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USGS2000

Characterization and speciation of mercury-bearing mine wastes using X-ray absorption spectroscopy

Mining of mercury deposits located in the California Coast Range has resulted in the release of mercury to the local environment and water supplies. The solubility, transport, and potential bioavailability of mercury are controlled by its chemical speciation, which can be directly determined for samples with total mercury concentrations greater than 100 mg kg-1 (ppm) using X-ray absorption spectroscopy (XAS). This technique has the additional benefits of being non-destructive to the sample, element-specific, relatively sensitive at low concentrations, and requiring minimal sample preparation. In this study, Hg L(III)-edge extended X-ray absorption fine structure (EXAFS) spectra were collected for several mercury mine tailings (calcines) in the California Coast Range. Total mercury concentrations of samples analyzed ranged from 230 to 1060 ppm. Speciation data (mercury phases present and relative abundances) were obtained by comparing the spectra from heterogeneous, roasted (calcined) mine tailings samples with a spectral database of mercury minerals and sorbed mercury complexes. Speciation analyses were also conducted on known mixtures of pure mercury minerals in order to assess the quantitative accuracy of the technique. While some calcine samples were found to consist exclusively of mercuric sulfide, others contain additional, more soluble mercury phases, indicating a greater potential for the release of mercury into solution. Also, a correlation was observed between samples from hot-spring mercury deposits, in which chloride levels are elevated, and the presence of mercury-chloride species as detected by the speciation analysis. The speciation results demonstrate the ability of XAS to identify multiple mercury phases in a heterogeneous sample, with a quantitative accuracy of ??25% for the mercury-containing phases considered. Use of this technique, in conjunction with standard microanalytical techniques such as X-ray diffraction and electron probe microanalysis, is beneficial in the prioritization and remediation of mercury-contaminated mine sites. (C) 2000 Elsevier Science B.V.

Science of the Total Environment↗

USGS2013

Microbiological reduction of Sb(V) in anoxic freshwater sediments

Microbiological reduction of millimolar concentrations of Sb(V) to Sb(III) was observed in anoxic sediments from two freshwater settings: (1) a Sb- and As-contaminated mine site (Stibnite Mine) in central Idaho and 2) an uncontaminated suburban lake (Searsville Lake) in the San Francisco Bay Area. Rates of Sb(V) reduction in anoxic sediment microcosms and enrichment cultures were enhanced by amendment with lactate or acetate as electron donors but not by H2, and no reduction occurred in sterilized controls. Addition of 2- 14 C-acetate to Stibnite Mine microcosms resulted in the production of 14 CO 2 coupled to Sb(V) reduction, suggesting that this process proceeds by a dissimilatory respiratory pathway in those sediments. Antimony(V) reduction in Searsville Lake sediments was not coupled to acetate mineralization and may be associated with Sb-resistance. The microcosms and enrichment cultures also reduced sulfate, and the precipitation of insoluble Sb(III)-sulfide complexes was a major sink for reduced Sb. The reduction of Sb(V) by Stibnite Mine sediments was inhibited by As(V), suggesting that As(V) is a preferred electron acceptor for the indigenous community. These findings indicate a novel pathway for anaerobic microbiological respiration and suggest that communities capable of reducing high concentrations of Sb(V) commonly occur naturally in the environment.

Environmental Science & Technology↗

USGS1987

Relationship between peat geochemistry and depositional environments, Cranberry Island, Maine

The Heath, Great Cranberry Island, Maine, offers a unique locality for studying lateral and vertical relationships between radically different peat types within 1 km 2 . The majority of The Heath is a Sphagnum moss-dominated raised bog. Surrounding the raised bog is a swamp/marsh complex containing grass, sedge, Sphagnum moss, alder, tamarack, and skunk cabbage. Swamp/ marsh-deposited peat occurs both around the margins of The Heath and under Sphagnum -dominated peat, which was deposited within the raised bog. A third peat type, dominated by herbaceous aquatics, is present underlying the swamp/marsh-dominated peat but is not present as a dominant botanical community of The Heath. The three peat types have major differences in petrographic characteristics, ash contents, and associated minerals. Sulfur contents range from a low of 0.19 wt.% (dry) within the raised bog to a high of 4.44 wt% (dry) near the west end of The Heath, where swamp/marsh peat occurring directly behind a storm beach berm has been influenced by marine waters. The presence of major geochemical variations within a 1-km 2 peat deposit suggests the need for in-depth characterization of potential peat resources prior to use.

