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At least 793 records · Page 44Linked to original sources
USGS2011

Rock formation characterization for CO2-EOR and carbon geosequestration; 3D seismic amplitude and coherency anomalies, Wellington Field, Kansas, USA

In this paper, we present a workflow for a Mississipian carbonates characterization case-study integrating post-stack seismic attributes, well-logs porosities, and seismic modeling to explore relating changes in small-scale "lithofacies" properties and/or sub-seismic resolution faulting to key amplitude and coherency 3D seismic attributes. The main objective of this study is to put emphasis on reservoir characterization that is both optimized for and subsequently benefiting from pilot tertiary CO2-EOR in preparation for future carbon geosequestration in a depleting reservoir and a deep saline aquifer. The extracted 3D seismic coherency attribute indicated anomalous features that can be interpreted as a lithofacies change or a sub-seismic resolution faulting. A 2D finite difference modeling has been undertaken to understand and potentially build discriminant attributes to map structural and/or lithofacies anomalies of interest especially when embarking upon CO2-EOR and/or carbon sequestration monitoring and management projects. ?? 2011 Society of Exploration Geophysicists.

SEG Technical Program Expanded Abstracts↗
USGS2022

Velocity modeling of supercritical pore fluids through porous media under reservoir conditions with applications for petroleum secondary migration and carbon sequestration plumes

Computational methods to characterize secondary migration in porous media traditionally rely on fluid transport equations with assumptions of time invariance, such as flowpath modeling of buoyancy vectors, statistical percolation algorithms, capillary pressure curves, or a form of Darcy’s Law which presumes instantaneous fluid transport. However, in petroleum systems modeling, the timeframe of secondary migration from source to reservoir is important to quantify in relation to other geologic factors such as timing of petroleum generation, fault movement, and seal formation. Additionally, quantifying migration velocities enables an estimation of the distance a plume of geologically sequestered carbon dioxide travels over time, as well as the identification of low-permeability strata appropriate for long-term containment. This study introduces a method to quantify transport velocities of supercritical fluids in low-permeability lithologies for a broad range of rock and fluid properties likely encountered in the sedimentary sequence. A time-dependent form of Darcy’s Law for pressure-driven viscous flow through homogeneous isotropic porous media was used to model flow velocities within a carrier bed. Thermodynamic equations of state were used to determine thermophysical properties of supercritical pore fluids under reservoir pressures ranging from 0–200 MPa (0–29,000 psi) to constrain the momentum equations. Three case studies were examined that (1) estimated fluid flow velocities of methane within the low-permeability Upper Jurassic Haynesville Formation, (2) defined permeability-based flow units to evaluate saline formations for long-term geologic carbon sequestration, and (3) calculated the migration distance of carbon dioxide plumes at the Decatur, Illinois injection and sequestration project.

SEG-AAPG Interpretation↗
USGS2002

The lacustrine carbon cycle as illuminated by the waters and sediments of two hydrologically distinct headwater lakes in north-central Minnesota, U.S.A

The accumulation rates of CaCO 3 and organic carbon (OC) in lake sediments are delicately balanced between production in the epilimnion and destruction in the hypolimnion. The cycling of these two forms of carbon makes a "carbon pump" that greatly affects the biogeochemical cycles of other elements. To further understand these biogeochemical dynamics, the lakes, streams, and wetlands of the Shingobee River headwater area of north-central Minnesota have been subjected to intensive hydrologic and biogeochemical studies. Williams Lake, situated close to the highest point in the regional flow system, is hydrologically closed, with no surface inlet or outlet, and ground water and precipitation as the only sources of water. Shingobee Lake, situated at the lowest point in the regional flow system, has the Shingobee River as an inlet and outlet. The surface waters of both lakes are oversaturated, and the bottom waters undersaturated, with respect to CaCO 3 during the summer. The small amount of CaCO 3 that is precipitated in the epilimnion of Williams Lake during the summer is dissolved in the undersaturated hypolimnion and sediments with the result that no CaCO 3 is incorporated into the profundal surface sediments. Because of the high phytoplankton productivity of Shingobee Lake, sufficient CaCO 3 is produced in the epilimnion that large amounts survive the corrosive hypolimnion and sediments, and an average of 46 wt. % accumulates in surface sediments. Another consequence of higher phytoplankton productivity in Shingobee Lake is that the hypolimnion becomes oxygen deficient within a month after overturn in both the spring and fall. Because of reducing conditions that develop in the hypolimnion of Shingobee Lake, high concentrations of dissolved Fe and Mn accumulate there during summer stratification. Precipitation of Fe and Mn oxyhydroxides during periods of fall and spring overturn results in high concentrations of Fe and Mn in surface sediments. In Williams Lake, high concentrations of Fe and Mn do not build up in the hypolimnion. The concentration of CaCO 3 is about 80 wt. % in lower Holocene sediments of both lakes. The lower Holocene sediments in both lakes also contain high concentrations of Fe and Mn, and the lower Holocene sediments of Shingobee are laminated. The waters of both lakes had identical values of δ 13 C and δ 18 O during the early Holocene, but the waters of Williams Lake "evolved" during the early Holocene, increasing about 10‰ in both δ 13 C and δ 18 O. Deposits of lacustrine marl occur as much as seven meters above the present elevation of Williams Lake, the highest of the two lakes. Taken together, these observations suggest that the lakes were once connected to form a larger lake called Lake Willobee with a hypolimnion that was anoxic, at least seasonally.

