Geology topics

Geoffrey S. Ellis

Publications and source records attributed to Geoffrey S. Ellis.

70 records · Page 4Linked to original sources

USGS2015

Organic sedimentation in modern lacustrine systems: A case study from Lake Malawi, East Africa

This study examines the relationship between depositional environment and sedimentary organic geochemistry in Lake Malawi, East Africa, and evaluates the relative significance of the various processes that control sedimentary organic matter (OM) in lacustrine systems. Total organic carbon (TOC) concentrations in recent sediments from Lake Malawi range from 0.01 to 8.80 wt% and average 2.83 wt% for surface sediments and 2.35 wt% for shallow core sediments. Hydrogen index (HI) values as determined by Rock-Eval pyrolysis range from 0 to 756 mg HC g−1 TOC and average 205 mg HC g−1 TOC for surface sediments and 228 mg HC g−1 TOC for shallow core samples. On average, variations in primary productivity throughout the lake may account for ~33% of the TOC content in Lake Malawi sediments (as much as 1 wt% TOC), and have little or no impact on sedimentary HI values. Similarly, ~33% to 66% of the variation in TOC content in Lake Malawi sediments appears to be controlled by anoxic preservation of OM (~1–2 wt% TOC), although some component of the water depth–TOC relationship may be due to physical sediment transport processes. Furthermore, anoxic preservation has a minimal effect on HI values in Lake Malawi sediments. Dilution of OM by inorganic sediment may account for ~16% of variability in TOC content in Lake Malawi sediments (~0.5 wt% TOC). The effect of inputs of terrestrial sediment on the organic character of surface sediments in these lakes is highly variable, and appears to be more closely related to the local depositional environment than the regional flux of terrestrial OM. Total nitrogen and TOC content in surface sediments collected throughout the lake are found to be highly correlated (r2 = 0.95), indicating a well-homogenized source of OM to the lake bottom. The recurring suspension and deposition of terrestrial sediment may account for significant amounts of OM deposited in offshore regions of the lake. This process effectively separates denser inorganic sediment from less dense OM and allows terrestrial OM to preferentially be transported farther offshore. The conclusion is that for the organic carbon content in these regions to be elevated a mixed terrestrial-lacustrine origin is required. The hydrodynamic separation of mineral and organic constituents is most pronounced in regions with shallow bathymetric gradients, consistent with previous findings from Lake Tanganyika.

Lake Malawi↗

USGS2015

Introduction to special section: China shale gas and shale oil plays

In the last 10 years, the success of shale gas and shale oil productions as a result of technological advances in horizontal drilling, hydraulic fracturing and nanoscale reservoir characterization have revolutionized the energy landscape in the United States. Resource assessment by the China Ministry of Land and Resources in 2010 and 2012 and by the U.S. Energy Information Administration in 2011 and 2013 indicates China’s shale gas resource is the largest in the world and shale oil resource in China is also potentially significant. Inspired by the success in the United States, China looks forward to replicating the U.S. experience to produce shale gas to power its economy and reduce greenhouse gas emissions. By 2014, China had drilled 400 wells targeting marine, lacustrine, and coastal swamp transitional shales spanning in age from the Precambrian to Cenozoic in the last five years. So far, China is the leading country outside of North America in the viable production of shale gas, with very promising prospects for shale gas and shale oil development, from the Lower Silurian Longmaxi marine shale in Fuling in the southeastern Sichuan Basin. Geological investigations by government and academic institutions as well as exploration and production activities from industry indicate that the tectonic framework, depositional settings, and geomechanical properties of most of the Chinese shales are more complex than many of the producing marine shales in the United States. These differences limit the applicability of geologic analogues from North America for use in Chinese shale oil and gas resource assessments, exploration strategies, reservoir characterization, and determination of optimal hydraulic fracturing techniques. Understanding the unique features of the geology, shale oil and gas resource potential, and reservoir characteristics is crucial for sweet spot identification, hydraulic fracturing optimization, and reservoir performance prediction. Even though China shale gas and shale oil exploration is still in an early stage, limited data are already available. We are pleased to have selected eight high-quality papers from fifteen submitted manuscripts for this timely section on the topic of China shale gas and shale oil plays. These selected papers discuss various subject areas including regional geology, resource potentials, integrated and multidisciplinary characterization of China shale reservoirs (geology, geophysics, geochemistry, and petrophysics) China shale property measurement using new techniques, case studies for marine, lacustrine, and transitional shale deposits in China, and hydraulic fracturing. One paper summarizes the regional geology and different tectonic and depositional settings of the major prospective shale oil and gas plays in China. Four papers concentrate on the geology, geochemistry, reservoir characterization, lithologic heterogeneity, and sweet spot identification in the Silurian Longmaxi marine shale in the Sichuan Basin in southwest China, which is currently the primary focus of shale gas exploration in China. One paper discusses the Ordovician Salgan Shale in the Tarim Basin in northwest China, and two papers focus on the reservoir characterization and hydraulic fracturing of Triassic lacustrine shale in the Ordos Basin in northern China. Each paper discusses a specific area.

