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Digital data in support of studies and assessments of coal and petroleum resources in the Appalachian basin

The Appalachian basin is a mature basin containing abundant oil, gas, and coal resources. Its fossil-fuel-bearing strata range in age from Cambrian to Permian and extend over the States of New York, Pennsylvania, Maryland, Ohio, West Virginia, Virginia, Kentucky, Tennessee, Georgia, and Alabama. The basin has provided abundant fossil fuels to support the Nation’s economic growth for at least 150 years and U.S. Geological Survey (USGS) assessments suggest that substantial untapped resources remain. A merger of new and old geologic data and ideas is required to locate and extract those remaining resources. This chapter brings together abundant existing datasets in a common and integrated spatial format to advance our understanding of the distribution, geologic framework, burial history, and geochemical character of the basin’s oil, gas, and coal resources. These datasets support the information and findings in chapters B through G of this volume, which include (1) geologic cross sections, seismic profiles, and burial history models that document the depositional and structural framework of the basin; (2) assessments of Carboniferous coal-bed gas and Devonian shale gas; (3) studies about the distribution of oil, gas, and coal fields and the geochemistry of natural gas and oil; and (4) a history of fossil-fuel production in the basin. The data that supported these studies were refined and made more accessible using geographic information system (GIS) tools. The following types of data are included: (1) the bedrock geology of States included within the boundary of the Appalachian basin, (2) the locations of oil and gas wells and fields, (3) data produced for the National Oil and Gas Assessment, and (4) the stratigraphy, geochemistry, and production of coal. Data layers are available in shapefile and Zipped Keyhole Markup Language (KMZ) formats, which can be viewed using ArcGIS, Google Earth, or any software package that supports these data formats. Metadata for these datasets are available in HTML and XML formats. Metadata files contain information about the sources of data used to create the dataset, the creation process steps, the data quality, the geographic coordinate system and horizontal datum used for the dataset, the values of attributes used in the dataset table, information about the publication and the publishing organization, and other information that may be useful to the reader. All links in the metadata were valid at the time of compilation. Some of these links may no longer be valid. No attempt has been made to determine the new online location (if one exists) for the data.

Appalachian basin↗

Thermal maturity of Jurassic shales from the Newark Basin, U.S.A.: Influence of hydrothermal fluids and implications to basin modeling

Organic geochemical investigations were conducted on a series of cores that systematically sampled the uppermost Jurassic strata from the northern Newark Basin. Each sedimentary unit consists of fluvial red sandstones and siltstones with cyclic deposits of interbedded black lacustrine shales and gray deltaic siltstones. In a suite of organic-rich shales from the Boonton, Towaco and Feltville Formations, organic maturation parameters were used to determine aspects of the thermal history of the Newark Basin. Comparisons of model calculations and measured maturities support 39 Ar/ 40 Ar-geochronometer studies that indicate a hydrothermal event occurred ∼175 Ma ago. An increase in the regional geothermal gradient to ∼7.5°C/100 m for ∼5 Ma best conforms to the organic geochemical observations. Biomarker compounds in Boonton and Towaco strata should have been relatively unaltered by this regional event, but anomalous molecular distributions in the organic-rich rocks may have resulted from localized heating by hydrothermal fluids. The effects of this interaction would be very subtle and may be indistinguishable from variations caused by differences in organic facies. Within this uncertainty, sterane and hopane isomerization and steroid aromatization reactions advanced in the Boonton and Towaco Formation strata primarily because of burial and normal geothermal heating that followed the hydrothermal event. Biomarker kinetic models indicate that ∼2400 m of Boonton and post-Boonton strata were eroded after basinal uplift commenced ∼50 Ma ago.

Applied Geochemistry↗

The geochemical atlas of Alaska, 2016

A rich legacy of geochemical data produced since the early 1960s covers the great expanse of Alaska; careful treatment of such data may provide significant and revealing geochemical maps that may be used for landscape geochemistry, mineral resource exploration, and geoenvironmental investigations over large areas. To maximize the spatial density and extent of data coverage for statewide mapping of element distributions, we compiled and integrated analyses of more than 175,000 sediment and soil samples from three major, separate sources: the U.S. Geological Survey, the National Uranium Resource Evaluation program, and the Alaska Division of Geological & Geophysical Surveys geochemical databases. Various types of heterogeneity and deficiencies in these data presented major challenges to our development of coherently integrated datasets for modeling and mapping of element distributions. Researchers from many different organizations and disparate scientific studies collected samples that were analyzed using highly variable methods throughout a time period of more than 50 years, during which many changes in analytical techniques were developed and applied. Despite these challenges, the U.S. Geological Survey has produced a new systematically integrated compilation of sediment and soil geochemical data with an average sample site density of approximately 1 locality per 10 square kilometers (km 2 ) for the entire State of Alaska, although density varies considerably among different areas. From that compilation, we have modeled and mapped the distributions of 68 elements, thus creating an updated geochemical atlas for the State.