International Journal of Coal Geology↗

USGS2011

Splint coals of the Central Appalachians: Petrographic and geochemical facies of the Peach Orchard No. 3 split coal bed, southern Magoffin County, Kentucky

The Bolsovian (Middle Pennsylvanian) Peach Orchard coal bed is one of the splint coals of the Central Appalachians. Splint coal is a name for the dull, inertinite-rich lithologies typical of coals of the region. The No. 3 Split was sampled at five locations in Magoffin County, Kentucky and analyzed for petrography and major and minor elements. The No. 3 Split coals contain semifusinite-rich lithologies, up to 48% (mineral-free basis) in one case. The nature of the semifusinite varies with position in the coal bed, containing more mineral matter of detrital origin in the uppermost durain. The maceral assemblage of these terminal durains is dominated by detrital fusinite and semifusinite, suggesting reworking of the maceral assemblage coincident with the deposition of the detrital minerals. However, a durain in the middle of the coal bed, while lithologically similar to the uppermost durains, has a degraded, macrinite-rich, texture. The inertinite macerals in the middle durain have less distinct edges than semifusinites in the uppermost terminal durains, suggesting degradation as a possible path to inertinite formation. The uppermost durain has higher ash and semifusinite contents at the eastern sites than at the western sites. The difference in the microscopic petrology indicates that megascopic petrology alone can be a deceptive indicator of depositional environments and that close attention must be paid to the individual macerals and their implications for the depositional setting, especially within the inertinite group.

International Journal of Coal Geology↗

USGS2011

Geology for a changing world 2010-2020-Implementing the U.S. Geological Survey science strategy

This report describes a science strategy for the geologic activities of the U.S. Geological Survey (USGS) for the years 2010-2020. It presents six goals with accompanying strategic actions and products that implement the science directions of USGS Circular 1309, 'Facing Tomorrow's Challenges-U.S. Geological Survey Science in the Decade 2007-2017.' These six goals focus on providing the geologic underpinning needed to wisely use our natural resources, understand and mitigate hazards and environmental change, and understand the relationship between humans and the environment. The goals emphasize the critical role of the USGS in providing long-term research, monitoring, and assessments for the Nation and the world. Further, they describe measures that must be undertaken to ensure geologic expertise and knowledge for the future. The natural science issues facing today's world are complex and cut across many scientific disciplines. The Earth is a system in which atmosphere, oceans, land, and life are all connected. Rocks and soils contain the answers to important questions about the origin of energy and mineral resources, the evolution of life, climate change, natural hazards, ecosystem structures and functions, and the movements of nutrients and toxicants. The science of geology has the power to help us understand the processes that link the physical and biological world so that we can model and forecast changes in the system. Ensuring the success of this strategy will require integration of geological knowledge with the other natural sciences and extensive collaboration across USGS science centers and with partners in Federal, State, and local agencies, academia, industry, nongovernmental organizations and, most importantly, the American public. The first four goals of this report describe the scientific issues facing society in the next 10 years and the actions and products needed to respond to these issues. The final two goals focus on the expertise and infrastructure needed to ensure the long-term sustainability of the geological sciences in the USGS. The ultimate goal of USGS science and of the strategy laid out in this document is to contribute to the development of a sustainable society that operates in harmony with the Earth systems that society depends upon. As we begin the second decade of the 21st century, our Nation faces growing challenges in resource availability, climate and environmental change, and natural hazards. Meeting these challenges will require strong collaboration across the natural and social sciences and extensive partnerships with both the public and private sectors. The six goals described in this document represent a mix of scientific focus areas and operational necessities that together provide a comprehensive roadmap for USGS geologic science to effectively contribute to the USGS mission, providing science for a changing world.