Interpretation↗

USGS2014

Vegetation controls on weathering intensity during the last deglacial transition in southeast Africa

Tropical climate is rapidly changing, but the effects of these changes on the geosphere are unknown, despite a likelihood of climatically-induced changes on weathering and erosion. The lack of long, continuous paleo-records prevents an examination of terrestrial responses to climate change with sufficient detail to answer questions about how systems behaved in the past and may alter in the future. We use high-resolution records of pollen, clay mineralogy, and particle size from a drill core from Lake Malawi, southeast Africa, to examine atmosphere-biosphere-geosphere interactions during the last deglaciation (~18–9 ka), a period of dramatic temperature and hydrologic changes. The results demonstrate that climatic controls on Lake Malawi vegetation are critically important to weathering processes and erosion patterns during the deglaciation. At 18 ka, afromontane forests dominated but were progressively replaced by tropical seasonal forest, as summer rainfall increased. Despite indication of decreased rainfall, drought-intolerant forest persisted through the Younger Dryas (YD) resulting from a shorter dry season. Following the YD, an intensified summer monsoon and increased rainfall seasonality were coeval with forest decline and expansion of drought-tolerant miombo woodland. Clay minerals closely track the vegetation record, with high ratios of kaolinite to smectite (K/S) indicating heavy leaching when forest predominates, despite variable rainfall. In the early Holocene, when rainfall and temperature increased (effective moisture remained low), open woodlands expansion resulted in decreased K/S, suggesting a reduction in chemical weathering intensity. Terrigenous sediment mass accumulation rates also increased, suggesting critical linkages among open vegetation and erosion during intervals of enhanced summer rainfall. This study shows a strong, direct influence of vegetation composition on weathering intensity in the tropics. As climate change will likely impact this interplay between the biosphere and geosphere, tropical landscape change could lead to deleterious effects on soil and water quality in regions with little infrastructure for mitigation.

PLoS ONE↗

USGS2014

Compositional and stable carbon isotopic fractionation during non-autocatalytic thermochemical sulfate reduction by gaseous hydrocarbons