Minnesota↗
USGS2024

Surface area of montmorillonite from the dynamic sorption of nitrogen and carbon dioxide

Surface area determinations were made on a montmorillonite with various cations emplaced on the exchangeable sites, utilizing nitrogen and carbon dioxide as adsorbates at 77 ° K and 195 ° K, respectively, in a dynamic system. From the fraction of a Mississippi montmorillonite less than about 1 μ in size, samples were prepared by replacing the original exchangeable cations with Li + , Na + , K + , Rb + , Cs + , Mg ++ , Ca ++ , Ba ++ , and NH 4 + , forming a series of homoionic montmorillonite species. Surface areas from 3-point B.E.T. plots (half-hour adsorption points), with nitrogen as the adsorbate, ranged from 61 m 2 /g for Li-montmorillonite to 138 m 2 /g for Cs-montmorillonite, thus reflecting a certain degree of nitrogen penetration between layers. Complete penetration should theoretically result in a surface area of over 300 m 2 /g for this clay with a nitrogen monolayer between each pair of platelets. The experimental data indicate that the extent of penetration is time-dependent and is also a function of the interlayer forces as governed by the size and charge of the replaceable cation. This finding negates the generally accepted concept that nitrogen at 77 ° K does not penetrate the layers and provides a measure only of the external surface of expandable clay minerals. A further measure of the variation of interlayer forces is provided by the adsorption of carbon dioxide at 195 ° K. Surface area values ranged from 99 m 2 /g for Li-montmorillonite to 315 m 2 /g for Csmontmorillonite. Although the carbon dioxide molecule is larger than the nitrogen molecule, its greater penetration apparently is a result of its being kinetically more energetic (with a larger diffusion coefficient) at its higher adsorption temperature. Similar differences have been found with both adsorbates in the study of microporous substances, such as coal, where activated diffusion is of considerable significance.

Clays and Clay Minerals↗
USGS2024

Surface area of vermiculite with nitrogen and carbon dioxide as adsorbates

Surface-area studies were made on several homoionic vermiculites with both nitrogen and carbon dioxide as adsorbates. These studies show that only very slight penetration occurs between individual vermiculite platelets. This is in contrast to an earlier investigation of montmorillonite where it was found that the degree of penetration between layers is quite high, particularly for carbon dioxide, and is governed by the size and charge of the interlayer cation. The inability of these adsorbates to penetrate substantially between vermiculite platelets is due primarily to this mineral's high surface-charge density. The extent of penetration of nitrogen and carbon dioxide at the edges of vermiculite platelets, though slight, is influenced by the coordinated water retained within the sample at a given degassing temperature. Forces between layers are weakened with increasing water content, which permits slightly greater penetration by adsorbate gases. Thus, the surface area of vermiculite, as determined by gas adsorption, is larger than the calculated external surface area based upon particle size and shape considerations. In addition, "extra" surface is provided by the lifting and scrolling of terminal platelets. These morphological features are shown in scanning electron micrographs of a naturally occuring vermiculite.

