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At least 865 records · Page 48Linked to original sources

USGS2000

Geochemical investigations by the U.S. Geological Survey on uranium mining, milling, and environmental restoration

Recent research by the U.S. Geological Survey has characterized contaminant sources and identified important geochemical processes that influence transport of radionuclides from uranium mining and milling wastes. 1) Selective extraction studies indicated that alkaline earth sulfates and hydrous ferric oxides are important hosts of 226 Ra in uranium mill tailings. The action of sulfate-reducing and ironreducing bacteria on these phases was shown to enhance release of radium, and this adverse result may temper decisions to dispose of uranium mill tailings in anaerobic environments. 2) Field studies have shown that although surface-applied sewage sludge/wood chip amendments aid in revegetating pyritic spoil, the nitrogen in sludge leachate can enhance pyrite oxidation, acidification of groundwater, and the consequent mobilization of metals and radionuclides. 3) In a U.S. Environmental Protection Agencyfunded study, three permeable reactive barriers consisting of phosphate-rich material, zero-valent iron, or amorphous ferric oxyhydroxide have been installed at an abandoned uranium upgrader facility near Fry Canyon, UT. Preliminary results indicate that each of the permeable reactive barriers is removing the majority of the uranium from the groundwater. 4) Studies on the geochemistry of rare earth elements as analogues for actinides such as uranium and thorium in acid mine drainage environments indicate high mobility under acid-weathering conditions but measurable attenuation associated with iron and aluminum colloid formation. Mass balances from field and laboratory studies are being used to quantify the amount of attenuation. 5) A field study in Colorado demonstrated the use of 234 U/ 238 U isotopic ratio measurements to evaluate contamination of shallow groundwater with uranium mill effluent.

Utah↗

USGS2011

USGS global change science strategy: A framework for understanding and responding to climate and land-use change

This U.S. Geological Survey (USGS) Global Change Science Strategy expands on the Climate Variability and Change science component of the USGS 2007 Science Strategy, “Facing Tomorrow’s Challenges: USGS Science in the Coming Decade” (U.S. Geological Survey, 2007). Here we embrace the broad definition of global change provided in the U.S. Global Change Research Act of 1990 (Public Law 101–606,104 Stat. 3096–3104)—“Changes in the global environment (including alterations in climate, land productivity, oceans or other water resources, atmospheric chemistry, and ecological systems) that may alter the capacity of the Earth to sustain life”—with a focus on climate and land-use change. There are three major characteristics of this science strategy. First, it addresses the science required to broadly inform global change policy, while emphasizing the needs of natural-resource managers and reflecting the role of the USGS as the science provider for the Department of the Interior and other resource-management agencies. Second, the strategy identifies core competencies, noting 10 critical capabilities and strengths the USGS uses to overcome key problem areas. We highlight those areas in which the USGS is a science leader, recognizing the strong partnerships and effective collaboration that are essential to address complex global environmental challenges. Third, it uses a query-based approach listing key research questions that need to be addressed to create an agenda for hypothesis-driven global change science organized under six strategic goals. Overall, the strategy starts from where we are, provides a vision for where we want to go, and then describes high-priority strategic actions, including outcomes, products, and partnerships that can get us there. Global change science is a well-defined research field with strong linkages to the ecosystems, water, energy and minerals, natural hazards, and environmental health components of the USGS Science Strategy (2007). When science strategies that cover these other components are developed, coordinated implementation will be necessary to achieve Bureau-level synergies and optimize capabilities and expertise. In October 2010, USGS realigned its management and budget structure to implement its 2007 Science Strategy. The new organizational structure, in which “Global Change” is one of seven key mission areas, lends itself to the advancement of the established six strategic goals. USGS global change science is formally represented by the “Climate and Land-Use Change” Mission Area in the FY 2012 budget (USGS, 2011). This plan was developed by the USGS Global Change Science Strategy Planning Team (SSPT) appointed by the USGS Director on March 4, 2010 and charged with developing a Global Change Science Strategy for the coming decade (McNutt, 2010). USGS managers and science staff are the main audience for this science strategy. This document is also intended to serve as the foundation for consistent USGS collaboration and communication with partners and stakeholders.

Open-File Report↗

USGS1994

Degradation of methyl bromide by methanotrophic bacteria in cell suspensions and soils

Cell suspensions of Methylococcus capsulatus mineralized methyl bromide (MeBr), as evidenced by its removal from the gas phase, the quantitative recovery of Br - in the spent medium, and the production of 14 CO 2 from [ 14 C]MeBr. Methyl fluoride (MeF) inhibited oxidation of methane as well as that of [ 14 C]MeBr. The rate of MeBr consumption by cells varied inversely with the supply of methane, which suggested a competitive relationship between these two substrates. However, MeBr did not support growth of the methanotroph. In soils exposed to high levels (10,000 ppm) of MeBr, methane oxidation was completely inhibited. At this concentration, MeBr removal rates were equivalent in killed and live controls, which indicated a chemical rather than biological removal reaction. At lower concentrations (1,000 ppm) of MeBr, methanotrophs were active and MeBr consumption rates were 10-fold higher in live controls than in killed controls. Soils exposed to trace levels (10 ppm) of MeBr demonstrated complete consumption within 5 h of incubation, while controls inhibited with MeF or incubated without O 2 had 50% lower removal rates. Aerobic soils oxidized [ 14 C]MeBr to 14 CO 2 , and MeF inhibited oxidation by 72%. Field experiments demonstrated slightly lower MeBr removal rates in chambers containing MeF than in chambers lacking MeF. Collectively, these results show that soil methanotrophic bacteria, as well as other microbes, can degrade MeBr present in the environment.