The possibility of autocatalysis during thermochemical sulfate reduction (TSR) by gaseous hydrocarbons was investigated by examination of previously reported laboratory and field data. This reaction was found to be a kinetically controlled non-autocatalytic process, and the apparent lack of autocatalysis is thought to be due to the absence of the required intermediate species. Kinetic parameters for chemical and carbon isotopic fractionations of gaseous hydrocarbons affected by TSR were calculated and found to be consistent with experimentally derived values for TSR involving long-chain hydrocarbons. Model predictions based on these kinetic values indicate that TSR by gaseous hydrocarbon requires high-temperature conditions. The oxidation of C 2–5 hydrocarbons by sulfate reduction is accompanied by carbon isotopic fractionation with the residual C 2–5 hydrocarbons becoming more enriched in 13 C. Kinetic parameters were calculated for the stable carbon isotopic fractionation of gaseous hydrocarbons that have experienced TSR. Model predictions based on these kinetics indicate that it may be difficult to distinguish the effects of TSR from those of thermal maturation at lower levels of hydrocarbon oxidation; however, unusually heavy δ 13 C 2+ values (>−10‰) can be diagnostic of high levels of conversion (>50%). Stoichiometric and stable carbon isotopic data show that methane is stable under the investigated reaction conditions and is likely a product of TSR by other gaseous hydrocarbons rather than a significant reactant. These results indicate that the overall TSR reaction mechanism for oxidation of organic substrates containing long-chain hydrocarbons involves three distinct phases as follows: (1) an initial slow and non-autocatalytic stage characterized by the reduction of reactive sulfate by long-chain saturated hydrocarbons; (2) a second autocatalytic reaction phase dominated by reactions involving reduced sulfur species and partially oxidized hydrocarbons; (3) and a final, or late-stage, TSR reaction in which hydrocarbon oxidation continues at a slower rate via the non-autocatalytic reduction of sulfate by gaseous hydrocarbons.

Geochimica et Cosmochimica Acta↗

USGS2014

Benzo[ b ]naphthothiophenes and alkyl dibenzothiophenes: molecular tracers for oil migration distances

The secondary migration of petroleum is one of the most critical geological processes responsible for the accumulation of hydrocarbons in a sedimentary basin. Pyrrolic nitrogen compounds such as carbazoles and benzocarbazoles are thought to be practical molecular indicators for estimating relative migration distances of oil. In light oils or condensates, however, considerable analytical errors are usually caused by low concentrations of NSO-compounds. Here we show that polycyclic sulfur aromatic hydrocarbons such as dibenzothiophene, C 1 ∼C 3 alkylated dibenzothiophenes and benzo[ b ]naphthothiophenes, which are present in relatively higher concentrations than the pyrrolic nitrogen compounds, exhibit changes in both absolute and relative concentrations that correlate with migration distances. The polycyclic sulfur aromatic hydrocarbons related parameters — benzo[ b ]naphtho[2,1- d ]thiophene/{benzo[ b ]naphtho[2,1- d ]thiophene + benzo[ b ]naphtho[1,2- d ]thiophene} (abbreviated as [2,1]BNT/([2,1]BNT+[1,2]BNT) and the concentration of total dibenzothiophenes plus benzo[ b ]naphthothiophenes — are proposed by this paper to trace the oil migration distances.

Tarim Basin;Tahe Oil Field↗

USGS2014

Experimental investigation of changes in methane adsorption of bitumen-free Woodford Shale with thermal maturation induced by hydrous pyrolysis

This study quantifies the effects of organic-matter (OM) thermal maturity on methane (CH 4 ) sorption, on the basis of five samples that were artificially matured through hydrous pyrolysis achieved by heating samples of immature Woodford Shale under five different time–temperature conditions. CH 4 -sorption isotherms at 35 °C, 50 °C, and 65 °C, and pressures up to 14 MPa on dry, solvent-extracted samples of the artificially matured Woodford Shale were measured. The results showed that CH 4 -sorption capacity, normalized to TOC, varied with thermal maturity, following the trend: maximum oil (367 °C) > oil cracking (400 °C) > maximum bitumen/early oil (333 °C) > early bitumen (300 °C) > immature stage (130 °C). The Langmuir constants for the samples at maximum-oil and oil-cracking stages are larger than the values for the bitumen-forming stages. The total pore volume, determined by N 2 physisorption at 77 K, increases with increased maturation: mesopores, 2–50 nm in width, were created during the thermal conversion of organic-matter and a dramatic increase in porosity appeared when maximum-bitumen and maximum-oil generation stages were reached. A linear relationship between thermal maturity and Brunauer–Emmett–Teller (BET) surface area suggests that the observed increase in CH 4 -sorption capacity may be the result of mesopores produced during OM conversion. No obvious difference is observed in pore-size distribution and pore volume for samples with pores <2.0 nm with the increase of thermal maturity based on CO 2 physisorption at 273 K. The isosteric heat of adsorption and the standard entropy for artificially matured samples ranged from 17.9 kJ mol −1 to 21.9 kJ mol −1 and from −85.4 J mol −1 K −1 to −101.8 J mol −1 K −1 , respectively. These values are similar to the values of immature Woodford kerogen concentrate previously observed, but are larger than naturally matured organic-rich shales. High-temperature hydrous pyrolysis might have induced Lewis acid sites on both organic and mineral surfaces, resulting to some extent, in chemical interactions between the adsorption site and the methane C–H bonds. The formation of abundant mesopores (2–50 nm) within organic matter during organic-matter thermal maturation makes a great contribution to the increase in both BET surface area and pore volume, and a significant increase in 2–6 nm pores occurs at maximum-oil-generation and oil-cracking to gas, ultimately controlling the methane-adsorption capacity. Therefore, consideration of pore-size effects and thermal maturity is very important for gas in place (GIP) prediction in organic-rich shales.