Circular↗

USGS1979

Environment of ore deposition in the Creede mining district, San Juan Mountains, Colorado; Part IV, source of fluids, from oxygen, hydrogen, and carbon isotope studies

The hydrogen isotopic composition of fluids responsible for formation of the near-surface silver-base metal vein deposits at Creede was measured by direct analysis of inclusion fluids in sphalerite, quartz, and rhodochrosite and was estimated from analyses of illite and chlorite. The oxygen isotopic composition was determined directly on inclusion fluids in sphalerite and was estimated from analyses of quartz, illite, rhodochrosite, siderite, and adularia. The carbon isotopic composition was estimated from analyses of rhodochrosite and siderite. The ranges in isotopic composition for water and CO 2 in the fluids associated with the formation of each of the minerals is given below (number of determinations given in parentheses):Mineral delta D (sub H 2 ) O ppm delta 18 O (sub H 2 ) O ppm delta 13 C (sub CO 2 ) ppmSphalerite -81 to -54 (4) -10.1 to -4.5 (4)Quartz -97 to -86 (4) -5.9 to 1.8 (18)Illite -62 to -50 (8) -1.6 to 1.2(7)Chlorite -64 to -55 (10) -2.2 to 0.8 (10)Adularia 4.2 (1)Rhodochrosite -82 to -78 (2) 4.2 to 9.4 (9) -5.7 to -4.2 (9)Siderite 4.9 to 9.9 (6) -6.9 to -2.7 (6)The delta D (sub H 2 ) O and delta 18 O (sub H 2 ) O values of fluids associated with the formation of sphalerite, quartz, illite/chlorite, and carbonate minerals differ substantially from one another, and these differences appear to have been maintained throughout the depositional history, regardless of the positions of the minerals in the paragenetic sequence.The data suggest that waters from three coexisting reservoirs fed the vein system alternately and episodically during vein formation, and apparently there was little mixing of the fluids from the different reservoirs. The hydrogen, oxygen, and carbon isotope data suggest that the carbonate waters were deep seated, probably dominantly magmatic, in origin. The sphalerite and illite/chlorite waters must have been dominantly meteoric in origin and substantially oxygen shifted by exchange with the volcanic country rocks. The quartz waters were also oxygen shifted meteoric waters but were some 40 per mil lower in deuterium content than the sphalerite and illite/chlorite waters.We propose that the quartz fluids entered the vein system from reservoirs beneath the mountainous areas to the north in the vicinity of the present Continental Divide, but that the sphalerite and illite/chlorite fluids entered the vein system from a topographically low area to the south along the structural moat of the Creede caldera. The difference in delta D between the two meteoric waters may reflect differences in altitude of the recharge areas for the two reservoirs or may be clue to isotopic evolution of the closed-basin lake and interstitial waters in the moat surrounding the Creede caldera.

Colorado↗

USGS2003

Arsenic in ground water: Geochemistry and occurrence

Interest in arsenic in ground water has greatly increased in the past decade because of the increased awareness of human health effects and the costs of avoidance or treatment of ground water supplies used for consumption. The goal of this book is to provide a description of the basic processes that affect arsenic occurrence and transport by providing sufficient background information on arsenic geochemistry and descriptions of hi- arsenic ground water, both affected and unaffected by human activity. An understanding of thermodynamics, adsorption, and the speciation of arsenic in solid phases, which are described in first three chapters, is needed to predict the fate of arsenic in ground water systems. Large-scale and deep movement of ground water can and has redistributed arsenic in the near surface environment, as described in the next two chapters. These large-scale systems can affect large volumes of both ground water and surface water, such as in the Yellowstone system, and can produce mineralised zones that subsequently release arsenic to ground water supplies. Regional identification of high-arsenic ground water and its consumption as described in the next three chapters clearly demonstrates a need for increased wat- quality monitoring, particularly in south and southeast Asia. Chapters 9-11 provide examples of high arsenic ground water associated with sulfide mineral oxidation and alkaline conditions. Finally, smaller scale studies of the effects of human activities that have produced high-arsenic ground water and methods for attenuation of ground water are presented

Book↗

USGS1996

MUDMASTER: A Program for Calculating Crystalline Size Distributions and Strain from the Shapes of X-Ray Diffraction Peaks