Applied and Environmental Microbiology↗

USGS2008

Isotope geochemistry of mercury in source rocks, mineral deposits and spring deposits of the California Coast Ranges, USA

We present here the first study of the isotopic composition of mercury in rocks, ore deposits, and active spring deposits from the California Coast Ranges, a part of Earth's crust with unusually extensive evidence of mercury mobility and enrichment. The Franciscan Complex and Great Valley Sequence, which form the bedrock in the California Coast Ranges, are intruded and overlain by Tertiary volcanic rocks including the Clear Lake Volcanic Sequence. These rocks contain two types of mercury deposits, hot-spring deposits that form at shallow depths (< 300??m) and silica-carbonate deposits that extend to depths of 1000??m. Active springs and geothermal areas continue to precipitate Hg and Au and are modern analogues to the fossil hydrothermal systems preserved in the ore deposits. The Franciscan Complex and Great Valley Sequence contain clastic sedimentary rocks with higher concentrations of mercury than volcanic rocks of the Clear Lake Volcanic Field. Mean mercury isotopic compositions (??202Hg) for all three rock units are similar, although the range of values in Franciscan Complex rocks is greater than in either Great Valley or Clear Lake rocks. Hot spring and silica-carbonate mercury deposits have similar average mercury isotopic compositions that are indistinguishable from averages for the three rock units, although ??202Hg values for the mercury deposits have a greater variance than the country rocks. Precipitates from spring and geothermal waters in the area have similarly large variance and a mean ??202Hg value that is significantly lower than the ore deposits and rocks. These observations indicate that there is little or no isotopic fractionation (< ?? 0.5???) during release of mercury from its source rocks into hydrothermal solutions. Isotopic fractionation does appear to take place during transport and concentration of mercury in deposits, however, especially in their uppermost parts. Boiling of hydrothermal fluids, separation of a mercury-bearing CO2 vapor or reduction and volatilization of Hg(0) in the near-surface environment are likely the most important processes causing the observed Hg isotope fractionation. This should result in the release of mercury with low ??202Hg values into the atmosphere from the top of these hydrothermal systems. Estimates of mass balance suggest that residual Hg reservoirs are not measurably enriched in heavy Hg isotopes as a result of this process because only a small amount of Hg (< 4%) leaves actively ore-forming systems. ?? 2008 Elsevier B.V. All rights reserved.

Earth and Planetary Science Letters↗

USGS2017

Origin and evolution of mineralizing fluids and exploration of the Cerro Quema Au-Cu deposit (Azuero Peninsula, Panama) from a fluid inclusion and stable isotope perspective

Cerro Quema is a high sulfidation epithermal Au-Cu deposit with a measured, indicated and inferred resource of 35.98 Mt. @ 0.77 g/t Au containing 893,600 oz. Au (including 183,930 oz. Au equiv. of Cu ore). It is characterized by a large hydrothermal alteration zone which is interpreted to represent the lithocap of a porphyry system. The innermost zone of the lithocap is constituted by vuggy quartz with advanced argillic alteration locally developed on its margin, enclosed by a well-developed zone of argillic alteration, grading to an external halo of propylitic alteration. The mineralization occurs in the form of disseminations and microveinlets of pyrite, chalcopyrite, enargite, tennantite, and trace sphalerite, crosscut by quartz, barite, pyrite, chalcopyrite, sphalerite and galena veins. Microthermometric analyses of two phase (L + V) secondary fluid inclusions in igneous quartz phenocrysts in vuggy quartz and advanced argillically altered samples indicate low temperature (140–216 °C) and low salinity (0.5–4.8 wt% NaCl eq.) fluids, with hotter and more saline fluids identified in the east half of the deposit (Cerro Quema area). Stable isotope analyses (S, O, H) were performed on mineralization and alteration minerals, including pyrite, chalcopyrite, enargite, alunite, barite, kaolinite, dickite and vuggy quartz. The range of δ 34 S of sulfides is from − 4.8 to − 12.7‰, whereas δ 34 S of sulfates range from 14.1 to 17.4‰. The estimated δ 34 S ΣS of the hydrothermal fluid is − 0.5‰. Within the advanced argillic altered zone the δ 34 S values of sulfides and sulfates are interpreted to reflect isotopic equilibrium at temperatures of ~ 240 °C. The δ 18 O values of vuggy quartz range from 9.0 to 17.5‰, and the δ 18 O values estimated for the vuggy quartz-forming fluid range from − 2.3 to 3.0‰, indicating that it precipitated from mixing of magmatic fluids with surficial fluids. The δ 18 O of kaolinite ranges from 12.7 to 18.1‰ and δD from − 103.3 to − 35.2‰, whereas the δ 18 O of dickite varies between 12.7 and 16.3‰ and δD from − 44 to − 30. Based on δ 18 O and δD, two types of kaolinite/dickite can be distinguished, a supergene type and a hypogene type. Combined, the analytical data indicate that the Cerro Quema deposit formed from magmatic-hydrothermal fluids derived from a porphyry copper-like intrusion located at depth likely towards the east of the deposit. The combination of stable isotope geochemistry and fluid inclusion analysis may provide useful exploration vectors for porphyry copper targets in the high sulfidation/lithocap environment.