Alaska↗

Antimony in mine wastes: Geochemistry, mineralogy, microbiology

Antimony (Sb) is a valuable mined commodity, used mostly in fire retardants, and considered a critical element. It is also a potential environment hazard classed as a carcinogen. Antimony is concentrated in tailings and waste rock from Sb mines as well as other locations, such as precious metal deposits, where Sb is present in the ore but not recovered. This review covers the aqueous geochemistry, isotope chemistry, mineralogy, and microbiology of Sb in the context of mine waste. The primary minerals stibnite and sulfosalts may release Sb in surface and groundwaters and result in contamination of soils, plants, and river sediments. In some cases, Sb mobility is limited by its adsorption and incorporation into Fe (oxyhydr)oxides. At higher Sb concentrations, precipitation of Sb secondary hosts such as tripuhyite (FeSbO 4 , relatively insoluble) and brandholzite (Mg[Sb(OH) 6 ] 2 · 6H 2 O, highly soluble) influence Sb concentrations in water associated with mine waste. Although Sb is nonessential to organisms, microorganisms are involved in oxidation, reduction, and methylation processes that can drive biogeochemical transformations. Limited toxicological information about Sb makes it challenging to establish regulations or guidelines limiting the concentration of Sb. Antimony is frequently associated with arsenic in mine waste, and remediation design is often based on the assumption that both metalloids behave in a similar way. However, new research suggests that in some environments, this is not the case, and Sb should be considered based on its unique biogeochemical behavior.

Economic Geology↗

Geochemical processes controlling selenium in ground water after mining, Powder River Basin, Wyoming, U.S.A.

Geochemical data for samples of overburden from three mines in the Powder River Basin indicate a statistically significant (0.01 confidence level) positive correlation ( r = 0.74) between Se and organic C. Results of factor analysis with varimax rotation on the major and trace element data from the rock samples indicate large (>50) varimax loadings for Se in two of the three factors. In Factor 1, the association of Se with constituents common to detrital grains indicates that water transporting the detrital particles into the Powder River Basin also carried dissolved Se. The large (>50) varimax loadings of Se and organic C in Factor 2 probably are due to the organic affinities characteristic of Se. Dissolved Se concentrations in water samples collected at one coal mine are directly related to the dissolved organic C concentrations. Hydrophilic acid concentrations in the water samples from the mine ranged from 35 to 43% of the total dissolved organic C, and hydrophobic acid concentrations ranged from 40 to 49% of the total dissolved organic C. The largest dissolved organic C concentrations in water from the same mine (34–302 mg/l), coupled with the large proportion of acidic components, may saturate adsorption sites on geothite and similar minerals that comprise the aquifer material, thus decreasing the extent of selenite (SeO 3 2− ) adsorption as a sink for Se as the redox state of ground water decreases.

Wyoming↗

Stream sediment geochemistry of four small drainages on the north shore of Kauai west of Hanalei

Geochemical compositions of fine-grained stream sediment from four drainages on the north shore of the island of Kauai, Hawaii, west of Hanalei and two back-beach sites were explored to increase understanding about land-based runoff and ecological risk from runoff to nearshore coral communities. Stream and beach sediment were collected between July 30 and August 2, 2016, and major, minor, and trace elements in the less than 63 micrometer-diameter fraction were analyzed by inductively coupled plasma optical emission spectroscopy and mass spectroscopy. The potentially toxic metals Cr, Cu, Ni, and Zn exceeded levels at which adverse biological effects could be observed; however, these metals seemed to be largely mineral-bound and thus were unlikely to harm organisms. Cd and Pb were below levels of ecological concern. Only a small amount of fine-grained sediment was retained on beaches west of Hanalei sampled in summer 2016 (mean=8.8 percent, median=0.4 percent, range=0–92.8 percent, n=41). Although the scarcity of fine-grained sediment precluded land-based runoff sourcing to the nearshore region, it did indicate that fine-grained sediment and associated contaminants did not accumulate over the long term in the sampled intertidal, subtidal, and reef-flat environments, which would reduce sediment-related pressures on coral communities there.

Hawaii↗

Compilation of gas geochemistry and isotopic analyses from The Geysers geothermal field: 1978-1991

We present 45 chemical and isotopic analyses from well discharges at The Geysers geothermal field and summarize the most notable geochemical trends. H 2 and H 2 S concentrations are highest in the Southeast Geysers, where steam samples have δD and δ 18 O values that reflect replenishment by meteoric water. In the Northwest Geysers, samples are enriched in gas/steam, CO 2 , CH 4 , and N 2 /Ar relative to the rest of the field, and contain steam that is elevated in δD and δ18O, most likely due to substantial contributions from Franciscan-derived fluids. The δ13C of CO 2 , trends in CH 4 vs. N 2 , and abundance of NH 3 indicate that the bulk of the non-condensable gases are derived from thermal breakdown of organic materials in Franciscan meta-sediments.