Particle size may strongly influence the physical and chemical properties of a substance (e.g. its rheology, surface area, cation exchange capacity, solubility, etc.), and its measurement in rocks may yield geological information about ancient environments (sediment provenance, degree of metamorphism, degree of weathering, current directions, distance to shore, etc.). Therefore mineralogists, geologists, chemists, soil scientists, and others who deal with clay-size material would like to have a convenient method for measuring particle size distributions. Nano-size crystals generally are too fine to be measured by light microscopy. Laser scattering methods give only average particle sizes; therefore particle size can not be measured in a particular crystallographic direction. Also, the particles measured by laser techniques may be composed of several different minerals, and may be agglomerations of individual crystals. Measurement by electron and atomic force microscopy is tedious, expensive, and time consuming. It is difficult to measure more than a few hundred particles per sample by these methods. This many measurements, often taking several days of intensive effort, may yield an accurate mean size for a sample, but may be too few to determine an accurate distribution of sizes. Measurement of size distributions by X-ray diffraction (XRD) solves these shortcomings. An X-ray scan of a sample occurs automatically, taking a few minutes to a few hours. The resulting XRD peaks average diffraction effects from billions of individual nano-size crystals. The size that is measured by XRD may be related to the size of the individual crystals of the mineral in the sample, rather than to the size of particles formed from the agglomeration of these crystals. Therefore one can determine the size of a particular mineral in a mixture of minerals, and the sizes in a particular crystallographic direction of that mineral.

Open-File Report↗

USGS2006

Geochemistry of bed and suspended sediment in the Mississippi river system: Provenance versus weathering and winnowing

Stream-bed sediment for the size fraction less than 150 μm, examined in 14,000 samples collected mostly from minor tributaries to the major rivers throughout the Mississippi River drainage system, is composed of 5 mineral fractions identified by factor analysis—Al-silicate minerals, quartz, calcite and dolomite, heavy minerals, and an Fe–Mn fraction. The Al-silicate fraction parallels its distribution in the regolith, emphasizing the local sediment source as a primary control to its distribution. Quartz and the heavy-mineral fraction, and associated trace elements, exhibit a complementary distribution to that of the Al-silicate fraction, with a level of enrichment in the bed sediment that is achieved through winnowing and sorting. The carbonate fraction has a distribution suggesting its dissolution during transport. Trace elements partitioned onto the Fe–Mn, possibly amorphous oxyhydride, fraction are introduced to the streams, in part, through human activity. Except for the heavy-mineral fraction, these fractions are identified in suspended sediment from the Mississippi River itself. Although comparison of the tributary bed sediment with the riverine suspended sediment is problematic, the geochemistry of the suspended sediment seems to corroborate the interpretation of the geochemistry of the bed sediment.

Arkansas basin, Ohio basin Tennessee basin, Lower ↗

USGS2011

Biology, status, and management of the yellowstone cutthroat trout

Yellowstone cutthroat trout Oncorhynchus clarkii bouvieri were historically distributed in the Yellowstone River drainage (Montana and Wyoming) and the Snake River drainage (Wyoming, Idaho, Utah, Nevada, and probably Washington). Individual populations evolved distinct life history characteristics in response to the diverse environments in which they were isolated after the last glaciation. Anthropogenic activities have resulted in a substantial decline (42% of the historical range is currently occupied; 28% is occupied by core [genetically unaltered] populations), but the number of extant populations, especially in headwater streams, has precluded listing of this taxon under the Endangered Species Act. Primary threats to persistence of Yellowstone cutthroat trout include (1) invasive species, resulting in hybridization, predation, disease, and interspecific competition; (2) habitat degradation from human activities such as agricultural practices, water diversions, grazing, dam construction, mineral extraction, grazing, timber harvest, and road construction; and (3) climate change, including an escalating risk of drought, wildfire, winter flooding, and rising temperatures. Extirpation of individual populations or assemblages has led to increasing isolation and fragmentation of remaining groups, which in turn raises susceptibility to the demographic influences of disturbance (both human and stochastic) and genetic factors. Primary conservation strategies include (1) preventing risks associated with invasive species by isolating populations of Yellowstone cutthroat trout and (2) connecting occupied habitats (where possible) to preserve metapopulation function and the expression of multiple life histories. Because persistence of isolated populations may be greater in the short term, current management is focused on isolating individual populations and restoring habitats; however, this approach implies that humans will act as dispersal agents if a population is extirpated because of stochastic events.