Azuero Peninsula↗

USGS1985

Geologic and hydrologic characterization and evaluation of the Basin and Range Province relative to the disposal of high-level radioactive waste: Part II, Geologic and hydrologic characterization

The geology and hydrology of the Basin and Range Province of the western conterminous United States are characterized in a series of data sets depicted in maps compiled for evaluation of prospective areas for further study of geohydrologic environments for isolation of high-level radioactive waste. The data sets include: (1) Average precipitation and evaporation; (2) surface distribution of selected rock types; (3) tectonic conditions; and (4) surface- and ground -water hydrology and Pleistocene lakes and marshes. Rocks mapped for consideration as potential host media for the isolation of high-level radioactive waste are widespread and include argillaceous rocks, granitic rocks, tuffaceous rocks, mafic extrusive rocks, evaporites, and laharic breccias. The unsaturated zone, where probably as thick as 150 meters (500 feet), was mapped for consideration as an environment for isolation of high-level waste. Unsaturated rocks of various lithologic types are widespread in the Province. Tectonic stability in the Quaternary Period is considered the key to assessing the probability of future tectonism with regard to high-level radioactive waste disposal. Tectonic conditions are characterized on the basis of the seismic record, heat-flow measurements, the occurrence of Quaternary faults, vertical crustal movement, and volcanic features. Tectonic activity, as indicated by seismicity, is greatest in areas bordering the western margin of the Province in Nevada and southern California, the eastern margin of the Province bordering the Wasatch Mountains in Utah and in parts of the Rio Grande valley. Late Cenozoic volcanic activity is widespread, being greatest bordering the Sierra Nevada in California and Oregon, and bordering the Wasatch Mountains in southern Utah and Idaho. he arid to semiarid climate of the Province results in few perennial streams and lakes. A large part of the surface drainage is interior and the many closed basins commonly are occupied by playas or dry lake beds. The Province is divided into ground-water flow units defined on the basis of ground-water divides, ground-water flow lines, and surface streams that receive ground-water discharge. Ground water contains less than 500 milligrams per liter of dissolved solids throughout most of the Province. Ground water is more mineralized in areas underlain by evaporitic rocks, overlain by playas, and near saline lakes. Ground water is of the calcium, magnesium, or sodium bicarbonate type in the areas where dissolved-solids concentrations are less than 500 milligrams per liter, and of the calcium, magnesium, or sodium sulfate or chloride type where dissolved-solids concentrations are greater than 500 milligrams per liter. Geologic and hydrologic evidence is found for about 100 lakes and marshes that existed during the Pleistocene Epoch. The possibility of a recurrence of pluvial conditions, such as existed in the Pleistocene, is of concern in repository siting because of possible changes in hydrologic conditions. The Pleistocene lakes and marshes provide clues to the hydrology during pluvial climates.

Arizona, California, Idaho, Nevada, New Mexico, Or↗

USGS2022

A novel method for conducting a geoenvironmental assessment of undiscovered ISR-amenable uranium Resources: Proof-of-concept in the Texas Coastal Plain

A geoenvironmental assessment methodology was developed to estimate waste quantities and disturbances that could be associated with the extraction of undiscovered uranium resources and identify areas on the landscape where uranium and other constituents of potential concern (COPCs) that may co-occur with uranium deposits in this region are likely to persist, if introduced into the environment. Prior to this work, a method was lacking to quantitively assess the environmental aspects associated with potential development of undiscovered uranium resources at a scale of a uranium resource assessment. The mining method of in situ recovery (ISR) was historically used to extract uranium from deposits in the Goliad Sand of the Texas Coastal Plain. For this reason, the study’s methodology projected the following types of wastes and disturbances commonly associated with ISR based on historical ISR mining records: the mine area, affected aquifer volume, mine pore volume, water pumped and disposed during uranium extraction and restoration, and radon emissions. Within the tract permissive for the occurrence of undiscovered uranium resources, maps and statistics of factors were derived that indicate the potential contaminant pathways. The percentage of days meeting the criteria for air stagnation indicate the potential for radon accumulation; the geochemical mobility of COPCs in groundwater in combination with effective recharge indicates the potential for infiltration of surface-derived COPCs; the geochemical mobility of COPCs in groundwater combined with hydraulic conductivity indicates the propensity for transmitting fluids away from contaminated or mined aquifers; and finally, geochemical mobility of COPCs in surface water combined with the factor for climatic erosivity (R factor) indicates the potential for COPCs to persist in surface waters due to runoff. This work resulted in a new methodology that can be applied to any undiscovered mineral resource to better understand possible wastes and disturbances associated with extraction and identify areas on the landscape where COPCs are likely to persist.