Geothermal Resources Council Transactions↗

BET surface area distributions in polar stream sediments: Implications for silicate weathering in a cold-arid environment

BET surface area values are critical for quantifying the amount of potentially reactive sediments available for chemical weathering and ultimately, prediction of silicate weathering fluxes. BET surface area values of fine-grained (<62.5 &mu;m) sediment from the hyporheic zone of polar glacial streams in the McMurdo Dry Valleys, Antarctica (Wright and Taylor Valleys) exhibit a wide range (2.5&ndash;70.6 m 2 /g) of surface area values. Samples from one (Delta Stream, Taylor Valley) of the four sampled stream transects exhibit high values (up to 70.6 m 2 /g), which greatly exceed surface area values from three temperate proglacial streams (0.3&ndash;12.1 m 2 /g). Only Clark stream in Wright Valley exhibits a robust trend with distance, wherein surface area systematically decreases (and particle size increases) in the mud fraction downstream, interpreted to reflect rapid dissolution processes in the weathering environment. The remaining transects exhibit a range in variability in surface area distributions along the length of the channel, likely related to variations in eolian input to exposed channel beds, adjacent snow drifts, and to glacier surfaces, where dust is trapped and subsequently liberated during summer melting. Additionally, variations in stream discharge rate, which mobilizes sediment in pulses and influences water:rock ratios, the origin and nature of the underlying drift material, and the contribution of organic acids may play significant roles in the production and mobilization of high-surface area sediment. This study highlights the presence of sediments with high surface area in cold-based glacier systems, which influences models of chemical denudation rates and the impact of glacial systems on the global carbon cycle.

Applied Geochemistry↗

Processes influencing the transport and fate of contaminated sediments in the coastal ocean– Boston Harbor and Massachusetts Bay

Most of the major urban centers of the United States including Boston, New York, Washington, Chicago, New Orleans, Miami, Los Angeles, San Francisco, and Seattle—are on a coast (fig. 1.1). All of these cities discharge treated sewage effluent into adjacent waters. In 2000, 74 percent of the U.S. population lived within 200 kilometers (km) of the coast. Between 1980 and 2002, the population density in coastal communities increased approximately 4.5 times faster than in noncoastal areas of the U.S. (Perkins, 2004). More people generate larger volumes of wastes, increase the demands on wastewater treatment, expand the area of impervious land surfaces, and use more vehicles that contribute contaminants to street runoff. According to the National Coastal Condition Report II (U.S. Environmental Protection Agency, 2005a), on the basis of coastal habitat, water and sediment quality, benthic index, and fish tissue, the overall national coastal condition is only poor to fair and the overall coastal condition in the highly populated Northeast is poor. Scientific information helps managers to prioritize and regulate coastal-ocean uses that include recreation, commercial fishing, transportation, waste disposal, and critical habitat for marine organisms. These uses are often in conflict with each other and with environmental concerns. Developing a strategy for managing competing uses while maintaining sustainability of coastal resources requires scientific understanding of how the coastal ocean system behaves and how it responds to anthropogenic influences. This report provides a summary of a multidisciplinary research program designed to improve our understanding of the transport and fate of contaminants in Massachusetts coastal waters. Massachusetts Bay and Boston Harbor have been a focus of U.S. Geological Survey (USGS) research because they provide a diverse geographic setting for developing a scientific understanding of the geology, geochemistry, and oceanography of coastal systems in general. Scientific data from this region can also be used to inform decisions about important economic, environmental, and political issues. From the economic viewpoint, the annual value of tourism and shipping in Massachusetts and Cape Cod Bays is about $1.5 billion and $1.9 billion, respectively. Commercial and recreational fishing generates about $240 million per year in the same region (U.S. Environmental Protection Agency, 2005b). The environmental issue is the 300-year history of waste discharge from the Boston metropolitan area into the harbor. This history is punctuated by cycles of environmental degradation, public outcry, and improvements in the sewage treatment system. With each improvement, however, the continuous growth of population in greater Boston (fig. 1.2) and the resulting increase in the volume of waste exceeded the capacity of the treatment system, thereby setting the stage for a new contamination crisis. By the 1980s, the levels of contaminants in sediments of Boston Harbor were among the highest in the nation (National Oceanic and Atmospheric Administration, 1987). Fish were diseased, shellfish beds were closed, and swimming beaches were unsafe after heavy rains; in general, water quality and aesthetics were below acceptable standards. Legal and political issues have always been part of Boston Harbor’s history. The environmental conditions in the 1980s were highlighted in a 1983 legal suit brought by the city of Quincy against the Metropolitan District Commission (MDC, the state agency responsible for sewage treatment) and heads of three state agencies for discharging untreated or poorly treated sewage into the harbor (Dolin, 2004). The suit never went to trial, but through the actions of a Massachusetts Superior Court, the issue of Boston Harbor contamination remained on the political and public agenda. The judge called the harbor “unsafe, unsanitary, indecent, in violation of the law (Clean Water Act), and a danger to the health and welfare of the people” (Forman, 1984). To force the state legislature to implement a plan to improve harbor conditions, the judge threatened to place the MDC in receivership and curtail new sewage hookups for industry. Under intense lobbying by business, the legislature created the Massachusetts Water Resources Authority (MWRA) in December 1984. The independent MWRA was established to manage Boston’s waste treatment system and was given the authority to float bonds to pay for major improvements in the treatment system. In 1985, a Federal court began hearings on a suit brought by the Conservation Law Foundation, the Environmental Protection Agency (USEPA), and towns of Quincy and Winthrop against the MDC and MWRA (as heir to responsibilities of the MDC) for years of violation of the Clean Water Act. The judge ruled against the defendants and required all the parties to submit a construction plan and schedule for a new sewage treatment system. From these submissions, he developed a schedule for treatment system upgrades that would give the “citizens of this commonwealth a public assurance that Boston Harbor will be cleaned up within a defined period of time” (Dolin, 2004). The MWRA’s Boston Harbor cleanup program (Levy and Connor, 1992) has transformed the Boston sewage system. Key improvements were to (1) reduce contaminants at the industrial source; (2) remediate leaks in the sewage-collection system; (3) eliminate sewage sludge discharge to the harbor; (4) upgrade sewage treatment from primary to secondary; (5) construct a new ocean outfall 15.2 km offshore in Massachusetts Bay for discharge of treated effluent (fig. 1.3); and (6) implement improvements in the combined-sewer-overflow system. As part of the harbor cleanup program, the MWRA developed a comprehensive monitoring program (summarized in MWRA, 2004) to assess changes in the harbor and bays that specifically related to the new sewage system. Additional information about conditions and processes in the coastal system on a regional scale and over a long time period was and continues to be important in predicting and interpreting local change. Implementation of the MWRA’s program and the mission of the USGS to understand the geology of the nation’s offshore waters provided an opportunity to conduct a cooperative multidisciplinary research program. This USGS program addresses basic scientific questions as well as concerns raised by management regarding the design, implementation, and assessment of the new sewage treatment system. Already active in Boston Harbor during the late 1970s, the USGS expanded research into Massachusetts Bay with a multidisciplinary program in 1989.