Clays and Clay Minerals↗
USGS2021

Incorporation of uncertainty to improve projections of tidal wetland elevation and carbon accumulation with sea-level rise

Understanding the rates and patterns of tidal wetland elevation changes relative to sea-level is essential for understanding the extent of potential wetland loss over the coming years. Using an enhanced and more flexible modeling framework of an ecosystem model (WARMER-2), we explored sea-level rise (SLR) impacts on wetland elevations and carbon sequestration rates through 2100 by considering plant community transitions, salinity effects on productivity, and changes in sediment availability. We incorporated local experimental results for plant productivity relative to inundation and salinity into a species transition model, as well as site-level estimates of organic matter decomposition. The revised modeling framework includes an improved calibration scheme that more accurately reconstructs soil profiles and incorporates parameter uncertainty through Monte Carlo simulations. Using WARMER-2, we evaluated elevation change in three tidal wetlands in the San Francisco Bay Estuary, CA, USA along an estuarine tidal and salinity gradient with varying scenarios of SLR, salinization, and changes in sediment availability. We also tested the sensitivity of marsh elevation and carbon accumulation rates to different plant productivity functions. Wetland elevation at all three sites was sensitive to changes in sediment availability, but sites with greater initial elevations or space for upland transgression persisted longer under higher SLR rates than sites at lower elevations. Using a multi-species wetland vegetation transition model for organic matter contribution to accretion, WARMER-2 projected increased elevations relative to sea levels (resilience) and higher rates of carbon accumulation when compared with projections assuming no future change in vegetation with SLR. A threshold analysis revealed that all three wetland sites were likely to eventually transition to an unvegetated state with SLR rates above 7 mm/yr. Our results show the utility in incorporating additional estuary-specific parameters to bolster confidence in model projections. The new WARMER-2 modeling framework is widely applicable to other tidal wetland ecosystems and can assist in teasing apart important drivers of wetland elevation change under SLR.

California↗
USGS2012

Carbon storage, timber production, and biodiversity: comparing ecosystem services with multi-criteria decision analysis

Increasingly, land managers seek ways to manage forests for multiple ecosystem services and functions, yet considerable challenges exist in comparing disparate services and balancing trade-offs among them. We applied multi-criteria decision analysis (MCDA) and forest simulation models to simultaneously consider three objectives: (1) storing carbon, (2) producing timber and wood products, and (3) sustaining biodiversity. We used the Forest Vegetation Simulator (FVS) applied to 42 northern hardwood sites to simulate forest development over 100 years and to estimate carbon storage and timber production. We estimated biodiversity implications with occupancy models for 51 terrestrial bird species that were linked to FVS outputs. We simulated four alternative management prescriptions that spanned a range of harvesting intensities and forest structure retention. We found that silvicultural approaches emphasizing less frequent harvesting and greater structural retention could be expected to achieve the greatest net carbon storage but also produce less timber. More intensive prescriptions would enhance biodiversity because positive responses of early successional species exceeded negative responses of late successional species within the heavily forested study area. The combinations of weights assigned to objectives had a large influence on which prescriptions were scored as optimal. Overall, we found that a diversity of silvicultural approaches is likely to be preferable to any single approach, emphasizing the need for landscape-scale management to provide a full range of ecosystem goods and services. Our analytical framework that combined MCDA with forest simulation modeling was a powerful tool in understanding trade-offs among management objectives and how they can be simultaneously accommodated.

Ecological Applications↗
USGS2014

Terrestrial carbon is a resource, but not a subsidy, for lake zooplankton

Inputs of terrestrial organic carbon (t-OC) into lakes are often considered a resource subsidy for aquatic consumer production. Although there is evidence that terrestrial carbon can be incorporated into the tissues of aquatic consumers, its ability to enhance consumer production has been debated. Our research aims to evaluate the net effect of t-OC input on zooplankton. We used a survey of zooplankton production and resource use in ten lakes along a naturally occurring gradient of t-OC concentration to address these questions. Total and group-specific zooplankton production was negatively related to t-OC. Residual variation in zooplankton production that was not explained by t-OC was negatively related to terrestrial resource use (allochthony) by zooplankton. These results challenge the designation of terrestrial carbon as a resource subsidy; rather, the negative effect of reduced light penetration on the amount of suitable habitat and the low resource quality of t-OC appear to diminish zooplankton production. Our findings suggest that ongoing continental-scale increases in t-OC concentrations of lakes will likely have negative impacts on the productivity of aquatic food webs.