Texas↗

USGS1993

Intensity and duration of chemical weathering: An example from soil clays of the southeastern Koolau Mountains, Oahu, Hawaii

Orographic precipitation on the southern flank of the southeastern Koolau Mountains produces a pronounced precipitation gradient. The corresponding gradient in the intensity of the chemical weathering environment provides an opportunity to address the effects of varying chemical weathering intensity on the composition of clay-size weathering products in soils developed on basalt. In addition, little-modified remnants of the constructional surface of the Koolau Volcano, isolated by stream dissection, remain as facets on the southern ends of the parallel ridges of the study area. By comparing clay mineralogy of soils developed on these older geomorphic surfaces with those developed on the younger sharp-crested ridges and steep side slopes, the effects of weathering duration on clay mineralogy can also be addressed. Soil clays in this part of the Koolau Mountains are mineralogically complex; principal phases include smectite, kaolinite, and halloysite, but pure end member phases are uncommon. Rather, most phases contain some amount of mixed layering. Smectite may contain small (<5%) amounts of randomly interstratified halloysite. Similarly, kaolinite commonly contains a small proportion of halloysite interlayers. A complex halloysitic phase shows evidence of interstratification with both smectite and kaolinite. Nonphyllosilicates found in the clay fraction include gibbsite, goethite, rare quartz, and perhaps cristobalite. The gradient in precipitation is reflected in soil clay mineralogy by varying proportions of dominantly smectitic, kaolinitic, and halloysitic phases. In regions of relatively low precipitation (<2,000 mm/yr), soils are dominated by the smectitic and halloysitic phases. With increased precipitation (as much as ∼4,000 mm/yr), kaolinitic and halloysitic phases become the dominant clay minerals, and goethite and gibbsite become increasingly abundant. Older soils developed on geomorphic surfaces representing the original constructional surface of Koolau Volcano are markedly more leached than those from younger landscapes in the same precipitation regime. Although smectite may be present, kaolinite is the dominant phase, and accumulations of Fe and Ti occur in the uppermost soil levels. Enrichment of Zr and Ti in these soils, as compared to concentrations in the original basaltic parent material, indicates that as much as 75% of the parent material has been lost. Thus weathering duration may affect soil clay composition in the same way as weathering intensity. Because smectite and halloysite are expandable clay minerals, their presence in soils may decrease slope stability and influence the nature of slope processes. Soil avalanches occur on steep slopes throughout the study area, whereas slow-moving landslides appear to be restricted to gentler slopes in drier parts of the study area where smectite is abundant. The clay mineralogy of soils thus appears to influence the nature of slope processes in the southeastern Koolau Mountains.

Special Paper of the Geological Society of America↗

USGS1958

Origin of manganese deposits of Busuanga Island, Philippines

The manganese deposits of Busuanga Island, Palawan, are tabular and broadly lenticular bodies which lie conformably within a thick sequence of deformed abort beds. The purpose of this study is to determine the probable mode of origin of the deposits. Similar deposits in other parts of the world have been described by others as products of several different genetic processes. Field and laboratory methods of research were employed in the course of the investigation. Detailed geologic mapping was done on the surface and underground, and many samples of rocks and ores were obtained. Later, intensive study of samples from four typical deposits and from the rooks in the surrounding areas was undertaken, using a variety of laboratory techniques. Microscopic study of thin sections and polished surfaces was supplemented by X-ray and chemical work. More than one hundred X-ray diffraction powder photographs were made to identify minerals, and qualitative chemical studies were made of a number of aamples by use of the X-ray spectrograph. In addition, quantitative chemical analyses were made of certain samples. Finally, published accounts of the occurrence and geological behavior of manganese and silica were consulted to aid in interpretation of the data at hand. Oherty layers in the manganese deposits are lithologically similar to the chart wallrooks and country rook beds. Radiolarian fossils are common in the chart and are also found in some ore specimens. Manganese content of the wallrocks and the country rock beds, however, in essentially nil. The manganese deposits contain mostly psilomelane-type oxides in their near-surface parts, and in the deepest mines this ore grades downward into siliceous protore. In three of the deposits studied, the protore consists mainly of braanite and quartz; in the fourth deposit, hausmannite and the silicate alleghatvite make up the milk of the protore. Some of the protoro is massive, but cherty stones are commonly well layered parallel to the wall rock structure. Grain size is very small, but, like the silica in the chert beds, becomes relatively coarse where the rocks are much deformed. No evidence of large-scale replacement or cross-cutting veins is found in the protores. It is concluded that the original manganiferous deposits were largely non-clastic or oolloidal marine sediments laid down in a reducing environment. The protorea were developed from these beds by processes of diagenesis and low-grade regional metamorphism. The protores were in turn altered to black oxide ore by near-surface agencies during the present erosion cycle. Particular interest is attached to the occurrence of alleghanyite and traces of pyroxmangite and hubnerite(?) in the protorea.