Idaho, Montana, Utah, Wyoming↗

USGS1992

Origin of stratiform sediment-hosted manganese carbonate ore deposits: Examples from Molango, Mexico, and TaoJiang, China

Carbonate and sulfide minerals from the Molango, Mexico, and TaoJiang, China, Mn deposits display similar and distinctive ??34S and ??13C patterns in intervals of manganese carbonate mineralization. ??13C-values for Mn-bearing carbonate range from -17.8 to +0.5??? (PDB), with the most negative values occurring in high-grade ore zones that are composed predominantly of rhodochrosite. In contrast, calcite from below, within and above Mn-carbonate zones at Molango has ??13C???0??? (PDB). Markedly negative ??13C data indicate that a large proportion of the carbon in Mn-carbonates was derived from organic matter oxidation. Diagenetic reactions using MnO2 and SO2-4 to oxidize sedimentary organic matter were the principle causes of such 12C enrichment. Pyrite content and sulfide ?? 34S-values also show distinctive variations. In unmineralized rocks, very negative ??34S-values (avg. < -21??? CDT) and abundant pyrite content suggest that pyrite formed from diagenetic, bacteriogenic sulfate reduction. In contrast, Mn-bearing horizons typically contain only trace amounts of pyrite (e.g., <0.5 wt% S with ??34S-values 34S-enriched, in some cases to nearly the value for contemporaneous seawater. 34S-enriched pyrite from the Mn-carbonate intervals indicates sulfide precipitation in an environment that underwent extensive SO2-4 reduction, and was largely a closed system with regard to exchange of sulfate and dissolved sulfide with normal seawater. The occasional occurrence of 34S-depleted pyrite within Mn-carbonate zones dominated by 34S-enriched pyrite is evidence that closed-system conditions were intermittent and limited to local pore waters and did not involve entire sedimentary basins. Mn-carbonate precipitation may have occluded porosity in the surficial sediments, thus establishing an effective barrier to SO2-4 exchange with overlying seawater. Similar isotopic and mineralogic characteristics from both the Molango and TaoJiang deposits, widely separated in geologic time and space, suggest they were formed similarly by MnO2 precipitation at the margins of dysaerobic to anoxic marine basins. Mn-carbonate formed predominantly by early-diagenetic reduction of Mn-oxides via oxidation of organic matter in near-surface sediments. In addition to MnCO3 precipitation, organic matter oxidation reactions resulted in oxidation of FeS to Fe-oxides such as magnetite, maghemite and hematite. The latter process explains anomalously low pyrite content and abundant Fe-oxide minerals in ore zones dominated by rhodochrosite. ?? 1992.

Chemical Geology↗

USGS2012

Index for characterizing post-fire soil environments in temperate coniferous forests

Many scientists and managers have an interest in describing the environment following a fire to understand the effects on soil productivity, vegetation growth, and wildlife habitat, but little research has focused on the scientific rationale for classifying the post-fire environment. We developed an empirically-grounded soil post-fire index (PFI) based on available science and ecological thresholds. Using over 50 literature sources, we identified a minimum of five broad categories of post-fire outcomes: (a) unburned, (b) abundant surface organic matter ( > 85% surface organic matter), (c) moderate amount of surface organic matter ( ≥ 40 through 85%), (d) small amounts of surface organic matter ( < 40%), and (e) absence of surface organic matter (no organic matter left). We then subdivided each broad category on the basis of post-fire mineral soil colors providing a more fine-tuned post-fire soil index. We related each PFI category to characteristics such as soil temperature and duration of heating during fire, and physical, chemical, and biological responses. Classifying or describing post-fire soil conditions consistently will improve interpretations of fire effects research and facilitate communication of potential responses or outcomes (e.g., erosion potential) from fires of varying severities.