Michigan;Wisconsin↗
USGS2001

Stratigraphy and lithofacies of Lisburne Group carbonate rocks (Carboniferous - Permian) in the National Petroleum Reserve - Alaska

Carbonate rocks of the Lisburne Group (Carboniferous-Permian) occur widely throughout northern Alaska. In the NPRA, seismic mapping and well penetrations show that the Lisburne occurs throughout the subsurface except in northernmost NPRA where it is missing by depositional onlap. Lisburne strata encountered in 11 exploratory wells in the northern part of the NPRA are essentially undeformed, consist of limestone and lesser dolostone, sandstone, siltstone, and shale, encompass a wide array of chiefly shallow-water facies, and range in age from Early Mississippian to Permian. Basins and platforms that formed during Mississippian (and possibly Devonian) time greatly affected depositional patterns of the Lisburne. Total thickness of the Lisburne in northern NPRA wells varies from almost 4000 ft in the Ikpikpuk-Umiat Basin to 300 ft on the north edge of the Fish Creek Platform. Lisburne strata of Mississippian age are found in northeastern NPRA, comprise three subunits (lower limestone, middle dolostone, and upper limestone) and are oldest (Osagean) in the Ikpikpuk-Umiat Basin. All wells that penetrated the Lisburne in northern NPRA encountered rocks of Pennsylvanian age; these intervals are mainly limestone and characterized by decameter-scale shallowing-upward sequences. Lisburne sections of prob-able Early-middle Permian age range from thin (≤60 ft) intervals of dolostone and limestone in the Fish Creek Platform area to thick (500-1000 ft) successions of interbedded limestone and siliciclastic sediment in the Ikpikpuk-Umiat Basin and northwestern NPRA. Abundant non-carbonate detritus, primarily quartz and chert with locally notable plagioclase feldspar and metamorphic lithic clasts, occurs throughout the Lisburne Group in northern NPRA. Per-mian strata and a persistent non-carbonate detrital component are also seen in the Lisburne in subsurface beneath the Chukchi Sea (Hanna Trough) to the northwest, but are not found in Lisburne successions elsewhere in Alaska.

Alaska↗
USGS2026

An integrated mudstone facies classification scheme and revised interpretation of the sedimentologic processes driving carbon burial in the Cenomanian–Turonian Greenhorn Formation, Colorado, U.S.A.

Standardizing facies descriptions has proven key to integrating interpretations of depositional processes and environments from sedimentologic observations with geochemistry data for mudstone lithologies. Because of their fine-grained nature, high degree of compaction, and heterogeneous composition, standardizing methods for mudstone descriptions has proven difficult, but it is critical to formulating meaningful interpretations of the processes that govern the accumulation of organic-rich lithologies and their role in both petroleum systems and the global carbon cycle. In this study, we have developed a modified facies classification scheme for mudstone lithologies that incorporates sedimentologic and compositional observation at the hand-sample and thin-section scales with geochemical measurements, including bulk organic and inorganic geochemistry, to characterize these rocks and their variability more completely for improved interpretations of depositional environments during a low-order sea-level transgression. The facies described in this study are of the Cenomanian–Turonian Greenhorn Formation in the USGS #1 Portland Core drilled in Fremont County, Colorado. Strata of the Greenhorn Formation span Oceanic Anoxic Event 2 (OAE-2) and the preceding interval. Lithologies range from organic-rich argillaceous mudstones with varied sedimentary structures to organic-lean, highly bioturbated limestones. Six facies were identified, each differentiated by varied sedimentary structures and geochemical composition. These facies occur in a predictable stratigraphic stacking pattern that represents a low-order sea-level transgression with interpreted depositional environments ranging from terrigenous-dominated pro-delta and muddy continental shelf at the base of the interval to pelagic offshore marine at the top of the Greenhorn Formation. Though the facies are consistent with previous interpretations of depositional environments at this locale in the Cretaceous Western Interior Seaway during the Greenhorn cyclothem, the sedimentary processes governing the accumulation of organic-rich strata that have defined this interval are significantly revised. Variability in the proximity and intensity of bottom currents driven by storms and geostrophic flows were key to the accumulation of each facies, with significant sediment transport occurring even through deposition in the most oxygen-depleted bottom waters. The methodology and interpretations provided here are now being employed to basin-scale predictions of organic enrichment utilizing calibrated petrophysical methods. The approach and results from this study improve understanding of how organic and inorganic carbon was sequestered during perturbations to the global carbon cycle associated with events such as OAE-2.