Busuanga Island↗

USGS2012

The Kanuti ophiolite, Alaska

The Kanuti ophiolite is a mafic-ultramafic thrust sheet of probable Jurassic age, formerly considered to be the upper part of the Yukon-Koyukuk ophiolite belt (Angayucham terrane). It is here called the Kanuti ophiolite after the Kanuti River region on the southeastern flank of the Yukon-Koyukuk Basin. The thrust sheet crops out discontinuously for a distance of more than 900 km along the northern and southeastern margins of the basin. It is probably correlative with similar ophiolite thrust sheets to the north in the western Brooks Range and to the south in the Ruby geanticline. Technically, the ophiolite is considered to be the Kanuti thrust panel of the Angayucham-Totzitna terrane. The Kanuti consistently overlies another extensive thrust sheet, consisting mostly of pillow basalt and radiolarian chert of Devonian to Jurassic age (Narvak thrust panel). This sheet is thrust over a third sheet consisting of probable Devonian phyllite and metagraywacke, which is in turn thrust over older metamorphic rocks (Slate Creek thrust panel). The Kanuti ophiolite is a partial ophiolite that consists of a lower residual mantle suite and an upper magmatic suite, but dikes, extrusives, and sediments are absent. The residual mantle suite is composed of harzburgite and dunite with refractory mineral compositions. The harzburgite is attributed to partial melting and extraction of basaltic magma; residual dunite is attributed to partial melting or to reaction of orthopyroxene out of harzburgite in contact with ascending melt diapirs. The magmatic suite consists of layered ultramafic and gabbroic rocks, containing minerals having limited iron enrichment. The absence of large volumes of magmatic rocks intermediate in composition between cumulus ultramafics and evolved gabbros favors periodic introduction of magma, rather than closed system fractional crystallization. The ultramafic rocks of both the residual mantle and magmatic suites are tectonites, which have undergone high-temperature deformation involving isoclinal folding on all scales and related syntectonic recrystallization. The olivine fabric is consistent with the glide system {0kl} [100], which has been produced experimentally at 800°–1190°C at 20 kbar. Olivine Z axes and subparallel isoclinal fold axes have consistent, northeast trends throughout the Kanuti region (>100 km NE-SW) and may be close to the original upper mantle flow direction, despite later low-angle thrust faulting. The order of crystallization in the cumulus ultramafic rocks of the magmatic suite is olivine, clinopyroxene, plagioclase, and orthopyroxene. The high Mg numbers of clinopyroxene (0.85–0.93) coexisting with olivine suggest that the cumulus ultramafic rocks crystallized at relatively high pressures (>10 kbar). The effects of parental magma composition cannot be evaluated, but the small difference in Mg numbers of coexisting olivine and clinopyroxene in the cumulus ultramafic rocks and in residual harzburgite suggests that regardless of absolute pressures, the pressure difference between the melting that produced the basalt magma and the initial fractional crystallization of the magma is small. Because of the limited range in rock types in the ophiolite, the tectonic environment cannot be interpreted unambiguously. However, the structural and petrological data are best reconciled with an origin in a volcanic arc tectonic setting.

Journal of Geophysical Research Solid Earth↗

USGS2015

Microbiological oxidation of antimony(III) with oxygen or nitrate by bacteria isolated from contaminated mine sediments

Bacterial oxidation of arsenite [As(III)] is a well-studied and important biogeochemical pathway that directly influences the mobility and toxicity of arsenic in the environment. In contrast, little is known about microbiological oxidation of the chemically similar anion antimonite [Sb(III)]. In this study, two bacterial strains, designated IDSBO-1 and IDSBO-4, which grow on tartrate compounds and oxidize Sb(III) using either oxygen or nitrate, respectively, as a terminal electron acceptor, were isolated from contaminated mine sediments. Both isolates belonged to the Comamonadaceae family and were 99% similar to previously described species. We identify these novel strains as Hydrogenophaga taeniospiralis strain IDSBO-1 and Variovorax paradoxus strain IDSBO-4. Both strains possess a gene with homology to the aioA gene, which encodes an As(III)-oxidase, and both oxidize As(III) aerobically, but only IDSBO-4 oxidized Sb(III) in the presence of air, while strain IDSBO-1 could achieve this via nitrate respiration. Our results suggest that expression of aioA is not induced by Sb(III) but may be involved in Sb(III) oxidation along with an Sb(III)-specific pathway. Phylogenetic analysis of proteins encoded by the aioA genes revealed a close sequence similarity (90%) among the two isolates and other known As(III)-oxidizing bacteria, particularly Acidovorax sp. strain NO1. Both isolates were capable of chemolithoautotrophic growth using As(III) as a primary electron donor, and strain IDSBO-4 exhibited incorporation of radiolabeled [ 14 C]bicarbonate while oxidizing Sb(III) from Sb(III)-tartrate, suggesting possible Sb(III)-dependent autotrophy. Enrichment cultures produced the Sb(V) oxide mineral mopungite and lesser amounts of Sb(III)-bearing senarmontite as precipitates.