Massachusetts↗

Lithofacies, age, depositional setting, and geochemistry of the Otuk Formation in the Red Dog district, northwestern Alaska

Complete penetration of the Otuk Formation in a continuous drill core (diamond-drill hole, DDH 927) from the Red Dog District illuminates the facies, age, depositional environment, source rock potential, and isotope stratigraphy of this unit in northwestern Alaska. The section, in the Wolverine Creek plate of the Endicott Mountains Allochthon (EMA), is ~82 meters (m) thick and appears structurally uncomplicated. Bedding dips are generally low and thicknesses recorded are close to true thicknesses. Preliminary synthesis of sedimentologic, paleontologic, and isotopic data suggests that the Otuk succession in DDH 927 is a largely complete, albeit condensed, marine Triassic section in conformable contact with marine Permian and Jurassic strata. The Otuk Formation in DDH 927 gradationally overlies gray siliceous mudstone of the Siksikpuk Formation (Permian, based on regional correlations) and underlies black organic-rich mudstone of the Kingak(?) Shale (Jurassic?, based on regional correlations). The informal shale, chert, and limestone members of the Otuk are recognized in DDH 927, but the Jurassic Blankenship Member is absent. The lower (shale) member consists of 28 m of black to light gray, silty shale with as much as 6.9 weight percent total organic carbon (TOC). Thin limy layers near the base of this member contain bivalve fragments (Claraia sp.?) consistent with an Early Triassic (Griesbachian-early Smithian) age. Gray radiolarian chert dominates the middle member (25 m thick) and yields radiolarians of Middle Triassic (Anisian and Ladinian) and Late Triassic (Carnian-late middle Norian) ages. Black to light gray silty shale, like that in the lower member, forms interbeds that range from a few millimeters to 7 centimeters in thickness through much of the middle member. A distinctive, 2.4-m-thick interval of black shale and calcareous radiolarite ~17 m above the base of the member has as much as 9.8 weight percent TOC, and a 1.9-m-thick interval of limy to cherty mudstone immediately above this contains radiolarians, foraminifers, conodonts, and halobiid bivalve fragments. The upper (limestone) member (29 m thick) is lime mudstone with monotid bivalves and late Norian radiolarians, overlain by gray chert that contains Rhaetian (latest Triassic) radiolarians; Rhaetian strata have not previously been documented in the Otuk. Rare gray to black shale interbeds in the upper member have as much as 3.4 weight percent TOC. At least 35 m of black mudstone overlies the limestone member; these strata lack interbeds of oil shale and chert that are characteristic of the Blankenship, and instead they resemble the Kingak Shale. Vitrinite reflectance values (2.45 and 2.47 percent Ro) from two samples of black shale in the chert member indicate that these rocks reached a high level of thermal maturity within the dry gas window. Regional correlations indicate that lithofacies in the Otuk Formation vary with both structural and geographic position. For example, the shale member of the Otuk in the Wolverine Creek plate includes more limy layers and less barite (as blades, nodules, and lenses) than equivalent strata in the structurally higher Red Dog plate of the EMA, but it has fewer limy layers than the shale member in the EMA ~450 kilometers (km) to the east at Tiglukpuk Creek. The limestone member of the Otuk is thicker in the Wolverine Creek plate than in the Red Dog plate and differs from this member in EMA sections to the east in containing an upper cherty interval that lacks monotids; a similar interval is seen at the top of the Otuk Formation ~125 km to the west (Lisburne Peninsula). Our observations are consistent with the interpretations of previous researchers that Otuk facies become more distal in higher structural positions and that within a given structural level more distal facies occur to the west. Recent paleogeographic reconstructions indicate that the Otuk accumulated at a relatively high paleolatitude with a bivalve fauna typical of the Boreal realm. A suite of δ 13 C org (carbon isotopic composition of carbon) data (n=38) from the upper Siksikpuk Formation through the Otuk Formation and into the Kingak(?) Shale in DDH 927 shows a pattern of positive and negative excursions similar to those reported elsewhere in Triassic strata. In particular, a distinct negative excursion at the base of the Otuk (from ‒23.8 to ‒31.3‰ (permil, or parts per thousand)) likely correlates with a pronounced excursion that marks the Permian-Triassic boundary at many localities worldwide. Another feature of the Otuk δ 13 C org record that may correlate globally is a series of negative and positive excursions in the lower member. At the top of the Otuk in DDH 927, the δ 13 C org values are extremely low and may correlate with a negative excursion that is widely observed at the Triassic-Jurassic boundary.