Colorado↗
USGS2014

Carbonate margin, slope, and basin facies of the Lisburne Group (Carboniferous-Permian) in northern Alaska

The Lisburne Group (Carboniferous-Permian) consists of a carbonate platform that extends for >1000 km across northern Alaska, and diverse margin, slope, and basin facies that contain world-class deposits of Zn and Ba, notable phosphorites, and petroleum source rocks. Lithologic, paleontologic, isotopic, geochemical, and seismic data gathered from outcrop and subsurface studies during the past 20 years allow us to delineate the distribution, composition, and age of the off-platform facies, and to better understand the physical and chemical conditions under which they formed. The southern edge of the Lisburne platform changed from a gently sloping, homoclinal ramp in the east to a tectonically complex, distally steepened margin in the west that was partly bisected by the extensional Kuna Basin (~200 by 600 km). Carbonate turbidites, black mudrocks, and radiolarian chert accumulated in this basin; turbidites were generated mainly during times of eustatic rise in the late Early and middle Late Mississippian. Interbedded black mudrocks (up to 20 wt% total organic carbon), granular and nodular phosphorite (up to 37 wt% P 2 O 5 ), and fine-grained limestone rich in radiolarians and sponge spicules formed along basin margins during the middle Late Mississippian in response to a nutrient-rich, upwelling regime. Detrital zircons from a turbidite sample in the western Kuna Basin have mainly Neoproterozoic through early Paleozoic U-Pb ages (~900-400 Ma), with subordinate populations of Mesoproterozoic and late Paleoproterozoic grains. This age distribution is similar to that found in slightly older rocks along the northern and western margins of the basin. It also resembles age distributions reported from Carboniferous and older strata elsewhere in northwestern Alaska and on Wrangel Island. Geochemical and isotopic data indicate that suboxic, denitrifying conditions prevailed in the Kuna Basin and along its margins. High V/Mo, Cr/Mo, and Re/Mo ratios (all marine fractions [MF]) and low MnO contents (<0.01 wt%) characterize Lisburne black mudrocks. Low Qmf/Vmf ratios (mostly 0.8-4.0) suggest moderately to strongly denitrifying conditions in suboxic bottom waters during siliciclastic and phosphorite sedimentation. Elevated to high Mo contents (31-135 ppm) in some samples are consistent with seasonal to intermittent sulfidic conditions in bottom waters, developed mainly along the basin margin. High d 15 N values (6-120) imply that the waters supplying nutrients to primary producers in the photic zone had a history of denitrification either in the water column or in underlying sediments. Demise of the Lisburne platform was diachronous and reflects tectonic, eustatic, and environmental drivers. Southwestern, south-central, and northwestern parts of the platform drowned during the Late Mississippian, coincident with Zn and Ba metallogenesis within the Kuna Basin and phosphogenesis along basin margins. This drowning was temporary (except in the southwest) and likely due to eutrophication associated with upwelling and sea-level rise enhanced by regional extension, which allowed suboxic, denitrifying waters to form on platform margins. Final drowning in the southcentral area occurred in the Early Pennsylvanian and also may have been linked to regional extension. In the northwest, platform sedimentation persisted into the Permian; its demise there appears to have been due to increased siliciclastic input. Climatic cooling may have produced additional stress on parts of the Lisburne platform biota during Pennsylvanian and Permian times.

Alaska↗
USGS2016

Determining the spatial variability of wetland soil bulk density, organic matter, and the conversion factor between organic matter and organic carbon across coastal Louisiana, U.S.A.

Soil bulk density (BD), soil organic matter (SOM) content, and a conversion factor between SOM and soil organic carbon (SOC) are often used in estimating SOC sequestration and storage. Spatial variability in BD, SOM, and the SOM–SOC conversion factor affects the ability to accurately estimate SOC sequestration, storage, and the benefits ( e.g., land building area and vertical accretion) associated with wetland restoration efforts, such as marsh creation and sediment diversions. There are, however, only a few studies that have examined large-scale spatial variability in BD, SOM, and SOM–SOC conversion factors in coastal wetlands. In this study, soil cores, distributed across the entire coastal Louisiana (approximately 14,667 km 2 ) were used to examine the regional-scale spatial variability in BD, SOM, and the SOM–SOC conversion factor. Soil cores for BD and SOM analyses were collected during 2006–09 from 331 spatially well-distributed sites in the Coastwide Reference Monitoring System network. Soil cores for the SOM–SOC conversion factor analysis were collected from 15 sites across coastal Louisiana during 2006–07. Results of a split-plot analysis of variance with incomplete block design indicated that BD and SOM varied significantly at a landscape level, defined by both hydrologic basins and vegetation types. Vertically, BD and SOM varied significantly among different vegetation types. The SOM–SOC conversion factor also varied significantly at the landscape level. This study provides critical information for the assessment of the role of coastal wetlands in large regional carbon budgets and the estimation of carbon credits from coastal restoration.