Forests↗

USGS2005

An astrobiological perspective on Meridiani Planum

Sedimentary rocks exposed in the Meridiani Planum region of Mars record aqueous and eolian deposition in ancient dune and interdune playa-like environments that were arid, acidic, and oxidizing. On Earth, microbial populations have repeatedly adapted to low pH and both episodic and chronic water limitation, suggesting that, to a first approximation, the Meridiani plain may have been habitable during at least part of the interval when deposition and early diagenesis took place. On the other hand, the environmental conditions inferred for Meridiani deposition would have posed a challenge for prebiotic chemical reactions thought to have played a role in the origin of life on Earth. Orbital observations suggest that the combination of sulfate minerals and hematite found in Meridiani rocks may be unusual on the martian surface; however, there is reason to believe that acidity, aridity, and oxidizing conditions were broadly distributed on ancient Mars. When these conditions were established and how much environmental heterogeneity existed on early Mars remain to be determined. Because sulfates and iron oxides can preserve detailed geochemical records of environmental history as well as chemical, textural and microfossil signatures of biological activity, Meridiani Planum is an attractive candidate for Mars sample return. ?? 2005 Elsevier B.V. All rights reserved.

Earth and Planetary Science Letters↗

USGS2009

USGS Science: Addressing Our Nation's Challenges

With 6.6 billion people already living on Earth, and that number increasing every day, human influence on our planet is ever more apparent. Changes to the natural world combined with increasing human demands threaten our health and safety, our national security, our economy, and our quality of life. As a planet and a Nation, we face unprecedented challenges: loss of critical and unique ecosystems, the effects of climate change, increasing demand for limited energy and mineral resources, increasing vulnerability to natural hazards, the effects of emerging diseases on wildlife and human health, and growing needs for clean water. The time to respond to these challenges is now, but policymakers and decisionmakers face difficult choices. With competing priorities to balance, and potentially serious - perhaps irreversible - consequences at stake, our leaders need reliable scientific information to guide their decisions. As the Nation's earth and natural science agency, the USGS monitors and conducts scientific research on natural hazards and resources and how these elements and human activities influence our environment. Because the challenges we face are complex, the science needed to better understand and deal with these challenges must reflect the complex interplay among natural and human systems. With world-class expertise in biology, geology, geography, hydrology, geospatial information, and remote sensing, the USGS is uniquely capable of conducting the comprehensive scientific research needed to better understand the interdependent interactions of Earth's systems. Every day, the USGS helps decisionmakers to minimize loss of life and property, manage our natural resources, and protect and enhance our quality of life. This brochure provides examples of the challenges we face and how USGS science helps decisionmakers to address these challenges.

General Information Product↗

USGS2020

Evidence for primitive magma storage and eruption following prolonged equilibration in thickened crust

In continental arcs, the exposure of primitive eruptive products at the surface is typically a result of rapid magmatic transfer through the crust. As a result, the initially primitive magma experiences minimal crustal residence and thus insignificant differentiation towards more evolved products. This rapid transfer of primitive magma through thickened crust is commonly recorded from smaller, monogenetic cinder cones. Manantial Pelado (35.5° S) is a long-lived stratocone in the Southern Andean Volcanic Zone (SVZ) overlying thick continental crust (45–50 km) that produces almost exclusively mafic material. As Manantial Pelado is surrounded by extensive silicic volcanism, the study of its mafic exposure as a stratocone can be used to further understand magmatic origins of long-lived volcanic systems. Our study uses textural, geochemical, and geochronological data from lavas collected from Manantial Pelado to characterize its magmatic petrogenesis, assess the primitive nature, and explain processes in the crust within the SVZ. A geologic description of the volcano reveals a mostly monotonous eruptive history of basaltic andesites that are now accessible through glacially carved valleys. New 40 Ar/ 39 Ar dating constrains most of the volcano’s cone constructing phase to last from ~ 220 to 190 ka. At ~ 30 ka, small-volume activity and different petrography of more intermediate magmas were present reflecting a change in the volcano’s character. A combination of the whole-rock and mineral-scale data reveals that basaltic andesites at Manantial Pelado are among the most primitive magmas in the thickened crust of the SVZ. Evidence for this primitive signature consists of textural and zonation patterns in olivine, the presence of Cr-spinel in olivine cores, and elevated Fo and Ni content within olivine cores. This data combined with elemental diffusion modeling provides evidence for a primitive signature for these lavas. Intermediate Fo olivines with uniform core compositions (Fo 80–84 ) suggest that basaltic andesites reside in the crust in quasi-closed system environments for extended storage prior to eruption (~ 25–6000 years). Diffusive equilibration in those intermediate Fo olivines masks the primitive nature of the magmas. These results suggest that mafic magmas can have a protracted storage history in the crust that does not significantly alter their primitive bulk composition before reaching the surface. We argue that these are important processes in understanding the magmatic origin of long-lived systems and the presence of compositionally homogenous olivines at intermediate Fo content may represent cryptic evidence for recharge with primitive magmas that experienced prolonged crustal storage.