Alaska↗

Chemostratigraphy of the Cretaceous Hue Shale in Arctic Alaska: Exploring paleoceanographic controls on trace element enrichment, organic matter accumulation, and source-rock evolution

We document chemostratigraphy in an outcrop of late Albian to early Campanian (∼103–82 Ma) marine source rocks to better understand paleoenvironmental controls on trace element (TE) enrichment and organic matter accumulation in the distal Colville foreland basin of Arctic Alaska and how those drivers are linked to arc volcanism and successions of Cretaceous oceanographic and climatic biogeochemical events. This unique, 113-m-thick section of Cretaceous Hue Shale deposited during a series of previously undocumented Arctic Cretaceous oceanic anoxic events (Lease et al., 2024) is the only known exposure of thermally immature (0.48–0.52% R o , random vitrinite reflectance) Hue Shale in Arctic Alaska. Strata comprise mainly clay-rich mudstone with elevated total organic carbon (TOC) and hydrogen index values reaching 26.3 wt% (mean = 7.5 wt%) and 689 mg hydrocarbon (HC)/g TOC (mean = 385 mg HC/g TOC), respectively. Maceral composition consists predominantly of fluorescent amorphous organic matter, with abundant brightly fluorescent alginite, including Tasmanites , acritarchs, and Leiosphaeridia . Discrete layers of volcanic ash (preserved as bentonite) are present throughout the section and provide quantitative age control based on U–Pb dates. Chemostratigraphic trends are investigated to advance our understanding of local oceanographic conditions and controls on stratigraphic and temporal heterogeneity of Brookian source rocks. Concurrent sedimentary enrichment in Mo, U, V, Pb, and Cu across the Albian–Cenomanian boundary of the exposed basal gamma-ray zone, may reflect anoxic to euxinic benthic redox conditions favoring organic matter accumulation and preservation. Fluctuating degrees of anoxia-euxinia are inferred throughout the overlying Hue Shale succession, reflected by varying patterns of TE enrichment and TE–TOC covariation. Elevated C org /P molar ratios (>250) across most of the section, with several values exceeding 690, signify that enhanced biological productivity is sustained throughout deposition. Enhanced productivity, recorded by both C org /P and excess Ba, also parallels increases in source rock richness (elevated TOC and S 2 values) during the late Albian–early Cenomanian and late Cenomanian – Turonian. Enhanced productivity and variations in oceanic circulation/stratification likely both drove changes in benthic redox conditions that favored organic carbon accumulation and preservation. Increased continental arc volcanism (e.g., Okhotsk–Chukotka volcanic belt) and High Arctic Large Igneous Province magmatic eruptions throughout the Cretaceous, inferred to have influenced nutrient cycling and local aqueous nutrient availability, also have been invoked as potential drivers of organic carbon burial and source-rock development across the sedimentary sequence. Results presented here document the organic-rich and oil-prone source-rock quality of the Hue Shale in the distal part of the Colville foreland basin and bolster the potential for a Cretaceous petroleum system beneath the eastern North Slope.