Louisiana↗
USGS2015

Hydrothermal, biogenic, and seawater components in metalliferous black shales of the Brooks Range, Alaska: Synsedimentary metal enrichment in a carbonate ramp setting

Trace element and Os isotope data for Lisburne Group metalliferous black shales of Middle Mississippian (early Chesterian) age in the Brooks Range of northern Alaska suggest that metals were sourced chiefly from local seawater (including biogenic detritus) but also from externally derived hydrothermal fluids. These black shales are interbedded with phosphorites and limestones in sequences 3 to 35 m thick; deposition occurred mainly on a carbonate ramp during intermittent upwelling under varying redox conditions, from suboxic to anoxic to sulfidic. Deposition of the black shales at ~335 Ma was broadly contemporaneous with sulfide mineralization in the Red Dog and Drenchwater Zn-Pb-Ag deposits, which formed in a distal marginal basin. Relative to the composition of average black shale, the metalliferous black shales ( n = 29) display large average enrichment factors (>10) for Zn (10.1), Cd (11.0), and Ag (20.1). Small enrichments (>2–<10) are shown by V, Cr, Ni, Cu, Mo, Pd, Pt, U, Se, Y, and all rare earth elements except Ce, Nd, and Sm. A detailed stratigraphic profile over 23 m in the Skimo Creek area (central Brooks Range) indicates that samples from at and near the top of the section, which accumulated during a period of major upwelling and is broadly correlative with the stratigraphic levels of the Red Dog and Drenchwater Zn-Pb-Ag deposits, have the highest Zn/TOC (total organic carbon), Cu/TOC, and Tl/TOC ratios for calculated marine fractions (no detrital component) of these three metals. Average authigenic (detrital-free) contents of Mo, V, U, Ni, Cu, Cd, Pb, Ge, Re, Se, As, Sb, Tl, Pd, and Au show enrichment factors of 4.3 × 10 3 to 1.2 × 10 6 relative to modern seawater. Such moderate enrichments, which are common in other metalliferous black shales, suggest wholly marine sources (seawater and biogenic material) for these metals, given similar trends for enrichment factors in organic-rich sediments of modern upwelling zones on the Namibian, Peruvian, and Chilean shelves. The largest enrichment factors for Zn and Ag are much higher (1.4 × 10 7 and 2.9 × 10 7 , respectively), consistent with an appreciable hydrothermal component. Other metals such as Cu, Pb, and Tl that are concentrated in several black shale samples, and are locally abundant in the Red Dog and Drenchwater Zn-Pb-Ag deposits, may have a partly hydrothermal origin but this cannot be fully established with the available data. Enrichments in Cr (up to 7.8 × 10 6 ) are attributed to marine and not hydrothermal processes. The presence in some samples of large enrichments in Eu (up to 6.1 × 10 7 ) relative to modern seawater and of small positive Eu anomalies (Eu/Eu* up to 1.12) are considered unrelated to hydrothermal activity, instead being linked to early diagenetic processes within sulfidic pore fluids. Initial Os isotope ratios ( 187 Os/ 188 Os) calculated for a paleontologically based depositional age of 335 Ma reveal moderately unradiogenic values of 0.24 to 0.88 for four samples of metalliferous black shale. A proxy for the ratio of coeval early Chesterian seawater is provided by initial ( 187 Os/ 188 Os) 335 Ma ratios of four unaltered black shales of the coeval Kuna Formation that average 1.08, nearly identical to the initial ratio of 1.06 for modern seawater. Evaluation of possible sources of unradiogenic Os in the metalliferous black shales suggests that the most likely source was mafic igneous rocks that were leached by externally derived hydrothermal fluids. This unradiogenic Os is interpreted to have been leached by deeply circulating hydrothermal fluids in the Kuna basin, followed by venting of the fluids into overlying seawater. We propose that metal-bearing hydrothermal fluids that formed Zn-Pb-Ag deposits such as Red Dog or Drenchwater vented into seawater in a marginal basin, were carried by upwelling currents onto the margins of a shallow-water carbonate platform, and were then deposited in organic-rich muds, together with seawater- and biogenically derived components, by syngenetic sedimentary processes. Metal concentration in the black shales was promoted by high biologic productivity, sorption onto organic matter, diffusion across redox boundaries, a low sedimentation rate, and availability of H 2 S in bottom waters and pore fluids.

