rate of 0.66 m/1,000 yr. Accumulation rates in domed deposits such as these are affected not only by factors controlling volume of biomass and aerobic decay but also by stream erosion and fires that remove peat. Such disconformities (see Fig. 2) within the deposit may be recognized by sudden vertical changes in degree of decomposition and/or the presence of charcoal. The trace-element content of peat deposits is affected by the environments of their settings. Samples of peat that have an ash content of less than 25% dry weight and that are from small, almost level swamp deposits along the Atlantic Coastal Plain of North Carolina were compared with similar samples from small domed bogs in Maine, a glaciated area. Samples from Nort Carolina, which are from deposits in thick fluvial and nearshore marine sediments far from the bedrock source, are generally higher in Ti, Cr and Pb. The Maine samples from deposits in glacial drift close to the bedrock source contain more Zn, Mn, P, Ca, Na and Fe. The kind and amount of trace elements within the deposits appear to relate largely to depositional setting, to kinds of bedrock source, and to the modes of transportation from source to peat swamp. Trace-element concentrations in the extensive Sumatra peat deposit, which represents a potentially commercial coal bed, are similar to those found in Appalachian coals except for As and Au, which are higher in the former. This similarity most likely implies that geochemical controls on mineral matter controlled the concentrations in both. Most peat deposits found in the world today are not precursors of economic coal beds because they are too local in extent, lack beds of commercial-quality peat greater than 6 m thick, and/or are too far from sea level to be rapidly by marine or marginal marine sediments before destruction by erosion and decomposition. However, the two domed deposits in Sarawak and Sumatra described above are parts of extensive, thick, low-sulfur, fuel-quality peat deposits, which have bases below the levels of rivers on coastal deltas. These are likely to be preserved in their lower part and to become precursors of tropical coal seams of potential economic importance. The lenticular and tabular peat deposits of the Atlantic and Gulf Coastal Plains, which have little chance of survival, have features resembling those in Tertiary peat deposits in alluvial settings of western North America. The quality, shape, and extent of modern and ancient peat deposits are controlled by the same factors - humidity, vegetation type, ground- and surface-water regimes, and physiographic and geologic setting. Thus, a study of modern peat deposits may help in studies of the areal distribution and the thickness and quality of ancient coal beds.

International Journal of Coal Geology↗