Alaska↗

The U.S.Geological Survey Energy Resources Program

Energy resources are an essential component of modern society. Adequate, reliable, and affordable energy supplies obtained using environmentally sustainable practices underpin economic prosperity, environmental quality and human health, and political stability. National and global demands for all forms of energy are forecast to increase significantly over the next several decades. Throughout its history, our Nation has faced important, often controversial, decisions regarding the competing uses of public lands, the supply of energy to sustain development and enable growth, and environmental stewardship. The U.S. Geological Survey (USGS) Energy Resources Program (ERP) provides information to address these challenges by supporting scientific investigations of energy resources, such as research on the geology, geochemistry, and geophysics of oil, gas, coal, heavy oil and natural bitumen, oil shale, uranium, and geothermal resources, emerging resources such as gas hydrates, and research on the effects associated with energy resource occurrence, production, and (or) utilization. The results from these investigations provide impartial, robust scientific information about energy resources and support the U.S. Department of the Interior's (DOI's) mission of protecting and responsibly managing the Nation's natural resources. Primary consumers of ERP information and products include the DOI land- and resource-management Bureaus; other Federal, State, and local agencies; the U.S. Congress and the Administration; nongovernmental organizations; the energy industry; academia; international organizations; and the general public.

Fact Sheet↗

The effects of Hurricane Irene and Tropical Storm Lee on the bed sediment geochemistry of U.S. Atlantic coastal rivers

Hurricane Irene and Tropical Storm Lee, both of which made landfall in the U.S. between late August and early September 2011, generated record or near record water discharges in 41 coastal rivers between the North Carolina/South Carolina border and the U.S./Canadian border. Despite the discharge of substantial amounts of suspended sediment from many of these rivers, as well as the probable influx of substantial amounts of eroded material from the surrounding basins, the geochemical effects on the <63-µm fractions of the bed sediments appear relatively limited [<20% of the constituents determined (256 out of 1394)]. Based on surface area measurements, this lack of change occurred despite substantial alterations in both the grain size distribution and the composition of the bed sediments. The sediment-associated constituents which display both concentration increases and decreases include: total sulfur (TS), Hg, Ag, total organic carbon (TOC), total nitrogen (TN), Zn, Se, Co, Cu, Pb, As, Cr, and total carbon (TC). As a group, these constituents tend to be associated either with urbanization/elevated population densities and/or wastewater/solid sludge. The limited number of significant sediment-associated chemical changes that were detected probably resulted from two potential processes: (1) the flushing of in-stream land-use affected sediments that were replaced by baseline material more representative of local geology and/or soils (declining concentrations), and/or (2) the inclusion of more heavily affected material as a result of urban nonpoint-source runoff and/or releases from flooded treatment facilities (increasing concentrations). Published 2013. This article is a U.S. Government work and is in the public domain in the USA.

Hydrological Processes↗

Stable isotope geochemistry of sphalerite and other mineral matter in coal beds of the Illinois and Forest City basins

Cleat and clastic dikes of Middle Pennsylvanian-age coal beds of the Illinois and Forest City basins of Illinois, Iowa, Missouri, and Kansas locally contain appreciable amounts of sphalerite within a kaolinite-pyrite-sphalerite (+ or - pyrite)-calcite paragenetic sequence. The sphalerite and associated minerals are of interest as a partial record of the history of fluids in the sedimentary basin and as possible indicators of Mississippi Valley-type mineralization. Moreover, zinc from the sphalerite may represent an exploitable by-product of coal mining and combustion.Pyrite is abundant in these coals both as fine-grained disseminated framboids that formed during early diagenesis and as coarser grained cleat fillings, etc., that formed much later. The delta 34 S values of this later pyrite, the sphalerite, and the coal organic matter range from -12 to 19 per mil. Within individual samples, however, pyrite, sphalerite, and organic matter sulfur delta 34 S values are nearly identical. This similarity strongly suggests related origins. The delta 34 S values of pyrite, sphalerite, and organic matter from coals of the Illinois basin and the central and southern Forest City basin range from -12 to 0 per mil. This range is not unique to the sphalerite-bearing coals; pyrite and organic matter from sphalerite-free high sulfur coals have similar delta 34 S values (Price and Shieh, 1979). We believe that sulfur produced by the breakdown of organosulfur compounds in the coal is incorporated into the epigenetic sulfides. In the northern Forest City basin, however, many samples have delta 34 S values between 8 and 19 per mil. These are similar to the delta 34 S values of sphalerite and pyrite from the Upper Mississippi Valley Zn-Pb district which lies northeast of the Forest City basin and north of the Illinois basin. This similarity suggests input from a Mississippi Valley-type hydrothermal system.Cleat kaolinite has delta D values of -36 to -24 per mil and delta 18 O values of 19.2 to 20.2 per mil. Assuming that clearing postdated the lignite rank of coalification implies that kaolinite was deposited between 40 degrees and 100 degrees C. At the lower temperatures, the kaolinite fluid would have had an isotopic composition similar to seawater; at the higher temperatures, it would have had a composition similar to the sphalerite-depositing fluid. Sphalerite was deposited from a fluid that was chemically and isotopically similar to the fluids responsible for the main-stage ores of the Upper Mississippi Valley Zn-Pb district (75 degrees -113 degrees C, approximately 21 equiv wt % NaCl, delta D = -65 to -3ppm, and delta 18 O = -0.9-9.9ppm). The isotopic compositions (delta 13 C = -12.4 to -2.7ppm and delta 18 O = 21.1-25.8ppm) and paragenetic positions of the cleat calcite samples are similar to those of the late-stage calcite of the Upper Mississippi Valley Zn-Pb and Illinois-Kentucky fluorspar districts. Calcite inclusion fluids had delta D (sub H 2 O) values of -80 and -58 per mil, implying a meteoric water source. At probable temperatures of 15 degrees to 75 degrees C, this calcite formed from fluids having calculated delta 18 O (sub H 2 O) values of -9 to 1 per mil, implying slight to moderate exchange with sedimentary rocks. The diagenetic-epigenetic history of fluids recorded by the cleat minerals probably began with a slightly evolved seawater, followed by a metal-bearing deep basin brine, and concluded with a cooler, slightly evolved, meteoric-water fluid.