Alaska↗
USGS1966

Stratified deposits of the oxides and carbonates of manganese

Compared with the stratified deposits of iron minerals, those of manganese minerals have received little attention until recent years. Before 1930, students of the stratified deposits of manganese minerals have generally concluded that the contained manganese was derived from the decomposition of the rocks that formed the borders of the basins. Only in a few places have geologists recognized that if these rocks were the principal source of the contained manganese the basins should contain also enormous quantities of iron minerals, whereas most of the large deposits of manganese contain little iron. Even though more than 100 years ago some geologists proposed that the iron contained in some deposits of stratified iron minerals was probably derived from hydrothermal waters related to centers of volcanism, not until about 1930 was this source of manganese in similar deposits seriously proposed. This mode of origin was given the name "volcanogene sedimentaire" by French geologists working in Morocco. Since then, other names, such as "exhalative sedimentaire," have been used by geologists working in several European districts. Because of the development of new techniques for the study of the chemical and physical features of the minerals, and because close attention to the lithologic environments of the beds is being given more and more during recent years, it has seemed advisable to review the features of stratified deposits of the manganese minerals in many parts of the world and over a wide range in age. This study indicates that at least three sources may have contributed the manganese in the large deposits of iron-free oxides and carbonates : (1) the rocks that form the borders of the basins, either marine or continental; (2) the nearby underlying sediments, largely of igneous origin, decomposed by warm waters largely derived from depth; and (3) waters of hydrothermal origin derived from great depths during epochs of volcanism from which iron minerals with little manganese are deposited in deep zones, then minerals with much iron and more manganese at intermediate depths, and, finally, manganese minerals with little iron near the surface. As the hot waters of many thermal springs contain more manganese than iron, such waters could yield the pure manganese oxides and carbonates found in stratified deposits . Several kinds of evidence indicate that most of the manganese in the large stratified deposits of the oxides and carbonates of manganese in many parts of the world has been derived from hydrothermal waters from depth related to centers of volcanism. Obviously, manganese derived from decay of the rocks on the lands adjacent to large basins-marine and continental -may have been added to that derived from centers of volcanism to form the sedimentary deposits found in the basins.

Economic Geology↗
USGS1973

Silica-carbonate alteration of serpentine: Wall rock alteration in mercury deposits of the California Coast Ranges

Chemical, isotopic, and thermodynamic properties have been measured of CO 2 -rich ground waters in the central California Coast Ranges. The acidic CO 2 -rich waters react with serpentine to form silica-carbonate rock, the host rock of many mercury deposits in the Coast Range of California. In part the waters are of a metamorphic origin and in part the waters are locally derived meteoric waters. The CO 2 is entirely derived from metamorphic reactions at depth. Depending on the relative importance of several reactions, the relative abundances of silica and carbonate minerals vary in the silica-carbonate rock. If the CO 2 -rich fluids react directly with peridotite or dunite, massive magnesite deposits may form. © 1973 Society of Economic Geologists, Inc.

California↗
USGS2015

Annual and seasonal distribution of intertidal foraminifera and stable carbon isotope geochemistry, Bandon Marsh, Oregon, USA