Marine and Petroleum Geology↗

USGS2013

Effect of organic matter properties, clay mineral type and thermal maturity on gas adsorption in organic-rich shale systems

A series of CH 4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH 4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH 4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH 4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH 4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH 4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH 4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH 4 molecules for sorption on organic matter is stronger than for most common clay minerals. Thus, it is expected that CH 4 molecules may preferentially occupy surface sites on organic matter. However, active sites on clay mineral surfaces are easily blocked by water. As a consequence, organic-rich shales possess a larger CH 4 -sorption capacity than clay-rich rocks lacking organic matter. The thermodynamic parameters obtained in this study can be incorporated into model predictions of the maximum Langmuir pressure and CH 4 - sorption capacity of shales under reservoir temperature and pressure conditions.

Conference Paper↗

USGS2013

Late Quaternary stratigraphy, sedimentology, and geochemistry of an underfilled lake basin in the Puna (north-west Argentina)

Depositional models of ancient lakes in thin-skinned retroarc foreland basins rarely benefit from appropriate Quaternary analogues. To address this, we present new stratigraphic, sedimentological and geochemical analyses of four radiocarbon-dated sediment cores from the Pozuelos Basin (PB; northwest Argentina) that capture the evolution of this low-accommodation Puna basin over the past ca. 43 cal kyr. Strata from the PB are interpreted as accumulations of a highly variable, underfilled lake system represented by lake-plain/littoral, profundal, palustrine, saline lake and playa facies associations. The vertical stacking of facies is asymmetric, with transgressive and thin organic-rich highstand deposits underlying thicker, organic-poor regressive deposits. The major controls on depositional architecture and basin palaeogeography are tectonics and climate. Accommodation space was derived from piggyback basin-forming flexural subsidence and Miocene-Quaternary normal faulting associated with incorporation of the basin into the Andean hinterland. Sediment and water supply was modulated by variability in the South American summer monsoon, and perennial lake deposits correlate in time with several well-known late Pleistocene wet periods on the Altiplano/Puna plateau. Our results shed new light on lake expansion–contraction dynamics in the PB in particular and provide a deeper understanding of Puna basin lakes in general.

Basin Research↗

USGS2012

Lacustrine records of Holocene flood pulse dynamics in the Upper Paraguay River watershed (Pantanal wetlands, Brazil)