Economic Geology↗

Hydrogeologic framework, arsenic distribution, and groundwater geochemistry of the glacial-sediment aquifer at the Auburn Road landfill superfund site, Londonderry, New Hampshire

Leachate continues to be generated from landfills at the Auburn Road Landfill Superfund Site in Londonderry, New Hampshire. Impermeable caps on the three landfills at the site inhibit direct infiltration of precipitation; however, high water-table conditions allow groundwater to interact with landfill materials from below, creating leachate and ultimately reducing conditions in downgradient groundwater. Reducing conditions can facilitate arsenic transport by allowing it to stay in solution or by liberating arsenic adsorbed to surfaces and from geologic sources, such as glacial sediments and bedrock. The site occupies a 180-acre parcel of land containing streams, ponds, wetlands, and former gravel pits located in glacial sediment. Four areas, totaling 14 acres, including three landfills and one septage lagoon, were used for waste disposal. The site was closed in 1980 after volatile organic compounds associated with industrial waste dumping were detected. The site was added to the U.S. Environmental Protection Agency National Priority List in 1982, and the landfills were capped in 1996. Although volatile organic compound concentrations in groundwater have declined substantially, some measurable concentrations remain. Temporally variable and persistent elevated arsenic concentrations have been measured in groundwater affected by the landfill leachate. Microbial consumption of carbon found in leachate is a driver of reducing conditions that liberate arsenic at the site. In addition to sources of carbon in landfill leachate, wetland areas throughout the site also could contribute carbon to groundwater, but it is currently unknown if any of the wetland areas have downward or reversing gradients that could allow the infiltration of surface water to groundwater. Red-stained sediments and water indicate iron-rich groundwater discharge to surface water and are also associated with elevated concentrations of arsenic in sediment and groundwater. Ironrich groundwater seeps have been observed in the wetland, streams, and pond downgradient of the landfills. Piezometers were installed in some of these locations to confirm groundwater discharge, measure vertical-flow gradients, and to provide a way to sample the discharging groundwater. Understanding the movement of leachate in groundwater is complicated by the presence of preferential flow paths through aquifer materials with differing hydraulic properties; these preferential flow paths can affect rates of recharge, geochemical conditions, and contaminant fluxes. In areas adjacent to the three capped landfills, infiltration of precipitation containing oxygenated water through permeable deltaic sediments in the former gravel pit area causes increases in dissolved oxygen concentrations and decreases in arsenic concentrations. Layered deltaic sediments produce anisotropic hydraulic characteristics and zones of high hydraulic conductivity. The glacial-sediment aquifer also includes glaciolacustrine sediments that have low permeability and limit infiltration at the surface Discharge of leachate-affected groundwater may be limited in areas of organic muck on the bottom of Whispering Pines Pond because the muck may act as a semiconfining layer. Geophysical survey results were used to identify several areas with continuous beds of muck and an underlying highresistivity layer on top of a layer of low resistivity that may represent leachate-affected groundwater. The high-resistivity layer is likely groundwater associated with oxygenated recharge, which would cause arsenic to adsorb onto aquifer sediments and reduce concentrations of dissolved arsenic in groundwater. Surface and borehole geophysical data collected in 2011 were used to identify potentially high-permeability or contaminated zones in the aquifer (preferential flowpaths) as well as low-permeability zones that may promote contamination through back diffusion. Some groundwater in parts of the glacial-sediment aquifer where the leachate plumes were present had low electrical resistivity, low dissolved oxygen, and high concentrations of arsenic. Low-resistivity zones in the underlying bedrock were associated with fractures that also may contain leachate. Although surveying the fractured bedrock was not a specific objective of this study, the results suggest that such a survey would help to determine if leachate and associated concentrations of arsenic are migrating downward into the fractured-bedrock-aquifer system. An uncalibrated, one-dimensional, reactive-transport model was used to assess several conditions that affect arsenic mobility. The results indicate that reductive dissolution and desorption from glacial sediments control dissolved arsenic concentrations. Parameter sensitivity analysis was used to identify key data that are needed in order to accurately assess the time required for arsenic concentrations to fall to levels below the maximum contaminant level at the site. Quantifying this time will require accurate characterization of carbon, sediment-surface sorption sites, and groundwater fluxes at the site.