Idaho↗

USGS2025

Shallow geologic framework of the Mississippi Sound and the potential for sediment resources

The Mississippi Sound, an estuarine environment located between the mainland and barrier islands bordering the northern Gulf of America (formerly the Gulf of Mexico), serves as a vital ecosystem for the States of Mississippi and Alabama. Spanning approximately 100 kilometers from east to west and covering 1,400 square kilometers, the sound is home to marine industry and ports, and its shallow and brackish waters sustain a diverse array of marine life. Barrier islands along the southern edge of the sound separate the microtidal estuary from the Gulf of America. This protection from gulf wave action mediates current flow within the sound, resulting in predominantly fine-grained sediment deposition along the seafloor. This study, conducted by the U.S. Geological Survey in cooperation with the U.S. Army Corps of Engineers, provides insight on fluvial and tidal processes spanning the past 5,000 years. The report synthesizes existing research to provide a comprehensive overview of the sound geology, from Pleistocene origins to present-day morphology, and utilizes high-resolution single channel seismic profiles and sediment data to identify and map sedimentary deposits and morphologic features at and below the seafloor. Despite its ecological significance, the Mississippi Sound faces environmental challenges, including water-quality issues, habitat degradation, storm-induced erosion, and the ongoing threats of sea-level rise and environmental changes. This study uses the present-day understanding of the sound's geology to inform coastal management decisions, hazard assessment, and potential mineral resources.

Louisiana, Mississippi↗

USGS2015

Pore characteristics of Wilcox Group Coal, U.S. Gulf Coast Region: Implications for the occurrence of coalbed gas

Pore characteristics of 27 subbituminous coal samples (16 mesh splits) from the Paleocene–Eocene Wilcox Group of north Louisiana (Ouachita and Caldwell Parishes) and south Texas (Zavala County) were examined in relation to desorbed gas content. Coal gas of the Wilcox Group is primarily biogenic in origin; thermogenic gas also may be present in some areas. On an as-received basis, desorbed gas contents range from 0.59 to 1.28 m 3 /t for Ouachita Parish samples, 0.37 to 5.19 m 3 /t for the Caldwell Parish samples, and 0.02 to 0.06 m 3 /t for the Zavala County samples. For Louisiana coal samples, micropore surface area and volume are correlated to the desorbed gas content of the Wilcox Group coal (correlations: r = 0.50 and 0.47, respectively), suggesting that micropore surface area and volume are important in terms of gas-holding capacity. Adsorption by micropores appears to be the primary form of gas storage for the Louisiana coal samples. Micropore surface area and volumes also are strongly correlated with the carbon/ash yield ratio (r = 0.97 and 0.94, respectively), indicating that gas sorption occurs primarily on organic matter. Mineral matter appears to reduce the sorption capacity of the coal. Micropore width decreases with depth (r = − 0.63), probably as the result of increasing pressure and coal rank with depth. For the Louisiana coal samples, mesopore surface area is negatively correlated with the carbon/ash yield ratio (r = − 0.70), suggesting that mesopores are preferentially associated with mineral matter. Average mesopore size is correlated with desorbed gas (r = 0.80) for the relatively shallow Ouachita Parish samples (average depth = 441 m, 1446 ft); these results suggest that the permeability of the Wilcox coal is greater in the shallow stratigraphic intervals compared to deeper intervals. Additionally, mesopore size decreases with depth (r = − 0.80). For Ouachita Parish coal samples, negative correlations of gas with mesopore surface area (r = − 0.74) and mesopore volume (r = − 0.56) strongly suggest that gas is not adsorbed in mesopores, and that free gas may be present in larger mesopores, macropores, or fractures of the Wilcox coal. Results also suggest that moisture in Ouachita Parish samples is present in mesopores; moisture in mesopores may have blocked gas adsorption. The low-gas south Texas samples (average depth = 313 m, 1026 ft) are markedly different from the Louisiana samples. Specifically, micropore surface area and micropore volume are negatively correlated with desorbed gas for the Texas samples (r =− 0.21 and − 0.36, respectively). Geologic or environmental conditions probably were not conducive to the generation or storage of microbial gas in the Zavala County coals. The geologic settings (i.e., salinity of formation water, groundwater recharge, permeability of coal) of each study area are important factors that need to be considered in relation to the potential for generation or storage of microbial gas. In south Texas, tectonic stress may have led to a reduction in permeability in the Wilcox Group coal, creating an unfavorable environment for the generation or preservation of microbial gas. The subbituminous rank of the Zavala coals is also too low for significant thermogenic gas generation to have occurred.