The Pantanal is the world's largest tropical wetland and a biodiversity hotspot, yet its response to Quaternary environmental change is unclear. To address this problem, sediment cores from shallow lakes connected to the UpperParaguayRiver (PR) were analyzed and radiocarbon dated to track changes in sedimentary environments. Stratal relations, detrital particle size, multiple biogeochemical indicators, and sponge spicules suggest fluctuating lake-level lowstand conditions between ~ 11,000 and 5300 cal yr BP, punctuated by sporadic and in some cases erosive flood flows. A hiatus has been recorded from ~ 5300 to 2600 cal yr BP, spurred by confinement of the PR within its channel during an episode of profound regional drought. Sustained PR flooding caused a transgression after ~ 2600 cal yr BP, with lake-level highstand conditions appearing during the Little Ice Age. Holocene PR floodpulsedynamics are best explained by variability in effective precipitation, likely driven by insolation and tropical sea-surface temperature gradients. Our results provide novel support for hypotheses on: (1) stratigraphic discontinuity of floodplain sedimentary archives; (2) late Holocene methane flux from Southern Hemisphere wetlands; and (3) pre-colonial indigenous ceramics traditions in western Brazil.

Pantanal Wetlands;Paraguay River↗

USGS2012

Kinetics of uncatalyzed thermochemical sulfate reduction by sulfur-free paraffin

To determine kinetic parameters of sulfate reduction by hydrocarbons (HC) without the initial presence of low valence sulfur, we carried out a series of isothermal gold-tube hydrous-pyrolysis experiments at 320, 340, and 360 °C under a constant confined pressure of 24.1 MPa. The reactants used consisted of saturated HC (sulfur-free) and CaSO 4 in an aqueous solution buffered to three different pH conditions without the addition of elemental sulfur (S 8 ) or H 2 S as initiators. H 2 S produced in the course of reaction was proportional to the extent of the reduction of CaSO 4 that was initially the only sulfur-containing reactant. Our results show that the in situ pH of the aqueous solution (herein, in situ pH refers to the calculated pH value of the aqueous solution at certain experimental conditions) can significantly affect the rate of the thermochemical sulfate reduction (TSR) reaction. A substantial increase in the TSR reaction rate was observed with a decrease in the in situ pH. Our experimental results show that uncatalyzed TSR is a first-order reaction. The temperature dependence of experimentally measured H 2 S yields from sulfate reduction was fit with the Arrhenius equation. The determined activation energy for HC (sulfur-free) reacting with View the MathML sourceHSO 4 − in our experiments is 246.6 kJ/mol at pH values ranging from 3.0 to 3.5, which is slightly higher than the theoretical value of 227.0 kJ/mol using ab initio quantum chemical calculations on a similar reaction. Although the availability of reactive sulfate significantly affects the rate of reaction, a consistent rate constant was determined by accounting for the HSO 4 − ion concentration. Our experimental and theoretical approach to the determination of the kinetics of TSR is further validated by a reevaluation of several published experimental TSR datasets without the initial presence of native sulfur or H 2 S. When the effect of reactive sulfate concentration is appropriately accounted for, the published experimental TSR data yield kinetic parameters that are consistent with our values. Assuming MgSO 4 contact-ion-pair ([MgSO 4 ]CIP) as the reactive form of sulfate in petroleum reservoir formation waters, a simple extrapolation of our experimentally derived HSO 4 − reduction kinetics as a proxy for [MgSO 4 ]CIP to geologically reasonable conditions predicts onset temperatures (130–140 °C) that are comparable to those observed in nature.

Geochimica et Cosmochimica Acta↗

USGS2012

Effect of organic-matter type and thermal maturity on methane adsorption in shale-gas systems