New Hampshire↗

Seasonal variability in the surface sediments of Mobile Bay, Alabama, recorded by geochemistry and foraminifera, 2009–2010

A study was undertaken in order to document and quantify recent environmental change in Mobile Bay, Alabama. The study was part of the Northern Gulf of Mexico (NGOM) Ecosystem Change and Hazard Susceptibility project, a regional project funded by the Coastal and Marine Geology Program to understand how natural forcings and anthropogenic modifications influence coastal ecosystems and their susceptibility to coastal hazards. Mobile Bay is a large drowned-river estuary that has been modified significantly by humans to accommodate the Port of Mobile. Examples include repeated dredging of a large shipping channel down the central axis of the bay and construction of a causeway across the head of the bay and at the foot of the bayhead delta. In addition to modifications, the bay is also known to have episodic periods of low oxygen (hypoxia) that result in significant mortality to fish and benthic organisms (May, 1973). For this study a series of surface sediment samples were collected. Surface benthic foraminiferal and bulk geochemical data provide the modern baseline conditions of the bay and can be used as a reference to changing environmental parameters in the past (Osterman and Smith, in press) and into the future. This report archives data collected as part of the Mobile Bay Study that may be used in future environmental change studies.

Alabama↗

Soil mineralogy and geochemistry along a north-south transect in Alaska and the relation to source-rock terrane

Soils collected along a predominately north-south transect in Alaska were used to evaluate regional differences in the soil mineralogy and geochemistry in the context of a geotectonic framework for Alaska. The approximately 1,395-kilometer-long transect followed the Dalton, Elliott, and Richardson Highways from near Prudhoe Bay to Valdez. Sites were selected with a site spacing of approximately 10 road-kilometers; soil was sampled by soil horizon at 175 sites. Terrane boundaries were estimated from digitized versions of the lithotectonic terrane map of Alaska (Silberling and others, 1994). Terrane assignments for each site were based on the site’s distance along the transect. We also present data for 15 minerals or mineral groups and 58 elements, as well as total, inorganic, and organic carbon. Quantitative mineralogy of the mineral-soil horizons was characterized by X-ray diffraction. Elemental contents were determined by a combination of inductively coupled plasma-atomic emission spectrometry (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS) analysis following a multi-acid or sodium-sinter decomposition of the samples. Total carbon and carbonate carbon contents were determined using an automated carbon analyzer and coulometric titration, respectively; organic carbon content was obtained by calculating the difference between total and carbonate carbon. Mercury and selenium were analyzed using cold-vapor atomic absorption (CV-AA), and hydride-generation atomic absorption spectrometry (HG-AAS), respectively. The mineralogical and geochemical patterns from these soils are used to assess the relation between soil characteristics and the geology of surrounding terranes.

Alaska↗

Geochemistry of artificial-recharge tests in the Oakes aquifer near Oakes, southeastern North Dakota

As part of an artificial-recharge feasibility study, water from the James River was introduced into the Oakes aquifer of southeastern North Dakota by infiltration through a recharge basin. Chemical composition of water in the recharge basin and ground water from two separate flow paths beneath the basin was determined from samples taken during two artificial-recharge tests. Changes between recharge-basin water and ground water from the termination of the flow paths during the spring 1987 test included increases in alkalinity, calcium, sodium, and silica and decreases in pH and dissolved oxygen. Interpretation of processes modifying the chemical composition of recharge water was complicated by mixing of recharge water with pre-existing ground water within the Oakes aquifer. In the summer 1987 test, the recharge basin was lined with a decomposing organic mat. The purpose of the organic mat was to sustain large infiltration rates for a longer period of time and to evaluate the effect of a decomposing organic mat on water quality during sustained recharge-basin operation. Larger infiltration rates with the organic mat in place allowed recharge water to reach the termination of the flow paths prior to apparent mixing with pre-existing ground water for a period of as much as approximately 405 hours of recharge-basin operation. Changes between recharge-basin water and ground water from the termination of the flow paths during the summer 1987 organic-mat test included increases in alkalinity, calcium, and silica and decreases in pH, dissolved oxygen, and total organic carbon. Detected changes between recharge-basin water and ground water from the termination of the flow paths were interpreted using a mass-balance geochemical model. Chemical changes of at least 2 milligrams per liter were modeled in terms of reactions, including those due to respiration of micro-organisms, dissolution of carbon dioxide, possible production of organic acids, dissolution of amorphous silica, cation exchange, and dissolution of carbonate minerals. Generation of organic acids within the decomposing organic mat may cause dissolution of dolomite in the subsurface.

Water-Resources Investigations Report↗