Arkansas, Louisiana, Mississippi, Texas↗

USGS2017

Undiscovered porphyry copper resources in the Urals—A probabilistic mineral resource assessment

A probabilistic mineral resource assessment of metal resources in undiscovered porphyry copper deposits of the Ural Mountains in Russia and Kazakhstan was done using a quantitative form of mineral resource assessment. Permissive tracts were delineated on the basis of mapped and inferred subsurface distributions of igneous rocks assigned to tectonic zones that include magmatic arcs where the occurrence of porphyry copper deposits within 1 km of the Earth's surface are possible. These permissive tracts outline four north-south trending volcano-plutonic belts in major structural zones of the Urals. From west to east, these include permissive lithologies for porphyry copper deposits associated with Paleozoic subduction-related island-arc complexes preserved in the Tagil and Magnitogorsk arcs, Paleozoic island-arc fragments and associated tonalite-granodiorite intrusions in the East Uralian zone, and Carboniferous continental-margin arcs developed on the Kazakh craton in the Transuralian zone. The tracts range from about 50,000 to 130,000 km 2 in area. The Urals host 8 known porphyry copper deposits with total identified resources of about 6.4 million metric tons of copper, at least 20 additional porphyry copper prospect areas, and numerous copper-bearing skarns and copper occurrences. Probabilistic estimates predict a mean of 22 undiscovered porphyry copper deposits within the four permissive tracts delineated in the Urals. Combining estimates with established grade and tonnage models predicts a mean of 82 million metric tons of undiscovered copper. Application of an economic filter suggests that about half of that amount could be economically recoverable based on assumed depth distributions, availability of infrastructure, recovery rates, current metals prices, and investment environment.

Urals↗

USGS2004

Use of short-term (5-Minute) and long-term (18-Hour) leaching tests to characterize, fingerprint, and rank mine-waste material from historical mines in the Deer Creek, Snake River, and Clear Creek Watersheds in and around the Montezuma Mining District, Colorado

Precipitation-induced runoff from historical mine-waste located adjacent to the headwaters of the Snake River, Deer Creek, Saints John Creek, Grizzly Gulch, Stevens Gulch, and Leavenworth Creek contributes to the degradation of water quality in these streams. Because historical mine-waste piles have had long-term exposure to the atmosphere, it is surmised that runoff from these piles, induced by meteorological events such as cloudbursts and snowmelt, may cause mobility of acid and metals into a watershed due to dissolution of soluble minerals. For this study, 13 mine-waste composite samples from various mine-wastes in these drainage basins were leached using both a short-term and a long-term leach test. Analytical results from this combination of leach tests are tools that allow the investigator to quantify (fingerprint) which geochemical components could be expected in runoff from these piles if they were leached by a cloudburst (5-minute leach test), as well as what the ?worst-case? geochemical profile would look like if the material were subject to extended leaching and breakdown of the mine-waste material (18-hour leach test). Also, this combination of leach tests allows the geoscientist the ability to see geochemical changes in the mine-waste leachate over time. That is, does the leachate become more or less acidic over time; does the specific conductance increase or decrease; and are there changes in the concentrations of major or trace elements? Further, use of a ranking scheme described herein will aid in prediction of which historical mine-waste piles have the greatest potential for impact on a watershed should runoff occur. Because of long-term weathering of these historical mine-waste piles, geochemical profiles, leachate time-trends, and relative ranking of the mine-wastes produced from analysis of the leachates are Hageman_SIR_2508.doc 1 7/21/2004 2:50 PM indicative of how the mine-waste piles can be expected to act in the environment and may help to identify the ?bad actors??this may aid in understanding the reasons for water-quality differences between the drainages.

Scientific Investigations Report↗

USGS1997

Effects of interaction between ultramafic tectonite and mafic magma on Nd-Pb-Sr isotopic systems in the Neoproterozoic Chaya Massif, Baikal-Muya ophiolite belt

Sm-Nd, Rb-Sr and U-Pb isotopic systems have been studied in minerals and whole rocks of harzburgites and mafic cumulates from the Chaya Massif, Baikal-Muya ophiolite belt, eastern Siberia, in order to determine the relationship between mantle ultramafic and crustal mafic sections. Geological relations in the Chaya Massif indicate that the mafic magmas were emplaced into, and interacted with older solid peridotite. Hand picked, acid-leached, primary rock-forming and accessory minerals (olivine, orthopyroxene, clinopyroxene and plagioclase) from the two harzburgite samples show coherent behavior and yield 147 Sm/ 144 Nd- 143 Nd/ 144 Nd and 238 U/ 204 Pb- 206 Pb/ 204 Pb mineral isochrons, corresponding to ages of 640 ± 58 Ma (95% confidence level) and 620 ± 71 Ma, respectively. These values are indistinguishable from the crystallization age of the Chaya mafic units of 627 ± 25 Ma (a weighted average of internal isochron Sm-Nd ages of four mafic cumulates). The Rb-Sr and Sm-Nd isotopic systems in the harzburgite whole-rock samples were disturbed by hydrothermal alteration. These alteration-related isotopic shifts mimic the trend of variations in primary isotopic compositions in the mafic sequence, thus emphasizing that isotopic data for ultramafic rocks should be interpreted with great caution. On the basis of initial Sr and Nd values, ultramafic and mafic rocks of the Chaya Massif can be divided into two groups: (1) harzburgites and the lower mafic unit gabbronorites withε Nd = +6.6 to +7.1 andε Sr = −11 to −16; and (2) websterite of the lower unit and gabbronorites of the upper mafic unit:ε Nd = +4.6 to +6.1 andε Sr = −8 to −9. Initial Pb isotopic ratios are identical in all rocks studied, with mean values of 206 Pb/ 204 Pb= 16.994 ± 0.023 and 207 Pb/ 204 Pb= 15.363 ± 0.015. The similarity of ages and initial isotopic ratios within the first group indicates that the isotopic systems in the pre-existing depleted peridotite were reset by extensive interaction with basaltic magma during formation of the mafic crustal sequence. The isotopic data agree with a hypothesized formation of the Chaya Massif in a suprasubduction-zone environment.