Manantial Pelado↗

USGS1995

Petrography, geochemistry, and depositional setting of the San Pedro and Santo Tomas coal zones: Anomalous algae-rich coals in the middle part of the Claiborne Group (Eocene) of Webb County, Texas

Two coal zones, the San Pedro and the overlying Santo Tomas, are present for nearly 35 km in outcrop, surface and underground mines, and shallow drill holes along the strike of the middle part of the Claiborne Group (Eocene) in Webb County, Texas. A sandstone-dominated interval of 25 to 35 m separates the two coal zones, which range up to 3 m in thickness. Each coal zone contains carbonaceous shales, thin (<0.75 m) impure coal beds, and thin (<0.85 m) but commercially significant nonbanded coal beds. The nonbanded coals are different from other Tertiary coals of the Gulf of Mexico Coastal Plain: unlike lignites that are typical of the older Wilcox Group (Paleocene-Eocene) and younger Jackson Group (Eocene), nonbanded coals of the Claiborne Group have high vitrinite-reflectance values (0.53 R max ) and high calorific yields (average 6670 kcal/kg or 12,000 Btu, dry basis). The coals are weakly agglomerating (free-swelling index is 1.5–2.0) and have an apparent rank of high-volatile bituminous. The coal-bearing portion of the middle Claiborne Group in the Rio Grande area represents a fining-upward transition from sandstone-dominated, marine-influenced, lower delta plain depositional environments to more inland, mudstone-rich, predominantly freshwater deltaic settings. Discontinuities within the San Pedro coal zone are attributed mainly to the influence of contemporaneous deposition of distributary mouth-bar sand bodies. The less variable nature of the Santo Tomas coal zone reflects its origin in the upper part of an interlobe basin that received only minor clastic influx. Petrographic attributes of the nonbanded coals indicate that they formed subaqueously in fresh to possibly brackish waters. A highly degraded groundmass composed of eugelinite is the main petrographic component (approximately 71%, mineral-matter-free basis). An enriched liptinite fraction (approximately 23%) probably accounts for unusually high calorific values. There is negligible inertinite. Petrographic study of polished blocks indicates that approximately 10 percent of the nonbanded coal from both coal zones is composed of green algae fructifications, which also occur in clastic rocks of the coal-bearing interval. Such algal material cannot be identified or quantified by conventional coal petrographic techniques that utilize particle pellets or by palynological analyses that include acid preparation.

International Journal of Coal Geology↗

USGS2012

An exploration hydrogeochemical study at the giant Pebble porphyry Cu-Au-Mo deposit, Alaska, USA, using high-resolution ICP-MS

A hydrogeochemical study using high resolution ICP-MS was undertaken at the giant Pebble porphyry Cu-Au-Mo deposit and surrounding mineral occurrences. Surface water and groundwater samples from regional background and the deposit area were collected at 168 sites. Rigorous quality control reveals impressive results at low nanogram per litre (ng/l) levels. Sites with pH values below 5.1 are from ponds in the Pebble West area, where sulphide-bearing rubble crop is thinly covered. Relative to other study area waters, anomalous concentrations of Cu, Cd, K, Ni, Re, the REE, Tl, SO 4 2− and F − are present in water samples from Pebble West. Samples from circum-neutral waters at Pebble East and parts of Pebble West, where cover is much thicker, have anomalous concentrations of Ag, As, In, Mn, Mo, Sb, Th, U, V, and W. Low-level anomalous concentrations for most of these elements were also found in waters surrounding nearby porphyry and skarn mineral occurrences. Many of these elements are present in low ng/l concentration ranges and would not have been detected using traditional quadrupole ICP-MS. Hydrogeochemical exploration paired with high resolution ICP-MS is a powerful new tool in the search for concealed deposits.