A series of methane (CH 4 ) adsorption experiments on bulk organic rich shales and their isolated kerogens were conducted at 35 °C, 50 °C and 65 °C and CH 4 pressure of up to 15 MPa under dry conditions. Samples from the Eocene Green River Formation, Devonian–Mississippian Woodford Shale and Upper Cretaceous Cameo coal were studied to examine how differences in organic matter type affect natural gas adsorption. Vitrinite reflectance values of these samples ranged from 0.56–0.58 %R o . In addition, thermal maturity effects were determined on three Mississippian Barnett Shale samples with measured vitrinite reflectance values of 0.58, 0.81 and 2.01 %R o . For all bulk and isolated kerogen samples, the total amount of methane adsorbed was directly proportional to the total organic carbon (TOC) content of the sample and the average maximum amount of gas sorption was 1.36 mmol of methane per gram of TOC. These results indicate that sorption on organic matter plays a critical role in shale-gas storage. Under the experimental conditions, differences in thermal maturity showed no significant effect on the total amount of gas sorbed. Experimental sorption isotherms could be fitted with good accuracy by the Langmuir function by adjusting the Langmuir pressure (P L ) and maximum sorption capacity (Γ max ). The lowest maturity sample (%R o = 0.56) displayed a Langmuir pressure (P L ) of 5.15 MPa, significantly larger than the 2.33 MPa observed for the highest maturity (%R o > 2.01) sample at 50 °C. The value of the Langmuir pressure (P L ) changes with kerogen type in the following sequence: type I > type II > type III. The thermodynamic parameters of CH 4 adsorption on organic rich shales were determined based on the experimental CH 4 isotherms. For the adsorption of CH4 on organic rich shales and their isolated kerogen, the heat of adsorption (q) and the standard entropy (Δs 0 ) range from 7.3–28.0 kJ/mol and from −36.2 to −92.2 J/mol/K, respectively.

Organic Geochemistry↗

USGS2011

Limnogeology in Brazil's "forgotten wilderness": A synthesis from the large floodplain lakes of the Pantanal

Sediment records from floodplain lakes have a large and commonly untapped potential for inferring wetland response to global change. The Brazilian Pantanal is a vast, seasonally inundated savanna floodplain system controlled by the flood pulse of the Upper Paraguay River. Little is known, however, about how floodplain lakes within the Pantanal act as sedimentary basins, or what influence hydroclimatic variables exert on limnogeological processes. This knowledge gap was addressed through an actualistic analysis of three large, shallow (<5 m) floodplain lakes in the western Pantanal: Lagoa Gaíva, Lagoa Mandioré and Baia Vermelha. The lakes are dilute (CO3 2- > Si 4+ > Ca 2+ ), mildly alkaline, freshwater systems, the chemistries and morphometrics of which evolve with seasonal flooding. Lake sills are bathymetric shoals marked by siliciclastic fans and marsh vegetation. Flows at the sills likely undergo seasonal reversals with the changing stage of the Upper Paraguay River. Deposition in deeper waters, typically encountered in proximity to margin-coincident topography, is dominated by reduced silty-clays with abundant siliceous microfossils and organic matter. Stable isotopes of carbon and nitrogen, plus hydrogen index measured on bulk organic matter, suggest that contributions from algae (including cyanobacteria) and other C3-vegetation dominate in these environments. The presence of lotic sponge spicules, together with patterns of terrigenous sand deposition and geochemical indicators of productivity, points to the importance of the flood pulse for sediment and nutrient delivery to the lakes. Flood-pulse plumes, waves and bioturbation likewise affect the continuity of sedimentation. Short-lived radioisotopes indicate rates of 0.11-0.24 cm year -1 at sites of uninterrupted deposition. A conceptual facies model, developed from insights gained from modern seasonal processes, can be used to predict limnogeological change when the lakes become isolated on the floodplain or during intervals associated with a strengthened flood pulse. Amplification of the seasonal cycle over longer time scales suggests carbonate, sandy lowstand fan and terrestrial organic matter deposition during arid periods, whereas deposition of lotic sponges, mixed aquatic organic matter, and highstand deltas characterizes wet intervals. The results hold substantial value for interpreting paleolimnological records from floodplain lakes linked to large tropical rivers with annual flooding cycles.