Siberia↗

USGS2007

Peru Mercury Inventory 2006

In 2004, a specific need for data on mercury use in South America was indicated by the United Nations Environmental Programme-Chemicals (UNEP-Chemicals) at a workshop on regional mercury pollution that took place in Buenos Aires, Argentina. Mercury has long been mined and used in South America for artisanal gold mining and imported for chlor-alkali production, dental amalgam, and other uses. The U.S. Geological Survey (USGS) provides information on domestic and international mercury production, trade, prices, sources, and recycling in its annual Minerals Yearbook mercury chapter. Therefore, in response to UNEP-Chemicals, the USGS, in collaboration with the Economic Section of the U.S. Embassy, Lima, has herein compiled data on Peru's exports, imports, and byproduct production of mercury. Peru was selected for this inventory because it has a 2000-year history of mercury production and use, and continues today as an important source of mercury for the global market, as a byproduct from its gold mines. Peru is a regional distributor of imported mercury and user of mercury for artisanal gold mining and chlor-alkali production. Peruvian customs data showed that 22 metric tons (t) of byproduct mercury was exported to the United States in 2006. Transshipped mercury was exported to Brazil (1 t), Colombia (1 t), and Guyana (1 t). Mercury was imported from the United States (54 t), Spain (19 t), and Kyrgyzstan (8 t) in 2006 and was used for artisanal gold mining, chlor-alkali production, dental amalgam, or transshipment to other countries in the region. Site visits and interviews provided information on the use and disposition of mercury for artisanal gold mining and other uses. Peru also imports mercury-containing batteries, electronics and computers, fluorescent lamps, and thermometers. In 2006, Peru imported approximately 1,900 t of a wide variety of fluorescent lamps; however, the mercury contained in these lamps, a minimum of approximately 76 kilograms (kg), and in other products such as batteries and computer electronics is not recycled and may ultimately be released to the environment.

Open-File Report↗

USGS1995

Areal distribution of selected trace elements, salinity, and major ions in shallow ground water, Tulare Basin, Southern San Joaquin Valley, California

The distribution of salinity and selected trace elements in shallow ground water in the Tulare Basin, California, was assessed to evaluate potential problems related to disposal in evaporation ponds of irrigation drain water containing elevated concentrations of selenium and other trace elements. The constituents of primary concern were selenium, arsenic, and salinity; uranium, boron, and molybdenum also were evaluated. Samples from 117 shallow wells were analyzed, and the results for samples from 110 of the wells were interpreted in relation to surficial geology, sediment depositional environment, soil characteristics, and hydrologic processes to determine the geochemical and hydrologic factors affecting the distribution of these constituents in ground water. In general, shallow ground water in areas where concentrations of salinity and most trace elements are elevated is influenced primarily by sediments derived from marine sedimentary rocks originating in the Coast Range, San Emigdio Mountains, and Tehachapi Mountains, and probably by unusual exposures of similar marine formations in the Sierra Nevada. Ground water in areas where concentrations of salinity and trace elements are significantly lower generally is influenced by igneous and metamorphic rocks exposed in the Sierra Nevada. In addition to sources of sediments, evaporation of shallow ground water, as indicated by isotopic enrichment of oxygen-18 and deuterium, increases salinity and concentrations of conservative trace elements such as selenium (under oxidizing conditions) and boron. Redox conditions affect the oxidation state of all trace elements of concern, except boron, and were found to be a major influence on trace-element solubility. Under oxidized conditions, selenate predominates and behaves conservatively, and arsenate predominates and is affected by sorption reactions that can limit arsenic solubility. Under reduced conditions, selenium is reduced to insoluble elemental selenium and arsenite predominates and generally is more soluble than arsenate. Elevated concentrations of uranium in shallow ground water probably are associated with uranium deposits in Kern County and other parts of the basin where oxidized conditions cause the more soluble uranyl species to predominate. Boron was correlated with salinity and behaved conservatively, whereas adsorption and precipitation of molybdenum minerals probably limited molybdenum solubility. Interrelations among constituents were examined with principal component analysis. The first two principal components explained 50.7 percent of the variance in the data. The first principal component was related to salinity, and the second principal component was related to redox conditions, reflecting two of the major influences on shallow groundwater quality found in this study.

California↗