We investigated the influence of inter-annual and seasonal differences on the distribution of live and dead foraminifera, and the inter-annual variability of stable carbon isotopes (d13C), total organic carbon (TOC) values and carbon to nitrogen (C/N) ratios in bulk sediments from intertidal environments of Bandon Marsh (Oregon, USA). Living and dead foraminiferal species from 10 stations were analyzed over two successive years in the summer (dry) and fall (wet) seasons. There were insignificant inter-annual and seasonal variations in the distribution of live and dead species. But there was a noticeable decrease in calcareous assemblages (Haynesina sp.) between live populations and dead assemblages, indicating that most of the calcareous tests were dissolved after burial; the agglutinated assemblages were comparable between constituents. The live populations and dead assemblages were dominated by Miliammina fusca in the tidal flat and low marsh, Jadammina macrescens, Trochammina inflata and M. fusca in the high marsh, and Trochamminita irregularis and Balticammina pseudomacrescens in the highest marsh to upland. Geochemical analyses (d13C, TOC and C/N of bulk sedimentary organic matter) show no significant influence of inter-annual variations but a significant correlation of d13C values (R = 20.820, p , 0.001), TOC values (R = 0.849, p , 0.001) and C/N ratios (R = 0.885, p , 0.001) to elevation with respect to the tidal frame. Our results suggest that foraminiferal assemblages and d13C and TOC values, as well as C/N ratios, in Bandon Marsh are useful in reconstructing paleosea-levels on the North American Pacific coast.

Oregon↗
USGS2004

Dissolved organic carbon and disinfection by-product precursor release from managed peat soils

A wetland restoration demonstration project examined the effects of a permanently flooded wetland on subsidence of peat soils. The project, started in 1997, was done on Twitchell Island, in the Sacramento-San Joaquin Delta of California. Conversion of agricultural land to a wetland has changed many of the biogeochemical processes controlling dissolved organic carbon (DOC) release from the peat soils, relative to the previous land use. Dissolved organic C in delta waters is a concern because it reacts with chlorine, added as a disinfectant in municipal drinking waters, to form carcinogenic disinfection byproducts (DBPs), including trihalomethanes (THMs) and haloacetic acids (HAAs). This study explores the effects of peat soil biogeochemistry on DOC and DBP release under agricultural and wetland management. Results indicate that organic matter source, extent of soil organic matter decomposition, and decomposition pathways all are factors in THM formation. The results show that historical management practices dominate the release of DOC and THM precursors. However, within-site differences indicate that recent management decisions can contribute to changes in DOC quality and THM precursor formation. Not all aromatic forms of carbon are highly reactive and certain environmental conditions produce the specific carbon structures that form THMs. Both HAA and THM precursors are elevated in the DOC released under wetland conditions. The findings of this study emphasize the need to further investigate the roles of organic matter sources, microbial decomposition pathways, and decomposition status of soil organic matter in the release of DOC and DBP precursors from delta soils under varying land-use practices.

California↗
USGS2008

Land management impacts on dairy-derived dissolved organic carbon in ground water

Dairy operations have the potential to elevate dissolved organic carbon (DOC) levels in ground water, where it may interact with organic and inorganic contaminants, fuel denitrification, and may present problems for drinking water treatment. Total and percent bioavailable DOC and total and carbon-specific trihalomethane (THM) formation potential (TTHMFP and STHMFP, respectively) were determined for shallow ground water samples from beneath a dairy farm in the San Joaquin Valley, California. Sixteen wells influenced by specific land management areas were sampled over 3 yr. Measured DOC concentrations were significantly elevated over the background as measured at an upgradient monitoring well, ranging from 13 to 55 mg L-1 in wells downgradient from wastewater ponds, 8 to 30 mg L-1 in corral wells, 5 to 12 mg L-1 in tile drains, and 4 to 15 mg L-1 in wells associated with manured fields. These DOC concentrations were at the upper range or greatly exceeded concentrations in most surface water bodies used as drinking water sources in California. DOC concentrations in individual wells varied by up to a factor of two over the duration of this study, indicating a dynamic system of sources and degradation. DOC bioavailability over 21 d ranged from 3 to 10%, comparable to surface water systems and demonstrating the potential for dairy-derived DOC to influence dissolved oxygen concentrations (nearly all wells were hypoxic to anoxic) and denitrification. TTHMFP measurements across all management units ranged from 141 to 1731 ??g L-1, well in excess of the maximum contaminant level of 80 ??g L-1 established by the Environmental Protection Agency. STHMFP measurements demonstrated over twofold variation (???4 to ???8 mmol total THM/mol DOC) across the management areas, indicating the dependence of reactivity on DOC composition. The results indicate that land management strongly controls the quantity and quality of DOC to reach shallow ground water and hence should be considered when managing ground water resources and in any efforts to mitigate contamination of ground water with carbon-based contaminants, such as pesticides and pharmaceuticals. Copyright ?? 2008 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America. All rights reserved.

Journal of Environmental Quality↗