Bahia Vermelha, Brazilian Pantanal, Lagoa Gaiva, L↗

USGS2010

Assessment of undiscovered natural gas resources of the Arkoma Basin province and geologically related areas

Using a geology-based assessment methodology, the U.S. Geological Survey estimated mean volumes of 38 trillion cubic feet (TCF) of undiscovered natural gas, 159 million barrels of natural gas liquid (MMBNGL), and no oil in accumulations of 0.5 million barrels (MMBO) or larger in the Arkoma Basin Province and related areas. More than 97 percent of the undiscovered gas occurs in continuous accumulations-70 percent in shale gas formations, 18 percent in a basin-centered accumulation with tight sandstone reservoirs, and 9 percent in coal beds. Less than 3 percent of the natural gas occurs in conventional accumulations.

Fact Sheet↗

USGS2010

Gas storage in the Upper Devonian-Lower Mississippian Woodford Shale, Arbuckle Mountains, Oklahoma: how much of a role do the cherts play?

How gas is stored in shale-gas systems is a critical element in characterizing these potentially prolific, low-porosity/permeability reservoirs. An integrated mineralogic, geochemical, and porosity/permeability study is of the Upper Devonian-Lower Mississippian Woodford Shale, Arbuckle Mountains, southern Oklahoma, at locations previously described through detailed stratigraphic and spectral gamma surveys, was undertaken to provide insights into possible mechanisms by which natural gas might be stored in Woodford reservoirs in the adjacent Anadarko Basin. The outcrops in the Arbuckle Mountains are an ideal location to study the Woodford because here the formation is immature or marginally mature for oil generation (Comer and Hinch, 1987; Lewan, 1987), so deep burial and thermal maturation are much less pronounced than is the case for the Woodford in the basin, and as such the samples we studied are not overprinted by possible alterations resulting from deep burial and heating.

Conference Paper↗

USGS2004

Organic contaminants associated with suspended sediment collected during five cruises of the Mississippi River and its principal tributaries, May 1988 to June 1990

Suspended-sediment samples were obtained from sites along the Mississippi River and its principal tributaries to determine the presence of halogenated hydrophobic organic compounds on the suspended sediment smaller than 63 micrometers. Sample collection involved pumping discharge-weighted volumes of river water along a cross section of the river into a continuous-flow centrifuge to isolate the suspended sediment. The suspended sediment was analyzed by gas chromatography/mass spectrometry for pentachlorobenzene, hexachlorobenzene, pentachloroanisole, chlorothalonil, pentachlorophenol, dachthal, chlordane, nonachlor, and penta-, hexa-, hepta-, and octachlorobiphenyls. Samples collected during June 1989 and February-March 1990 also were analyzed for U.S. Environmental Protection Agency priority pollutants, including polycyclic aromatic hydrocarbons, phthalate esters, and triazines. Samples were collected at sites on the Mississippi River from above St. Louis, Missouri to below New Orleans, Louisiana, and on the Illinois, Missouri, Ohio, Wabash, Cumberland, Tennessee, White, Arkansas, and Yazoo Rivers. Masses of selected halogenated hydrophobic organic compounds associated with the suspended sediment at each site are presented in this report in tabular format, along with suspended-sediment concentration, water discharge, and organic-carbon content.

Mississippi River↗

USGS1995

Evaluation of lipid-containing semipermeable membrane devices for monitoring organochlorine contaminants in the Upper Mississippi river

Organochlorine contaminants sequestered in lipid-containing semipermeable membrane devices (SPMDs) were compared to those found in tangential-flow ultrafilter permeates as part of a pilot study at 10 sites in the Upper Mississippi River system. Caged and feral fish from three primary sites were also analyzed for comparison. Concentrated organochlorine (OC) compounds were readily extracted from the SPMDs by dialysis into hexane, and samples were analyzed by gas chromatography-negative chemical ionization-mass spectrometry. Fish and water samples were processed by conventional methods. Reasonable agreement was found between analyte SPMD-derived water concentrations and measured values of ultrafilter permeates; however, concentrations of the same analytes in caged fish did not appear to be proportional to water concentrations derived from SPMDs and ultrafilter permeates. The greatest number of OC compounds was detected in SPMDs; fewer were detected in caged fish and feral fish.

Illinois, Iowa, Minnesota, Missouri, Wisconsin↗