Alaska↗

USGS2016

Mineral thermometry and fluid inclusion studies of the Pea Ridge iron oxide-apatite–rare earth element deposit, Mesoproterozoic St. Francois Mountains Terrane, southeast Missouri, USA

Mineral thermometry and fluid inclusion studies were conducted on variably altered and mineralized samples from the Mesoproterozoic Pea Ridge iron oxide-apatite (IOA)-rare earth element (REE) deposit in order to constrain P-T conditions, fluid chemistry, and the source of salt and volatiles during early magnetite and later REE mineralization. Scanning electron microscopy (SEM)-cathodoluminescence and SEM-backscatter electron images show that quartz and rutile precipitated before, during, and after magnetite and REE mineral growth. Ti-in-quartz and Zr-in-rutile equilibration temperatures range from ≤350° to 750°C in the amphibole, magnetite, hematite, and silicified zones where T increased during magnetite and quartz growth and dropped precipitously after fracturing and brecciation. Late drusy quartz cements within a REE-rich breccia pipe record the lowest T (≤315°–400°C). Liquid-, vapor-rich, and hypersaline (±hematite, calcite) fluid inclusions are common and liquid CO 2 is present locally. Salinities define three populations: saline (10–27 wt % NaCl equiv), hypersaline (34–>60 wt % NaCl equiv), and dilute (0–10 wt % NaCl equiv ). The wide range of eutectic melting temperatures (−67° to −19°C) suggests that saline inclusions trapped variable proportions of a CaCl-MgCl-FeCl-bearing fluid end member and an NaCl-KCl fluid end member. Homogenization temperatures and pressures of these saline inclusions suggest they were trapped when fluids unmixed into brine and vapor at T <350°C, P <15 MPa, and a depth of ~1.5 km. Hypersaline inclusions were trapped at low T and P (~200°C and ~1 MPa) along the V + L + H curve when the system vented to the paleosurface. Data for dilute inclusions in late drusy quartz from the REE-rich breccia pipe are indicative of a boiling epithermal environment. The Na/Cl, Na/K, and Cl/Br ratios of fluid inclusion extracts provide evidence for mixtures of magmatic hydrothermal fluids and evaporated seawater. Extracts from magnetite, hematite, and pyrite plot in the magmatic-hydrothermal field, indicating that Fe was derived from a magmatic source. Their enrichments in Mg and Ca are consistent with a mafic magmatic source. The positive correlation between Na/Mg and Na/Ca ratios may be due to halite saturation or albitization of igneous rocks. Extracts from barite in the REE-rich breccia pipes are enriched in Na and Br and plot near the seawater evaporation trend. He is highly enriched relative to Ne and Ar in fluid inclusion extracts, which precludes air as a source of He. Although the He is mostly of crustal origin, pyrite with a 3 He/ 4 He (R/R A ) of 0.1 contains up to 12% mantle He. Many extracts have low 20 Ne/ 22 Ne ratios due to nucleogenic production of 22 Ne in high F/O minerals such as fluorapatite or F biotite. The arrays of data for 3 He/ 4 He (R/R A ) and 22 Ne/ 20 Ne suggest that volatiles were derived from two sources, a moderate F mafic magma containing mantle He and a high F silicic magma with crustal He. Together with other evidence cited in this report, these data (1) support a magmatic hydrothermal origin for the Mesoproterozoic magnetite-apatite deposit with ore fluids derived from a concealed mafic to intermediate-composition intrusion, (2) suggest that the REE minerals in breccia pipes were either derived from apatite or precipitated in response to decompression and cooling during breccia pipe formation, (3) provide evidence for the influx of basinal brine, magmatic fluids from granitic intrusions, and meteoric water after breccia pipe formation, and (4) show that Pea Ridge was relatively unaffected by the late Paleozoic Mississippi Valley-type (MVT) Pb-Zn system in overlying Cambrian sedimentary rocks.

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